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鉴定和表征参与地衣芽孢杆菌新细菌胞外多糖生物合成的 6 种糖基转移酶。

Identification and characterization of six glycosyltransferases involved in the biosynthesis of a new bacterial exopolysaccharide in Paenibacillus elgii.

机构信息

Zhejiang Province Key Laboratory of Plant Secondary Metabolism and Regulation, College of Life Sciences, Zhejiang Sci-Tech University, Hangzhou, 310018, China.

The department of development technology of marine resources, College of Life Sciences, Zhejiang Sci-Tech University, Hangzhou, 310018, China.

出版信息

Appl Microbiol Biotechnol. 2018 Feb;102(3):1357-1366. doi: 10.1007/s00253-017-8673-y. Epub 2017 Dec 3.

Abstract

Paenibacillus elgii B69 produces a new xylose-containing exopolysaccharide (EPS) that effectively removes the pollutants from wastewater through flocculation. However, information about the biosynthesis of this EPS is limited. In this study, sequence analysis showed six putative glycosyltransferases (GTs) genes in polysaccharide gene clusters involved in glycosidic linkages of repeating units. Each gene was deleted and phenotypes were examined to understand the functions of these genes. Two of the genes were deleted successfully to encode a priming glucose GT and a side-chain xylose GT, but other genes were unsuccessfully deleted because of the accumulation of toxic intermediate products. The six genes were cloned and expressed in Escherichia coli, and the corresponding enzymes were purified. The activity of GTs was analyzed through mass spectrometry by using the purified membrane fraction as a lipid carrier receptor after a hexasaccharide repeated unit was reconstructed in vitro. The specificities of six different GTs and the building order of the hexasaccharide were characterized. This study provided a basis for future research on the biosynthetic pathway of EPS in Paenibacillus or other genera.

摘要

短小芽孢杆菌 B69 产生一种新型的含木糖胞外多糖(EPS),通过絮凝有效地去除废水中的污染物。然而,关于这种 EPS 的生物合成信息有限。在这项研究中,序列分析显示多糖基因簇中涉及重复单元糖苷键连接的六个假定糖基转移酶(GT)基因。每个基因都被删除,并观察表型以了解这些基因的功能。成功删除了两个基因,分别编码一个启动葡萄糖 GT 和一个侧链木糖 GT,但由于有毒中间产物的积累,其他基因的删除不成功。六个基因被克隆并在大肠杆菌中表达,并纯化了相应的酶。通过使用重建的六糖重复单元作为脂质载体受体,在体外分析了 GTs 的活性,使用纯化的膜部分通过质谱进行。表征了六种不同 GT 的特异性和六糖的构建顺序。这项研究为进一步研究短小芽孢杆菌或其他属的 EPS 生物合成途径提供了基础。

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