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You searched for subject:(Directed evolution). Showing records 1 – 30 of 129 total matches.

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University of Manchester

1. Doherty, Claire. The use of directed evolution towards altering the substrate specificity of acyl-coenzyme A : isopenicillin N acyl transferase and transforming it from generalist to specialist.

Degree: PhD, 2011, University of Manchester

 Acyl Coenzyme A: Isopenicillin N Acyl Transferase (AT) is a key enzyme in the biosynthesis of β-lactam antibiotics in penicillin producing organisms such as P.… (more)

Subjects/Keywords: 615.19; Directed Evolution; Acyl Transferase

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Doherty, C. (2011). The use of directed evolution towards altering the substrate specificity of acyl-coenzyme A : isopenicillin N acyl transferase and transforming it from generalist to specialist. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/the-use-of-directed-evolution-towards-altering-the-substrate-specificity-of-acylcoenzyme-a-isopenicillin-n-acyl-transferase-and-transforming-it-from-generalist-to-specialist(48bdd12d-f8dd-4bb1-b31b-dae1139cea97).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.529192

Chicago Manual of Style (16th Edition):

Doherty, Claire. “The use of directed evolution towards altering the substrate specificity of acyl-coenzyme A : isopenicillin N acyl transferase and transforming it from generalist to specialist.” 2011. Doctoral Dissertation, University of Manchester. Accessed July 23, 2019. https://www.research.manchester.ac.uk/portal/en/theses/the-use-of-directed-evolution-towards-altering-the-substrate-specificity-of-acylcoenzyme-a-isopenicillin-n-acyl-transferase-and-transforming-it-from-generalist-to-specialist(48bdd12d-f8dd-4bb1-b31b-dae1139cea97).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.529192.

MLA Handbook (7th Edition):

Doherty, Claire. “The use of directed evolution towards altering the substrate specificity of acyl-coenzyme A : isopenicillin N acyl transferase and transforming it from generalist to specialist.” 2011. Web. 23 Jul 2019.

Vancouver:

Doherty C. The use of directed evolution towards altering the substrate specificity of acyl-coenzyme A : isopenicillin N acyl transferase and transforming it from generalist to specialist. [Internet] [Doctoral dissertation]. University of Manchester; 2011. [cited 2019 Jul 23]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-use-of-directed-evolution-towards-altering-the-substrate-specificity-of-acylcoenzyme-a-isopenicillin-n-acyl-transferase-and-transforming-it-from-generalist-to-specialist(48bdd12d-f8dd-4bb1-b31b-dae1139cea97).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.529192.

Council of Science Editors:

Doherty C. The use of directed evolution towards altering the substrate specificity of acyl-coenzyme A : isopenicillin N acyl transferase and transforming it from generalist to specialist. [Doctoral Dissertation]. University of Manchester; 2011. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-use-of-directed-evolution-towards-altering-the-substrate-specificity-of-acylcoenzyme-a-isopenicillin-n-acyl-transferase-and-transforming-it-from-generalist-to-specialist(48bdd12d-f8dd-4bb1-b31b-dae1139cea97).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.529192


University of Manchester

2. Doherty, Claire. The Use of Directed Evolution Towards Altering the Substrate Specificity of Acyl-Coenzyme A: Isopenicillin N Acyl Transferase and Transforming it from Generalist to Specialist.

Degree: 2011, University of Manchester

Acyl Coenzyme A: Isopenicillin N Acyl Transferase (AT) is a key enzyme in the biosynthesis of β-lactam antibiotics in penicillin producing organisms such as P.… (more)

Subjects/Keywords: Directed Evolution; Acyl Transferase

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APA (6th Edition):

Doherty, C. (2011). The Use of Directed Evolution Towards Altering the Substrate Specificity of Acyl-Coenzyme A: Isopenicillin N Acyl Transferase and Transforming it from Generalist to Specialist. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:118477

Chicago Manual of Style (16th Edition):

Doherty, Claire. “The Use of Directed Evolution Towards Altering the Substrate Specificity of Acyl-Coenzyme A: Isopenicillin N Acyl Transferase and Transforming it from Generalist to Specialist.” 2011. Doctoral Dissertation, University of Manchester. Accessed July 23, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:118477.

MLA Handbook (7th Edition):

Doherty, Claire. “The Use of Directed Evolution Towards Altering the Substrate Specificity of Acyl-Coenzyme A: Isopenicillin N Acyl Transferase and Transforming it from Generalist to Specialist.” 2011. Web. 23 Jul 2019.

Vancouver:

Doherty C. The Use of Directed Evolution Towards Altering the Substrate Specificity of Acyl-Coenzyme A: Isopenicillin N Acyl Transferase and Transforming it from Generalist to Specialist. [Internet] [Doctoral dissertation]. University of Manchester; 2011. [cited 2019 Jul 23]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:118477.

Council of Science Editors:

Doherty C. The Use of Directed Evolution Towards Altering the Substrate Specificity of Acyl-Coenzyme A: Isopenicillin N Acyl Transferase and Transforming it from Generalist to Specialist. [Doctoral Dissertation]. University of Manchester; 2011. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:118477


Queens University

3. Perry, Meagan. Improving Protein Solubility via Directed Evolution .

Degree: Chemistry, 2009, Queens University

 A major hurdle facing in vitro protein characterization is obtaining soluble protein from targets that tend to aggregate and form insoluble inclusion bodies. Soluble protein… (more)

Subjects/Keywords: Directed Evolution; Protein Solubility

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APA (6th Edition):

Perry, M. (2009). Improving Protein Solubility via Directed Evolution . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/5276

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Perry, Meagan. “Improving Protein Solubility via Directed Evolution .” 2009. Thesis, Queens University. Accessed July 23, 2019. http://hdl.handle.net/1974/5276.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Perry, Meagan. “Improving Protein Solubility via Directed Evolution .” 2009. Web. 23 Jul 2019.

Vancouver:

Perry M. Improving Protein Solubility via Directed Evolution . [Internet] [Thesis]. Queens University; 2009. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/1974/5276.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Perry M. Improving Protein Solubility via Directed Evolution . [Thesis]. Queens University; 2009. Available from: http://hdl.handle.net/1974/5276

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Texas – Austin

4. Gollihar, Jimmy Dale, Jr. Methods in protein engineering and screening : from rational design to directed evolution and beyond.

