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最小whiE聚酮合酶的异位表达产生了一系列大小和形状各异的芳香聚酮化合物文库。

Ectopic expression of the minimal whiE polyketide synthase generates a library of aromatic polyketides of diverse sizes and shapes.

作者信息

Shen Y, Yoon P, Yu T W, Floss H G, Hopwood D, Moore B S

机构信息

Department of Chemistry, Box 351700, University of Washington, Seattle, WA 98195-1700, USA.

出版信息

Proc Natl Acad Sci U S A. 1999 Mar 30;96(7):3622-7. doi: 10.1073/pnas.96.7.3622.

Abstract

The single recombinant expressing the Streptomyces coelicolor minimal whiE (spore pigment) polyketide synthase (PKS) is uniquely capable of generating a large array of well more than 30 polyketides, many of which, so far, are novel to this recombinant. The characterized polyketides represent a diverse set of molecules that differ in size (chain length) and shape (cyclization pattern). This combinatorial biosynthetic library is, by far, the largest and most complex of its kind described to date and indicates that the minimal whiE PKS does not independently control polyketide chain length nor dictate the first cyclization event. Rather, the minimal PKS enzyme complex must rely on the stabilizing effects of additional subunits (i.e., the cyclase whiE-ORFVI) to ensure that the chain reaches the full 24 carbons and cyclizes correctly. This dramatic loss of control implies that the growing polyketide chain does not remain enzyme bound, resulting in the spontaneous cyclization of the methyl terminus. Among the six characterized dodecaketides, four different first-ring cyclization regiochemistries are represented, including C7/C12, C8/C13, C10/C15, and C13/C15. The dodecaketide TW93h possesses a unique 2,4-dioxaadamantane ring system and represents a new structural class of polyketides with no related structures isolated from natural or engineered organisms, thus supporting the claim that engineered biosynthesis is capable of producing novel chemotypes.

摘要

表达天蓝色链霉菌最小whiE(孢子色素)聚酮合酶(PKS)的单一重组体独特地能够产生大量超过30种的聚酮化合物,其中许多聚酮化合物,到目前为止,对于该重组体来说是新的。已鉴定的聚酮化合物代表了一组不同的分子,它们在大小(链长)和形状(环化模式)上有所不同。这个组合生物合成文库是迄今为止所描述的同类文库中最大且最复杂的,表明最小的whiE聚酮合酶并不独立控制聚酮化合物链的长度,也不决定第一次环化事件。相反,最小的聚酮合酶酶复合物必须依赖于其他亚基(即环化酶whiE-ORFVI)的稳定作用,以确保链达到完整的24个碳原子并正确环化。这种显著的控制丧失意味着不断增长的聚酮化合物链不会保持与酶结合,导致甲基末端的自发环化。在六种已鉴定的十二酮化合物中,代表了四种不同的第一环环化区域化学,包括C7/C12、C8/C13、C10/C15和C13/C15。十二酮化合物TW93h具有独特的2,4-二氧杂金刚烷环系统,代表了一类新的聚酮化合物结构类型,没有从天然或工程生物体中分离出相关结构,因此支持了工程生物合成能够产生新型化学类型的说法。

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