Rosenthal R S, Jungkind D, Daneo-Moore L, Shockman G D
J Bacteriol. 1975 Oct;124(1):398-409. doi: 10.1128/jb.124.1.398-409.1975.
Growing protoplasts of Streptococcus faecalis 9790 were found to synthesize and excrete soluble peptidoglycan fragments. The presence of soluble peptidoglycan derivatives in culture supernatants was determined by (i) incorporation of three different radioactively labeled precursors (L-lysine, D-alanine, and acetate) into products which, after hen egg-white lysozyme hydrolysis, had the same KD values on gel filtration as muramidase hydrolysis products of isolated walls; (ii) inhibition of net synthesis of these products by cycloserine and vancomycin; and (iii) identification of disaccharide-peptide monomer using the beta-elimination reaction, gel filtration, and high-voltage paper electrophoresis. Under the conditions of these experiments the presence of newly synthesized, acid-precipitable (macromolecular) peptidoglycan was not detected. The predominance of monomer (70 to 80%) in lysozyme digests of peptidoglycan synthesized by protoplasts was in sharp contrast to digest of walls from intact streptococci which contain mostly peptide cross-linked products. Biosynthesis and release of relatively uncross-linked, soluble peptidoglycan fragments by protoplasts was related to the absence of suitable, preexisting acceptor wall.
粪肠球菌9790生长中的原生质体被发现能合成并分泌可溶性肽聚糖片段。通过以下方法确定培养上清液中可溶性肽聚糖衍生物的存在:(i)将三种不同的放射性标记前体(L-赖氨酸、D-丙氨酸和乙酸盐)掺入产物中,这些产物在经鸡卵清溶菌酶水解后,在凝胶过滤中的KD值与分离细胞壁的溶菌酶水解产物相同;(ii)环丝氨酸和万古霉素对这些产物净合成的抑制作用;(iii)使用β-消除反应、凝胶过滤和高压纸电泳鉴定二糖-肽单体。在这些实验条件下,未检测到新合成的、酸可沉淀的(大分子)肽聚糖的存在。原生质体合成的肽聚糖经溶菌酶消化后,单体占主导(70%至80%),这与完整链球菌细胞壁的消化形成鲜明对比,后者大多含有肽交联产物。原生质体合成并释放相对未交联的可溶性肽聚糖片段与缺乏合适的、预先存在的受体壁有关。