Degree: Biochemistry, 2017, University of Texas – Austin

 Humans have engineered organisms for thousands of years. The domestication of plants and animals are early examples of how humans have changed genotypes of organisms… (more)

Subjects/Keywords: Rational design; Directed evolution

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APA (6th Edition):

Gollihar, Jimmy Dale, J. (2017). Methods in protein engineering and screening : from rational design to directed evolution and beyond. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/61769

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Gollihar, Jimmy Dale, Jr. “Methods in protein engineering and screening : from rational design to directed evolution and beyond.” 2017. Thesis, University of Texas – Austin. Accessed July 23, 2019. http://hdl.handle.net/2152/61769.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Gollihar, Jimmy Dale, Jr. “Methods in protein engineering and screening : from rational design to directed evolution and beyond.” 2017. Web. 23 Jul 2019.

Vancouver:

Gollihar, Jimmy Dale J. Methods in protein engineering and screening : from rational design to directed evolution and beyond. [Internet] [Thesis]. University of Texas – Austin; 2017. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/2152/61769.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Gollihar, Jimmy Dale J. Methods in protein engineering and screening : from rational design to directed evolution and beyond. [Thesis]. University of Texas – Austin; 2017. Available from: http://hdl.handle.net/2152/61769

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Texas – Austin

5. Ellefson, Jared Wade. Engineering the central dogma using emulsion based directed evolution.

Degree: Cellular and Molecular Biology, 2016, University of Texas – Austin

 The central dogma of molecular biology forms the most basic (and fundamental) paradigm of how life operates. Despite its elegant simplicity, scientists are still uncovering… (more)

Subjects/Keywords: Directed evolution; Central dogma

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APA (6th Edition):

Ellefson, J. W. (2016). Engineering the central dogma using emulsion based directed evolution. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/39570

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ellefson, Jared Wade. “Engineering the central dogma using emulsion based directed evolution.” 2016. Thesis, University of Texas – Austin. Accessed July 23, 2019. http://hdl.handle.net/2152/39570.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ellefson, Jared Wade. “Engineering the central dogma using emulsion based directed evolution.” 2016. Web. 23 Jul 2019.

Vancouver:

Ellefson JW. Engineering the central dogma using emulsion based directed evolution. [Internet] [Thesis]. University of Texas – Austin; 2016. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/2152/39570.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ellefson JW. Engineering the central dogma using emulsion based directed evolution. [Thesis]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/39570

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Victoria University of Wellington

6. Prosser, Gareth Adrian. Discovery and Optimisation of Bacterial Nitroreductases for Use in Anti-Cancer Gene Therapy.

Degree: 2011, Victoria University of Wellington

 Nitroaromatic prodrugs are biologically inert compounds that are attractive candidates for anti-cancer therapy by virtue of their ability to be converted to potent DNA alkylating… (more)

Subjects/Keywords: Nitroreductase; GDEPT; Directed evolution

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APA (6th Edition):

Prosser, G. A. (2011). Discovery and Optimisation of Bacterial Nitroreductases for Use in Anti-Cancer Gene Therapy. (Doctoral Dissertation). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/1718

Chicago Manual of Style (16th Edition):

Prosser, Gareth Adrian. “Discovery and Optimisation of Bacterial Nitroreductases for Use in Anti-Cancer Gene Therapy.” 2011. Doctoral Dissertation, Victoria University of Wellington. Accessed July 23, 2019. http://hdl.handle.net/10063/1718.

MLA Handbook (7th Edition):

Prosser, Gareth Adrian. “Discovery and Optimisation of Bacterial Nitroreductases for Use in Anti-Cancer Gene Therapy.” 2011. Web. 23 Jul 2019.

Vancouver:

Prosser GA. Discovery and Optimisation of Bacterial Nitroreductases for Use in Anti-Cancer Gene Therapy. [Internet] [Doctoral dissertation]. Victoria University of Wellington; 2011. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/10063/1718.

Council of Science Editors:

Prosser GA. Discovery and Optimisation of Bacterial Nitroreductases for Use in Anti-Cancer Gene Therapy. [Doctoral Dissertation]. Victoria University of Wellington; 2011. Available from: http://hdl.handle.net/10063/1718


University of Cambridge

7. Shafee, Thomas. Evolvability of a viral protease: experimental evolution of catalysis, robustness and specificity .

Degree: 2014, University of Cambridge

 The aim of this thesis is to investigate aspects of molecular evolution and enzyme engineering using the experimental evolution of Tobacco Etch Virus cysteine protease… (more)

Subjects/Keywords: Directed evolution; Evolution; Evolvability; Promiscuity; Experimental evolution; Robustness; Protease; Enzymology; Nucleophile

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APA (6th Edition):

Shafee, T. (2014). Evolvability of a viral protease: experimental evolution of catalysis, robustness and specificity . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/245207

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Shafee, Thomas. “Evolvability of a viral protease: experimental evolution of catalysis, robustness and specificity .” 2014. Thesis, University of Cambridge. Accessed July 23, 2019. https://www.repository.cam.ac.uk/handle/1810/245207.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Shafee, Thomas. “Evolvability of a viral protease: experimental evolution of catalysis, robustness and specificity .” 2014. Web. 23 Jul 2019.

Vancouver:

Shafee T. Evolvability of a viral protease: experimental evolution of catalysis, robustness and specificity . [Internet] [Thesis]. University of Cambridge; 2014. [cited 2019 Jul 23]. Available from: https://www.repository.cam.ac.uk/handle/1810/245207.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Shafee T. Evolvability of a viral protease: experimental evolution of catalysis, robustness and specificity . [Thesis]. University of Cambridge; 2014. Available from: https://www.repository.cam.ac.uk/handle/1810/245207

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

8. Chaikind, Brian Robb. Targeting bifurcated methyltransferases towards user-defined DNA sequences.

Degree: 2014, Johns Hopkins University

 There would be great value in targeting methylation toward user-defined DNA sequences. Directing methylation toward single CpG sites within a genome would provide a means… (more)

Subjects/Keywords: methyltransferases; protein engineering; directed evolution; zinc fingers

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APA (6th Edition):

Chaikind, B. R. (2014). Targeting bifurcated methyltransferases towards user-defined DNA sequences. (Thesis). Johns Hopkins University. Retrieved from http://jhir.library.jhu.edu/handle/1774.2/38017

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Chaikind, Brian Robb. “Targeting bifurcated methyltransferases towards user-defined DNA sequences.” 2014. Thesis, Johns Hopkins University. Accessed July 23, 2019. http://jhir.library.jhu.edu/handle/1774.2/38017.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Chaikind, Brian Robb. “Targeting bifurcated methyltransferases towards user-defined DNA sequences.” 2014. Web. 23 Jul 2019.

