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You searched for +publisher:"University of Texas – Austin" +contributor:("Liu, Hung-wen, 1952-"). Showing records 1 – 16 of 16 total matches.

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University of Texas – Austin

1. Kim, Nam Ho, 1975-. Mechanistic investigations of SpnF- and SpnL-catalyzed cyclizations in the biosynthesis of spinosyn A.

Degree: PhD, Pharmacy, 2013, University of Texas – Austin

 Spinosyn A is a particularly interesting natural product due to its structural complexity and potent insecticidal activity. The biosynthetic pathway of spinosyn A is interesting… (more)

Subjects/Keywords: Spinosyn A; Cyclization; Cycloaddition; SpnF; SpnL; Mechanism; Diels-Alder; Rauhut-Currier; Kinetic isotope effect; Mechanism-based inhibitor

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APA (6th Edition):

Kim, Nam Ho, 1. (2013). Mechanistic investigations of SpnF- and SpnL-catalyzed cyclizations in the biosynthesis of spinosyn A. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/28735

Chicago Manual of Style (16th Edition):

Kim, Nam Ho, 1975-. “Mechanistic investigations of SpnF- and SpnL-catalyzed cyclizations in the biosynthesis of spinosyn A.” 2013. Doctoral Dissertation, University of Texas – Austin. Accessed August 11, 2020. http://hdl.handle.net/2152/28735.

MLA Handbook (7th Edition):

Kim, Nam Ho, 1975-. “Mechanistic investigations of SpnF- and SpnL-catalyzed cyclizations in the biosynthesis of spinosyn A.” 2013. Web. 11 Aug 2020.

Vancouver:

Kim, Nam Ho 1. Mechanistic investigations of SpnF- and SpnL-catalyzed cyclizations in the biosynthesis of spinosyn A. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2013. [cited 2020 Aug 11]. Available from: http://hdl.handle.net/2152/28735.

Council of Science Editors:

Kim, Nam Ho 1. Mechanistic investigations of SpnF- and SpnL-catalyzed cyclizations in the biosynthesis of spinosyn A. [Doctoral Dissertation]. University of Texas – Austin; 2013. Available from: http://hdl.handle.net/2152/28735


University of Texas – Austin

2. Thibodeaux, Christopher James. Mechanistic studies of two enzymes that employ common coenzymes in uncommon ways.

Degree: PhD, Cell and Molecular Biology, 2010, University of Texas – Austin

 Enzymes are biological catalysts which greatly accelerate the rates of chemical reactions, oftentimes by many orders of magnitude over the uncatalyzed reaction. The remarkable catalytic… (more)

Subjects/Keywords: Enzyme catalysis; Isoprenoid biosynthesis; IDI-2; ACCD; Chemical mechanism

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APA (6th Edition):

Thibodeaux, C. J. (2010). Mechanistic studies of two enzymes that employ common coenzymes in uncommon ways. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/22160

Chicago Manual of Style (16th Edition):

Thibodeaux, Christopher James. “Mechanistic studies of two enzymes that employ common coenzymes in uncommon ways.” 2010. Doctoral Dissertation, University of Texas – Austin. Accessed August 11, 2020. http://hdl.handle.net/2152/22160.

MLA Handbook (7th Edition):

Thibodeaux, Christopher James. “Mechanistic studies of two enzymes that employ common coenzymes in uncommon ways.” 2010. Web. 11 Aug 2020.

Vancouver:

Thibodeaux CJ. Mechanistic studies of two enzymes that employ common coenzymes in uncommon ways. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2010. [cited 2020 Aug 11]. Available from: http://hdl.handle.net/2152/22160.

