Saul D J, Williams L C, Toogood H S, Daniel R M, Bergquist P L
Centre for Gene Technology, University of Auckland, New Zealand.
Biochim Biophys Acta. 1996 Jul 31;1308(1):74-80. doi: 10.1016/0167-4781(96)00074-7.
The gene for a highly thermostable neutral proteinase (Npr) was isolated from Bacillus sp. strain EA1 by the polymerase chain reaction using consensus primers based on the sequences of npr genes from related species. The gene was sequenced and shown to be closely related to a neutral proteinase gene from Bacillus caldolyticus strain YP-T; the mature form of the enzyme differing by only a single amino acid. Enzyme samples were prepared from both the native organisms and also from recombinant Escherichia coli expressing the two npr genes. The proteinase from strain EA1 was shown to be significantly more thermostable than that from B. caldolyticus and that this difference is the result of a single amino acid substitution which is situated proximal to a region of the enzyme known to be crucial to conferring thermal stability. The phylogenetic relationship of EA1 to other Bacilli is also described.
利用基于相关物种npr基因序列的共有引物,通过聚合酶链反应从芽孢杆菌属菌株EA1中分离出一种高度耐热中性蛋白酶(Npr)的基因。对该基因进行了测序,结果表明它与嗜热解芽孢杆菌菌株YP-T的中性蛋白酶基因密切相关;该酶的成熟形式仅相差一个氨基酸。从天然生物体以及表达这两个npr基因的重组大肠杆菌中都制备了酶样品。结果表明,菌株EA1的蛋白酶比嗜热解芽孢杆菌的蛋白酶具有更高的热稳定性,这种差异是由一个氨基酸取代导致的,该取代位于已知对赋予热稳定性至关重要的酶区域附近。还描述了EA1与其他芽孢杆菌的系统发育关系。