Weerakoon L K, Jayaswal R K
Department of Biological Sciences, Illinois State University, Normal 61790-4120, USA.
FEMS Microbiol Lett. 1995 Nov 1;133(1-2):9-15. doi: 10.1111/j.1574-6968.1995.tb07853.x.
The nucleotide sequence of a 1.1-kb DNA fragment upstream of a peptidoglycan hydrolase-encoding gene (lytA) from bacteriophage phi 11 of Staphylococcus aureus was determined to see if the upstream sequences are involved in the transfer of the lytA product through the cytoplasmic membrane. Sequencing revealed three open reading frames of 171, 147 and 435 bp with consensus Shine-Dalgarno sequences located upstream from the ATG start codons. The third open reading frame overlaps with the 5' end of lytA by 18 nucleotides. Comparison of the deduced amino acid sequences of the open reading frames with the amino acid sequences in the NCBI Entrez database did not show any significant homology to any sequenced polypeptides. However, the analysis of the peptides showed some structural similarities to the product of the holin gene family. Lysogens containing an insertional mutation in ORF3, upon induction, produced either no phage titer or very low phage titers, compared to the wild-type lysogen. Transformation of ORF3 mutated lysogens by a plasmid containing the intact ORF3 produced the same phage titer as wild-type lysogen, suggesting that the ORF3 product is involved in the process of cell lysis/phage release.
测定了金黄色葡萄球菌噬菌体phi 11中肽聚糖水解酶编码基因(lytA)上游1.1 kb DNA片段的核苷酸序列,以确定上游序列是否参与lytA产物通过细胞质膜的转运。测序揭示了三个开放阅读框,长度分别为171、147和435 bp,在ATG起始密码子上游具有一致的Shine-Dalgarno序列。第三个开放阅读框与lytA的5'端重叠18个核苷酸。将开放阅读框推导的氨基酸序列与NCBI Entrez数据库中的氨基酸序列进行比较,未发现与任何已测序多肽有明显同源性。然而,对这些肽段的分析显示与孔蛋白基因家族的产物有一些结构相似性。与野生型溶原菌相比,在ORF3中含有插入突变的溶原菌在诱导后产生的噬菌体滴度要么为零,要么非常低。用含有完整ORF3的质粒转化ORF3突变的溶原菌,产生的噬菌体滴度与野生型溶原菌相同,表明ORF3产物参与细胞裂解/噬菌体释放过程。