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耻垢分枝杆菌中假定的聚酮环化酶MSMEG_0129:纯化、结晶及X射线晶体学分析。

The putative polyketide cyclase MSMEG_0129 from Mycobacterium smegmatis: purification, crystallization and X-ray crystallographic analysis.

作者信息

Zheng Shuping, Zhou Ying, Fleming Joy, Zhou Yafeng, Liu Wei, Bi Lijun

机构信息

Key Laboratory of RNA Biology, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, People's Republic of China.

School of Stomatology and Medicine, Foshan University, Foshan, Guangdong 528000, People's Republic of China.

出版信息

Acta Crystallogr F Struct Biol Commun. 2017 Jul 1;73(Pt 7):437-442. doi: 10.1107/S2053230X17008937. Epub 2017 Jun 30.

Abstract

Mycobacterium tuberculosis Rv0164 has previously been identified as a human T-cell antigen that induces significant production of IFN-γ in human peripheral blood mononuclear cells. M. smegmatis MSMEG_0129 shares 59% sequence identity with Rv0164. Based on sequence alignment, both proteins are predicted to be members of the cyclase/dehydrase family, which is part of a large group of enzymes referred to as type II polyketide synthases (PKSs). In biosynthetic pathways mediated by type II PKSs, cyclases catalyze the conversion of linear poly-β-ketones to cyclized intermediates. To date, no mycobacterial type II PKSs have been reported. Here, the goal is to determine whether these proteins adopt similar folds to reported cyclase structures, and to this end MSMEG_0129 was cloned, expressed, purified and crystallized. An X-ray diffraction data set was collected to 1.95 Å resolution from a crystal belonging to space group P6, with unit-cell parameters a = 109.76, b = 109.76, c = 56.5 Å, α = 90, β = 90, γ = 120°. Further crystallographic analysis should establish a basis for investigating the structure and function of this putative mycobacterial type II PKS enzyme.

摘要

结核分枝杆菌Rv0164先前已被鉴定为一种人类T细胞抗原,可在人外周血单核细胞中诱导大量干扰素-γ的产生。耻垢分枝杆菌MSMEG_0129与Rv0164的序列同一性为59%。基于序列比对,这两种蛋白质均被预测为环化酶/脱水酶家族的成员,该家族是被称为II型聚酮合酶(PKSs)的一大类酶的一部分。在由II型PKSs介导的生物合成途径中,环化酶催化线性聚-β-酮转化为环化中间体。迄今为止,尚未有分枝杆菌II型PKSs的报道。在此,目标是确定这些蛋白质是否采用与已报道的环化酶结构相似的折叠方式,为此对MSMEG_0129进行了克隆、表达、纯化和结晶。从属于空间群P6的晶体收集了分辨率为1.95 Å的X射线衍射数据集,其晶胞参数为a = 109.76、b = 109.76、c = 56.5 Å,α = 90、β = 90、γ = 120°。进一步的晶体学分析应为研究这种假定的分枝杆菌II型PKS酶的结构和功能奠定基础。

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