Bibb M J, Molle V, Buttner M J
Department of Molecular Microbiology, John Innes Centre, Colney, Norwich NR4 7UH, United Kingdom.
J Bacteriol. 2000 Aug;182(16):4606-16. doi: 10.1128/JB.182.16.4606-4616.2000.
Sporulation mutants of Streptomyces coelicolor appear white because they are defective in the synthesis of the gray polyketide spore pigment, and such white (whi) mutants have been used to define 13 sporulation loci. whiN, one of five new whi loci identified in a recent screen of NTG (N-methyl-N'-nitro-N-nitrosoguanidine)-induced whi strains (N. J. Ryding et al., J. Bacteriol. 181:5419-5425, 1999), was defined by two mutants, R112 and R650. R650 produced frequent spores that were longer than those of the wild type. In contrast, R112 produced long, straight, undifferentiated hyphae, although rare spore chains were observed, sometimes showing highly irregular septum placement. Subcloning and sequencing showed that whiN encodes a member of the extracytoplasmic function subfamily of RNA polymerase sigma factors and that the sigma factor has an unusual N-terminal extension of approximately 86 residues that is not present in other sigma factors. A constructed whiN null mutant failed to form aerial mycelium (the "bald" phenotype) and, as a consequence, whiN was renamed bldN. This observation was not totally unexpected because, on some media, the R112 point mutant produced substantially less aerial mycelium than its parent, M145. The bldN null mutant did not fit simply into the extracellular signaling cascade proposed for S. coelicolor bld mutants. Expression of bldN was analyzed during colony development in wild-type and aerial mycelium-deficient bld strains. bldN was transcribed from a single promoter, bldNp. bldN transcription was developmentally regulated, commencing approximately at the time of aerial mycelium formation, and depended on bldG and bldH, but not on bldA, bldB, bldC, bldF, bldK, or bldJ or on bldN itself. Transcription from the p1 promoter of the response-regulator gene bldM depended on bldN in vivo, and the bldMp1 promoter was shown to be a direct biochemical target for sigma(BldN) holoenzyme in vitro.
天蓝色链霉菌的孢子形成突变体呈现白色,因为它们在灰色聚酮类孢子色素的合成上存在缺陷,并且这类白色(whi)突变体已被用于定义13个孢子形成位点。whiN是在最近对NTG(N-甲基-N'-硝基-N-亚硝基胍)诱导的whi菌株进行的筛选中鉴定出的五个新whi位点之一(N. J. Ryding等人,《细菌学杂志》181:5419 - 5425,1999),由两个突变体R112和R650定义。R650产生的孢子频繁,且比野生型的孢子长。相比之下,R112产生长而直的未分化菌丝,尽管观察到有罕见的孢子链,有时隔膜放置高度不规则。亚克隆和测序表明,whiN编码RNA聚合酶σ因子胞外功能亚家族的一个成员,并且该σ因子具有约86个残基的异常N端延伸,这在其他σ因子中不存在。构建的whiN缺失突变体无法形成气生菌丝(“光秃”表型),因此,whiN被重新命名为bldN。这一观察结果并非完全出乎意料,因为在某些培养基上,R112点突变体产生的气生菌丝比其亲本M145少得多。bldN缺失突变体并不简单地符合为天蓝色链霉菌bld突变体提出的细胞外信号级联反应。在野生型和气生菌丝缺陷型bld菌株的菌落发育过程中分析了bldN的表达。bldN从单个启动子bldNp转录。bldN转录受到发育调控,大约在气生菌丝形成时开始,并且依赖于bldG和bldH,但不依赖于bldA、bldB、bldC、bldF、bldK或bldJ,也不依赖于bldN本身。体内响应调节基因bldM的p1启动子的转录依赖于bldN,并且在体外bldMp1启动子被证明是σ(BldN)全酶的直接生化靶标。