Loessner M J, Gaeng S, Scherer S
Institut für Mikrobiologie, Forschungszentrum für Milch und Lebensmittel Weihenstephan, Technische Universität München, D-85350 Freising, Germany.
J Bacteriol. 1999 Aug;181(15):4452-60. doi: 10.1128/JB.181.15.4452-4460.1999.
We have cloned, sequenced, and characterized the genes encoding the lytic system of the unique Staphylococcus aureus phage 187. The endolysin gene ply187 encodes a large cell wall-lytic enzyme (71.6 kDa). The catalytic site, responsible for the hydrolysis of staphylococcal peptidoglycan, was mapped to the N-terminal domain of the protein by the expression of defined ply187 domains. This enzymatically active N terminus showed convincing amino acid sequence homology to an N-acetylmuramoyl-L-alanine amidase, whereas the C-terminal part, whose function is unknown, revealed striking relatedness to major staphylococcal autolysins. An additional reading frame was identified entirely embedded out of frame (+1) within the 5' region of ply187 and was shown to encode a small, hydrophobic protein of holin-like function. The hol187 gene features a dual-start motif, possibly enabling the synthesis of two products of different lengths (57 and 55 amino acids, respectively). Overproduction of Hol187 in Escherichia coli resulted in growth retardation, leakiness of the cytoplasmic membrane, and loss of de novo ATP synthesis. Compared to other holins identified to date, Hol187 completely lacks the highly charged C terminus. The secondary structure of the polypeptide is predicted to consist of two small, antiparallel, hydrophobic, transmembrane helices. These are supposed to be essential for integration into the membrane, since site-specific introduction of negatively charged amino acids into the first transmembrane domain (V7D G8D) completely abolished the function of the Hol187 polypeptide. With antibodies raised against a synthetic 18-mer peptide representing a central part of the protein, it was possible to detect Hol187 in the cytoplasmic membrane of phage-infected S. aureus cells. An important indication that the protein actually functions as a holin in vivo was that the gene (but not the V7D G8D mutation) was able to complement a phage lambda Sam mutation in a nonsuppressing E. coli HB101 background. Plaque formation by lambdagt11::hol187 indicated that both phage genes have analogous functions. The data presented here indicate that a putative holin is encoded on a different reading frame within the enzymatically active domain of ply187 and that the holin is synthesized during the late stage of phage infection and found in the cytoplasmic membrane, where it causes membrane lesions which are thought to enable access of Ply187 to the peptidoglycan of phage-infected Staphylococcus cells.
我们已经克隆、测序并鉴定了编码独特的金黄色葡萄球菌噬菌体187裂解系统的基因。内溶素基因ply187编码一种大型细胞壁裂解酶(71.6 kDa)。通过表达特定的ply187结构域,负责水解葡萄球菌肽聚糖的催化位点被定位到该蛋白的N端结构域。这个具有酶活性的N端与N - 乙酰胞壁酰 - L - 丙氨酸酰胺酶显示出令人信服的氨基酸序列同源性,而功能未知的C端部分则与主要的葡萄球菌自溶素显示出显著的相关性。在ply187的5'区域内,还鉴定出一个完全处于移码(+1)状态的额外阅读框,该阅读框编码一种具有类穿孔素功能的小疏水蛋白。hol187基因具有双起始基序,可能能够合成两种不同长度的产物(分别为57和55个氨基酸)。在大肠杆菌中过量表达Hol187会导致生长迟缓、细胞质膜渗漏以及从头合成ATP的能力丧失。与迄今鉴定的其他穿孔素相比,Hol187完全缺乏高度带电的C端。预测该多肽的二级结构由两个小的、反平行的、疏水的跨膜螺旋组成。这些螺旋被认为对于整合到膜中至关重要,因为将带负电荷的氨基酸位点特异性引入第一个跨膜结构域(V7D G8D)会完全消除Hol187多肽的功能。用针对代表该蛋白中心部分的合成18聚体肽产生的抗体,能够在噬菌体感染的金黄色葡萄球菌细胞的细胞质膜中检测到Hol187。该蛋白在体内实际作为穿孔素发挥作用的一个重要迹象是,该基因(而非V7D G8D突变)能够在非抑制性大肠杆菌HB101背景中互补噬菌体λ Sam突变。lambdagt11::hol187形成噬菌斑表明这两个噬菌体基因具有类似的功能。此处呈现的数据表明,一个假定的穿孔素编码于ply187酶活性结构域内的一个不同阅读框上,并且该穿孔素在噬菌体感染后期合成并存在于细胞质膜中,在那里它会导致膜损伤,据认为这使得Ply187能够进入噬菌体感染的葡萄球菌细胞的肽聚糖。