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微生物和植物中聚酮化合物次级代谢途径的基因。

Genes for polyketide secondary metabolic pathways in microorganisms and plants.

作者信息

Hopwood D A, Khosla C

机构信息

John Innes Institute, John Innes Centre, Norwich, UK.

出版信息

Ciba Found Symp. 1992;171:88-106; discussion 106-12. doi: 10.1002/9780470514344.ch6.

Abstract

Recent advances in molecular genetics have led to the isolation, sequencing and functional analysis of genes encoding synthases that catalyse the formation of several classes of polyketides. The structures of the genes and their protein products differ strikingly in the various examples. For Streptomyces aromatic polyketides, exemplified by granaticin and tetracenomycin, the synthases correspond to Type II (bacterial and plant) fatty acid synthases in consisting of distinct proteins for such processes as condensation, acyl carrier function and ketoreduction. In contrast, for actinomycete macrolides such as erythromycin, similar catalytic functions are performed by a set of multifunctional proteins resembling Type I (animal) fatty acid synthases, but with every step in chain-building being catalysed by a different enzymic domain. Penicillium patulum has a simple Type I synthase for 6-methylsalicylic acid. For plant chalcones and stilbenes, a single small polypeptide acts as a condensing enzyme for carbon chain-building and may be unrelated to any of the other polyketide and fatty acid synthases. Thus, although these systems share a common general mechanism of chain assembly, they must differ in the ways that synthase 'programming' has evolved to determine chain length, choice of chain starter and extender units, and handling of successive keto groups during chain assembly, and so control the great diversity of possible chemical products.

摘要

分子遗传学的最新进展已导致对编码合成酶的基因进行分离、测序和功能分析,这些合成酶催化几类聚酮化合物的形成。在各种实例中,这些基因及其蛋白质产物的结构存在显著差异。以石榴菌素和四环素霉素为例的链霉菌芳香族聚酮化合物,其合成酶对应于II型(细菌和植物)脂肪酸合成酶,由用于缩合、酰基载体功能和酮还原等过程的不同蛋白质组成。相比之下,对于红霉素等放线菌大环内酯类化合物,一组类似于I型(动物)脂肪酸合成酶的多功能蛋白质执行类似的催化功能,但链构建的每一步都由不同的酶结构域催化。展青霉具有用于6-甲基水杨酸的简单I型合成酶。对于植物查耳酮和芪类化合物,单个小多肽作为碳链构建的缩合酶,可能与任何其他聚酮化合物和脂肪酸合成酶无关。因此,尽管这些系统共享链组装的共同一般机制,但它们在合成酶“编程”的进化方式上必然存在差异,以确定链长度、链起始单元和延伸单元的选择以及链组装过程中连续酮基的处理,从而控制可能的化学产物的巨大多样性。

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