Waugh S I, Paulsen D M, Mylona P V, Maynard R H, Premakumar R, Bishop P E
Department of Microbiology, North Carolina State University, Raleigh 27695-7615.
J Bacteriol. 1995 Mar;177(6):1505-10. doi: 10.1128/jb.177.6.1505-1510.1995.
vnfG and anfG encode the delta subunits of alternative nitrogenases 2 and 3 in Azotobacter vinelandii, respectively. As a first step towards elucidating the role of these subunits, diazotrophic growth and acetylene reduction studies were conducted on mutants containing alterations in the genes encoding these subunits. Mutants containing a stop codon (C36stop) or an in-frame deletion in anfG were unable to grow in N-free, Mo-deficient medium (Anf-). Mutants in which cysteine 36 of AnfG (a residue conserved between VnfG and AnfG) was changed to Ala or Ser were Anf+. Thus, this conserved cysteine is not essential for the function of AnfG in dinitrogenase 3. A mutant with a stop codon in vnfG (C17stop) grew after a lag of 25 h in N-free, Mo-deficient medium containing V2O5. However, a Nif- Anf- strain with this mutation was unable to grow under these conditions. This shows that the vnfG gene product is required for nitrogenase 2-dependent growth. Strains with mutations in vnfG and anfG reduced acetylene to different degrees. This indicates that the delta subunits are not required for acetylene reduction by nitrogenases 2 and 3.
vnfG 和 anfG 分别编码棕色固氮菌中交替型固氮酶2和3的δ亚基。作为阐明这些亚基作用的第一步,对编码这些亚基的基因发生改变的突变体进行了固氮生长和乙炔还原研究。含有终止密码子(C36stop)或 anfG 框内缺失的突变体无法在无氮、缺钼培养基(Anf-)中生长。AnfG 的半胱氨酸36(VnfG 和 AnfG 之间保守的一个残基)被替换为丙氨酸或丝氨酸的突变体是 Anf+。因此,这个保守的半胱氨酸对于固氮酶3中 AnfG 的功能不是必需 的。在含有V2O5的无氮、缺钼培养基中,具有 vnfG 终止密码子(C17stop)的突变体在延迟25小时后生长。然而,具有这种突变的Nif- Anf- 菌株在这些条件下无法生长。这表明 vnfG 基因产物是固氮酶2依赖性生长所必需的。vnfG 和 anfG 发生突变的菌株对乙炔的还原程度不同。这表明δ亚基不是固氮酶2和3还原乙炔所必需的。