Council of Science Editors:

Thibodeaux CJ. Mechanistic studies of two enzymes that employ common coenzymes in uncommon ways. [Doctoral Dissertation]. University of Texas – Austin; 2010. Available from: http://hdl.handle.net/2152/22160


University of Texas – Austin

3. Choi, Sei Hyun. Synthetic approaches to investigate the chemical mechanism in the biosynthesis of natural products.

Degree: PhD, Chemistry, 2012, University of Texas – Austin

 The study of the biosynthetic logic of natural products has established itself to be one of the more exciting areas of research and have become… (more)

Subjects/Keywords: Natural product; Chemical mechanism; Organic synthesis; Spinosyn; Diels-Alder reaction; Rauhut-Currier reaction; Apiose; AXS; Desii; Radical SAM enzyme

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APA (6th Edition):

Choi, S. H. (2012). Synthetic approaches to investigate the chemical mechanism in the biosynthesis of natural products. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/26079

Chicago Manual of Style (16th Edition):

Choi, Sei Hyun. “Synthetic approaches to investigate the chemical mechanism in the biosynthesis of natural products.” 2012. Doctoral Dissertation, University of Texas – Austin. Accessed August 11, 2020. http://hdl.handle.net/2152/26079.

MLA Handbook (7th Edition):

Choi, Sei Hyun. “Synthetic approaches to investigate the chemical mechanism in the biosynthesis of natural products.” 2012. Web. 11 Aug 2020.

Vancouver:

Choi SH. Synthetic approaches to investigate the chemical mechanism in the biosynthesis of natural products. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2012. [cited 2020 Aug 11]. Available from: http://hdl.handle.net/2152/26079.

Council of Science Editors:

Choi SH. Synthetic approaches to investigate the chemical mechanism in the biosynthesis of natural products. [Doctoral Dissertation]. University of Texas – Austin; 2012. Available from: http://hdl.handle.net/2152/26079

4. Kim, Hak Joong, 1974-. Investigation of the post-polyketide synthase (PKS) modifications during spinosyn A biosynthesis in Saccharopolyspora spinosa.

Degree: PhD, Chemistry, 2010, University of Texas – Austin

 Diverse biological activities of polyketide natural products are often associated with specific structural motifs, biosynthetically introduced after construction of the polyketide core. Therefore, investigation of… (more)

Subjects/Keywords: Polyketide; Biosynthesis; Spinosyn; Methyltransferase; Diels-Alderase; Rauhut-Currier reaction; Intramolecular C-C bond formation; Kinetics; Enzyme mechanism

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APA (6th Edition):

Kim, Hak Joong, 1. (2010). Investigation of the post-polyketide synthase (PKS) modifications during spinosyn A biosynthesis in Saccharopolyspora spinosa. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/22143

Chicago Manual of Style (16th Edition):

Kim, Hak Joong, 1974-. “Investigation of the post-polyketide synthase (PKS) modifications during spinosyn A biosynthesis in Saccharopolyspora spinosa.” 2010. Doctoral Dissertation, University of Texas – Austin. Accessed August 11, 2020. http://hdl.handle.net/2152/22143.

MLA Handbook (7th Edition):

Kim, Hak Joong, 1974-. “Investigation of the post-polyketide synthase (PKS) modifications during spinosyn A biosynthesis in Saccharopolyspora spinosa.” 2010. Web. 11 Aug 2020.

Vancouver:

Kim, Hak Joong 1. Investigation of the post-polyketide synthase (PKS) modifications during spinosyn A biosynthesis in Saccharopolyspora spinosa. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2010. [cited 2020 Aug 11]. Available from: http://hdl.handle.net/2152/22143.

Council of Science Editors:

Kim, Hak Joong 1. Investigation of the post-polyketide synthase (PKS) modifications during spinosyn A biosynthesis in Saccharopolyspora spinosa. [Doctoral Dissertation]. University of Texas – Austin; 2010. Available from: http://hdl.handle.net/2152/22143

5. Zhou, Ying, 1977-. Studies of the metal binding properties and DNA recognition mode of the unusual zinc fingers in poly(ADP-ribose) Polymerase-1 and the investigation of its interaction with apoptosis inducing factor (AIF).