Vancouver:

Chaikind BR. Targeting bifurcated methyltransferases towards user-defined DNA sequences. [Internet] [Thesis]. Johns Hopkins University; 2014. [cited 2019 Jul 23]. Available from: http://jhir.library.jhu.edu/handle/1774.2/38017.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Chaikind BR. Targeting bifurcated methyltransferases towards user-defined DNA sequences. [Thesis]. Johns Hopkins University; 2014. Available from: http://jhir.library.jhu.edu/handle/1774.2/38017

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Université Catholique de Louvain

9. Khan, Mohammad Shahneawz. In vivo promiscuity and directed evolution of oligomeric beta-decarboxylating dehydrogenases.

Degree: 2018, Université Catholique de Louvain

At the molecular level, natural evolution gave rise a wide variety of proteins endowed with exquisite properties. In this study, we envisioned to contribute a… (more)

Subjects/Keywords: Enzyme; Promiscuity; Directed Evolution; Beta-decarboxylating dehydrogenase

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APA (6th Edition):

Khan, M. S. (2018). In vivo promiscuity and directed evolution of oligomeric beta-decarboxylating dehydrogenases. (Thesis). Université Catholique de Louvain. Retrieved from http://hdl.handle.net/2078.1/202599

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Khan, Mohammad Shahneawz. “In vivo promiscuity and directed evolution of oligomeric beta-decarboxylating dehydrogenases.” 2018. Thesis, Université Catholique de Louvain. Accessed July 23, 2019. http://hdl.handle.net/2078.1/202599.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Khan, Mohammad Shahneawz. “In vivo promiscuity and directed evolution of oligomeric beta-decarboxylating dehydrogenases.” 2018. Web. 23 Jul 2019.

Vancouver:

Khan MS. In vivo promiscuity and directed evolution of oligomeric beta-decarboxylating dehydrogenases. [Internet] [Thesis]. Université Catholique de Louvain; 2018. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/2078.1/202599.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Khan MS. In vivo promiscuity and directed evolution of oligomeric beta-decarboxylating dehydrogenases. [Thesis]. Université Catholique de Louvain; 2018. Available from: http://hdl.handle.net/2078.1/202599

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Adelaide

10. Betteridge, Alice Livingston. Enhanced wine-making efficiency through fool-proof malolactic fermentation: evolution of superior lactic acid bacteria.

Degree: 2015, University of Adelaide

 Malolactic fermentation (MLF), also known as the secondary fermentation in winemaking, involves the enzymatic decarboxylation of L-malic to L-lactic acid, by lactic acid bacteria, usually… (more)

Subjects/Keywords: wine-making; oenococcus oeni; ethanol; directed evolution

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APA (6th Edition):

Betteridge, A. L. (2015). Enhanced wine-making efficiency through fool-proof malolactic fermentation: evolution of superior lactic acid bacteria. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/97994

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Betteridge, Alice Livingston. “Enhanced wine-making efficiency through fool-proof malolactic fermentation: evolution of superior lactic acid bacteria.” 2015. Thesis, University of Adelaide. Accessed July 23, 2019. http://hdl.handle.net/2440/97994.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Betteridge, Alice Livingston. “Enhanced wine-making efficiency through fool-proof malolactic fermentation: evolution of superior lactic acid bacteria.” 2015. Web. 23 Jul 2019.

Vancouver:

Betteridge AL. Enhanced wine-making efficiency through fool-proof malolactic fermentation: evolution of superior lactic acid bacteria. [Internet] [Thesis]. University of Adelaide; 2015. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/2440/97994.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Betteridge AL. Enhanced wine-making efficiency through fool-proof malolactic fermentation: evolution of superior lactic acid bacteria. [Thesis]. University of Adelaide; 2015. Available from: http://hdl.handle.net/2440/97994

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Manchester

11. Thompson, Matthew. Asymmetric Bioamination of Alcohols via Hydrogen-Borrowing.

Degree: 2018, University of Manchester

 The value of biocatalysis lies in the unparalleled specificity with which enzymes catalyse reactions. This high specificity allows for synthetic chemists to rapidly build molecular… (more)

Subjects/Keywords: Biocatalysis; Hydrogen Borrowing; Directed evolution; Enzyme Immobilisation

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APA (6th Edition):

Thompson, M. (2018). Asymmetric Bioamination of Alcohols via Hydrogen-Borrowing. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:314642

Chicago Manual of Style (16th Edition):

Thompson, Matthew. “Asymmetric Bioamination of Alcohols via Hydrogen-Borrowing.” 2018. Doctoral Dissertation, University of Manchester. Accessed July 23, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:314642.

MLA Handbook (7th Edition):

Thompson, Matthew. “Asymmetric Bioamination of Alcohols via Hydrogen-Borrowing.” 2018. Web. 23 Jul 2019.

Vancouver:

Thompson M. Asymmetric Bioamination of Alcohols via Hydrogen-Borrowing. [Internet] [Doctoral dissertation]. University of Manchester; 2018. [cited 2019 Jul 23]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:314642.

Council of Science Editors:

Thompson M. Asymmetric Bioamination of Alcohols via Hydrogen-Borrowing. [Doctoral Dissertation]. University of Manchester; 2018. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:314642


Victoria University of Wellington

12. Brown, Alistair. Engineering the indigoidine-synthesising enzyme BpsA for diverse applications in biotechnology.

Degree: 2018, Victoria University of Wellington

 Non-ribosomal peptide synthetases (NRPSs) are large, modular enzymes that synthesise bioactive peptides using an assembly line architecture, wherein each module is responsible for the incorporation… (more)

Subjects/Keywords: Directed evolution; Indigoidine; Nonribosomal peptide synthetase

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APA (6th Edition):

Brown, A. (2018). Engineering the indigoidine-synthesising enzyme BpsA for diverse applications in biotechnology. (Doctoral Dissertation). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/7088

Chicago Manual of Style (16th Edition):

Brown, Alistair. “Engineering the indigoidine-synthesising enzyme BpsA for diverse applications in biotechnology.” 2018. Doctoral Dissertation, Victoria University of Wellington. Accessed July 23, 2019. http://hdl.handle.net/10063/7088.

