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You searched for subject:( metabolic engineering). Showing records 121 – 150 of 315 total matches.

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121. Leone, Lisa M. Metabolic Modeling of Secondary Metabolism in Plant Systems.

Degree: 2014, University of Massachusetts

  In the first part of this research, we constructed a Genome scale Metabolic Model (GEM) of Taxus cuspidata, a medicinal plant used to produce… (more)

Subjects/Keywords: Plant Metabolic Engineering; Metabolic Modeling; Flux Balance Analysis; Secondary Metabolism; Methyl Jasmonate; Taxus; Biochemical and Biomolecular Engineering; Molecular, Cellular, and Tissue Engineering

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

APA (6th Edition):

Leone, L. M. (2014). Metabolic Modeling of Secondary Metabolism in Plant Systems. (Thesis). University of Massachusetts. Retrieved from https://scholarworks.umass.edu/masters_theses_2/27

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):

Leone, Lisa M. “Metabolic Modeling of Secondary Metabolism in Plant Systems.” 2014. Thesis, University of Massachusetts. Accessed November 11, 2019. https://scholarworks.umass.edu/masters_theses_2/27.

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

MLA Handbook (7th Edition):

Leone, Lisa M. “Metabolic Modeling of Secondary Metabolism in Plant Systems.” 2014. Web. 11 Nov 2019.

Vancouver:

Leone LM. Metabolic Modeling of Secondary Metabolism in Plant Systems. [Internet] [Thesis]. University of Massachusetts; 2014. [cited 2019 Nov 11]. Available from: https://scholarworks.umass.edu/masters_theses_2/27.

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

Council of Science Editors:

Leone LM. Metabolic Modeling of Secondary Metabolism in Plant Systems. [Thesis]. University of Massachusetts; 2014. Available from: https://scholarworks.umass.edu/masters_theses_2/27

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


Delft University of Technology

122. Oud, B. Reverse engineering of industrially relevant phenotypes in yeast: An integrated approach.

Degree: 2013, Delft University of Technology

 Reverse engineering is the study of discovering the structure, function and operation of a device or system with the express aim to reconstruct its key… (more)

Subjects/Keywords: reverse engeering; inverse metabolic engineering; evolutionary engineering; metabolic engineering; synthetic biology; biofuels; biochemicals

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APA (6th Edition):

Oud, B. (2013). Reverse engineering of industrially relevant phenotypes in yeast: An integrated approach. (Doctoral Dissertation). Delft University of Technology. Retrieved from http://resolver.tudelft.nl/uuid:d0782f7d-0445-41a8-bc64-a177c117ec1a ; urn:NBN:nl:ui:24-uuid:d0782f7d-0445-41a8-bc64-a177c117ec1a ; urn:NBN:nl:ui:24-uuid:d0782f7d-0445-41a8-bc64-a177c117ec1a ; http://resolver.tudelft.nl/uuid:d0782f7d-0445-41a8-bc64-a177c117ec1a

Chicago Manual of Style (16th Edition):

Oud, B. “Reverse engineering of industrially relevant phenotypes in yeast: An integrated approach.” 2013. Doctoral Dissertation, Delft University of Technology. Accessed November 11, 2019. http://resolver.tudelft.nl/uuid:d0782f7d-0445-41a8-bc64-a177c117ec1a ; urn:NBN:nl:ui:24-uuid:d0782f7d-0445-41a8-bc64-a177c117ec1a ; urn:NBN:nl:ui:24-uuid:d0782f7d-0445-41a8-bc64-a177c117ec1a ; http://resolver.tudelft.nl/uuid:d0782f7d-0445-41a8-bc64-a177c117ec1a.

MLA Handbook (7th Edition):

Oud, B. “Reverse engineering of industrially relevant phenotypes in yeast: An integrated approach.” 2013. Web. 11 Nov 2019.

Vancouver:

Oud B. Reverse engineering of industrially relevant phenotypes in yeast: An integrated approach. [Internet] [Doctoral dissertation]. Delft University of Technology; 2013. [cited 2019 Nov 11]. Available from: http://resolver.tudelft.nl/uuid:d0782f7d-0445-41a8-bc64-a177c117ec1a ; urn:NBN:nl:ui:24-uuid:d0782f7d-0445-41a8-bc64-a177c117ec1a ; urn:NBN:nl:ui:24-uuid:d0782f7d-0445-41a8-bc64-a177c117ec1a ; http://resolver.tudelft.nl/uuid:d0782f7d-0445-41a8-bc64-a177c117ec1a.

Council of Science Editors:

Oud B. Reverse engineering of industrially relevant phenotypes in yeast: An integrated approach. [Doctoral Dissertation]. Delft University of Technology; 2013. Available from: http://resolver.tudelft.nl/uuid:d0782f7d-0445-41a8-bc64-a177c117ec1a ; urn:NBN:nl:ui:24-uuid:d0782f7d-0445-41a8-bc64-a177c117ec1a ; urn:NBN:nl:ui:24-uuid:d0782f7d-0445-41a8-bc64-a177c117ec1a ; http://resolver.tudelft.nl/uuid:d0782f7d-0445-41a8-bc64-a177c117ec1a


Lincoln University

123. Mao, Longfei. Flux balance analysis to model microbial metabolism for electricity generation.

Degree: 2013, Lincoln University

 Microbial fuel cells (MFCs) are bioelectrochemcial devices that possess a similar design to a fuel cell, with an anode and a cathode connected through an… (more)

Subjects/Keywords: MFC; microbial fuel cell; Geobacter sulfurreducens; Chlamydomonas reinhardtii; Synechocystis sp. PCC 6803; Sachoromyoces cerevisiae; bioelectricity; flux balance analysis; flux variability analysis; flux minimization; FATMIN; mathematical optimization; metabolic model; Metabolic network analysis; Metabolic network redesign; metabolic engineering; in silico simulation; model-driven discovery

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APA (6th Edition):

Mao, L. (2013). Flux balance analysis to model microbial metabolism for electricity generation. (Thesis). Lincoln University. Retrieved from http://hdl.handle.net/10182/5718

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):

Mao, Longfei. “Flux balance analysis to model microbial metabolism for electricity generation.” 2013. Thesis, Lincoln University. Accessed November 11, 2019. http://hdl.handle.net/10182/5718.

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

MLA Handbook (7th Edition):

Mao, Longfei. “Flux balance analysis to model microbial metabolism for electricity generation.” 2013. Web. 11 Nov 2019.

Vancouver:

Mao L. Flux balance analysis to model microbial metabolism for electricity generation. [Internet] [Thesis]. Lincoln University; 2013. [cited 2019 Nov 11]. Available from: http://hdl.handle.net/10182/5718.