Degree: PhD, Cell and Molecular Biology, 2009, University of Texas – Austin

 Poly(ADP-ribosyl)ation, a covalent modification of proteins catalyzed by poly(ADP-ribose) polymerases (PARPs), plays a crucial role in regulating DNA repair, DNA replication, and cell death. Poly(ADP-ribose)… (more)

Subjects/Keywords: DNA repair; Poly(ADP-ribosyl)ation; Poly(ADP-ribose) polymerases; Poly(ADP-ribose) Polymerase-1; Zinc fingers; PARP; DNA-binding protein; DNA-binding properties; Apoptosis

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APA (6th Edition):

Zhou, Ying, 1. (2009). Studies of the metal binding properties and DNA recognition mode of the unusual zinc fingers in poly(ADP-ribose) Polymerase-1 and the investigation of its interaction with apoptosis inducing factor (AIF). (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/21906

Chicago Manual of Style (16th Edition):

Zhou, Ying, 1977-. “Studies of the metal binding properties and DNA recognition mode of the unusual zinc fingers in poly(ADP-ribose) Polymerase-1 and the investigation of its interaction with apoptosis inducing factor (AIF).” 2009. Doctoral Dissertation, University of Texas – Austin. Accessed August 11, 2020. http://hdl.handle.net/2152/21906.

MLA Handbook (7th Edition):

Zhou, Ying, 1977-. “Studies of the metal binding properties and DNA recognition mode of the unusual zinc fingers in poly(ADP-ribose) Polymerase-1 and the investigation of its interaction with apoptosis inducing factor (AIF).” 2009. Web. 11 Aug 2020.

Vancouver:

Zhou, Ying 1. Studies of the metal binding properties and DNA recognition mode of the unusual zinc fingers in poly(ADP-ribose) Polymerase-1 and the investigation of its interaction with apoptosis inducing factor (AIF). [Internet] [Doctoral dissertation]. University of Texas – Austin; 2009. [cited 2020 Aug 11]. Available from: http://hdl.handle.net/2152/21906.

Council of Science Editors:

Zhou, Ying 1. Studies of the metal binding properties and DNA recognition mode of the unusual zinc fingers in poly(ADP-ribose) Polymerase-1 and the investigation of its interaction with apoptosis inducing factor (AIF). [Doctoral Dissertation]. University of Texas – Austin; 2009. Available from: http://hdl.handle.net/2152/21906


University of Texas – Austin

6. White-Phillip, Jessica Ann. Glycosylation reactions in secondary metabolism : glycosylation events in C-mannosylation and the biosynthesis of kijanimicin.

Degree: PhD, Cell and Molecular Biology, 2010, University of Texas – Austin

 In this work, we examine two disparate aspects of glycosylation. The first project involves the elucidation of the glycosylation of the novel tetronolide natural product,… (more)

Subjects/Keywords: C-mannosylation; Kijanimicin glycosylation; TDP-L-digitoxose

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APA (6th Edition):

White-Phillip, J. A. (2010). Glycosylation reactions in secondary metabolism : glycosylation events in C-mannosylation and the biosynthesis of kijanimicin. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/30539

Chicago Manual of Style (16th Edition):

White-Phillip, Jessica Ann. “Glycosylation reactions in secondary metabolism : glycosylation events in C-mannosylation and the biosynthesis of kijanimicin.” 2010. Doctoral Dissertation, University of Texas – Austin. Accessed August 11, 2020. http://hdl.handle.net/2152/30539.

MLA Handbook (7th Edition):

White-Phillip, Jessica Ann. “Glycosylation reactions in secondary metabolism : glycosylation events in C-mannosylation and the biosynthesis of kijanimicin.” 2010. Web. 11 Aug 2020.

Vancouver:

White-Phillip JA. Glycosylation reactions in secondary metabolism : glycosylation events in C-mannosylation and the biosynthesis of kijanimicin. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2010. [cited 2020 Aug 11]. Available from: http://hdl.handle.net/2152/30539.

Council of Science Editors:

White-Phillip JA. Glycosylation reactions in secondary metabolism : glycosylation events in C-mannosylation and the biosynthesis of kijanimicin. [Doctoral Dissertation]. University of Texas – Austin; 2010. Available from: http://hdl.handle.net/2152/30539


University of Texas – Austin

7. Wu, Meilan. DNA recognition and mechanistic investigation of poly(ADP-ribose) polymerase-1.

Degree: PhD, Pharmaceutical Sciences, 2014, University of Texas – Austin

 Human PARP-1 is a nuclear protein containing six functional domains that catalyzes the poly(ADP-ribosyl)ation of a variety of protein substrates including itself. This process involves… (more)

Subjects/Keywords: Poly(ADP-ribosyl)ation; PARP-1

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APA (6th Edition):

Wu, M. (2014). DNA recognition and mechanistic investigation of poly(ADP-ribose) polymerase-1. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/62238

Chicago Manual of Style (16th Edition):

Wu, Meilan. “DNA recognition and mechanistic investigation of poly(ADP-ribose) polymerase-1.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed August 11, 2020. http://hdl.handle.net/2152/62238.