MLA Handbook (7th Edition):

Brown, Alistair. “Engineering the indigoidine-synthesising enzyme BpsA for diverse applications in biotechnology.” 2018. Web. 23 Jul 2019.

Vancouver:

Brown A. Engineering the indigoidine-synthesising enzyme BpsA for diverse applications in biotechnology. [Internet] [Doctoral dissertation]. Victoria University of Wellington; 2018. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/10063/7088.

Council of Science Editors:

Brown A. Engineering the indigoidine-synthesising enzyme BpsA for diverse applications in biotechnology. [Doctoral Dissertation]. Victoria University of Wellington; 2018. Available from: http://hdl.handle.net/10063/7088


Vanderbilt University

13. Birmingham, William Ross. Bioretrosynthetic Construction of a Non-Natural Nucleoside Analog Biosynthetic Pathway.

Degree: PhD, Biochemistry, 2013, Vanderbilt University

 Engineered biocatalysts have become increasingly sought after as replacements for individual chemical synthetic steps. However, their implementation in multistep sequences as biosynthetic pathways has proven… (more)

Subjects/Keywords: directed evolution; retrograde evolution; bioretrosynthesis; dideoxyinosine; phosphopentomutase; ribokinase

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APA (6th Edition):

Birmingham, W. R. (2013). Bioretrosynthetic Construction of a Non-Natural Nucleoside Analog Biosynthetic Pathway. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-11212013-085213/ ;

Chicago Manual of Style (16th Edition):

Birmingham, William Ross. “Bioretrosynthetic Construction of a Non-Natural Nucleoside Analog Biosynthetic Pathway.” 2013. Doctoral Dissertation, Vanderbilt University. Accessed July 23, 2019. http://etd.library.vanderbilt.edu/available/etd-11212013-085213/ ;.

MLA Handbook (7th Edition):

Birmingham, William Ross. “Bioretrosynthetic Construction of a Non-Natural Nucleoside Analog Biosynthetic Pathway.” 2013. Web. 23 Jul 2019.

Vancouver:

Birmingham WR. Bioretrosynthetic Construction of a Non-Natural Nucleoside Analog Biosynthetic Pathway. [Internet] [Doctoral dissertation]. Vanderbilt University; 2013. [cited 2019 Jul 23]. Available from: http://etd.library.vanderbilt.edu/available/etd-11212013-085213/ ;.

Council of Science Editors:

Birmingham WR. Bioretrosynthetic Construction of a Non-Natural Nucleoside Analog Biosynthetic Pathway. [Doctoral Dissertation]. Vanderbilt University; 2013. Available from: http://etd.library.vanderbilt.edu/available/etd-11212013-085213/ ;


University of California – Irvine

14. Ravikumar, Arjun. An orthogonal DNA replication system for in vivo continuous directed evolution.

Degree: Biomedical Engineering, 2018, University of California – Irvine

Directed evolution is a powerful approach for engineering biomolecules and understanding the basic principles of adaptation. However, experimental strategies for directed evolution are notoriously labor-intensive… (more)

Subjects/Keywords: Bioengineering; Molecular biology; biomolecular evolution; continuous evolution; directed evolution; drug resistance; error threshold; orthogonal replication

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APA (6th Edition):

Ravikumar, A. (2018). An orthogonal DNA replication system for in vivo continuous directed evolution. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/78b901hc

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ravikumar, Arjun. “An orthogonal DNA replication system for in vivo continuous directed evolution.” 2018. Thesis, University of California – Irvine. Accessed July 23, 2019. http://www.escholarship.org/uc/item/78b901hc.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ravikumar, Arjun. “An orthogonal DNA replication system for in vivo continuous directed evolution.” 2018. Web. 23 Jul 2019.

Vancouver:

Ravikumar A. An orthogonal DNA replication system for in vivo continuous directed evolution. [Internet] [Thesis]. University of California – Irvine; 2018. [cited 2019 Jul 23]. Available from: http://www.escholarship.org/uc/item/78b901hc.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ravikumar A. An orthogonal DNA replication system for in vivo continuous directed evolution. [Thesis]. University of California – Irvine; 2018. Available from: http://www.escholarship.org/uc/item/78b901hc

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


INP Toulouse

15. Ricordel, Marine. Sélection, Génération et Amélioration de Poxvirus Oncolytiques par Génie Génétique et Evolution Dirigée : Selection, generation and improvement of oncolytic poxviruses with viral engineering and directed evolution.

Degree: Docteur es, Pathologie, Toxicologie, Génétique et Nutrition, 2018, INP Toulouse

Les virus oncolytiques sont une nouvelle classe d’agents thérapeutiques pouvant être une alternative au traitement des cancers. Plusieurs virus oncolytiques sont actuellement développés en clinique,… (more)

Subjects/Keywords: Poxvirus; Virothérapie oncolytique; Tropisme tumoral; Evolution dirigée; Poxviruses; Oncolytic virotherapy; Tropism modification; Directed evolution

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Ricordel, M. (2018). Sélection, Génération et Amélioration de Poxvirus Oncolytiques par Génie Génétique et Evolution Dirigée : Selection, generation and improvement of oncolytic poxviruses with viral engineering and directed evolution. (Doctoral Dissertation). INP Toulouse. Retrieved from http://www.theses.fr/2018INPT0010

Chicago Manual of Style (16th Edition):

Ricordel, Marine. “Sélection, Génération et Amélioration de Poxvirus Oncolytiques par Génie Génétique et Evolution Dirigée : Selection, generation and improvement of oncolytic poxviruses with viral engineering and directed evolution.” 2018. Doctoral Dissertation, INP Toulouse. Accessed July 23, 2019. http://www.theses.fr/2018INPT0010.

