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A Turnstile Mechanism for the Controlled Growth of Biosynthetic Intermediates on Assembly Line Polyketide Synthases
[Image: see text] Vectorial polyketide biosynthesis on an assembly line polyketide synthase is the most distinctive property of this family of biological machines, while providing the key conceptual tool for the bioinformatic decoding of new antibiotic pathways. We now show that the action of the en...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4731828/ https://www.ncbi.nlm.nih.gov/pubmed/26878060 http://dx.doi.org/10.1021/acscentsci.5b00321 |
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author | Lowry, Brian Li, Xiuyuan Robbins, Thomas Cane, David E. Khosla, Chaitan |
author_facet | Lowry, Brian Li, Xiuyuan Robbins, Thomas Cane, David E. Khosla, Chaitan |
author_sort | Lowry, Brian |
collection | PubMed |
description | [Image: see text] Vectorial polyketide biosynthesis on an assembly line polyketide synthase is the most distinctive property of this family of biological machines, while providing the key conceptual tool for the bioinformatic decoding of new antibiotic pathways. We now show that the action of the entire assembly line is synchronized by a previously unrecognized turnstile mechanism that prevents the ketosynthase domain of each module from being acylated by a new polyketide chain until the product of the prior catalytic cycle has been passed to the downstream module from the corresponding acyl carrier protein domain. The turnstile is closed by virtue of tight coupling to the signature decarboxylative condensation reaction catalyzed by the ketosynthase domain of each polyketide synthase module. Reopening of the turnstile is coupled to the eventual chain translocation step that vacates the module. At the maximal rate of substrate turnover, one would expect the chain release step to initiate a cascade of chain translocation events that sequentially migrate back upstream, thereby repriming each module and setting up the assembly line for the next round of polyketide chain elongation. |
format | Online Article Text |
id | pubmed-4731828 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-47318282016-02-10 A Turnstile Mechanism for the Controlled Growth of Biosynthetic Intermediates on Assembly Line Polyketide Synthases Lowry, Brian Li, Xiuyuan Robbins, Thomas Cane, David E. Khosla, Chaitan ACS Cent Sci [Image: see text] Vectorial polyketide biosynthesis on an assembly line polyketide synthase is the most distinctive property of this family of biological machines, while providing the key conceptual tool for the bioinformatic decoding of new antibiotic pathways. We now show that the action of the entire assembly line is synchronized by a previously unrecognized turnstile mechanism that prevents the ketosynthase domain of each module from being acylated by a new polyketide chain until the product of the prior catalytic cycle has been passed to the downstream module from the corresponding acyl carrier protein domain. The turnstile is closed by virtue of tight coupling to the signature decarboxylative condensation reaction catalyzed by the ketosynthase domain of each polyketide synthase module. Reopening of the turnstile is coupled to the eventual chain translocation step that vacates the module. At the maximal rate of substrate turnover, one would expect the chain release step to initiate a cascade of chain translocation events that sequentially migrate back upstream, thereby repriming each module and setting up the assembly line for the next round of polyketide chain elongation. American Chemical Society 2016-01-06 2016-01-27 /pmc/articles/PMC4731828/ /pubmed/26878060 http://dx.doi.org/10.1021/acscentsci.5b00321 Text en Copyright © 2016 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Lowry, Brian Li, Xiuyuan Robbins, Thomas Cane, David E. Khosla, Chaitan A Turnstile Mechanism for the Controlled Growth of Biosynthetic Intermediates on Assembly Line Polyketide Synthases |
title | A Turnstile Mechanism for the Controlled Growth of
Biosynthetic Intermediates on Assembly Line Polyketide Synthases |
title_full | A Turnstile Mechanism for the Controlled Growth of
Biosynthetic Intermediates on Assembly Line Polyketide Synthases |
title_fullStr | A Turnstile Mechanism for the Controlled Growth of
Biosynthetic Intermediates on Assembly Line Polyketide Synthases |
title_full_unstemmed | A Turnstile Mechanism for the Controlled Growth of
Biosynthetic Intermediates on Assembly Line Polyketide Synthases |
title_short | A Turnstile Mechanism for the Controlled Growth of
Biosynthetic Intermediates on Assembly Line Polyketide Synthases |
title_sort | turnstile mechanism for the controlled growth of
biosynthetic intermediates on assembly line polyketide synthases |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4731828/ https://www.ncbi.nlm.nih.gov/pubmed/26878060 http://dx.doi.org/10.1021/acscentsci.5b00321 |
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