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利用 Calcofluor white M2R 染色和延时显微镜监测单个苜蓿中华根瘤菌中结瘤多糖的产生。

Monitoring succinoglycan production in single Sinorhizobium meliloti cells by Calcofluor white M2R staining and time-lapse microscopy.

机构信息

Department of Natural Sciences, FCEFQyN, National University of Río Cuarto, Río Cuarto, Córdoba, Argentina.

Department of Natural Sciences, FCEFQyN, National University of Río Cuarto, Río Cuarto, Córdoba, Argentina; Department of Molecular Biology, FCEFQyN, National University of Río Cuarto, Río Cuarto, Córdoba, Argentina.

出版信息

Carbohydr Polym. 2018 Feb 1;181:918-922. doi: 10.1016/j.carbpol.2017.11.059. Epub 2017 Nov 16.

Abstract

Here, we describe a simple, non-time consuming and inexpensive method for monitoring of Calcofluor white M2R-binding exopolysaccharides in individual bacterial cells. This method was demonstrated by time-lapse microscopy of succinoglycan-producing cells of the plant-symbiotic alpha-proteobacterium Sinorhizobium meliloti. The method is most likely applicable to other bacteria producing β-(1→3) and β-(1→4) linked polysaccharides.

摘要

在这里,我们描述了一种简单、耗时短且廉价的方法,用于监测单个细菌细胞中 Calcofluor white M2R 结合胞外多糖。该方法通过对植物共生的α-变形菌根瘤菌 Sinorhizobium meliloti 产生鼠李糖半乳聚糖的细胞进行延时显微镜观察来进行演示。该方法很可能适用于其他产生β-(1→3)和β-(1→4)键合多糖的细菌。

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