MLA Handbook (7th Edition):

Wu, Meilan. “DNA recognition and mechanistic investigation of poly(ADP-ribose) polymerase-1.” 2014. Web. 11 Aug 2020.

Vancouver:

Wu M. DNA recognition and mechanistic investigation of poly(ADP-ribose) polymerase-1. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2020 Aug 11]. Available from: http://hdl.handle.net/2152/62238.

Council of Science Editors:

Wu M. DNA recognition and mechanistic investigation of poly(ADP-ribose) polymerase-1. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/62238


University of Texas – Austin

8. Ko, Yeonjin. Unusual carbohydrate biosynthesis : mechanistic studies of DesII and the biosynthesis of formycin A.

Degree: PhD, Chemistry, 2017, University of Texas – Austin

 Carbohydrates are essential biomolecules in all living organisms. Besides serving as energy storage and structural building blocks in primary metabolism, carbohydrates represent the building blocks… (more)

Subjects/Keywords: DesII; Formycin; Formycin A; Carbohydrate biosynthesis; Biosynthetic pathways; Radical intermediates

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APA (6th Edition):

Ko, Y. (2017). Unusual carbohydrate biosynthesis : mechanistic studies of DesII and the biosynthesis of formycin A. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/47151

Chicago Manual of Style (16th Edition):

Ko, Yeonjin. “Unusual carbohydrate biosynthesis : mechanistic studies of DesII and the biosynthesis of formycin A.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed August 11, 2020. http://hdl.handle.net/2152/47151.

MLA Handbook (7th Edition):

Ko, Yeonjin. “Unusual carbohydrate biosynthesis : mechanistic studies of DesII and the biosynthesis of formycin A.” 2017. Web. 11 Aug 2020.

Vancouver:

Ko Y. Unusual carbohydrate biosynthesis : mechanistic studies of DesII and the biosynthesis of formycin A. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2020 Aug 11]. Available from: http://hdl.handle.net/2152/47151.

Council of Science Editors:

Ko Y. Unusual carbohydrate biosynthesis : mechanistic studies of DesII and the biosynthesis of formycin A. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://hdl.handle.net/2152/47151


University of Texas – Austin

9. Lin, Geng-Min. Unusual carbohydrate biosynthesis : studies of the flavin-dependent isomerase UGM, the radical S-adenosyl-L-methionine enzyme DesII, and the biosynthesis of herbicidins.

Degree: PhD, Chemistry, 2017, University of Texas – Austin

 Bacteria produce a great variety of unusual carbohydrates that are often found as parts of their cell surfaces or secondary metabolites. These components are crucial… (more)

Subjects/Keywords: Unusual carbohydrate; Biosynthesis; UDP-galactopyranose mutase; DesII; Radical SAM enzyme; Herbicidin

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APA (6th Edition):

Lin, G. (2017). Unusual carbohydrate biosynthesis : studies of the flavin-dependent isomerase UGM, the radical S-adenosyl-L-methionine enzyme DesII, and the biosynthesis of herbicidins. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/5870

Chicago Manual of Style (16th Edition):

Lin, Geng-Min. “Unusual carbohydrate biosynthesis : studies of the flavin-dependent isomerase UGM, the radical S-adenosyl-L-methionine enzyme DesII, and the biosynthesis of herbicidins.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed August 11, 2020. http://dx.doi.org/10.26153/tsw/5870.

MLA Handbook (7th Edition):

Lin, Geng-Min. “Unusual carbohydrate biosynthesis : studies of the flavin-dependent isomerase UGM, the radical S-adenosyl-L-methionine enzyme DesII, and the biosynthesis of herbicidins.” 2017. Web. 11 Aug 2020.

