Sibakov M, Palva I
Eur J Biochem. 1984 Dec 17;145(3):567-72. doi: 10.1111/j.1432-1033.1984.tb08594.x.
We have isolated and determined the 5'-end nucleotide sequence of the alpha-amylase gene from Bacillus licheniformis ATCC 14580. The alpha-amylase produced by this strain is thermostable and of liquefying type. The gene was originally cloned in a bacteriophage lambda 1059 vector. A subclone containing a 5.3 X 10(3)-base insert in pBR322 was further characterized. The nucleotide sequence coding for the 5' end of the structural gene together with the sequence coding for the upstream control regions was determined. The deduced N-terminal amino acid sequence was identical with the previously published amino acid sequence of B. licheniformis alpha-amylase. There was also very strong homology to the N-terminal sequence of Bacillus amyloliquefaciens alpha-amylase. The Mr of the thermostable alpha-amylase, as determined in vitro in a cell-free transcription/translation system of Escherichia coli, was about 55 000.
我们已从地衣芽孢杆菌ATCC 14580中分离并确定了α-淀粉酶基因的5'-末端核苷酸序列。该菌株产生的α-淀粉酶具有热稳定性且为液化型。该基因最初克隆于噬菌体λ1059载体中。对在pBR322中含有5.3×10³个碱基插入片段的亚克隆进行了进一步鉴定。确定了编码结构基因5'端的核苷酸序列以及编码上游控制区的序列。推导的N端氨基酸序列与先前发表的地衣芽孢杆菌α-淀粉酶的氨基酸序列相同。与解淀粉芽孢杆菌α-淀粉酶的N端序列也有很强的同源性。在大肠杆菌无细胞转录/翻译系统中体外测定的热稳定α-淀粉酶的Mr约为55000。