Vasantha N, Thompson L D, Rhodes C, Banner C, Nagle J, Filpula D
J Bacteriol. 1984 Sep;159(3):811-9. doi: 10.1128/jb.159.3.811-819.1984.
The genes for alkaline protease (apr[BamP]) and neutral protease (npr[BamP]) from Bacillus amyloliquefaciens have been isolated and expressed in Bacillus subtilis. The DNA sequences of apr[BamP] and npr[BamP] revealed, in each case, the presence of a large open reading frame. The inferred amino acid sequence of either gene contained a signal sequence and an additional polypeptide sequence ('pro' sequence) preceding the mature protein. Based on DNA sequence, the start point of translation has been identified as amino acid residue - 107 for apr[BamP] and -221 for npr[BamP]. To demonstrate that the start point of translation of apr[BamP] in vivo is probably at codon -107, codon -103 (AAA) was changed to an ochre (TAA) by site-directed mutagenesis. Alkaline protease was produced from this ochre mutant derivative of apr[BamP] only when the host strain was Su+. The presence of a pro sequence may be common to all of the secreted proteases from bacilli.
解淀粉芽孢杆菌的碱性蛋白酶(apr[BamP])基因和中性蛋白酶(npr[BamP])基因已被分离出来,并在枯草芽孢杆菌中表达。apr[BamP]和npr[BamP]的DNA序列在每种情况下都显示存在一个大的开放阅读框。任一基因推导的氨基酸序列在成熟蛋白之前都包含一个信号序列和一个额外的多肽序列(“前体”序列)。根据DNA序列,已确定apr[BamP]的翻译起始点为氨基酸残基-107,npr[BamP]的为-221。为了证明apr[BamP]在体内的翻译起始点可能在密码子-107处,通过定点诱变将密码子-103(AAA)改变为赭石型密码子(TAA)。只有当宿主菌株为Su+时,才从apr[BamP]的这种赭石型突变衍生物产生碱性蛋白酶。前体序列的存在可能是芽孢杆菌所有分泌型蛋白酶所共有的。