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丁烯基多杀菌素,抗生素生物合成基因基因工程的一个天然实例。

Butenyl-spinosyns, a natural example of genetic engineering of antibiotic biosynthetic genes.

作者信息

Hahn Donald R, Gustafson Gary, Waldron Clive, Bullard Brian, Jackson James D, Mitchell Jon

机构信息

Discovery Research, LLC, Dow AgroSciences, 9330 Zionsville Road., Indianapolis, IN, 46268-1054,

出版信息

J Ind Microbiol Biotechnol. 2006 Feb;33(2):94-104. doi: 10.1007/s10295-005-0016-9. Epub 2005 Sep 23.

Abstract

Spinosyns, a novel class of insect active macrolides produced by Saccharopolyspora spinosa, are used for insect control in a number of commercial crops. Recently, a new class of spinosyns was discovered from S. pogona NRRL 30141. The butenyl-spinosyns, also called pogonins, are very similar to spinosyns, differing in the length of the side chain at C-21 and in the variety of novel minor factors. The butenyl-spinosyn biosynthetic genes (bus) were cloned on four cosmids covering a contiguous 110-kb region of the NRRL 30141 chromosome. Their function in butenyl-spinosyn biosynthesis was confirmed by a loss-of-function deletion, and subsequent complementation by cloned genes. The coding sequences of the butenyl-spinosyn biosynthetic genes and the spinosyn biosynthetic genes from S. spinosa were highly conserved. In particular, the PKS-coding genes from S. spinosa and S. pogona have 91-94% nucleic acid identity, with one notable exception. The butenyl-spinosyn gene sequence codes for one additional PKS module, which is responsible for the additional two carbons in the C-21 tail. The DNA sequence of spinosyn genes in this region suggested that the S. spinosa spnA gene could have been the result of an in-frame deletion of the S. pogona busA gene. Therefore, the butenyl-spinosyn genes represent the putative parental gene structure that was naturally engineered by deletion to create the spinosyn genes.

摘要

多杀菌素是由刺糖多孢菌产生的一类新型昆虫活性大环内酯类化合物,用于多种经济作物的害虫防治。最近,从刺糖多孢菌NRRL 30141中发现了一类新的多杀菌素。丁烯基多杀菌素,也称为波戈宁,与多杀菌素非常相似,只是在C-21位侧链长度和多种新型次要因子上有所不同。丁烯基多杀菌素生物合成基因(bus)被克隆到四个黏粒上,这些黏粒覆盖了NRRL 30141染色体上一个连续的110 kb区域。通过功能缺失缺失以及随后克隆基因的互补,证实了它们在丁烯基多杀菌素生物合成中的功能。来自刺糖多孢菌的丁烯基多杀菌素生物合成基因和多杀菌素生物合成基因的编码序列高度保守。特别是,来自刺糖多孢菌和刺糖多孢菌的聚酮合酶编码基因具有91-94%的核酸同一性,但有一个显著例外。丁烯基多杀菌素基因序列编码一个额外的聚酮合酶模块,该模块负责C-21尾部额外的两个碳原子。该区域多杀菌素基因的DNA序列表明,刺糖多孢菌的spnA基因可能是刺糖多孢菌busA基因框内缺失的结果。因此,丁烯基多杀菌素基因代表了推定的亲本基因结构,该结构通过缺失自然改造以产生多杀菌素基因。

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