MLA Handbook (7th Edition):

Ricordel, Marine. “Sélection, Génération et Amélioration de Poxvirus Oncolytiques par Génie Génétique et Evolution Dirigée : Selection, generation and improvement of oncolytic poxviruses with viral engineering and directed evolution.” 2018. Web. 23 Jul 2019.

Vancouver:

Ricordel M. Sélection, Génération et Amélioration de Poxvirus Oncolytiques par Génie Génétique et Evolution Dirigée : Selection, generation and improvement of oncolytic poxviruses with viral engineering and directed evolution. [Internet] [Doctoral dissertation]. INP Toulouse; 2018. [cited 2019 Jul 23]. Available from: http://www.theses.fr/2018INPT0010.

Council of Science Editors:

Ricordel M. Sélection, Génération et Amélioration de Poxvirus Oncolytiques par Génie Génétique et Evolution Dirigée : Selection, generation and improvement of oncolytic poxviruses with viral engineering and directed evolution. [Doctoral Dissertation]. INP Toulouse; 2018. Available from: http://www.theses.fr/2018INPT0010

16. Jacquet, Pauline. Amélioration d'une enzyme hyperthermostable pour la dégradation des organophosphorés : Improvement of hyperthermostable enzyme for organophosphorus degradation.

Degree: Docteur es, Biologie. Biochimie structurale, 2017, Aix Marseille Université

Les organophosphorés (OPs) sont des composés neurotoxiques qui sont largement utilisés comme pesticides. Cette utilisation intensive a conduit à une importante pollution des sols et… (more)

Subjects/Keywords: SsoPox; Phosphotriestérase-Like lactonase; Evolution dirigée; SsoPox; Phosphotriesterase-Like lactonase; Directed evolution

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Jacquet, P. (2017). Amélioration d'une enzyme hyperthermostable pour la dégradation des organophosphorés : Improvement of hyperthermostable enzyme for organophosphorus degradation. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2017AIXM0618

Chicago Manual of Style (16th Edition):

Jacquet, Pauline. “Amélioration d'une enzyme hyperthermostable pour la dégradation des organophosphorés : Improvement of hyperthermostable enzyme for organophosphorus degradation.” 2017. Doctoral Dissertation, Aix Marseille Université. Accessed July 23, 2019. http://www.theses.fr/2017AIXM0618.

MLA Handbook (7th Edition):

Jacquet, Pauline. “Amélioration d'une enzyme hyperthermostable pour la dégradation des organophosphorés : Improvement of hyperthermostable enzyme for organophosphorus degradation.” 2017. Web. 23 Jul 2019.

Vancouver:

Jacquet P. Amélioration d'une enzyme hyperthermostable pour la dégradation des organophosphorés : Improvement of hyperthermostable enzyme for organophosphorus degradation. [Internet] [Doctoral dissertation]. Aix Marseille Université 2017. [cited 2019 Jul 23]. Available from: http://www.theses.fr/2017AIXM0618.

Council of Science Editors:

Jacquet P. Amélioration d'une enzyme hyperthermostable pour la dégradation des organophosphorés : Improvement of hyperthermostable enzyme for organophosphorus degradation. [Doctoral Dissertation]. Aix Marseille Université 2017. Available from: http://www.theses.fr/2017AIXM0618


University of Alberta

17. Hoi, Hiofan. Development of monomeric fluorescent proteins and fluorescent protein-based biosensors.

Degree: PhD, Department of Chemistry, 2013, University of Alberta

 Fluorescent protein (FP) technology is now an indispensible tool of biomedical research. Nevertheless, only a few members of the hundreds of existing FPs are generally… (more)

Subjects/Keywords: directed evolution; protein engineering; calcium indicator; genetically-encoded biosensor; fluorescent protein

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APA (6th Edition):

Hoi, H. (2013). Development of monomeric fluorescent proteins and fluorescent protein-based biosensors. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/5712m723w

Chicago Manual of Style (16th Edition):

Hoi, Hiofan. “Development of monomeric fluorescent proteins and fluorescent protein-based biosensors.” 2013. Doctoral Dissertation, University of Alberta. Accessed July 23, 2019. https://era.library.ualberta.ca/files/5712m723w.

MLA Handbook (7th Edition):

Hoi, Hiofan. “Development of monomeric fluorescent proteins and fluorescent protein-based biosensors.” 2013. Web. 23 Jul 2019.

Vancouver:

Hoi H. Development of monomeric fluorescent proteins and fluorescent protein-based biosensors. [Internet] [Doctoral dissertation]. University of Alberta; 2013. [cited 2019 Jul 23]. Available from: https://era.library.ualberta.ca/files/5712m723w.

Council of Science Editors:

Hoi H. Development of monomeric fluorescent proteins and fluorescent protein-based biosensors. [Doctoral Dissertation]. University of Alberta; 2013. Available from: https://era.library.ualberta.ca/files/5712m723w


Texas A&M University

18. Ghanem, Eman Mohamed. Directed evolution of phosphotriesterase for detoxification of the nerve agent VX.

Degree: 2006, Texas A&M University

 Phosphotriesterase (PTE) isolated from the soil bacterium Flavobacterium sp. is a member of the amidohydrolase superfamily. PTE catalyzes the hydrolysis of a broad spectrum of… (more)

Subjects/Keywords: Phosphotriesterase; organophosphates; Directed evolution

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APA (6th Edition):

Ghanem, E. M. (2006). Directed evolution of phosphotriesterase for detoxification of the nerve agent VX. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/4330

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ghanem, Eman Mohamed. “Directed evolution of phosphotriesterase for detoxification of the nerve agent VX.” 2006. Thesis, Texas A&M University. Accessed July 23, 2019. http://hdl.handle.net/1969.1/4330.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ghanem, Eman Mohamed. “Directed evolution of phosphotriesterase for detoxification of the nerve agent VX.” 2006. Web. 23 Jul 2019.

Vancouver:

Ghanem EM. Directed evolution of phosphotriesterase for detoxification of the nerve agent VX. [Internet] [Thesis]. Texas A&M University; 2006. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/1969.1/4330.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ghanem EM. Directed evolution of phosphotriesterase for detoxification of the nerve agent VX. [Thesis]. Texas A&M University; 2006. Available from: http://hdl.handle.net/1969.1/4330

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Colorado

19. Glebes, Tirzah Ya'el. Genome Engineering for Improved Furfural and Product Tolerance in Escherichia coli for Renewable Biofuel Applications.