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

Council of Science Editors:

Mao L. Flux balance analysis to model microbial metabolism for electricity generation. [Thesis]. Lincoln University; 2013. Available from: http://hdl.handle.net/10182/5718

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


University of Washington

124. Takahashi, Christopher Noboru. A Platform for Microbial Evolution and Characterization.

Degree: PhD, 2016, University of Washington

 In this document we describe a novel platform for the engineered evolution of microbes. Our platform consists of three major components, which we discuss in… (more)

Subjects/Keywords: Biofilms; Circuit characterization; Continuous cultule; Evolution; Metabolic engineering; Optimization; Biomedical engineering; Electrical engineering; Evolution & development; electrical engineering

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APA (6th Edition):

Takahashi, C. N. (2016). A Platform for Microbial Evolution and Characterization. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/35185

Chicago Manual of Style (16th Edition):

Takahashi, Christopher Noboru. “A Platform for Microbial Evolution and Characterization.” 2016. Doctoral Dissertation, University of Washington. Accessed November 11, 2019. http://hdl.handle.net/1773/35185.

MLA Handbook (7th Edition):

Takahashi, Christopher Noboru. “A Platform for Microbial Evolution and Characterization.” 2016. Web. 11 Nov 2019.

Vancouver:

Takahashi CN. A Platform for Microbial Evolution and Characterization. [Internet] [Doctoral dissertation]. University of Washington; 2016. [cited 2019 Nov 11]. Available from: http://hdl.handle.net/1773/35185.

Council of Science Editors:

Takahashi CN. A Platform for Microbial Evolution and Characterization. [Doctoral Dissertation]. University of Washington; 2016. Available from: http://hdl.handle.net/1773/35185


University of Colorado

125. Tarasava, Katia. Development of Novel Crispr-Based Methods for Transcriptional Control Over Bacterial Gene Expression.

Degree: PhD, 2019, University of Colorado

 One of the challenges of the 21st century is creating a sustainable economy that is able to serve the needs of a growing population with… (more)

Subjects/Keywords: bioplastics; crispr; crispri; metabolic engineering; synthetic biology; transcriptional engineering; Biomedical Engineering and Bioengineering; Materials Science and Engineering; Microbiology; Molecular Genetics

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

APA (6th Edition):

Tarasava, K. (2019). Development of Novel Crispr-Based Methods for Transcriptional Control Over Bacterial Gene Expression. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mats_gradetds/9

Chicago Manual of Style (16th Edition):

Tarasava, Katia. “Development of Novel Crispr-Based Methods for Transcriptional Control Over Bacterial Gene Expression.” 2019. Doctoral Dissertation, University of Colorado. Accessed November 11, 2019. https://scholar.colorado.edu/mats_gradetds/9.

MLA Handbook (7th Edition):

Tarasava, Katia. “Development of Novel Crispr-Based Methods for Transcriptional Control Over Bacterial Gene Expression.” 2019. Web. 11 Nov 2019.

Vancouver:

Tarasava K. Development of Novel Crispr-Based Methods for Transcriptional Control Over Bacterial Gene Expression. [Internet] [Doctoral dissertation]. University of Colorado; 2019. [cited 2019 Nov 11]. Available from: https://scholar.colorado.edu/mats_gradetds/9.

Council of Science Editors:

Tarasava K. Development of Novel Crispr-Based Methods for Transcriptional Control Over Bacterial Gene Expression. [Doctoral Dissertation]. University of Colorado; 2019. Available from: https://scholar.colorado.edu/mats_gradetds/9

126. Prasant Kumar. Metabolic engineering of Escherichia coli as Probiotics;.

Degree: Biochemistry, 2012, Maharaja Sayajirao University of Baroda

None

References p. i-xxvii

Advisors/Committee Members: Naresh Kumar G.

Subjects/Keywords: Biochemistry; Probiotics; Escherichia coli; Metabolic engineering

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APA (6th Edition):

Kumar, P. (2012). Metabolic engineering of Escherichia coli as Probiotics;. (Thesis). Maharaja Sayajirao University of Baroda. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/7480

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):

Kumar, Prasant. “Metabolic engineering of Escherichia coli as Probiotics;.” 2012. Thesis, Maharaja Sayajirao University of Baroda. Accessed November 11, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/7480.

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

MLA Handbook (7th Edition):

Kumar, Prasant. “Metabolic engineering of Escherichia coli as Probiotics;.” 2012. Web. 11 Nov 2019.

Vancouver:

Kumar P. Metabolic engineering of Escherichia coli as Probiotics;. [Internet] [Thesis]. Maharaja Sayajirao University of Baroda; 2012. [cited 2019 Nov 11]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/7480.

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

Council of Science Editors:

Kumar P. Metabolic engineering of Escherichia coli as Probiotics;. [Thesis]. Maharaja Sayajirao University of Baroda; 2012. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/7480

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


The Ohio State University

127. Liu, Xiaoguang. Production of butyric acid and hydrogen by metabolically engineered mutants of Clostridium tyrobutyricum.

Degree: PhD, Chemical Engineering, 2005, The Ohio State University

 The main goal of this research was to develop an economical process for butyric acid and hydrogen production by Clostridium tyrobutyricum. First, metabolically engineered mutants,… (more)

Subjects/Keywords: fermentation; metabolic engineering; butyric acid; hydrogen

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APA (6th Edition):

Liu, X. (2005). Production of butyric acid and hydrogen by metabolically engineered mutants of Clostridium tyrobutyricum. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1124114266

Chicago Manual of Style (16th Edition):

Liu, Xiaoguang. “Production of butyric acid and hydrogen by metabolically engineered mutants of Clostridium tyrobutyricum.” 2005. Doctoral Dissertation, The Ohio State University. Accessed November 11, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1124114266.

MLA Handbook (7th Edition):

Liu, Xiaoguang. “Production of butyric acid and hydrogen by metabolically engineered mutants of Clostridium tyrobutyricum.” 2005. Web. 11 Nov 2019.

Vancouver:

Liu X. Production of butyric acid and hydrogen by metabolically engineered mutants of Clostridium tyrobutyricum. [Internet] [Doctoral dissertation]. The Ohio State University; 2005. [cited 2019 Nov 11]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1124114266.

Council of Science Editors:

Liu X. Production of butyric acid and hydrogen by metabolically engineered mutants of Clostridium tyrobutyricum. [Doctoral Dissertation]. The Ohio State University; 2005. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1124114266


Université de Montréal

128. Ghosh, Dipankar. Improving the microbial production of biofuels through metabolic engineering .

Degree: 2013, Université de Montréal

 Les défis conjoints du changement climatique d'origine anthropique et la diminution des réserves de combustibles fossiles sont le moteur de recherche intense pour des sources… (more)

Subjects/Keywords: Biocarburants; Production d'hydrogène; Photofermentation; Fermentation; Génie métabolique; Biofuel; Hydrogen production; Photofermentation; Dark fermentation; Metabolic engineering

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APA (6th Edition):

Ghosh, D. (2013). Improving the microbial production of biofuels through metabolic engineering . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/10227

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):

Ghosh, Dipankar. “Improving the microbial production of biofuels through metabolic engineering .” 2013. Thesis, Université de Montréal. Accessed November 11, 2019. http://hdl.handle.net/1866/10227.

