Kennedy_1999_Science_284_1368

Reference

Title : Modulation of polyketide synthase activity by accessory proteins during lovastatin biosynthesis - Kennedy_1999_Science_284_1368
Author(s) : Kennedy J , Auclair K , Kendrew SG , Park C , Vederas JC , Hutchinson CR
Ref : Science , 284 :1368 , 1999
Abstract :

Polyketides, the ubiquitous products of secondary metabolism in microorganisms, are made by a process resembling fatty acid biosynthesis that allows the suppression of reduction or dehydration reactions at specific biosynthetic steps, giving rise to a wide range of often medically useful products. The lovastatin biosynthesis cluster contains two type I polyketide synthase genes. Synthesis of the main nonaketide-derived skeleton was found to require the previously known iterative lovastatin nonaketide synthase (LNKS), plus at least one additional protein (LovC) that interacts with LNKS and is necessary for the correct processing of the growing polyketide chain and production of dihydromonacolin L. The noniterative lovastatin diketide synthase (LDKS) enzyme specifies formation of 2-methylbutyrate and interacts closely with an additional transesterase (LovD) responsible for assembling lovastatin from this polyketide and monacolin J.

PubMedSearch : Kennedy_1999_Science_284_1368
PubMedID: 10334994
Gene_locus related to this paper: aspte-Q9Y7C9

Related information

Gene_locus aspte-Q9Y7C9

Citations formats

Kennedy J, Auclair K, Kendrew SG, Park C, Vederas JC, Hutchinson CR (1999)
Modulation of polyketide synthase activity by accessory proteins during lovastatin biosynthesis
Science 284 :1368

Kennedy J, Auclair K, Kendrew SG, Park C, Vederas JC, Hutchinson CR (1999)
Science 284 :1368