Eck R, Belter J
Martin-Luther-University Halle-Wittenberg, Institute of Microbiology, Halle/Saale, Germany.
Gene. 1993 Jan 15;123(1):87-92. doi: 10.1016/0378-1119(93)90544-d.
The catA gene, coding for the catechol 1,2-dioxygenase (C12O) of the bacterial strain Arthrobacter sp. mA3, was cloned and expressed in Escherichia coli. One plasmid containing a 6.1-kb EcoRI insert was selected by its ability to degrade catechol and to accumulate cis-cis-muconate. The DNA insert of this plasmid was mapped with restriction enzymes. The catA gene was subcloned on a 1.3-kb PstI-EcoRI fragment by deleting the adjacent restriction fragments. The nucleotide sequence of catA was determined. The C12O is coded for by a gene spanning 849 nucleotides and the deduced M(r) of the protein is 30,560. The polypeptide encoded by the cloned catA gene was expressed in an E. coli minicell system and detected by gel electrophoresis.
编码节杆菌属菌株mA3的儿茶酚1,2-双加氧酶(C12O)的catA基因被克隆并在大肠杆菌中表达。通过其降解儿茶酚和积累顺式-顺式粘康酸的能力,选择了一个含有6.1 kb EcoRI插入片段的质粒。用限制性内切酶对该质粒的DNA插入片段进行了图谱分析。通过删除相邻的限制性片段,将catA基因亚克隆到一个1.3 kb的PstI-EcoRI片段上。测定了catA的核苷酸序列。C12O由一个跨越849个核苷酸的基因编码,该蛋白质推导的M(r)为30,560。克隆的catA基因编码的多肽在大肠杆菌小细胞系统中表达,并通过凝胶电泳检测。