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

MLA Handbook (7th Edition):

Ghosh, Dipankar. “Improving the microbial production of biofuels through metabolic engineering .” 2013. Web. 11 Nov 2019.

Vancouver:

Ghosh D. Improving the microbial production of biofuels through metabolic engineering . [Internet] [Thesis]. Université de Montréal; 2013. [cited 2019 Nov 11]. Available from: http://hdl.handle.net/1866/10227.

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

Council of Science Editors:

Ghosh D. Improving the microbial production of biofuels through metabolic engineering . [Thesis]. Université de Montréal; 2013. Available from: http://hdl.handle.net/1866/10227

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


Georgia State University

129. Wei, Mohui. Transforming Dihydroxyacetone Phosphate-Dependent Aldolases Mediated Aldol Reactions From Flask Reaction Into Cell-Based Synthesis & Studying The Mechanism Of Chemical Desialylation In The Life Processes.

Degree: PhD, Chemistry, 2016, Georgia State University

  Dihydroxyacetone phosphate (DHAP)-dependent aldolases have been intensively studied and widely used in the synthesis of carbohydrates and complex polyhydroxylated molecules. However, the strict specificity… (more)

Subjects/Keywords: DHAP-dependent aldolase; Metabolic engineering; E. coli synthetic machinery; Electrochemical desialylation; Desialylation mechanism

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APA (6th Edition):

Wei, M. (2016). Transforming Dihydroxyacetone Phosphate-Dependent Aldolases Mediated Aldol Reactions From Flask Reaction Into Cell-Based Synthesis & Studying The Mechanism Of Chemical Desialylation In The Life Processes. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_diss/121

Chicago Manual of Style (16th Edition):

Wei, Mohui. “Transforming Dihydroxyacetone Phosphate-Dependent Aldolases Mediated Aldol Reactions From Flask Reaction Into Cell-Based Synthesis & Studying The Mechanism Of Chemical Desialylation In The Life Processes.” 2016. Doctoral Dissertation, Georgia State University. Accessed November 11, 2019. https://scholarworks.gsu.edu/chemistry_diss/121.

MLA Handbook (7th Edition):

Wei, Mohui. “Transforming Dihydroxyacetone Phosphate-Dependent Aldolases Mediated Aldol Reactions From Flask Reaction Into Cell-Based Synthesis & Studying The Mechanism Of Chemical Desialylation In The Life Processes.” 2016. Web. 11 Nov 2019.

Vancouver:

Wei M. Transforming Dihydroxyacetone Phosphate-Dependent Aldolases Mediated Aldol Reactions From Flask Reaction Into Cell-Based Synthesis & Studying The Mechanism Of Chemical Desialylation In The Life Processes. [Internet] [Doctoral dissertation]. Georgia State University; 2016. [cited 2019 Nov 11]. Available from: https://scholarworks.gsu.edu/chemistry_diss/121.

Council of Science Editors:

Wei M. Transforming Dihydroxyacetone Phosphate-Dependent Aldolases Mediated Aldol Reactions From Flask Reaction Into Cell-Based Synthesis & Studying The Mechanism Of Chemical Desialylation In The Life Processes. [Doctoral Dissertation]. Georgia State University; 2016. Available from: https://scholarworks.gsu.edu/chemistry_diss/121


Case Western Reserve University

130. Fernandez, Charles Anthony. Isotopomer modeling and analysis in metabolic systems.

Degree: PhD, Biomedical Engineering, 1995, Case Western Reserve University

 Various methods are developed to analyze metabolic fluxes in isolated and intact metabolic systems using metabolically active molecules labeled with stable isotopes. Models that predict… (more)

Subjects/Keywords: Engineering, Biomedical; Isotopomer modeling; Metabolic Systems

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APA (6th Edition):

Fernandez, C. A. (1995). Isotopomer modeling and analysis in metabolic systems. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1058544437

Chicago Manual of Style (16th Edition):

Fernandez, Charles Anthony. “Isotopomer modeling and analysis in metabolic systems.” 1995. Doctoral Dissertation, Case Western Reserve University. Accessed November 11, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1058544437.

MLA Handbook (7th Edition):

Fernandez, Charles Anthony. “Isotopomer modeling and analysis in metabolic systems.” 1995. Web. 11 Nov 2019.

Vancouver:

Fernandez CA. Isotopomer modeling and analysis in metabolic systems. [Internet] [Doctoral dissertation]. Case Western Reserve University; 1995. [cited 2019 Nov 11]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1058544437.

Council of Science Editors:

Fernandez CA. Isotopomer modeling and analysis in metabolic systems. [Doctoral Dissertation]. Case Western Reserve University; 1995. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1058544437


Penn State University

131. Xu, Yu. SYNECHOCOCCUS SP. PCC 7002: A ROBUST AND VERSATILE CYANOBACTERIAL PLATFORM FOR BIOFUELS DEVELOPMENT.

Degree: PhD, Biochemistry, Microbiology, and Molecular Biology, 2010, Penn State University

 A cyanobacterial platform for biofuels or biofuel-related applications has been established in a marine cyanobacterium, Synechococcus sp. PCC 7002. To better understand H2-production mechanisms, the… (more)

Subjects/Keywords: carbohydrate; metabolic engineering; biofuel; cyanobacteria; hydrogen; gene expression; organic acid; co-culturing

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APA (6th Edition):

Xu, Y. (2010). SYNECHOCOCCUS SP. PCC 7002: A ROBUST AND VERSATILE CYANOBACTERIAL PLATFORM FOR BIOFUELS DEVELOPMENT. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/11032

Chicago Manual of Style (16th Edition):

Xu, Yu. “SYNECHOCOCCUS SP. PCC 7002: A ROBUST AND VERSATILE CYANOBACTERIAL PLATFORM FOR BIOFUELS DEVELOPMENT.” 2010. Doctoral Dissertation, Penn State University. Accessed November 11, 2019. https://etda.libraries.psu.edu/catalog/11032.

MLA Handbook (7th Edition):

Xu, Yu. “SYNECHOCOCCUS SP. PCC 7002: A ROBUST AND VERSATILE CYANOBACTERIAL PLATFORM FOR BIOFUELS DEVELOPMENT.” 2010. Web. 11 Nov 2019.

