Lunsford R D, Roble A G
Oral Infection and Immunity Branch, National Institute of Dental Research, Bethesda, Maryland, USA.
J Bacteriol. 1997 May;179(10):3122-6. doi: 10.1128/jb.179.10.3122-3126.1997.
Tn4001 mutagenesis identified a new competence gene in Streptococcus gordonii Challis designated comYA. A comYA mutant was completely deficient in transformation and exhibited decreased levels of DNA binding and hydrolysis. The deduced 319-amino-acid ComYA protein exhibited 57% similarity and 33% identity to the ComGA transporter protein of Bacillus subtilis and contained the Walker A-box motif conserved in ATP-binding proteins as well as aspartic acid boxes Asp-1 and Asp-2 present in some components of the general secretory pathway of gram-negative bacteria. comYA appeared to be part of a putative operon encompassing a comGB homolog, designated comYB, together with sequences that could encode ComGC- and ComGD-like peptides designated ComYC and ComYD, respectively, as well as other components. The putative ComYC and ComYD peptides had leader sequences similar to the type IV N-methylphenylalanine pilins of gram-negative bacteria, but unlike other examples in this class, including B. subtilis, they contained an alanine at position -1 of the leader instead of the usual glycine residue. Northern analysis identified a single 6.0-kb comYA-containing transcript strictly dependent on exogenous competence factor for expression in ComA1 cells. An identical pattern of expression was seen in wild-type Challis cells grown under conditions of maximal competence but not in cells that were noncompetent.
Tn4001诱变在戈登氏链球菌Challis中鉴定出一个新的感受态基因,命名为comYA。comYA突变体在转化方面完全缺陷,并且DNA结合和水解水平降低。推导的319个氨基酸的ComYA蛋白与枯草芽孢杆菌的ComGA转运蛋白具有57%的相似性和33%的同一性,包含ATP结合蛋白中保守的沃克A框基序以及革兰氏阴性菌一般分泌途径某些组分中存在的天冬氨酸框Asp-1和Asp-2。comYA似乎是一个推定操纵子的一部分,该操纵子包含一个comGB同源物,命名为comYB,以及分别可编码ComGC样和ComGD样肽(命名为ComYC和ComYD)的序列以及其他组分。推定的ComYC和ComYD肽具有与革兰氏阴性菌IV型N-甲基苯丙氨酸菌毛蛋白相似的前导序列,但与包括枯草芽孢杆菌在内的该类其他例子不同的是,它们在前导序列的-1位含有丙氨酸而非通常的甘氨酸残基。Northern分析鉴定出一个单一的含6.0-kb comYA的转录本,其表达严格依赖于外源性感受态因子,在ComA1细胞中表达。在最大感受态条件下生长的野生型Challis细胞中观察到相同的表达模式,但在无感受态的细胞中未观察到。