Keil H
Department of Biology and Biochemistry, Brunel University, Uxbridge, Middlesex, UK.
J Gen Microbiol. 1990 Apr;136(4):607-13. doi: 10.1099/00221287-136-4-607.
Azotobacter vinelandii strain 206 degrades benzoate via the meta-cleavage pathway. In a genomic library derived from this organism a clone was obtained which carried and expressed the gene for the third enzyme in this pathway, catechol 2,3-dioxygenase (EC 1.13.11.2), on a 5.9 kb SalI restriction fragment. The structural gene was more precisely mapped on an internal 1.6 kb EcoRI fragment which, after insertion into expression vectors, directed the synthesis of a 33 kDa polypeptide. The gene showed very little or no homology with isofunctional genes derived from Pseudomonas. Comprehensive substrate specificity analysis showed significant differences between the specific activities obtained from the cloned gene product and extracts derived from Azotobacter itself.
维涅兰德固氮菌206菌株通过间位裂解途径降解苯甲酸酯。在来源于该微生物的基因组文库中,获得了一个克隆,其在一个5.9 kb的SalI限制性片段上携带并表达了该途径中第三种酶即儿茶酚2,3 -双加氧酶(EC 1.13.11.2)的基因。该结构基因更精确地定位在一个内部1.6 kb的EcoRI片段上,将其插入表达载体后,指导合成了一种33 kDa的多肽。该基因与来源于假单胞菌的同功能基因几乎没有同源性。全面的底物特异性分析表明,从克隆的基因产物获得的比活性与固氮菌自身提取物的比活性之间存在显著差异。