Hofer B, Ruge M, Dreiseikelmann B
Universität Bielefeld, Fakultät für Biologie, Lehrstuhl für Mikrobiologie/Gentechnologie, Germany.
J Bacteriol. 1995 Jun;177(11):3080-6. doi: 10.1128/jb.177.11.3080-3086.1995.
Previous work has shown that the sieA gene of Salmonella bacteriophage P22 is located between the genes mnt and 16. We cloned DNA fragments of the region into multicopy vectors and tested the transformants for mediating superinfection exclusion. Subcloning, phenotypical tests, and DNA sequencing resulted in the identification of the sieA gene. There are two possible initiation codons within one open reading frame of 492 or 480 bp. The deduced amino acid sequence leads to a hypothetical polypeptide with a calculated molecular mass of 18.8 or 18.3 kDa, respectively. According to three hydrophobic regions, all of which are long enough to span the membrane, the product of sieA should be a protein of the inner membrane of a P22-lysogenic cell of Salmonella typhimurium. The SieA protein was moderately overproduced from an expression vector in cultures of Escherichia coli and could be recovered from the membrane fraction.
先前的研究表明,沙门氏菌噬菌体P22的sieA基因位于mnt和16基因之间。我们将该区域的DNA片段克隆到多拷贝载体中,并测试转化体介导的超感染排除作用。通过亚克隆、表型测试和DNA测序鉴定出了sieA基因。在一个492或480 bp的开放阅读框内有两个可能的起始密码子。推导的氨基酸序列分别产生一个计算分子量为18.8或18.3 kDa的假想多肽。根据三个疏水区,它们都足够长以跨越细胞膜,sieA的产物应该是鼠伤寒沙门氏菌P22溶原细胞内膜的一种蛋白质。SieA蛋白在大肠杆菌培养物中由表达载体适度过量表达,并可从膜部分回收。