Pronk A F, Stouthamer A H, Van Verseveld H W, Boogerd F C
Department of Microbiology, BioCentrum Amsterdam, Vrije Universiteit, Amsterdam, The Netherlands.
J Bacteriol. 1995 Jan;177(1):75-81. doi: 10.1128/jb.177.1.75-81.1995.
When Azorhizobium caulinodans was grown in chemostat cultures with N2 as the N source at a constant dilution rate of 0.1 h-1 in media with a constant concentration (50 mM) of succinate and variable concentrations (1.5 to 585 microM) of nicotinate, neither the growth yield on succinate, the specific rate of O2 consumption, nor the specific rate of CO2 production showed linear regression with the concentration of nicotinate. Moreover, for transient continuous cultures in which the nicotinate concentration was gradually lowered, growth parameters remained unchanged until an apparently critical level of 0.7 microM nicotinate was reached. Below this nicotinate level, an immediate washout of the chemostat population began. A. caulinodans nicotinate hydroxylase-negative mutant 61007, unable to catabolize nicotinate, and the wild type behaved similarly. Thus, for continuous cultures supplied with N2 as the N source, submicromolar concentrations of nicotinate both sustained pyridine nucleotide biosynthesis at sufficient levels and precluded the use of nicotinate as a catabolic substrate. Furthermore, when more nicotinate was provided, dual succinate-nicotinate limitation in continuous cultures did not occur. Finally, when nicotinate is present in suboptimal concentrations, the specific growth rate is directly proportional to the amount of nicotinate present per unit of biomass. By contrast, in batch cultures with different nicotinate concentrations and with either succinate or lactate as the carbon and energy source, anomalous growth curves were obtained. With a low concentration (1.5 microM) of nicotinate, growth on N2 occurred, albeit at low rates. With a high concentration (195 microM) of nicotinate, growth on N2 was temporarily stimulated, but nicotinate was quickly exhausted and growth was thereafter nicotinate limited. Continuous supplementation of batch cultures with nicotinate allowed only transient exponential growth followed by linear growth. Thus, also for batch cultures, nicotinate catabolism is dispensable, although a high concentration of nicotinate temporarily stimulates growth on N2. Ut us concluded that A. caulinodans is a true diazotroph.
当茎瘤固氮根瘤菌在恒化器培养中以 N₂ 作为氮源,在琥珀酸盐浓度恒定(50 mM)且烟酸浓度可变(1.5 至 585 μM)的培养基中,以 0.1 h⁻¹ 的恒定稀释率生长时,琥珀酸盐上的生长产量、氧气消耗比速率或二氧化碳产生比速率均未显示出与烟酸浓度的线性回归关系。此外,对于烟酸浓度逐渐降低的瞬态连续培养,生长参数保持不变,直到达到明显临界水平的 0.7 μM 烟酸。低于此烟酸水平,恒化器中的菌群体立即开始被冲出。无法分解代谢烟酸的茎瘤固氮根瘤菌烟酸羟化酶阴性突变体 61007 和野生型表现相似。因此,对于以 N₂ 作为氮源的连续培养,亚微摩尔浓度的烟酸既能将吡啶核苷酸生物合成维持在足够水平,又能阻止将烟酸用作分解代谢底物。此外,当提供更多烟酸时,连续培养中不会出现琥珀酸盐 - 烟酸双重限制。最后,当烟酸以次优浓度存在时,比生长速率与每单位生物量中存在的烟酸量成正比。相比之下,在具有不同烟酸浓度且以琥珀酸盐或乳酸盐作为碳源和能源的分批培养中,获得了异常的生长曲线。在低浓度(1.5 μM)的烟酸条件下,在 N₂ 上发生生长,尽管速率较低。在高浓度(195 μM)的烟酸条件下,在 N₂ 上的生长暂时受到刺激,但烟酸很快耗尽,此后生长受到烟酸限制。向分批培养中连续补充烟酸仅允许瞬态指数生长,随后是线性生长。因此,对于分批培养也是如此,尽管高浓度的烟酸会暂时刺激在 N₂ 上的生长,但烟酸分解代谢是可有可无的。我们得出结论,茎瘤固氮根瘤菌是一种真正的固氮菌。