Degree: PhD, 2014, University of Colorado

  As engineers, we are interested in designing controlled, predictable, and maintainable strategies for performing or improving tasks. Genome engineering aims to use these same… (more)

Subjects/Keywords: biofuels; directed evolution; furfural; genome engineering; Chemical Engineering

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APA (6th Edition):

Glebes, T. Y. (2014). Genome Engineering for Improved Furfural and Product Tolerance in Escherichia coli for Renewable Biofuel Applications. (Doctoral Dissertation). University of Colorado. Retrieved from http://scholar.colorado.edu/chen_gradetds/3

Chicago Manual of Style (16th Edition):

Glebes, Tirzah Ya'el. “Genome Engineering for Improved Furfural and Product Tolerance in Escherichia coli for Renewable Biofuel Applications.” 2014. Doctoral Dissertation, University of Colorado. Accessed July 23, 2019. http://scholar.colorado.edu/chen_gradetds/3.

MLA Handbook (7th Edition):

Glebes, Tirzah Ya'el. “Genome Engineering for Improved Furfural and Product Tolerance in Escherichia coli for Renewable Biofuel Applications.” 2014. Web. 23 Jul 2019.

Vancouver:

Glebes TY. Genome Engineering for Improved Furfural and Product Tolerance in Escherichia coli for Renewable Biofuel Applications. [Internet] [Doctoral dissertation]. University of Colorado; 2014. [cited 2019 Jul 23]. Available from: http://scholar.colorado.edu/chen_gradetds/3.

Council of Science Editors:

Glebes TY. Genome Engineering for Improved Furfural and Product Tolerance in Escherichia coli for Renewable Biofuel Applications. [Doctoral Dissertation]. University of Colorado; 2014. Available from: http://scholar.colorado.edu/chen_gradetds/3


Universidade Federal de Viçosa

20. Larissa Mattos Trevizano. Melhoramento por evolução dirigida da termoestabilidade da xilanase xynA de Orpinomyces sp. PC-2.

Degree: 2009, Universidade Federal de Viçosa

 Xilana é o polissacarídeo hemicelulósico mais comum da parede celular de plantas. Este polissacarídeo é composto por uma cadeia principal constituída exclusivamente por resíduos de… (more)

Subjects/Keywords: Xilanase; Evolução dirigida; Orpinomyces sp.; BIOQUIMICA; Directed evolution; Xylanase; Orpinomyces sp.

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APA (6th Edition):

Trevizano, L. M. (2009). Melhoramento por evolução dirigida da termoestabilidade da xilanase xynA de Orpinomyces sp. PC-2. (Thesis). Universidade Federal de Viçosa. Retrieved from http://www.tede.ufv.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=5540

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Trevizano, Larissa Mattos. “Melhoramento por evolução dirigida da termoestabilidade da xilanase xynA de Orpinomyces sp. PC-2.” 2009. Thesis, Universidade Federal de Viçosa. Accessed July 23, 2019. http://www.tede.ufv.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=5540.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Trevizano, Larissa Mattos. “Melhoramento por evolução dirigida da termoestabilidade da xilanase xynA de Orpinomyces sp. PC-2.” 2009. Web. 23 Jul 2019.

Vancouver:

Trevizano LM. Melhoramento por evolução dirigida da termoestabilidade da xilanase xynA de Orpinomyces sp. PC-2. [Internet] [Thesis]. Universidade Federal de Viçosa; 2009. [cited 2019 Jul 23]. Available from: http://www.tede.ufv.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=5540.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Trevizano LM. Melhoramento por evolução dirigida da termoestabilidade da xilanase xynA de Orpinomyces sp. PC-2. [Thesis]. Universidade Federal de Viçosa; 2009. Available from: http://www.tede.ufv.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=5540

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Penn State University

21. Moore, Gregory Lee. Modeling and Optimization in Directed Evolution Protocols and Protein Engineering.

Degree: PhD, Chemical Engineering, 2005, Penn State University

 The central theme of this thesis aims toward the systematic development of integrated approaches for proactively designing protein libraries with focused diversity for directed evolution(more)

Subjects/Keywords: directed evolution; protein engineering; optimization

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APA (6th Edition):

Moore, G. L. (2005). Modeling and Optimization in Directed Evolution Protocols and Protein Engineering. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/6525

Chicago Manual of Style (16th Edition):

Moore, Gregory Lee. “Modeling and Optimization in Directed Evolution Protocols and Protein Engineering.” 2005. Doctoral Dissertation, Penn State University. Accessed July 23, 2019. https://etda.libraries.psu.edu/catalog/6525.

MLA Handbook (7th Edition):

Moore, Gregory Lee. “Modeling and Optimization in Directed Evolution Protocols and Protein Engineering.” 2005. Web. 23 Jul 2019.

Vancouver:

Moore GL. Modeling and Optimization in Directed Evolution Protocols and Protein Engineering. [Internet] [Doctoral dissertation]. Penn State University; 2005. [cited 2019 Jul 23]. Available from: https://etda.libraries.psu.edu/catalog/6525.

Council of Science Editors:

Moore GL. Modeling and Optimization in Directed Evolution Protocols and Protein Engineering. [Doctoral Dissertation]. Penn State University; 2005. Available from: https://etda.libraries.psu.edu/catalog/6525


University of California – Irvine

22. Gansmiller, Andrew Michael. Towards Selections for Enzyme Turnovers.

Degree: Chemistry, 2015, University of California – Irvine

 Enzyme engineering is a field with a wide variety of applications, including medicine, alternative energy, waste disposal, and chemical synthesis. Despite rapid advancements in the… (more)

Subjects/Keywords: Chemistry; Biochemistry; Molecular biology; Directed Evolution; Enzyme Engineering; Phage Display

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APA (6th Edition):

Gansmiller, A. M. (2015). Towards Selections for Enzyme Turnovers. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/335747r4

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Gansmiller, Andrew Michael. “Towards Selections for Enzyme Turnovers.” 2015. Thesis, University of California – Irvine. Accessed July 23, 2019. http://www.escholarship.org/uc/item/335747r4.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Gansmiller, Andrew Michael. “Towards Selections for Enzyme Turnovers.” 2015. Web. 23 Jul 2019.

