Archdeacon J, Talty J, Boesten B, Danchin A, O'Gara F
Microbiology Department, University College Cork, Ireland.
FEMS Microbiol Lett. 1995 May 1;128(2):177-84. doi: 10.1111/j.1574-6968.1995.tb07519.x.
A second adenylate cyclase (cya2) gene was isolated from a Rhizobium meliloti F34 gene bank. Complemented E. coli delta cya mutants were capable of utilizing a number of, but not all, carbon sources known to be regulated by cAMP. DNA hybridization studies showed cya2 to be unique to R. meliloti strains. The cya2 nucleotide sequence was determined and found to encode a protein of 363 amino acids. Residues were identified within the C-terminal domain which are conserved in both eukaryotic adenylate and guanylate cyclases, including a putative ATP binding site. Similar residues were also found in the prokaryotic R. meliloti Cya1 protein. A R. meliloti cya1/cya2 double mutant was constructed and characterized; however, cAMP production was still observed in this strain indicating the presence of a third cya gene.
从苜蓿根瘤菌F34基因文库中分离出第二个腺苷酸环化酶(cya2)基因。互补的大肠杆菌Δcya突变体能够利用一些但并非全部已知受cAMP调节的碳源。DNA杂交研究表明cya2是苜蓿根瘤菌菌株所特有的。测定了cya2核苷酸序列,发现其编码一个由363个氨基酸组成的蛋白质。在C末端结构域内鉴定出了在真核腺苷酸环化酶和鸟苷酸环化酶中均保守的残基,包括一个假定的ATP结合位点。在原核苜蓿根瘤菌Cya1蛋白中也发现了类似的残基。构建并表征了苜蓿根瘤菌cya1/cya2双突变体;然而,在该菌株中仍观察到cAMP的产生,这表明存在第三个cya基因。