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Permanent link (DOI): https://doi.org/10.7939/R35P56

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Synthesis and investigation of viral cysteine protease inhibitors and biosynthetic studies on subtilosin A Open Access

Descriptions

Other title
Subject/Keyword
Cyclic peptides -- Synthesis
Peptide antibiotics -- Synthesis
Cysteine proteinases -- Inhibitors -- Synthesis
Cysteine proteinases -- Inhibitors -- Evaluation
Bacillus subtilis -- Genetics
SARS (Disease) -- Chemotherapy
Type of item
Thesis
Degree grantor
University of Alberta
Author or creator
Miyyapuram, Venugopal
Supervisor and department
Dr. John C. Vederas (Department of Chemistry)
Examining committee member and department
Dr. Erika Plettner (Department of Chemistry, Simon Fraser University, British Columbia)
Dr. Frederick G. West (Department of Chemistry)
Dr. Robert E. Campbell (Department of Chemistry)
Dr. Jillian M. Buriak (Department of Chemistry)
Dr. David Bressler (Department of Agriculture, Food and Nutrional Science)
Department
Department of Chemistry
Specialization

Date accepted
2009-10-06T18:42:37Z
Graduation date
2009-11
Degree
Doctor of Philosophy
Degree level
Doctoral
Abstract
ABSTRACT This thesis discusses the synthesis and evaluation of cysteine protease inhibitors, the asymmetric reduction of pseudoxazolones, and the study of the mechanism of subtilosin A biosynthesis. Five classes of compounds, including pyridinylamines and ethers, have been designed with the aim of developing non-covalent inhibitors of SARS–CoV 3CLpro, a chymotrypsin-like cysteine protease vital to the life cycle of the SARS coronavirus. These compounds were synthesized and screened against SARS–CoV 3CLpro. 3-Bromo-5-[5-(4-nitro-phenyl)-furan-2-ylmethoxy]-pyridine (37), 5-Bromo-N-((5-(4-nitrophenyl)furan-2-yl)methyl)pyridin-3-amine (54), N-((5-(4-Aminophenyl)furan-2-yl)methyl)-5-bromopyridin-3-amine (61) and N-{5-[5-(4-Nitro-phenyl)-furan-2-ylmethylene]-4-oxo-2-thioxo-thiazolidin-3-yl}-acetamide (67) show very good inhibition with IC50 values ranging from 12 μM to 31 μM. Mechanism studies suggest that these compounds are reversible inhibitors. Inhibitors against Israel acute paralysis virus (IAPV), which is associated with Colony Collapse Disorder (CCD) in honeybees, have been designed with a glutamine residue at the P1 position based on sequence comparisons between IAPV 3Cpro and known 3C proteases. Two fluorogenic peptide substrates, Abz-QTTTQAG-Y(NO2)-E (95) and Abz-EVSMQVD-Y(NO2)-D (98), were synthesized. However, both compounds show no activity. As a different strategy, a peptidyl fluoromethyl ketone, Ac-Val-Thr(OBn)-Leu-6-fluoro-N,N-dimethyl-S-oxohexanamide (77), incorporating the SARS recognition sequence, has also been synthesized, and testing of its activity is in progress. Asymmetric reduction of pseudoxazolones containing an imine moiety can serve as a method for preparing enantiopure amino acids. Several conditions were tried but without success. Although the results are not encouraging, attempts to prepare pseudoxazolone derivatives with increased reactivity led to synthesis of highly substituted olefins. Subtilosin A, a ribosomally synthesized antimicrobial cyclic peptide from Bacillus subtilis, is posttranslationally modified to contain unusual thioether cross-links between cysteine sulfurs and alpha-carbons of phenylalanines and threonine. The sbo-alb gene locus is required for the production of subtilosin A as well as for immunity, but the exact roles of these genes are unclear. In order to elucidate the roles of albA, albE and albF genes that may be responsible for the posttranslational modifications, three potential substrates were designed and synthesized. In addition to these biosynthetic studies, subtilosin A1, a T6I mutant of subtilosin A, was purified and characterized. It was found to show hemolytic activity and altered bactericidal activity compared to that of the parent.
Language
English
DOI
doi:10.7939/R35P56
Rights
License granted by Venugopal Rao Miyyapuram (vrm@ualberta.ca) on 2009-09-29T19:44:43Z (GMT): Permission is hereby granted to the University of Alberta Libraries to reproduce single copies of this thesis and to lend or sell such copies for private, scholarly or scientific research purposes only. Where the thesis is converted to, or otherwise made available in digital form, the University of Alberta will advise potential users of the thesis of the above terms. The author reserves all other publication and other rights in association with the copyright in the thesis, and except as herein provided, neither the thesis nor any substantial portion thereof may be printed or otherwise reproduced in any material form whatsoever without the author's prior written permission.
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