Vancouver:

Gansmiller AM. Towards Selections for Enzyme Turnovers. [Internet] [Thesis]. University of California – Irvine; 2015. [cited 2019 Jul 23]. Available from: http://www.escholarship.org/uc/item/335747r4.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Gansmiller AM. Towards Selections for Enzyme Turnovers. [Thesis]. University of California – Irvine; 2015. Available from: http://www.escholarship.org/uc/item/335747r4

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of California – Berkeley

23. Wolski, Paul William. Engineering and Identification of Ionic Liquid-Tolerant Cellulases for Biofuels Production.

Degree: Comparative Biochemistry, 2013, University of California – Berkeley

 AbstractEngineering and Identification of Ionic Liquid-Tolerant Cellulases for Biofuels ProductionbyPaul William WolskiDoctor of Philosophy in Comparative BiochemistryUniversity of California, BerkeleyProfessor Douglas S. Clark, Chair Cellulose… (more)

Subjects/Keywords: Biogeochemistry; Chemical engineering; Biofuel; Cellulase; Directed Evolution; Enzyme; Ionic Liquid

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Wolski, P. W. (2013). Engineering and Identification of Ionic Liquid-Tolerant Cellulases for Biofuels Production. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/4m17q46c

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Wolski, Paul William. “Engineering and Identification of Ionic Liquid-Tolerant Cellulases for Biofuels Production.” 2013. Thesis, University of California – Berkeley. Accessed July 23, 2019. http://www.escholarship.org/uc/item/4m17q46c.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Wolski, Paul William. “Engineering and Identification of Ionic Liquid-Tolerant Cellulases for Biofuels Production.” 2013. Web. 23 Jul 2019.

Vancouver:

Wolski PW. Engineering and Identification of Ionic Liquid-Tolerant Cellulases for Biofuels Production. [Internet] [Thesis]. University of California – Berkeley; 2013. [cited 2019 Jul 23]. Available from: http://www.escholarship.org/uc/item/4m17q46c.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Wolski PW. Engineering and Identification of Ionic Liquid-Tolerant Cellulases for Biofuels Production. [Thesis]. University of California – Berkeley; 2013. Available from: http://www.escholarship.org/uc/item/4m17q46c

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Tampere University

24. Lehtonen, Soili. Avidin as an Alternative Scaffold : Development of avidin-based small molecule binding proteins, antidins .

Degree: 2017, Tampere University

 Vasta-aineet ovat immuunipuolustusjärjestelmämme tuottamia erityisiä sitojaproteiineja, jotka kykenevät tunnistamaan lähes minkä tahansa vieraan molekyylin. Niitä onkin hyödynnetty jo melkein vuosisadan ajan sekä arvokkaina laboratorio-reagensseina biotieteissä… (more)

Subjects/Keywords: avidiini; suunnattu evoluutio; faaginäyttö; avidin; alternative scaffold; directed evolution; phage display

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APA (6th Edition):

Lehtonen, S. (2017). Avidin as an Alternative Scaffold : Development of avidin-based small molecule binding proteins, antidins . (Doctoral Dissertation). Tampere University. Retrieved from http://tampub.uta.fi/handle/10024/101930

Chicago Manual of Style (16th Edition):

Lehtonen, Soili. “Avidin as an Alternative Scaffold : Development of avidin-based small molecule binding proteins, antidins .” 2017. Doctoral Dissertation, Tampere University. Accessed July 23, 2019. http://tampub.uta.fi/handle/10024/101930.

MLA Handbook (7th Edition):

Lehtonen, Soili. “Avidin as an Alternative Scaffold : Development of avidin-based small molecule binding proteins, antidins .” 2017. Web. 23 Jul 2019.

Vancouver:

Lehtonen S. Avidin as an Alternative Scaffold : Development of avidin-based small molecule binding proteins, antidins . [Internet] [Doctoral dissertation]. Tampere University; 2017. [cited 2019 Jul 23]. Available from: http://tampub.uta.fi/handle/10024/101930.

Council of Science Editors:

Lehtonen S. Avidin as an Alternative Scaffold : Development of avidin-based small molecule binding proteins, antidins . [Doctoral Dissertation]. Tampere University; 2017. Available from: http://tampub.uta.fi/handle/10024/101930

25. Dorr, Brent Matthew. Directed Evolution of Sortase Activity and Specificity.

Degree: PhD, Chemistry, 2014, Harvard University

Nature employs complex networks of protein-tailoring enzymes to effect the post-translational modification of proteins in vivo. By comparison, modern chemical methods rely upon either nonspecific… (more)

Subjects/Keywords: Chemistry; Molecular biology; Biochemistry; Bioconjugation; Chemical Biology; Directed Evolution; Sortase

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APA (6th Edition):

Dorr, B. M. (2014). Directed Evolution of Sortase Activity and Specificity. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:12274116

Chicago Manual of Style (16th Edition):

Dorr, Brent Matthew. “Directed Evolution of Sortase Activity and Specificity.” 2014. Doctoral Dissertation, Harvard University. Accessed July 23, 2019. http://nrs.harvard.edu/urn-3:HUL.InstRepos:12274116.

MLA Handbook (7th Edition):

Dorr, Brent Matthew. “Directed Evolution of Sortase Activity and Specificity.” 2014. Web. 23 Jul 2019.

Vancouver:

Dorr BM. Directed Evolution of Sortase Activity and Specificity. [Internet] [Doctoral dissertation]. Harvard University; 2014. [cited 2019 Jul 23]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:12274116.

Council of Science Editors:

Dorr BM. Directed Evolution of Sortase Activity and Specificity. [Doctoral Dissertation]. Harvard University; 2014. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:12274116


Université Catholique de Louvain

26. Woronoff, Gabrielle. Development of methods for the directed evolution of penicillin G acylase by in vitro compartmentalization.