Vancouver:

Lin G. Unusual carbohydrate biosynthesis : studies of the flavin-dependent isomerase UGM, the radical S-adenosyl-L-methionine enzyme DesII, and the biosynthesis of herbicidins. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2020 Aug 11]. Available from: http://dx.doi.org/10.26153/tsw/5870.

Council of Science Editors:

Lin G. Unusual carbohydrate biosynthesis : studies of the flavin-dependent isomerase UGM, the radical S-adenosyl-L-methionine enzyme DesII, and the biosynthesis of herbicidins. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://dx.doi.org/10.26153/tsw/5870


University of Texas – Austin

10. Sun, He, Ph. D. Studies of unusual catalysis : a tale of four enzymes from diverse biosynthesis pathways.

Degree: PhD, Pharmaceutical Sciences, 2013, University of Texas – Austin

 The diverse reactions that enzymes catalyze have fascinated enzymologists for decades. Continuing investigations in the biosynthesis of both primary and secondary metabolites have led to… (more)

Subjects/Keywords: Unusual; Catalysis; Enzyme; Biosynthesis; Mechanism; Characterization; UDP-galactopyranose mutase; Sulfur carrier protein activating enzyme; Cobalamin-dependent radical S-adenosyl-L-methionine enzymes

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APA (6th Edition):

Sun, He, P. D. (2013). Studies of unusual catalysis : a tale of four enzymes from diverse biosynthesis pathways. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/63875

Chicago Manual of Style (16th Edition):

Sun, He, Ph D. “Studies of unusual catalysis : a tale of four enzymes from diverse biosynthesis pathways.” 2013. Doctoral Dissertation, University of Texas – Austin. Accessed August 11, 2020. http://hdl.handle.net/2152/63875.

MLA Handbook (7th Edition):

Sun, He, Ph D. “Studies of unusual catalysis : a tale of four enzymes from diverse biosynthesis pathways.” 2013. Web. 11 Aug 2020.

Vancouver:

Sun, He PD. Studies of unusual catalysis : a tale of four enzymes from diverse biosynthesis pathways. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2013. [cited 2020 Aug 11]. Available from: http://hdl.handle.net/2152/63875.

Council of Science Editors:

Sun, He PD. Studies of unusual catalysis : a tale of four enzymes from diverse biosynthesis pathways. [Doctoral Dissertation]. University of Texas – Austin; 2013. Available from: http://hdl.handle.net/2152/63875


University of Texas – Austin

11. Lin, Chia-I. Biosynthetic studies of lincomycin A, a thiosugar-containing natural product.

Degree: PhD, Chemistry, 2019, University of Texas – Austin

 The dissertation describes biosynthetic studies of lincomycin A, a thiosugarcontaining natural product. Lincomycin A was isolated from Streptomyces lincolnensis and has been used clinically as… (more)

Subjects/Keywords: Biosynthesis; Lincomycin; Thiosugar

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APA (6th Edition):

Lin, C. (2019). Biosynthetic studies of lincomycin A, a thiosugar-containing natural product. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/2237

Chicago Manual of Style (16th Edition):

Lin, Chia-I. “Biosynthetic studies of lincomycin A, a thiosugar-containing natural product.” 2019. Doctoral Dissertation, University of Texas – Austin. Accessed August 11, 2020. http://dx.doi.org/10.26153/tsw/2237.

MLA Handbook (7th Edition):

Lin, Chia-I. “Biosynthetic studies of lincomycin A, a thiosugar-containing natural product.” 2019. Web. 11 Aug 2020.

Vancouver:

Lin C. Biosynthetic studies of lincomycin A, a thiosugar-containing natural product. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2019. [cited 2020 Aug 11]. Available from: http://dx.doi.org/10.26153/tsw/2237.

Council of Science Editors:

Lin C. Biosynthetic studies of lincomycin A, a thiosugar-containing natural product. [Doctoral Dissertation]. University of Texas – Austin; 2019. Available from: http://dx.doi.org/10.26153/tsw/2237


University of Texas – Austin

12. -9265-9181. Characterization of two radical S-adenosyl-L-methionine enzymes in the biosynthesis of aminoglycosides.

