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PMID: 7791871 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Rational design of aromatic polyketide natural products by recombinant assembly of enzymatic subunits.

Nature ·Vol. 375 ·No. 6532 ·1995-06-15 ·Pages 549-54

McDaniel R, Ebert-Khosla S, Hopwood DA, Khosla C

Abstract

Recent advances in understanding of bacterial aromatic polyketide biosynthesis allow the development of a set of design rules for the rational manipulation of chain synthesis, reduction of keto groups and early cyclization steps by genetic engineering. The concept of rational design is illustrated by the preparation of Streptomyces strains that produce two new polyketides by expression of combinations of appropriate enzymatic subunits from naturally occurring polyketide synthases. The potential for generating molecular diversity within this class of molecules by genetic engineering is enormous.

MeSH Terms
Genetic Engineering/methods Multienzyme Complexes/genetics,metabolism Multigene Family Oxidoreductases/genetics,metabolism Plasmids Polycyclic Compounds/metabolism Streptomyces/genetics
Chemicals
Multienzyme Complexes Polycyclic Compounds Oxidoreductases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
McDaniel R
Department of Chemical Engineering, Stanford University, California 94305-5025, USA.
Ebert-Khosla S
Hopwood D A
Khosla C
Article Info
Journal
Nature
Abbr.
Nature
ISSN
0028-0836
Published
1995-06-15
Pages
549-54
Language
English
Region
England
NLM ID
0410462
Subset
IM
Corrections
CommentIn
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