Degree: 2012, Université Catholique de Louvain

Enzymatic catalysts have been finely tuned for their specific function though natural evolution, by iterative mutations and selections cycles. Directed evolution mimics natural evolution at… (more)

Subjects/Keywords: Directed evolution; Penicillin G acylase; Dropletb-based microfluidics; In vitro compartmentalization

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APA (6th Edition):

Woronoff, G. (2012). Development of methods for the directed evolution of penicillin G acylase by in vitro compartmentalization. (Thesis). Université Catholique de Louvain. Retrieved from http://hdl.handle.net/2078.1/110274

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Woronoff, Gabrielle. “Development of methods for the directed evolution of penicillin G acylase by in vitro compartmentalization.” 2012. Thesis, Université Catholique de Louvain. Accessed July 23, 2019. http://hdl.handle.net/2078.1/110274.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Woronoff, Gabrielle. “Development of methods for the directed evolution of penicillin G acylase by in vitro compartmentalization.” 2012. Web. 23 Jul 2019.

Vancouver:

Woronoff G. Development of methods for the directed evolution of penicillin G acylase by in vitro compartmentalization. [Internet] [Thesis]. Université Catholique de Louvain; 2012. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/2078.1/110274.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Woronoff G. Development of methods for the directed evolution of penicillin G acylase by in vitro compartmentalization. [Thesis]. Université Catholique de Louvain; 2012. Available from: http://hdl.handle.net/2078.1/110274

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of British Columbia

27. MacPherson, Iain. Evolution of copper-containing nitrite reductase .

Degree: 2007, University of British Columbia

 Copper-containing nitrite reductase (NiR) is a homotrimer of two cupredoxin domains and catalyzes the single electron reduction of NO2- to NO during dissimilatory denitrification. To… (more)

Subjects/Keywords: protein engineering; directed evolution

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APA (6th Edition):

MacPherson, I. (2007). Evolution of copper-containing nitrite reductase . (Thesis). University of British Columbia. Retrieved from http://hdl.handle.net/2429/259

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

MacPherson, Iain. “Evolution of copper-containing nitrite reductase .” 2007. Thesis, University of British Columbia. Accessed July 23, 2019. http://hdl.handle.net/2429/259.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

MacPherson, Iain. “Evolution of copper-containing nitrite reductase .” 2007. Web. 23 Jul 2019.

Vancouver:

MacPherson I. Evolution of copper-containing nitrite reductase . [Internet] [Thesis]. University of British Columbia; 2007. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/2429/259.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

MacPherson I. Evolution of copper-containing nitrite reductase . [Thesis]. University of British Columbia; 2007. Available from: http://hdl.handle.net/2429/259

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Texas – Austin

28. -8181-7589. Improved selections and assessments for engineering orthogonal translation systems.

Degree: Biochemistry, 2019, University of Texas – Austin

 Over twenty-five years have passed since researchers first demonstrated that introduction of a heterologous tRNA and tRNA synthetase pair could be used as an effective… (more)

Subjects/Keywords: Non-canonical amino acids; Orthogonal translation systems; Directed evolution; Selections

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

-8181-7589. (2019). Improved selections and assessments for engineering orthogonal translation systems. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/72474

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

-8181-7589. “Improved selections and assessments for engineering orthogonal translation systems.” 2019. Thesis, University of Texas – Austin. Accessed July 23, 2019. http://hdl.handle.net/2152/72474.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

-8181-7589. “Improved selections and assessments for engineering orthogonal translation systems.” 2019. Web. 23 Jul 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-8181-7589. Improved selections and assessments for engineering orthogonal translation systems. [Internet] [Thesis]. University of Texas – Austin; 2019. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/2152/72474.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

-8181-7589. Improved selections and assessments for engineering orthogonal translation systems. [Thesis]. University of Texas – Austin; 2019. Available from: http://hdl.handle.net/2152/72474

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation


Université Catholique de Louvain

29. Trabelsi, Heykel. Directed evolution of a DD-peptidase into a β-lactamase.

Degree: 2014, Université Catholique de Louvain

Understanding how proteins or more specifically enzymes evolve is still a challenging scientific issue. This thesis aimed at finding an artificial evolutionary trajectory between phylogenetically… (more)

Subjects/Keywords: Directed evolution; DD-peptidase; β-lactamase; Penicillin binding protein; Fitness

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Trabelsi, H. (2014). Directed evolution of a DD-peptidase into a β-lactamase. (Thesis). Université Catholique de Louvain. Retrieved from http://hdl.handle.net/2078.1/151945

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Trabelsi, Heykel. “Directed evolution of a DD-peptidase into a β-lactamase.” 2014. Thesis, Université Catholique de Louvain. Accessed July 23, 2019. http://hdl.handle.net/2078.1/151945.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Trabelsi, Heykel. “Directed evolution of a DD-peptidase into a β-lactamase.” 2014. Web. 23 Jul 2019.

Vancouver:

Trabelsi H. Directed evolution of a DD-peptidase into a β-lactamase. [Internet] [Thesis]. Université Catholique de Louvain; 2014. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/2078.1/151945.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Trabelsi H. Directed evolution of a DD-peptidase into a β-lactamase. [Thesis]. Université Catholique de Louvain; 2014. Available from: http://hdl.handle.net/2078.1/151945

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Illinois – Urbana-Champaign

30. Tang, Weng Lin. Engineering of an efficient and enantioselective biocatalyst for the preparation of chiral pharmaceutical intermediates.

Degree: PhD, 0300, 2011, University of Illinois – Urbana-Champaign

 This Ph.D. thesis focuses on the engineering of an efficient and enantioselective biocatalyst via direct evolution and genetic engineering for the enantioselective hydroxylation of non-activated… (more)

Subjects/Keywords: Directed Evolution; P450; High throughput screening; protein engineering

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Tang, W. L. (2011). Engineering of an efficient and enantioselective biocatalyst for the preparation of chiral pharmaceutical intermediates. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/26297

Chicago Manual of Style (16th Edition):

Tang, Weng Lin. “Engineering of an efficient and enantioselective biocatalyst for the preparation of chiral pharmaceutical intermediates.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 23, 2019. http://hdl.handle.net/2142/26297.

MLA Handbook (7th Edition):

Tang, Weng Lin. “Engineering of an efficient and enantioselective biocatalyst for the preparation of chiral pharmaceutical intermediates.” 2011. Web. 23 Jul 2019.

Vancouver:

Tang WL. Engineering of an efficient and enantioselective biocatalyst for the preparation of chiral pharmaceutical intermediates. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/2142/26297.

Council of Science Editors:

Tang WL. Engineering of an efficient and enantioselective biocatalyst for the preparation of chiral pharmaceutical intermediates. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/26297

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