Vancouver:

Xu Y. SYNECHOCOCCUS SP. PCC 7002: A ROBUST AND VERSATILE CYANOBACTERIAL PLATFORM FOR BIOFUELS DEVELOPMENT. [Internet] [Doctoral dissertation]. Penn State University; 2010. [cited 2019 Nov 11]. Available from: https://etda.libraries.psu.edu/catalog/11032.

Council of Science Editors:

Xu Y. SYNECHOCOCCUS SP. PCC 7002: A ROBUST AND VERSATILE CYANOBACTERIAL PLATFORM FOR BIOFUELS DEVELOPMENT. [Doctoral Dissertation]. Penn State University; 2010. Available from: https://etda.libraries.psu.edu/catalog/11032


UCLA

132. Li, Xiaoqian. Engineering of Synthetic Reverse Glyoxylate Shunt Module for enhanced carbon incorporation in cyanobacteria.

Degree: Chemical Engineering, 2016, UCLA

 Synthetic Biology and Metabolic engineering research aim to elucidate the underlying principle of biological systems and enable a predicable cellular behavior through artificial design. In… (more)

Subjects/Keywords: Chemical engineering; carbon fixation; carbon incorporation; metabolic pathway design; reverse glyoxylate shunt; Synechococcus elongatus PCC7942

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APA (6th Edition):

Li, X. (2016). Engineering of Synthetic Reverse Glyoxylate Shunt Module for enhanced carbon incorporation in cyanobacteria. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/6k0975v7

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):

Li, Xiaoqian. “Engineering of Synthetic Reverse Glyoxylate Shunt Module for enhanced carbon incorporation in cyanobacteria.” 2016. Thesis, UCLA. Accessed November 11, 2019. http://www.escholarship.org/uc/item/6k0975v7.

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

MLA Handbook (7th Edition):

Li, Xiaoqian. “Engineering of Synthetic Reverse Glyoxylate Shunt Module for enhanced carbon incorporation in cyanobacteria.” 2016. Web. 11 Nov 2019.

Vancouver:

Li X. Engineering of Synthetic Reverse Glyoxylate Shunt Module for enhanced carbon incorporation in cyanobacteria. [Internet] [Thesis]. UCLA; 2016. [cited 2019 Nov 11]. Available from: http://www.escholarship.org/uc/item/6k0975v7.

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

Council of Science Editors:

Li X. Engineering of Synthetic Reverse Glyoxylate Shunt Module for enhanced carbon incorporation in cyanobacteria. [Thesis]. UCLA; 2016. Available from: http://www.escholarship.org/uc/item/6k0975v7

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


University of California – Berkeley

133. Yee, Nathan Alexander. Investigating Cancer Sialylation in Embryonic Zebrafish.

Degree: Chemistry, 2017, University of California – Berkeley

 Changes in glycosylation have been well-documented with regard to the onset and progression of cancer. Pervasive amongst these is the overexpression of cell surface sialic… (more)

Subjects/Keywords: Chemistry; Biology; bioorthogonal chemistry; cancer; fluorescence imaging; metabolic engineering; sialic acid; zebrafish

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APA (6th Edition):

Yee, N. A. (2017). Investigating Cancer Sialylation in Embryonic Zebrafish. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/7br6w966

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):

Yee, Nathan Alexander. “Investigating Cancer Sialylation in Embryonic Zebrafish.” 2017. Thesis, University of California – Berkeley. Accessed November 11, 2019. http://www.escholarship.org/uc/item/7br6w966.

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

MLA Handbook (7th Edition):

Yee, Nathan Alexander. “Investigating Cancer Sialylation in Embryonic Zebrafish.” 2017. Web. 11 Nov 2019.

Vancouver:

Yee NA. Investigating Cancer Sialylation in Embryonic Zebrafish. [Internet] [Thesis]. University of California – Berkeley; 2017. [cited 2019 Nov 11]. Available from: http://www.escholarship.org/uc/item/7br6w966.

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

Council of Science Editors:

Yee NA. Investigating Cancer Sialylation in Embryonic Zebrafish. [Thesis]. University of California – Berkeley; 2017. Available from: http://www.escholarship.org/uc/item/7br6w966

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

134. Tran, Kien Trung. Biofuels Production and Bioremediation using Glycerol by Genetic Engineering and Biochemical Approaches : 遺伝子工学と生物化学的アプローチによるグリセロールを活用したバイオ燃料生産とバイオレメディエーション.

Degree: 博士(工学), 2017, Kyushu Institute of Technology / 九州工業大学

Glycerol is the main byproduct from biodiesel production and expected to be a cheap feedstock for the production of useful substances. Furthermore, waste glycerol (WG)… (more)

Subjects/Keywords: Glycerol; Bio-hydrogen; Escherichia coli; Waste activated sludge; Metabolic engineering; Transposon mutagenesis

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APA (6th Edition):

Tran, K. T. (2017). Biofuels Production and Bioremediation using Glycerol by Genetic Engineering and Biochemical Approaches : 遺伝子工学と生物化学的アプローチによるグリセロールを活用したバイオ燃料生産とバイオレメディエーション. (Thesis). Kyushu Institute of Technology / 九州工業大学. Retrieved from http://hdl.handle.net/10228/5600

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):

Tran, Kien Trung. “Biofuels Production and Bioremediation using Glycerol by Genetic Engineering and Biochemical Approaches : 遺伝子工学と生物化学的アプローチによるグリセロールを活用したバイオ燃料生産とバイオレメディエーション.” 2017. Thesis, Kyushu Institute of Technology / 九州工業大学. Accessed November 11, 2019. http://hdl.handle.net/10228/5600.

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

MLA Handbook (7th Edition):

Tran, Kien Trung. “Biofuels Production and Bioremediation using Glycerol by Genetic Engineering and Biochemical Approaches : 遺伝子工学と生物化学的アプローチによるグリセロールを活用したバイオ燃料生産とバイオレメディエーション.” 2017. Web. 11 Nov 2019.

Vancouver:

Tran KT. Biofuels Production and Bioremediation using Glycerol by Genetic Engineering and Biochemical Approaches : 遺伝子工学と生物化学的アプローチによるグリセロールを活用したバイオ燃料生産とバイオレメディエーション. [Internet] [Thesis]. Kyushu Institute of Technology / 九州工業大学; 2017. [cited 2019 Nov 11]. Available from: http://hdl.handle.net/10228/5600.

