Yang M, Galizzi A, Henner D
Nucleic Acids Res. 1983 Jan 25;11(2):237-49. doi: 10.1093/nar/11.2.237.
The gene coding for amylase (EC.3.2.1.1) has been isolated and sequenced from Bacillus subtilis by cloning in lambda Charon4A and pBR322. The entire coding sequence and large preceding and following regions, comprising the presumed transcriptional and translational regulatory regions, were sequenced. The coding sequence shows a large open reading frame with a translated molecular weight of 72,800 and a presumed signal sequence of approximately thirty-two amino acids. When the intact gene is present in Escherichia coli, it confers the ability to degrade starch, indicating that the gene is expressed in a functional state.
通过克隆到λ噬菌体Charon4A和pBR322中,已从枯草芽孢杆菌中分离并测序了编码淀粉酶(EC.3.2.1.1)的基因。对整个编码序列以及包括假定的转录和翻译调控区域在内的上下游大片段区域进行了测序。编码序列显示出一个大的开放阅读框,其翻译后的分子量为72,800,并且有一个约32个氨基酸的假定信号序列。当完整基因存在于大肠杆菌中时,它赋予了降解淀粉的能力,这表明该基因以功能状态表达。