摘要
黄海黄杆菌 YS- 94 12 - 130具有稳定的分泌低温碱性蛋白酶的能力。将其染色体 DNA用 Sau3A 部分酶切后 ,低熔点琼脂糖回收 2 - 10 Kb的 DNA片段 ,用 Klenow大片段酶半补齐 ,与用 Sal 酶切且半补齐的质粒 p UC19连接后 ,转化 E.Coli.JM10 9,构建基因文库。用酪蛋白平板法和酶联免疫吸附 ( EL ISA)的活性筛选方法从基因文库中筛选到一株产海洋低温碱性酶的阳性克隆 (命名为p HH1)。序列测定分析表明 ,此重组质粒包含有长度为 768bp低温碱性蛋白酶基因的完整的开放读码框架 ( ORF)和上游基因调控序列。此片段编码由 2 56个氨基酸组成的酶 ,计算分子量为 330 0 0 Dal。通过 Southern杂交证实了此片段来自于黄海黄杆菌 YS- 94 12 - 130基因组 DNA。
F. yellowsea YS 9412 130 stably secreted low temperature alkaline protease. For the preparation of gene libraries, genomic DNA from F. yellowesea YS 9412 130 was digested partially with Sau3AⅠ,and the fragments from 2Kb to 10kb were recovered.The cohesive ends partially filled in by klenow fragment of DNA polymeraseⅠ(PolⅠk). DNA of plasmid pUC19 was cleaved with SalⅠand subsequently partially filled in with PolⅠk. The plasmid and the genomic DNAs were mixed and ligated. Then the recombinant plasmid transformed E.coli.JM109. One positive clone was obtained from the libraries with casein flat and ELISA sieve method. The analysis of sequence detection show that the positive clone includs the Open Read Frame of low temperature alkaline protease gene. The fragment coded the enzyme of 256 amino acid, the molecular weight of which is 33 000Dal. Through Southern hybridization, the fragment is confirmed to come from F.yellowsea YS 9412 130 genomic DNA.
出处
《海洋水产研究》
CSCD
2000年第4期46-53,共8页
Marine Fisheries Research
基金
国家"海洋 86 3"项目! (86 3-819-0 6 -0 1)资助
关键词
低温碱性蛋白酶
基因克隆
序列测定
Marine low temperature alkaline protease Gene cloning Sequencing
