Modular polyketide synthase contains two reaction chambers that operate asynchronously
Author(s) -
Saket R. Bagde,
Irimpan I. Mathews,
J. Christopher Fromme,
ChuYoung Kim
Publication year - 2021
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.abi8532
Subject(s) - polyketide , polyketide synthase , chemistry , stereochemistry , atp synthase , acyl carrier protein , biosynthesis , enzyme , active site , angstrom , crystallography , biochemistry
Big molecules build small Actinomycete bacteria are prolific producers of bioactive small molecules such as polyketide antibiotics. These molecules are built by the addition of short carbon units to a growing, protein-tethered chain, either iteratively as in fatty acid synthesis or in a modular fashion by a hand-off from one distinct enzyme complex to the next. Bagdeet al . and Coganet al . report structures of polyketide synthase modules in action, taking advantage of antibody stabilization of one of the domains. Both groups visualized multiple conformational states and an asymmetric arrangement of domains, providing insight into how these molecular assembly machines transfer substrates from one active site to another. —MAF
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