Hulett F M
J Bacteriol. 1984 Jun;158(3):978-82. doi: 10.1128/jb.158.3.978-982.1984.
The structural gene for alkaline phosphatase (orthophosphoric monoester phosphohydrolase; EC 3.1.3.1) of Bacillus licheniformis MC14 was cloned into the Pst1 site of pMK2004 from chromosomal DNA. The gene was cloned on an 8.5-kilobase DNA fragment. A restriction map was developed, and the gene was subcloned on a 4.2-kilobase DNA fragment. The minimum coding region of the gene was localized to a 1.3-kilobase region. Western blot analysis was used to show that the gene coded for a 60,000-molecular-weight protein which cross-reacts with anti-alkaline phosphatase prepared against the salt-extractable membrane alkaline phosphatase of B. licheniformis MC14 .
地衣芽孢杆菌MC14碱性磷酸酶(正磷酸单酯磷酸水解酶;EC 3.1.3.1)的结构基因从染色体DNA克隆到pMK2004的Pst1位点。该基因克隆在一个8.5千碱基的DNA片段上。构建了限制酶图谱,并将该基因亚克隆到一个4.2千碱基的DNA片段上。该基因的最小编码区定位在一个1.3千碱基的区域。蛋白质免疫印迹分析表明,该基因编码一种分子量为60000的蛋白质,它与针对地衣芽孢杆菌MC14盐可提取膜碱性磷酸酶制备的抗碱性磷酸酶发生交叉反应。