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利用液相色谱/质谱联用技术,通过FDLA和PMP衍生化对属于小单孢菌科的三个属,即小单孢菌属、链状游动放线菌属和库奇游动放线菌属的细胞壁肽聚糖结构进行分析。

Analyses of the cell-wall peptidoglycan structures in three genera Micromonospora, Catenuloplanes, and Couchioplanes belonging to the family Micromonosporaceae by derivatization with FDLA and PMP using LC/MS.

作者信息

Také Akira, Nakashima Takuji, Inahashi Yuki, Shiomi Kazuro, Takahashi Yōko, Ōmura Satoshi, Matsumoto Atsuko

机构信息

Graduate School of Infection Control Sciences, Kitasato University.

出版信息

J Gen Appl Microbiol. 2016 Sep 12;62(4):199-205. doi: 10.2323/jgam.2016.02.007. Epub 2016 Jul 29.

Abstract

It is the major characteristic of the cell-wall peptidoglycan structure in members of the family Micromonosporaceae that N-acetylmuramic acid (MurNAc) of glycan strand is replaced with N-glycolylmuramic acid (MurNGlyc). Consequently, it is difficult to use enzymatic methods for their peptidoglycan analyses. We therefore developed analysis method of peptidoglycan without using cell wall lytic enzymes as example to take the 3 genera, Micromonospora, Catenuloplanes, and Couchioplanes belonging to the family Micromonosporaceae, and their peptidoglycans were partially hydrolyzed with 4 M HCl at 60°C for 16 h followed by derivatization with N(α)-(5-fluoro-2,4-dinitrophenyl)-D-leucinamide (FDLA) or 1-phenyl-3-methyl-5-pyrazolone (PMP) and LC/MS analysis. Peptidoglycan of the genus Micromonospora consisted of a MurNGlyc-Gly-D-Glu-meso-diaminopimelyl (DAP)-D-Ala peptide stem and direct linkage between D-Ala and meso-DAP. In contrast, peptidoglycans of the genera Catenuloplanes and Couchioplanes consisted of a MurNGlyc-Gly-D-Glu-L-Lys-D-Ala peptide stem, and cross-linkage between D-Ala and L-Lys was mediated by an L-Ser residue. This method can be used to analyze the cell-wall peptidoglycan structure of other bacteria as well. By derivatization with FDLA or PMP followed by LC/MS analysis, the structure can be determined using only 0.2 mg of purified peptidoglycan.

摘要

小单孢菌科成员细胞壁肽聚糖结构的主要特征是聚糖链中的N-乙酰胞壁酸(MurNAc)被N-糖基胞壁酸(MurNGlyc)取代。因此,很难用酶法对其肽聚糖进行分析。因此,我们开发了一种不使用细胞壁裂解酶的肽聚糖分析方法,以小单孢菌科的小单孢菌属、链状小单孢菌属和库奇小单孢菌属这3个属为例,将它们的肽聚糖在60℃下用4 M盐酸部分水解16小时,然后用N(α)-(5-氟-2,4-二硝基苯基)-D-亮氨酰胺(FDLA)或1-苯基-3-甲基-5-吡唑啉酮(PMP)进行衍生化,再进行液相色谱/质谱分析。小单孢菌属的肽聚糖由MurNGlyc-Gly-D-Glu-内消旋二氨基庚二酸(DAP)-D-Ala肽茎以及D-Ala和内消旋DAP之间的直接连接组成。相比之下,链状小单孢菌属和库奇小单孢菌属的肽聚糖由MurNGlyc-Gly-D-Glu-L-Lys-D-Ala肽茎组成,D-Ala和L-Lys之间的交联由L-Ser残基介导。该方法也可用于分析其他细菌的细胞壁肽聚糖结构。通过用FDLA或PMP进行衍生化,然后进行液相色谱/质谱分析,仅使用0.2 mg纯化的肽聚糖就能确定其结构。

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