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

Council of Science Editors:

Tran KT. Biofuels Production and Bioremediation using Glycerol by Genetic Engineering and Biochemical Approaches : 遺伝子工学と生物化学的アプローチによるグリセロールを活用したバイオ燃料生産とバイオレメディエーション. [Thesis]. Kyushu Institute of Technology / 九州工業大学; 2017. Available from: http://hdl.handle.net/10228/5600

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


Harvard University

135. Boyle, Patrick M. Network-Scale Engineering: Systems Approaches to Synthetic Biology.

Degree: PhD, Cell and Developmental Biology, 2012, Harvard University

 The field of Synthetic Biology seeks to develop engineering principles for biological systems. Modular biological parts are repurposed and recombined to develop new synthetic biological… (more)

Subjects/Keywords: bioenergy; metabolic engineering; metabolomics; synthetic biology; systems biology; cellular biology; systematic biology; genetics

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APA (6th Edition):

Boyle, P. M. (2012). Network-Scale Engineering: Systems Approaches to Synthetic Biology. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:9393259

Chicago Manual of Style (16th Edition):

Boyle, Patrick M. “Network-Scale Engineering: Systems Approaches to Synthetic Biology.” 2012. Doctoral Dissertation, Harvard University. Accessed November 11, 2019. http://nrs.harvard.edu/urn-3:HUL.InstRepos:9393259.

MLA Handbook (7th Edition):

Boyle, Patrick M. “Network-Scale Engineering: Systems Approaches to Synthetic Biology.” 2012. Web. 11 Nov 2019.

Vancouver:

Boyle PM. Network-Scale Engineering: Systems Approaches to Synthetic Biology. [Internet] [Doctoral dissertation]. Harvard University; 2012. [cited 2019 Nov 11]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:9393259.

Council of Science Editors:

Boyle PM. Network-Scale Engineering: Systems Approaches to Synthetic Biology. [Doctoral Dissertation]. Harvard University; 2012. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:9393259

136. Dusseaux, Simon. Ingénierie métabolique de Clostridium acetobutylicum pour la production d'isopropanol : Metabolic engineering of C. acetobutylicum for the production of isopropanol.

Degree: Docteur es, Ingénierie Microbienne et Enzymatique, 2014, Toulouse, INSA

Une stratégie d’ingénierie du métabolisme de C. acetobutylicum a été développée afin de construire une souche capable de produire de l’isopropanol à partir de sucres… (more)

Subjects/Keywords: Ingénierie métabolique; C. acetobutylicum; Isopropanol; Biocarburant; Metabolic engineering; C. acetobutylicum; Isopropanol; Biofuel; 572; 660.6

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APA (6th Edition):

Dusseaux, S. (2014). Ingénierie métabolique de Clostridium acetobutylicum pour la production d'isopropanol : Metabolic engineering of C. acetobutylicum for the production of isopropanol. (Doctoral Dissertation). Toulouse, INSA. Retrieved from http://www.theses.fr/2014ISAT0031

Chicago Manual of Style (16th Edition):

Dusseaux, Simon. “Ingénierie métabolique de Clostridium acetobutylicum pour la production d'isopropanol : Metabolic engineering of C. acetobutylicum for the production of isopropanol.” 2014. Doctoral Dissertation, Toulouse, INSA. Accessed November 11, 2019. http://www.theses.fr/2014ISAT0031.

MLA Handbook (7th Edition):

Dusseaux, Simon. “Ingénierie métabolique de Clostridium acetobutylicum pour la production d'isopropanol : Metabolic engineering of C. acetobutylicum for the production of isopropanol.” 2014. Web. 11 Nov 2019.

Vancouver:

Dusseaux S. Ingénierie métabolique de Clostridium acetobutylicum pour la production d'isopropanol : Metabolic engineering of C. acetobutylicum for the production of isopropanol. [Internet] [Doctoral dissertation]. Toulouse, INSA; 2014. [cited 2019 Nov 11]. Available from: http://www.theses.fr/2014ISAT0031.

Council of Science Editors:

Dusseaux S. Ingénierie métabolique de Clostridium acetobutylicum pour la production d'isopropanol : Metabolic engineering of C. acetobutylicum for the production of isopropanol. [Doctoral Dissertation]. Toulouse, INSA; 2014. Available from: http://www.theses.fr/2014ISAT0031

137. Collas, Florent. Production of isopropanol, butanol and ethanol by metabolic engineered Clostridia : Production of isopropanol, butanol and ethanol by metabolic engineered Clostridia.

Degree: Docteur es, Microbiologie et Biologie moléculaire, 2012, Paris, AgroParisTech

Au cours des dernières décennies, la fermentation IBE (isopropanol, butanol and éthanol) a connu un regain d'intérêt en vue de la production de carburants ou… (more)

Subjects/Keywords: Clostridia; Solvants; Isopropanol; Modification génétique; Butanol; Clostridia; Solvent; Isopropanol; Metabolic engineering; Butanol; 579.364

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APA (6th Edition):

Collas, F. (2012). Production of isopropanol, butanol and ethanol by metabolic engineered Clostridia : Production of isopropanol, butanol and ethanol by metabolic engineered Clostridia. (Doctoral Dissertation). Paris, AgroParisTech. Retrieved from http://www.theses.fr/2012AGPT0070

Chicago Manual of Style (16th Edition):

Collas, Florent. “Production of isopropanol, butanol and ethanol by metabolic engineered Clostridia : Production of isopropanol, butanol and ethanol by metabolic engineered Clostridia.” 2012. Doctoral Dissertation, Paris, AgroParisTech. Accessed November 11, 2019. http://www.theses.fr/2012AGPT0070.

MLA Handbook (7th Edition):

Collas, Florent. “Production of isopropanol, butanol and ethanol by metabolic engineered Clostridia : Production of isopropanol, butanol and ethanol by metabolic engineered Clostridia.” 2012. Web. 11 Nov 2019.

Vancouver:

Collas F. Production of isopropanol, butanol and ethanol by metabolic engineered Clostridia : Production of isopropanol, butanol and ethanol by metabolic engineered Clostridia. [Internet] [Doctoral dissertation]. Paris, AgroParisTech; 2012. [cited 2019 Nov 11]. Available from: http://www.theses.fr/2012AGPT0070.

Council of Science Editors:

Collas F. Production of isopropanol, butanol and ethanol by metabolic engineered Clostridia : Production of isopropanol, butanol and ethanol by metabolic engineered Clostridia. [Doctoral Dissertation]. Paris, AgroParisTech; 2012. Available from: http://www.theses.fr/2012AGPT0070


Ohio University

138. Kulkarni, Aditya S. Metabolic Studies of Albomycin Biosynthesis.

Degree: PhD, Biological Sciences (Arts and Sciences), 2015, Ohio University

 Albomycin is a sulfur containing metabolite produced by Streptomcyes sp. ATCC 700974. It is a structurally unique molecule with potent antibiotic activity. Unfortunately, it is… (more)

Subjects/Keywords: Microbiology; Molecular Biology; Biochemistry; Albomycin; sulfur metabolism; secondary metabolite biosynthesis; metabolic engineering; Streptomyces

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APA (6th Edition):

Kulkarni, A. S. (2015). Metabolic Studies of Albomycin Biosynthesis. (Doctoral Dissertation). Ohio University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1439979936

Chicago Manual of Style (16th Edition):

Kulkarni, Aditya S. “Metabolic Studies of Albomycin Biosynthesis.” 2015. Doctoral Dissertation, Ohio University. Accessed November 11, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1439979936.