Degree: PhD, Chemistry, 2016, University of Texas – Austin

 Biosynthetic studies of natural products are essential to the discovery and development of new drugs, because by understanding biosynthetic pathways and the enzymes that characterize… (more)

Subjects/Keywords: Biosynthesis; Aminoglycoside; Radical SAM; Enzyme

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APA (6th Edition):

-9265-9181. (2016). Characterization of two radical S-adenosyl-L-methionine enzymes in the biosynthesis of aminoglycosides. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68375

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

Chicago Manual of Style (16th Edition):

-9265-9181. “Characterization of two radical S-adenosyl-L-methionine enzymes in the biosynthesis of aminoglycosides.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed August 11, 2020. http://hdl.handle.net/2152/68375.

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

MLA Handbook (7th Edition):

-9265-9181. “Characterization of two radical S-adenosyl-L-methionine enzymes in the biosynthesis of aminoglycosides.” 2016. Web. 11 Aug 2020.

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

Vancouver:

-9265-9181. Characterization of two radical S-adenosyl-L-methionine enzymes in the biosynthesis of aminoglycosides. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2020 Aug 11]. Available from: http://hdl.handle.net/2152/68375.

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

Council of Science Editors:

-9265-9181. Characterization of two radical S-adenosyl-L-methionine enzymes in the biosynthesis of aminoglycosides. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/68375

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


University of Texas – Austin

13. Liu, Cheng-Hao. Probing chemical mechanism of two enzyme-catalyzed reactions by chiral substrate analogues.

Degree: PhD, Chemistry, 2014, University of Texas – Austin

 Enzymes are biological catalysts which greatly accelerate the rate of chemical reactions with remarkable substrate specificity and stereoselectivity. To optimize their catalytic abilities, many enzymes… (more)

Subjects/Keywords: Enzyme mechanism; Chiral substrate; ACC deaminase; PLP; Difluorocyclopropane; Tight-binding inhibitor; IspH; chiral methyl analysis; Iron-sulfur cluster

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APA (6th Edition):

Liu, C. (2014). Probing chemical mechanism of two enzyme-catalyzed reactions by chiral substrate analogues. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/63859

Chicago Manual of Style (16th Edition):

Liu, Cheng-Hao. “Probing chemical mechanism of two enzyme-catalyzed reactions by chiral substrate analogues.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed August 11, 2020. http://hdl.handle.net/2152/63859.

MLA Handbook (7th Edition):

Liu, Cheng-Hao. “Probing chemical mechanism of two enzyme-catalyzed reactions by chiral substrate analogues.” 2014. Web. 11 Aug 2020.

Vancouver:

Liu C. Probing chemical mechanism of two enzyme-catalyzed reactions by chiral substrate analogues. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2020 Aug 11]. Available from: http://hdl.handle.net/2152/63859.

Council of Science Editors:

Liu C. Probing chemical mechanism of two enzyme-catalyzed reactions by chiral substrate analogues. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/63859


University of Texas – Austin

14. Romo, Anthony James. Discovery of the amipurimycin and miharamycins biosynthetic gene clusters and insight into the biosynthesis of nogalamycin.

Degree: PhD, Pharmaceutical Sciences, 2019, University of Texas – Austin

 Advancements in our ability to obtain high quality bacterial whole genome sequences have increased the rate natural product biosynthetic gene clusters are identified, but these… (more)

Subjects/Keywords: Next generation sequencing; Peptidyl nucleoside antibiotics; Gene cluster; Streptomyces

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APA (6th Edition):

Romo, A. J. (2019). Discovery of the amipurimycin and miharamycins biosynthetic gene clusters and insight into the biosynthesis of nogalamycin. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/2198

Chicago Manual of Style (16th Edition):

Romo, Anthony James. “Discovery of the amipurimycin and miharamycins biosynthetic gene clusters and insight into the biosynthesis of nogalamycin.” 2019. Doctoral Dissertation, University of Texas – Austin. Accessed August 11, 2020. http://dx.doi.org/10.26153/tsw/2198.

