Abstract
Streptomyces is a genus of soil dwelling bacteria with the ability to produce natural products that have found widespread use in medicine. Annotation of Streptomyces genome sequences has revealed far more biosynthetic gene clusters than previously imagined, offering exciting possibilities for future combinatorial biosynthesis. Experiments to manipulate modular biosynthetic clusters to create novel chemistries often result in no detectable product or product yield is extremely low. Understanding the coupling between components in these hybrid enzymes will be crucial for efficient synthesis of new compounds. We are using new algebraic approaches to predict protein properties, and homologous recombination to exploit natural evolutionary constraints to generate novel functional enzymes. The methods and techniques developed could easily be adapted to study modular, multi-interacting complex systems where appreciable biochemical and comparative sequence data are available, for example, clinically significant non-ribosomally synthesised peptides and polyketides.
Keywords: streptomyces, hidden markov models, genetic recombination, enzyme structure-function, novel antibiotics
Current Medicinal Chemistry
Title: Plasticity of the Streptomyces Genome-Evolution and Engineering of New Antibiotics
Volume: 12 Issue: 14
Author(s): Daslav Hranueli, John Cullum, Bojan Basrak, Pavle Goldstein and Paul F. Long
Affiliation:
Keywords: streptomyces, hidden markov models, genetic recombination, enzyme structure-function, novel antibiotics
Abstract: Streptomyces is a genus of soil dwelling bacteria with the ability to produce natural products that have found widespread use in medicine. Annotation of Streptomyces genome sequences has revealed far more biosynthetic gene clusters than previously imagined, offering exciting possibilities for future combinatorial biosynthesis. Experiments to manipulate modular biosynthetic clusters to create novel chemistries often result in no detectable product or product yield is extremely low. Understanding the coupling between components in these hybrid enzymes will be crucial for efficient synthesis of new compounds. We are using new algebraic approaches to predict protein properties, and homologous recombination to exploit natural evolutionary constraints to generate novel functional enzymes. The methods and techniques developed could easily be adapted to study modular, multi-interacting complex systems where appreciable biochemical and comparative sequence data are available, for example, clinically significant non-ribosomally synthesised peptides and polyketides.
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Cite this article as:
Hranueli Daslav, Cullum John, Basrak Bojan, Goldstein Pavle and Long F. Paul, Plasticity of the Streptomyces Genome-Evolution and Engineering of New Antibiotics, Current Medicinal Chemistry 2005; 12 (14) . https://dx.doi.org/10.2174/0929867054367176
DOI https://dx.doi.org/10.2174/0929867054367176 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
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