Parquet C, Flouret B, Leduc M, Hirota Y, van Heijenoort J
Eur J Biochem. 1983 Jun 15;133(2):371-7. doi: 10.1111/j.1432-1033.1983.tb07472.x.
Various experiments were carried out in an attempt to determine the possible physiological function of the N-acetylmuramoyl-L-alanine amidase purified from Escherichia coli K12 on the basis of its activity on N-acetylmuramoyl-L-alanyl-D-gamma-glutamyl-meso-diaminopimelic acid [MurNAc-LAla-DGlu(msA2pm)]. A Km value of 0.04 mM was determined with this substrate. Specificity studies revealed that compounds with a MurNAc-LAla linkage are the most probable substrates of this enzyme in vivo. Purified amidase had no effect on purified peptidoglycan and only low levels (1-2.5%) of cleaved MurNAc-LAla linkages were detected in peptidoglycan isolated from normally growing cells. However, the action of the amidase in vivo on peptidoglycan was clearly detectable during autolysis. The amidase activity of cells treated by osmotic shock, ether or toluene, as well as that of mutants with altered outer membrane composition was investigated. Attempts to reveal a transfer reaction catalysed by amidase were unsuccessful. Furthermore, by its location and specificity, amidase was clearly not involved in the formation of UDP-MurNAc. The possibility that it might be functioning in vivo as a hydrolase degrading exogeneous peptidoglycan fragments in the periplasma was substantiated by the fact that MurNAc itself and MurNAc-peptides could sustain growth of E. coli as sole carbon and nitrogen sources. Finally, out of 200 thermosensitive mutants examined for altered amidase activity, only two strains had less than 50% of the normal level of activity, whereas ten strains were found to possess more than 50%. In fact, two of the overproducers encountered presented a 4-5-fold increase in activity.
进行了各种实验,试图根据从大肠杆菌K12中纯化的N-乙酰胞壁酰-L-丙氨酸酰胺酶对N-乙酰胞壁酰-L-丙氨酰-D-γ-谷氨酰-内消旋二氨基庚二酸[MurNAc-LAla-DGlu(msA2pm)]的活性来确定其可能的生理功能。用该底物测定的Km值为0.04 mM。特异性研究表明,具有MurNAc-LAla连接的化合物最有可能是该酶在体内的底物。纯化的酰胺酶对纯化的肽聚糖没有影响,并且在从正常生长的细胞中分离的肽聚糖中仅检测到低水平(1-2.5%)的MurNAc-LAla连接的裂解。然而,在自溶过程中,酰胺酶在体内对肽聚糖的作用是明显可检测到的。研究了经渗透休克、乙醚或甲苯处理的细胞以及外膜组成改变的突变体的酰胺酶活性。揭示由酰胺酶催化的转移反应的尝试未成功。此外,根据其位置和特异性,酰胺酶显然不参与UDP-MurNAc的形成。MurNAc本身和MurNAc-肽可以作为唯一的碳源和氮源维持大肠杆菌的生长,这一事实证实了它可能在体内作为一种水解酶降解周质中外源肽聚糖片段的可能性。最后,在检测酰胺酶活性改变的200个温度敏感突变体中,只有两个菌株的活性低于正常水平的50%,而有十个菌株的活性高于50%。事实上,所遇到的两个高产菌株的活性增加了4-5倍。