INRA, UMR1319 Micalis, 78352 Jouy-en-Josas, France.
J Biol Chem. 2013 Jul 12;288(28):20416-26. doi: 10.1074/jbc.M112.446344. Epub 2013 Jun 3.
Peptidoglycan hydrolases (PGHs) are responsible for bacterial cell lysis. Most PGHs have a modular structure comprising a catalytic domain and a cell wall-binding domain (CWBD). PGHs of bacteriophage origin, called endolysins, are involved in bacterial lysis at the end of the infection cycle. We have characterized two endolysins, Lc-Lys and Lc-Lys-2, identified in prophages present in the genome of Lactobacillus casei BL23. These two enzymes have different catalytic domains but similar putative C-terminal CWBDs. By analyzing purified peptidoglycan (PG) degradation products, we showed that Lc-Lys is an N-acetylmuramoyl-L-alanine amidase, whereas Lc-Lys-2 is a γ-D-glutamyl-L-lysyl endopeptidase. Remarkably, both lysins were able to lyse only Gram-positive bacterial strains that possess PG with D-Ala(4)→D-Asx-L-Lys(3) in their cross-bridge, such as Lactococcus casei, Lactococcus lactis, and Enterococcus faecium. By testing a panel of L. lactis cell wall mutants, we observed that Lc-Lys and Lc-Lys-2 were not able to lyse mutants with a modified PG cross-bridge, constituting D-Ala(4)→L-Ala-(L-Ala/L-Ser)-L-Lys(3); moreover, they do not lyse the L. lactis mutant containing only the nonamidated D-Asp cross-bridge, i.e. D-Ala(4)→D-Asp-L-Lys(3). In contrast, Lc-Lys could lyse the ampicillin-resistant E. faecium mutant with 3→3 L-Lys(3)-D-Asn-L-Lys(3) bridges replacing the wild-type 4→3 D-Ala(4)-D-Asn-L-Lys(3) bridges. We showed that the C-terminal CWBD of Lc-Lys binds PG containing mainly D-Asn but not PG with only the nonamidated D-Asp-containing cross-bridge, indicating that the CWBD confers to Lc-Lys its narrow specificity. In conclusion, the CWBD characterized in this study is a novel type of PG-binding domain targeting specifically the D-Asn interpeptide bridge of PG.
肽聚糖水解酶(PGHs)负责细菌细胞的裂解。大多数 PGHs 具有模块化结构,包括催化结构域和细胞壁结合结构域(CWBD)。噬菌体来源的 PGHs,称为内溶素,参与感染周期结束时的细菌裂解。我们已经鉴定了两种内溶素,Lc-Lys 和 Lc-Lys-2,它们存在于乳杆菌 BL23 基因组中的噬菌体中。这两种酶具有不同的催化结构域,但具有相似的假定 C 末端 CWBD。通过分析纯化的肽聚糖(PG)降解产物,我们表明 Lc-Lys 是 N-乙酰基胞壁酰-L-丙氨酸酰胺酶,而 Lc-Lys-2 是 γ-D-谷氨酰-L-赖氨酰内肽酶。值得注意的是,这两种溶菌酶只能裂解具有 D-Ala(4)→D-Asx-L-Lys(3) 交叉桥的革兰氏阳性细菌菌株,例如乳球菌、乳球菌和粪肠球菌。通过测试乳球菌细胞壁突变体的一组,我们观察到 Lc-Lys 和 Lc-Lys-2 不能裂解具有修饰的 PG 交叉桥的突变体,其构成 D-Ala(4)→L-Ala-(L-Ala/L-Ser)-L-Lys(3);此外,它们不能裂解仅含有非酰胺化的 D-Asp 交叉桥的乳球菌突变体,即 D-Ala(4)→D-Asp-L-Lys(3)。相比之下,Lc-Lys 可以裂解含有 3→3 L-Lys(3)-D-Asn-L-Lys(3)桥取代野生型 4→3 D-Ala(4)-D-Asn-L-Lys(3)桥的氨苄青霉素抗性粪肠球菌突变体。我们表明,Lc-Lys 的 C 末端 CWBD 结合主要含有 D-Asn 的 PG,但不结合仅含有非酰胺化的 D-Asp 交叉桥的 PG,表明 CWBD 赋予 Lc-Lys 其狭窄的特异性。总之,本研究中鉴定的 CWBD 是一种新型的 PG 结合结构域,专门针对 PG 的 D-Asn 肽间桥。