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PMID: 10205055 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Dissecting and exploiting intermodular communication in polyketide synthases.

Science (New York, N.Y.) ·Vol. 284 ·No. 5413 ·1999-04-16 ·Pages 482-5

Gokhale RS, Tsuji SY, Cane DE, Khosla C

Abstract

Modular polyketide synthases catalyze the biosynthesis of medicinally important natural products through an assembly-line mechanism. Although these megasynthases display very precise overall selectivity, we show that their constituent modules are remarkably tolerant toward diverse incoming acyl chains. By appropriate engineering of linkers, which exist within and between polypeptides, it is possible to exploit this tolerance to facilitate the transfer of biosynthetic intermediates between unnaturally linked modules. This protein engineering strategy also provides insights into the evolution of modular polyketide synthases.

MeSH Terms
Amino Acid Sequence Catalysis Escherichia coli/enzymology,genetics Evolution, Molecular Genes, Bacterial Lactones/metabolism Macrolides/metabolism Molecular Sequence Data Multienzyme Complexes/chemistry,genetics,metabolism Nuclear Magnetic Resonance, Biomolecular Peptides/metabolism Protein Engineering Recombinant Fusion Proteins/chemistry,metabolism Streptomyces/enzymology
Chemicals
Lactones Macrolides Multienzyme Complexes Peptides Recombinant Fusion Proteins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Gokhale R S
Department of Chemical Engineering, Stanford University, Stanford CA 94305-5025, USA.
Tsuji S Y
Cane D E
Khosla C
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1999-04-16
Pages
482-5
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NCI NIH HHS · CA66736 · United States
NIGMS NIH HHS · GM22172 · United States
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