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26元环多烯大环内酯匹马霉素的生物合成基因簇。一种由两个被功能化基因分隔的亚簇编码的新型聚酮合酶组织。

The biosynthetic gene cluster for the 26-membered ring polyene macrolide pimaricin. A new polyketide synthase organization encoded by two subclusters separated by functionalization genes.

作者信息

Aparicio J F, Colina A J, Ceballos E, Martín J F

机构信息

Institute of Biotechnology INBIOTEC, Science Park of León, Avda. del Real, n degrees 1, 24006 León, Spain.

出版信息

J Biol Chem. 1999 Apr 9;274(15):10133-9. doi: 10.1074/jbc.274.15.10133.

Abstract

The biosynthetic gene cluster for the 26-membered ring of the polyene macrolide pimaricin extends for about 110 kilobase pairs of contiguous DNA in the genome of Streptomyces natalensis. Two sets of polyketide synthase (PKS) genes are separated by a group of small polyketide-functionalizing genes. Two of the polyketide synthase genes, pimS0 and pimS1, have been fully sequenced and disrupted proving the involvement of each of these genes in pimaricin biosynthesis. The pimS0 gene encodes a relatively small acetate-activating PKS (approximately 193 kDa) that appears to work as a loading protein which "presents" the starter unit to the second PKS subunit. The pimS1 gene encodes a giant multienzyme (approximately 710 kDa) harboring 15 activities responsible for the first four cycles of chain elongation in pimaricin biosynthesis, resulting in formation of the polyene chromophore.

摘要

在纳塔尔链霉菌基因组中,聚烯大环内酯匹马霉素26元环的生物合成基因簇延伸约110千碱基对的连续DNA。两组聚酮合酶(PKS)基因被一组小的聚酮功能化基因隔开。其中两个聚酮合酶基因pimS0和pimS1已被完全测序并破坏,证明这些基因各自参与了匹马霉素的生物合成。pimS0基因编码一种相对较小的乙酸激活PKS(约193 kDa),它似乎作为一种装载蛋白,将起始单元“呈现”给第二个PKS亚基。pimS1基因编码一种巨大的多酶(约710 kDa),具有15种活性,负责匹马霉素生物合成中链延伸的前四个循环,从而形成多烯发色团。

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