MLA Handbook (7th Edition):

Kulkarni, Aditya S. “Metabolic Studies of Albomycin Biosynthesis.” 2015. Web. 11 Nov 2019.

Vancouver:

Kulkarni AS. Metabolic Studies of Albomycin Biosynthesis. [Internet] [Doctoral dissertation]. Ohio University; 2015. [cited 2019 Nov 11]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1439979936.

Council of Science Editors:

Kulkarni AS. Metabolic Studies of Albomycin Biosynthesis. [Doctoral Dissertation]. Ohio University; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1439979936


Iowa State University

139. Boggess, Erin. Methods for analysis of derivative strains from metabolic evolution experiments.

Degree: 2018, Iowa State University

 One of the largest challenges in genomics studies is determining the relationship between genotype and phenotype and then applying this knowledge to design principles. Metabolic(more)

Subjects/Keywords: Evolution; Gene regulatory networks; Metabolic engineering; Mutation analysis; Reverse enginering; Strain design; Bioinformatics

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APA (6th Edition):

Boggess, E. (2018). Methods for analysis of derivative strains from metabolic evolution experiments. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/16766

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):

Boggess, Erin. “Methods for analysis of derivative strains from metabolic evolution experiments.” 2018. Thesis, Iowa State University. Accessed November 11, 2019. https://lib.dr.iastate.edu/etd/16766.

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

MLA Handbook (7th Edition):

Boggess, Erin. “Methods for analysis of derivative strains from metabolic evolution experiments.” 2018. Web. 11 Nov 2019.

Vancouver:

Boggess E. Methods for analysis of derivative strains from metabolic evolution experiments. [Internet] [Thesis]. Iowa State University; 2018. [cited 2019 Nov 11]. Available from: https://lib.dr.iastate.edu/etd/16766.

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

Council of Science Editors:

Boggess E. Methods for analysis of derivative strains from metabolic evolution experiments. [Thesis]. Iowa State University; 2018. Available from: https://lib.dr.iastate.edu/etd/16766

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


Boston University

140. Zhao, Qi. Control and optimization methods in biomedical systems: from cells to humans.

Degree: PhD, Systems Engineering, 2016, Boston University

 Optimization and control theory are well developed techniques to quantize, model, understand and optimize real world systems and they have been widely used in engineering,… (more)

Subjects/Keywords: Biomedical engineering; Inverse optimization; Metabolic network; Pharmacokinetics; Predictive model; Microbial ecosystem; Nonlinear opimization

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APA (6th Edition):

Zhao, Q. (2016). Control and optimization methods in biomedical systems: from cells to humans. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/17071

Chicago Manual of Style (16th Edition):

Zhao, Qi. “Control and optimization methods in biomedical systems: from cells to humans.” 2016. Doctoral Dissertation, Boston University. Accessed November 11, 2019. http://hdl.handle.net/2144/17071.

MLA Handbook (7th Edition):

Zhao, Qi. “Control and optimization methods in biomedical systems: from cells to humans.” 2016. Web. 11 Nov 2019.

Vancouver:

Zhao Q. Control and optimization methods in biomedical systems: from cells to humans. [Internet] [Doctoral dissertation]. Boston University; 2016. [cited 2019 Nov 11]. Available from: http://hdl.handle.net/2144/17071.

Council of Science Editors:

Zhao Q. Control and optimization methods in biomedical systems: from cells to humans. [Doctoral Dissertation]. Boston University; 2016. Available from: http://hdl.handle.net/2144/17071


The Ohio State University

141. Seethapathi, Nidhi, Seethapathi. Transients, Variability, Stability and Energy in Human Locomotion.

Degree: PhD, Mechanical Engineering, 2018, The Ohio State University

 Most research in human locomotion is limited to steady-state, constant speed and symmetric locomotion behaviors. However, walking and running in everyday life requires us to… (more)

Subjects/Keywords: Mechanical Engineering; locomotion, metabolic energy, amputee, rehabilitation, asymmetric walking, stability, control, running

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APA (6th Edition):

Seethapathi, Nidhi, S. (2018). Transients, Variability, Stability and Energy in Human Locomotion. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1534590933898397

Chicago Manual of Style (16th Edition):

Seethapathi, Nidhi, Seethapathi. “Transients, Variability, Stability and Energy in Human Locomotion.” 2018. Doctoral Dissertation, The Ohio State University. Accessed November 11, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1534590933898397.

MLA Handbook (7th Edition):

Seethapathi, Nidhi, Seethapathi. “Transients, Variability, Stability and Energy in Human Locomotion.” 2018. Web. 11 Nov 2019.

Vancouver:

Seethapathi, Nidhi S. Transients, Variability, Stability and Energy in Human Locomotion. [Internet] [Doctoral dissertation]. The Ohio State University; 2018. [cited 2019 Nov 11]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1534590933898397.

Council of Science Editors:

Seethapathi, Nidhi S. Transients, Variability, Stability and Energy in Human Locomotion. [Doctoral Dissertation]. The Ohio State University; 2018. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1534590933898397


Virginia Tech

142. Yen, Jiun Yang. Model-guided Analysis of Plant Metabolism and Design of Metabolic Engineering Strategies.

Degree: PhD, Biological Systems Engineering, 2017, Virginia Tech

 Advances in bioinformatics and computational biology have enabled integration of an enormous amount of known biological interactions. This has enabled researchers to use models and… (more)

Subjects/Keywords: genome-scale model; metabolic engineering; plant; Arabidopsis thaliana; energy metabolism; flux balance analysis

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APA (6th Edition):

Yen, J. Y. (2017). Model-guided Analysis of Plant Metabolism and Design of Metabolic Engineering Strategies. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/85179

Chicago Manual of Style (16th Edition):

Yen, Jiun Yang. “Model-guided Analysis of Plant Metabolism and Design of Metabolic Engineering Strategies.” 2017. Doctoral Dissertation, Virginia Tech. Accessed November 11, 2019. http://hdl.handle.net/10919/85179.

MLA Handbook (7th Edition):

Yen, Jiun Yang. “Model-guided Analysis of Plant Metabolism and Design of Metabolic Engineering Strategies.” 2017. Web. 11 Nov 2019.

Vancouver:

Yen JY. Model-guided Analysis of Plant Metabolism and Design of Metabolic Engineering Strategies. [Internet] [Doctoral dissertation]. Virginia Tech; 2017. [cited 2019 Nov 11]. Available from: http://hdl.handle.net/10919/85179.

