THE BIOSYNTHETIC GENE-CLUSTER FOR THE POLYKETIDE IMMUNOSUPPRESSANT RAPAMYCIN

被引:393
作者
SCHWECKE, T
APARICIO, JF
MOLNAR, I
KONIG, A
KHAW, LE
HAYDOCK, SF
OLIYNYK, M
CAFFREY, P
CORTES, J
LESTER, JB
BOHM, GA
STAUNTON, J
LEADLAY, PF
机构
[1] UNIV CAMBRIDGE, DEPT BIOCHEM, CAMBRIDGE CB2 1QW, ENGLAND
[2] UNIV CAMBRIDGE, CAMBRIDGE CTR MOLEC RECOGNIT, CAMBRIDGE CB2 1QW, ENGLAND
[3] UNIV CAMBRIDGE, CHEM LAB, CAMBRIDGE CB2 1EW, ENGLAND
[4] UNIV CAMBRIDGE, CAMBRIDGE CTR MOLEC RECOGNIT, CAMBRIDGE CB2 1EW, ENGLAND
基金
英国惠康基金;
关键词
STREPTOMYCES; PEPTIDE SYNTHETASE; POLYKETIDE SYNTHASE; FK506;
D O I
10.1073/pnas.92.17.7839
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The macrocyclic polyketides rapamycin and FK506 are potent immunosuppressants that prevent T-cell proliferation through specific binding to intracellular protein receptors (immunophilins). The cloning and specific alteration of the biosynthetic genes for these polyketides might allow the biosynthesis of clinically valuable analogues, We report here that three clustered polyketide synthase genes responsible for rapamycin biosynthesis in Streptomyces hygroscopicus together encode 14 homologous sets of enzyme activities (modules), each catalyzing a specific round of chain elongation. An adjacent gene encodes a pipecolate-incorporating enzyme, which completes the macrocycle. The total of 70 constituent active sites makes this the most complex multienzyme system identified so far. The DNA region sequenced (107.3 kbp) contains 24 additional open reading frames, some of which code for proteins governing other key steps in rapamycin biosynthesis.
引用
收藏
页码:7839 / 7843
页数:5
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