Massidda O, Dardenne O, Whalen M B, Zorzi W, Coyette J, Shockman G D, Daneo-Moore L
Department of Microbiology and Immunology, Temple University School of Medicine, Philadelphia, PA 19140, USA.
FEMS Microbiol Lett. 1998 Sep 15;166(2):355-60. doi: 10.1111/j.1574-6968.1998.tb13912.x.
A reexamination of the nucleotide sequence of the psr gene of Enterococcus hirae revealed the presence of two additional nucleotides at residues 1190 and 1191. As a result, instead of a stop codon after 148 aa, the psr gene product would contain 293 aa residues. The revised size of the gene product was confirmed by subsequently cloning and expressing the psr gene in Escherichia coli. The derived amino acid sequence of the revised psr gene product was found to be similar to several other proteins in the combined GenBank/EMBL database. The protein products of some of these genes are thought to play regulatory role(s) in exo or capsular polysaccharide synthesis and/or in cell wall metabolism. All the putative homologs of the revised Psr appear to have a putative membrane-anchoring domain at their N-termini. Amino acid blocks with high degrees of similarity have been identified in the aligned sequences, and it is suggested that these common motifs could be of structural or functional importance.
对平肠球菌psr基因核苷酸序列的重新检查发现,在第1190和1191位残基处额外存在两个核苷酸。结果,psr基因产物在148个氨基酸后不是终止密码子,而是将包含293个氨基酸残基。通过随后在大肠杆菌中克隆和表达psr基因,证实了基因产物的修正大小。在合并的GenBank/EMBL数据库中,发现修正后的psr基因产物的推导氨基酸序列与其他几种蛋白质相似。其中一些基因的蛋白质产物被认为在胞外或荚膜多糖合成和/或细胞壁代谢中起调节作用。修正后的Psr的所有假定同源物在其N末端似乎都有一个假定的膜锚定结构域。在比对序列中已鉴定出具有高度相似性的氨基酸块,并且表明这些共同基序可能具有结构或功能重要性。