Roten C A, Pagni M, Margot P, Touri F, Karamata D
Institut de génétique et de biologie microbiennes, Lausanne, Switzerland.
Anal Biochem. 1994 Dec;223(2):208-11. doi: 10.1006/abio.1994.1575.
A radioassay for the determination of the peptidoglycan cross-linking index (CLI) was devised. It is based on specific radioactive labeling of diaminopimelic acid (DAP) by diverting [14C]aspartate into the DAP pathway, while inhibiting incorporation of label into other cell wall components. Purified [14C]DAP-labeled cell walls were treated with fluorodinitrobenzene, hydrolyzed, and chromatographed by TLC. The radioactivity in well-separated mono dinitrophenyl-diaminopimelate (DNP-DAP) and DAP spots was counted and the CLI was determined from the ratio of DAP to the total of mono DNP-DAP and DAP counts. The method, suitable for bacteria such as Bacillus subtilis unable to incorporate exogenous DAP, can be applied to other systems. A CLI of 50.8 +/- 1.3% and 55.5 +/- 0.9% was obtained for B. subtilis 168 cells growing exponentially in rich and minimal medium, respectively. Comparison of these to results previously obtained on B. subtilis suggested the existence of a hitherto unreported peptidoglycan endopeptidase activity.
设计了一种用于测定肽聚糖交联指数(CLI)的放射分析方法。该方法基于通过将[14C]天冬氨酸转入二氨基庚二酸(DAP)途径对DAP进行特异性放射性标记,同时抑制标记物掺入其他细胞壁成分。用氟二硝基苯处理纯化的[14C]DAP标记的细胞壁,水解后通过薄层层析进行色谱分析。对分离良好的单二硝基苯基 - 二氨基庚二酸(DNP - DAP)和DAP斑点中的放射性进行计数,并根据DAP与单DNP - DAP和DAP计数总和的比率确定CLI。该方法适用于无法掺入外源DAP的枯草芽孢杆菌等细菌,也可应用于其他系统。在丰富培养基和基本培养基中指数生长的枯草芽孢杆菌168细胞的CLI分别为50.8 +/- 1.3%和55.5 +/- 0.9%。将这些结果与先前在枯草芽孢杆菌上获得的结果进行比较,表明存在一种迄今未报道的肽聚糖内肽酶活性。