Council of Science Editors:

Yen JY. Model-guided Analysis of Plant Metabolism and Design of Metabolic Engineering Strategies. [Doctoral Dissertation]. Virginia Tech; 2017. Available from: http://hdl.handle.net/10919/85179


The Ohio State University

143. Lehtinen, Kevin M. Human stepping response to perturbations during quiet standing:experiments and predictions from metabolic energy optimization.

Degree: MS, Mechanical Engineering, 2016, The Ohio State University

 The mechanical complexity of humans allows for many possible ways of stabilizing quiet standing. Here, we test the hypothesis that humans, when pushed or pulled… (more)

Subjects/Keywords: Mechanical Engineering; Human stepping response, perturbations, quiet standing, experiments and predictions, metabolic energy optimization

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APA (6th Edition):

Lehtinen, K. M. (2016). Human stepping response to perturbations during quiet standing:experiments and predictions from metabolic energy optimization. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1469131665

Chicago Manual of Style (16th Edition):

Lehtinen, Kevin M. “Human stepping response to perturbations during quiet standing:experiments and predictions from metabolic energy optimization.” 2016. Masters Thesis, The Ohio State University. Accessed November 11, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1469131665.

MLA Handbook (7th Edition):

Lehtinen, Kevin M. “Human stepping response to perturbations during quiet standing:experiments and predictions from metabolic energy optimization.” 2016. Web. 11 Nov 2019.

Vancouver:

Lehtinen KM. Human stepping response to perturbations during quiet standing:experiments and predictions from metabolic energy optimization. [Internet] [Masters thesis]. The Ohio State University; 2016. [cited 2019 Nov 11]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1469131665.

Council of Science Editors:

Lehtinen KM. Human stepping response to perturbations during quiet standing:experiments and predictions from metabolic energy optimization. [Masters Thesis]. The Ohio State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1469131665


University of Toronto

144. Pandit, Aditya. An in silico Characterization of Microbial Electrosynthesis for Metabolic Engineering of Biochemicals.

Degree: 2012, University of Toronto

A critical concern in metabolic engineering is the need to balance the demand and supply of redox intermediates. Bioelectrochemical techniques offer a promising method to… (more)

Subjects/Keywords: in silico; bioelectrosynthesis; metabolic engineering; flux balance analysis; microbial electrosynthesis; SPEEQ; 0542

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APA (6th Edition):

Pandit, A. (2012). An in silico Characterization of Microbial Electrosynthesis for Metabolic Engineering of Biochemicals. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/32616

Chicago Manual of Style (16th Edition):

Pandit, Aditya. “An in silico Characterization of Microbial Electrosynthesis for Metabolic Engineering of Biochemicals.” 2012. Masters Thesis, University of Toronto. Accessed November 11, 2019. http://hdl.handle.net/1807/32616.

MLA Handbook (7th Edition):

Pandit, Aditya. “An in silico Characterization of Microbial Electrosynthesis for Metabolic Engineering of Biochemicals.” 2012. Web. 11 Nov 2019.

Vancouver:

Pandit A. An in silico Characterization of Microbial Electrosynthesis for Metabolic Engineering of Biochemicals. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2019 Nov 11]. Available from: http://hdl.handle.net/1807/32616.

Council of Science Editors:

Pandit A. An in silico Characterization of Microbial Electrosynthesis for Metabolic Engineering of Biochemicals. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/32616


University of Waterloo

145. Mozell, Bradley. Production of 3-hydroxy acids from acetate in engineered Escherichia coli.

Degree: 2018, University of Waterloo

 Acetate serves as an uncommon carbon source for metabolic engineering of value-added chemicals. As a carbon source, acetate has unique advantages since it is not… (more)

Subjects/Keywords: Acetate; Escherichia coli; 3-hydroxy acid; metabolic engineering; 3-hydroxybutyrate; 3-hydroxyvalerate

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APA (6th Edition):

Mozell, B. (2018). Production of 3-hydroxy acids from acetate in engineered Escherichia coli. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/13900

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):

Mozell, Bradley. “Production of 3-hydroxy acids from acetate in engineered Escherichia coli.” 2018. Thesis, University of Waterloo. Accessed November 11, 2019. http://hdl.handle.net/10012/13900.

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

MLA Handbook (7th Edition):

Mozell, Bradley. “Production of 3-hydroxy acids from acetate in engineered Escherichia coli.” 2018. Web. 11 Nov 2019.

Vancouver:

Mozell B. Production of 3-hydroxy acids from acetate in engineered Escherichia coli. [Internet] [Thesis]. University of Waterloo; 2018. [cited 2019 Nov 11]. Available from: http://hdl.handle.net/10012/13900.

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

Council of Science Editors:

Mozell B. Production of 3-hydroxy acids from acetate in engineered Escherichia coli. [Thesis]. University of Waterloo; 2018. Available from: http://hdl.handle.net/10012/13900

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


University of Minnesota

146. Bloch, Sarah E. Plant phenylpropanoid biosynthesis in Escherichia coli: engineering novel pathways and tools.

Degree: PhD, Biochemistry, Molecular Bio, and Biophysics, 2014, University of Minnesota

 Plant phenylpropanoid natural products are important in the discovery of safe and effective therapeutics. Most plant natural products cannot be economically mass produced via extraction… (more)

Subjects/Keywords: Bacterial microcompartments; Biosynthesis; Metabolic engineering; Microbial production; Natural products; Phenylpropanoid; Biochemistry, molecular bio, and biophysics

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APA (6th Edition):

Bloch, S. E. (2014). Plant phenylpropanoid biosynthesis in Escherichia coli: engineering novel pathways and tools. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/168157

Chicago Manual of Style (16th Edition):

Bloch, Sarah E. “Plant phenylpropanoid biosynthesis in Escherichia coli: engineering novel pathways and tools.” 2014. Doctoral Dissertation, University of Minnesota. Accessed November 11, 2019. http://hdl.handle.net/11299/168157.

MLA Handbook (7th Edition):

Bloch, Sarah E. “Plant phenylpropanoid biosynthesis in Escherichia coli: engineering novel pathways and tools.” 2014. Web. 11 Nov 2019.

Vancouver:

Bloch SE. Plant phenylpropanoid biosynthesis in Escherichia coli: engineering novel pathways and tools. [Internet] [Doctoral dissertation]. University of Minnesota; 2014. [cited 2019 Nov 11]. Available from: http://hdl.handle.net/11299/168157.

Council of Science Editors:

Bloch SE. Plant phenylpropanoid biosynthesis in Escherichia coli: engineering novel pathways and tools. [Doctoral Dissertation]. University of Minnesota; 2014. Available from: http://hdl.handle.net/11299/168157


University of Illinois – Urbana-Champaign

147. Turner, Timothy Lee. Engineering and evaluation of yeast strains for the production of lactic acid from cellulosic sugars.

