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Enhanced heterologous polyketide production in<Emphasis Type="Italic"> Streptomyces</Emphasis> by exploiting plasmid co-integration
Authors:Email author" target="_blank">Zhihao?HuEmail author  David?A?Hopwood  C?Richard?Hutchinson
Institution:(1) Kosan Biosciences, 3832 Bay Center Place, Hayward, CA 94545, USA;(2) Present address: John Innes Centre, Department of Molecular Microbiology, University of East Anglia, Norwich, NR4 7UH, UK
Abstract:A plasmid named pSMALL was discovered in a Streptomyces coelicolor strain that significantly enhanced the levels of production of 15-methyl-6-deoxyerythronolide B, a polyketide lactone normally produced in low amounts by engineered polyketide synthase (PKS) genes. It is a co-integrate between a conventional SCP2*-derived Streptomyces expression plasmid, pJRJ2, and SCP2@, a variant of the parental SCP2* plasmid. SCP2@ has a 45-bp deletion 35 bp upstream of the start codon of the repI gene in the replication region; and this correlated with an enhanced plasmid copy number and polyketide overproduction by its derivatives. This discovery was exploited to construct pBOOST, a high-copy-number cloning vector that can be used to achieve greatly elevated (at least 25-fold), stable metabolite production by PKS genes cloned in SCP2*-derived vectors by forming co-integrates with them.
Keywords:Co-integration  SCP2  Heterologous expression
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