MLA Handbook (7th Edition):

Romo, Anthony James. “Discovery of the amipurimycin and miharamycins biosynthetic gene clusters and insight into the biosynthesis of nogalamycin.” 2019. Web. 11 Aug 2020.

Vancouver:

Romo AJ. Discovery of the amipurimycin and miharamycins biosynthetic gene clusters and insight into the biosynthesis of nogalamycin. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2019. [cited 2020 Aug 11]. Available from: http://dx.doi.org/10.26153/tsw/2198.

Council of Science Editors:

Romo AJ. Discovery of the amipurimycin and miharamycins biosynthetic gene clusters and insight into the biosynthesis of nogalamycin. [Doctoral Dissertation]. University of Texas – Austin; 2019. Available from: http://dx.doi.org/10.26153/tsw/2198

15. Zlotkowski, Katherine Hannah. Chemical biology studies of neuroregenerative small molecules using Caenorhabditis elegans.

Degree: PhD, Chemistry, 2015, University of Texas – Austin

 The debilitating effects of spinal cord injury can be attributed to a lack of regeneration in the central nervous system. Identification of growth-promoting pathways, particularly… (more)

Subjects/Keywords: Chemical biology; C. elegans; Small molecules; Spinal cord injury; Regeneration; Clovanemagnolol; Vinaxanthone; Neuronal growth; In vivo assay; Mechanism of action; Laser axotomy; Structure-activity relationship

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

APA (6th Edition):

Zlotkowski, K. H. (2015). Chemical biology studies of neuroregenerative small molecules using Caenorhabditis elegans. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/30511

Chicago Manual of Style (16th Edition):

Zlotkowski, Katherine Hannah. “Chemical biology studies of neuroregenerative small molecules using Caenorhabditis elegans.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed August 11, 2020. http://hdl.handle.net/2152/30511.

MLA Handbook (7th Edition):

Zlotkowski, Katherine Hannah. “Chemical biology studies of neuroregenerative small molecules using Caenorhabditis elegans.” 2015. Web. 11 Aug 2020.

Vancouver:

Zlotkowski KH. Chemical biology studies of neuroregenerative small molecules using Caenorhabditis elegans. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2020 Aug 11]. Available from: http://hdl.handle.net/2152/30511.

Council of Science Editors:

Zlotkowski KH. Chemical biology studies of neuroregenerative small molecules using Caenorhabditis elegans. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/30511

16. Lin, Ke-Yi. Molecular mechanism of poly(ADP-ribosyl)ation catalyzed by human poly(ADP-ribose) polymerase-1.

Degree: PhD, Pharmaceutical Sciences, 2015, University of Texas – Austin

 Human poly(ADP-ribose) polymerase-1 (PARP-1) is an abundant nuclear enzyme which catalyzes protein poly(ADP-ribosyl)ation upon binding to DNA. NAD+ is used as a co-substrate in the… (more)

Subjects/Keywords: PARP-1; Poly(ADP-ribosyl)ation; Enzyme mechanism; Single-molecule

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

APA (6th Edition):

Lin, K. (2015). Molecular mechanism of poly(ADP-ribosyl)ation catalyzed by human poly(ADP-ribose) polymerase-1. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/62239

Chicago Manual of Style (16th Edition):

Lin, Ke-Yi. “Molecular mechanism of poly(ADP-ribosyl)ation catalyzed by human poly(ADP-ribose) polymerase-1.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed August 11, 2020. http://hdl.handle.net/2152/62239.

MLA Handbook (7th Edition):

Lin, Ke-Yi. “Molecular mechanism of poly(ADP-ribosyl)ation catalyzed by human poly(ADP-ribose) polymerase-1.” 2015. Web. 11 Aug 2020.

Vancouver:

Lin K. Molecular mechanism of poly(ADP-ribosyl)ation catalyzed by human poly(ADP-ribose) polymerase-1. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2020 Aug 11]. Available from: http://hdl.handle.net/2152/62239.

Council of Science Editors:

Lin K. Molecular mechanism of poly(ADP-ribosyl)ation catalyzed by human poly(ADP-ribose) polymerase-1. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/62239

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