Degree: PhD, Food Science & Human Nutrition, 2016, University of Illinois – Urbana-Champaign

 Terrestrial biomass consists largely of lignocellulosic materials. Abundant in nature, lignocellulosic biomass can be cultivated easily on land otherwise unsuitable for traditional crops or be… (more)

Subjects/Keywords: Yeast; Lactic acid; Metabolic engineering; JEN1; ADY2; Xylose; Cellobiose; Lignocellulosic; Saccharomyces cerevisiae

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APA (6th Edition):

Turner, T. L. (2016). Engineering and evaluation of yeast strains for the production of lactic acid from cellulosic sugars. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/92933

Chicago Manual of Style (16th Edition):

Turner, Timothy Lee. “Engineering and evaluation of yeast strains for the production of lactic acid from cellulosic sugars.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed November 11, 2019. http://hdl.handle.net/2142/92933.

MLA Handbook (7th Edition):

Turner, Timothy Lee. “Engineering and evaluation of yeast strains for the production of lactic acid from cellulosic sugars.” 2016. Web. 11 Nov 2019.

Vancouver:

Turner TL. Engineering and evaluation of yeast strains for the production of lactic acid from cellulosic sugars. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Nov 11]. Available from: http://hdl.handle.net/2142/92933.

Council of Science Editors:

Turner TL. Engineering and evaluation of yeast strains for the production of lactic acid from cellulosic sugars. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/92933


University of Delaware

148. Fast, Alan Gregory. Engineering bacterial CO2 fixation to enhance biofuel and biochemical yields .

Degree: 2017, University of Delaware

 The mass production of biofuels and chemicals through microbial fermentation is renewable solution to combat climate change through decreased greenhouse gas emissions. The primary factor… (more)

Subjects/Keywords: Pure sciences; Biological sciences; Applied sciences; Biofuels; Carbon fixation; Metabolic engineering; Wood-Ljungdahl pathway

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APA (6th Edition):

Fast, A. G. (2017). Engineering bacterial CO2 fixation to enhance biofuel and biochemical yields . (Doctoral Dissertation). University of Delaware. Retrieved from http://udspace.udel.edu/handle/19716/23119

Chicago Manual of Style (16th Edition):

Fast, Alan Gregory. “Engineering bacterial CO2 fixation to enhance biofuel and biochemical yields .” 2017. Doctoral Dissertation, University of Delaware. Accessed November 11, 2019. http://udspace.udel.edu/handle/19716/23119.

MLA Handbook (7th Edition):

Fast, Alan Gregory. “Engineering bacterial CO2 fixation to enhance biofuel and biochemical yields .” 2017. Web. 11 Nov 2019.

Vancouver:

Fast AG. Engineering bacterial CO2 fixation to enhance biofuel and biochemical yields . [Internet] [Doctoral dissertation]. University of Delaware; 2017. [cited 2019 Nov 11]. Available from: http://udspace.udel.edu/handle/19716/23119.

Council of Science Editors:

Fast AG. Engineering bacterial CO2 fixation to enhance biofuel and biochemical yields . [Doctoral Dissertation]. University of Delaware; 2017. Available from: http://udspace.udel.edu/handle/19716/23119


Rice University

149. Sun, Ruiqiang. Improved Understanding of Apoptosis and Metabolism in Chinese Hamster Ovary Cell Culture.

Degree: MS, Engineering, 2011, Rice University

 Mammalian cell culture has gained importance in biotechnology for the development of therapeutic and diagnostic agents. Among them, Chinese hamster ovary (CHO) cells are regarded… (more)

Subjects/Keywords: Applied sciences; Biological sciences; Apoptosis; Metabolic flux; Cell separation; Systematic biology; Chemical engineering; Bioinformatics

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APA (6th Edition):

Sun, R. (2011). Improved Understanding of Apoptosis and Metabolism in Chinese Hamster Ovary Cell Culture. (Masters Thesis). Rice University. Retrieved from http://hdl.handle.net/1911/70459

Chicago Manual of Style (16th Edition):

Sun, Ruiqiang. “Improved Understanding of Apoptosis and Metabolism in Chinese Hamster Ovary Cell Culture.” 2011. Masters Thesis, Rice University. Accessed November 11, 2019. http://hdl.handle.net/1911/70459.

MLA Handbook (7th Edition):

Sun, Ruiqiang. “Improved Understanding of Apoptosis and Metabolism in Chinese Hamster Ovary Cell Culture.” 2011. Web. 11 Nov 2019.

Vancouver:

Sun R. Improved Understanding of Apoptosis and Metabolism in Chinese Hamster Ovary Cell Culture. [Internet] [Masters thesis]. Rice University; 2011. [cited 2019 Nov 11]. Available from: http://hdl.handle.net/1911/70459.

Council of Science Editors:

Sun R. Improved Understanding of Apoptosis and Metabolism in Chinese Hamster Ovary Cell Culture. [Masters Thesis]. Rice University; 2011. Available from: http://hdl.handle.net/1911/70459


Brigham Young University

150. Hu, Peng. Thermodynamic, Sulfide, Redox Potential, and pH Effects on Syngas Fermentation.

Degree: PhD, 2011, Brigham Young University

 Recently, work in ethanol production is exploring the fermentation of syngas (primarily CO, CO2, and H2) following gasification of cellulosic biomass. The syngas fermentation by… (more)

Subjects/Keywords: ethanol; syngas; fermentation; Wood-Ljungdahl metabolic pathway; thermodynamics; redox potential; pH; Chemical Engineering

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

APA (6th Edition):

Hu, P. (2011). Thermodynamic, Sulfide, Redox Potential, and pH Effects on Syngas Fermentation. (Doctoral Dissertation). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=3918&context=etd

Chicago Manual of Style (16th Edition):

Hu, Peng. “Thermodynamic, Sulfide, Redox Potential, and pH Effects on Syngas Fermentation.” 2011. Doctoral Dissertation, Brigham Young University. Accessed November 11, 2019. https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=3918&context=etd.

MLA Handbook (7th Edition):

Hu, Peng. “Thermodynamic, Sulfide, Redox Potential, and pH Effects on Syngas Fermentation.” 2011. Web. 11 Nov 2019.

Vancouver:

Hu P. Thermodynamic, Sulfide, Redox Potential, and pH Effects on Syngas Fermentation. [Internet] [Doctoral dissertation]. Brigham Young University; 2011. [cited 2019 Nov 11]. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=3918&context=etd.

Council of Science Editors:

Hu P. Thermodynamic, Sulfide, Redox Potential, and pH Effects on Syngas Fermentation. [Doctoral Dissertation]. Brigham Young University; 2011. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=3918&context=etd

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