Demydchuk Yuliya, Sun Yuhui, Hong Hui, Staunton James, Spencer Jonathan B, Leadlay Peter F
Department of Biochemistry, University of Cambridge, Tennis Court Road, Cambridge CB2 1GA, UK.
Chembiochem. 2008 May 5;9(7):1136-45. doi: 10.1002/cbic.200700715.
The biosynthetic gene cluster for tetronomycin (TMN), a polyether ionophoric antibiotic that contains four different types of ring, including the distinctive tetronic acid moiety, has been cloned from Streptomyces sp. NRRL11266. The sequenced tmn locus (113 234 bp) contains six modular polyketide synthase (PKS) genes and a further 27 open-reading frames. Based on sequence comparison to related biosynthetic gene clusters, the majority of these can be assigned a plausible role in TMN biosynthesis. The identity of the cluster, and the requirement for a number of individual genes, especially those hypothesised to contribute a glycerate unit to the formation of the tetronate ring, were confirmed by specific gene disruption. However, two large genes that are predicted to encode together a multifunctional PKS of a highly unusual type seem not to be involved in this pathway since deletion of one of them did not alter tetronomycin production. Unlike previously characterised polyether PKS systems, oxidative cyclisation appears to take place on the modular PKS rather than after transfer to a separate carrier protein, while tetronate ring formation and concomitant chain release share common mechanistic features with spirotetronate biosynthesis.
从链霉菌属NRRL11266中克隆出了用于生产特罗诺霉素(TMN)的生物合成基因簇,特罗诺霉素是一种聚醚离子载体抗生素,含有四种不同类型的环,包括独特的特ronic酸部分。已测序的tmn基因座(113234 bp)包含六个模块化聚酮合酶(PKS)基因和另外27个开放阅读框。基于与相关生物合成基因簇的序列比较,其中大多数在TMN生物合成中可被赋予合理的作用。通过特定的基因破坏证实了该基因簇的身份以及对许多单个基因的需求,特别是那些被假设为特ronic酸环形成贡献甘油酸单元的基因。然而,预计共同编码一种高度不寻常类型的多功能PKS的两个大基因似乎不参与该途径,因为其中一个基因的缺失并未改变特罗诺霉素的产量。与先前表征的聚醚PKS系统不同,氧化环化似乎发生在模块化PKS上,而不是转移到单独的载体蛋白之后,而特ronic酸环的形成和伴随的链释放与螺特ronic酸生物合成具有共同的机制特征。