Wainwright Laura M, Elvers Karen T, Park Simon F, Poole Robert K
Department of Molecular Biology and Biotechnology, The University of Sheffield, Sheffield S10 2TN, UK.
School of Biomedical and Molecular Sciences, University of Surrey, Guildford GU2 7XH, UK.
Microbiology (Reading). 2005 Dec;151(Pt 12):4079-4091. doi: 10.1099/mic.0.28266-0.
Of the three groups of haemoglobins identified in micro-organisms (single-domain globins, flavohaemoglobins and truncated globins), the last group is the least well understood. The function of the truncated haemoglobin (Ctb) encoded by Cj0465c in the microaerophilic food-borne bacterial pathogen Campylobacter jejuni was investigated by constructing a ctb mutant and characterizing its phenotype. The effects of the ctb mutation on the kinetics of terminal oxidase function in C. jejuni were investigated using oxyleghaemoglobin and oxymyoglobin as sensitive reporters of O2 consumption. The Vmax of ctb mutant cells for O2, calculated using either globin, was greater than that of wild-type cells at extracellular O2 concentrations up to approximately 1 microM, suggesting a role for Ctb in moderating O2 supply for reduction by high-affinity terminal oxidases. However, cells mutated in ctb were disadvantaged when grown under conditions of high aeration, as revealed by measurements of growth yields and rates in batch culture. Furthermore, the rate at which ctb mutant cells consumed O2 in an O2 electrode (10-200 microM O2) was approximately half the rate displayed by wild-type cells, reflecting a role for Ctb in respiration at physiologically relevant external O2 concentrations. However, a lack of sensitivity of the mutant to paraquat or H2O2 indicated that increased oxidative stress under such conditions was not the cause of these phenotypes. O2 affinities of cells (Km values of approximately 40 nM and 1 microM) were unaffected by mutation of either Ctb or the full-length C. jejuni globin, Cgb. Although the gene encoding Ctb was found to be upregulated by S-nitrosoglutathione (GSNO) and the NO-donating compound S-nitroso-N-acetylpenicillamine (SNAP), a ctb mutant did not display sensitivity to a number of nitrosative stress-generating compounds. The authors conclude that Ctb is involved in moderating O2 flux within C. jejuni.
在微生物中鉴定出的三类血红蛋白(单结构域球蛋白、黄素血红蛋白和截短球蛋白)中,最后一类的了解最少。通过构建ctb突变体并表征其表型,研究了微需氧食源细菌病原体空肠弯曲菌中由Cj0465c编码的截短血红蛋白(Ctb)的功能。使用氧合血红蛋白和氧合肌红蛋白作为氧气消耗的敏感报告物,研究了ctb突变对空肠弯曲菌末端氧化酶功能动力学的影响。在细胞外氧气浓度高达约1微摩尔时,使用任一球蛋白计算得出的ctb突变体细胞对氧气的Vmax均大于野生型细胞,这表明Ctb在调节高亲和力末端氧化酶用于还原的氧气供应中发挥作用。然而,如分批培养中生长产量和速率的测量所示,在高通气条件下生长时,ctb突变的细胞处于劣势。此外,ctb突变体细胞在氧气电极中消耗氧气的速率(10 - 200微摩尔氧气)约为野生型细胞的一半,这反映了Ctb在生理相关的外部氧气浓度下呼吸中的作用。然而,突变体对百草枯或过氧化氢缺乏敏感性表明,在此类条件下氧化应激增加并非这些表型的原因。细胞的氧气亲和力(Km值约为40纳摩尔和1微摩尔)不受Ctb或空肠弯曲菌全长球蛋白Cgb突变的影响。尽管发现编码Ctb的基因被亚硝基谷胱甘肽(GSNO)和一氧化氮供体化合物亚硝基 - N - 乙酰青霉胺(SNAP)上调,但ctb突变体对多种产生亚硝化应激的化合物不敏感。作者得出结论,Ctb参与调节空肠弯曲菌内的氧气通量。