Smith A J, Hoare D S
J Bacteriol. 1968 Mar;95(3):844-55. doi: 10.1128/jb.95.3.844-855.1968.
Acetate (1 to 10 mm) had no effect on the rate of nitrite oxidation or exponential growth by Nitrobacter agilis. However, acetate-1-(14)C and -2-(14)C were both assimilated by growing cultures, and acetate carbon contributed 33 to 39% of newly synthesized cell carbon. Carbon from acetate was incorporated into all of the major cell constituents, including most of the amino acids of cell protein and poly-beta-hydroxybutyrate (PHB). Cultures grown in the presence of acetate showed a significant increase in turbidity, attributable in part to protein synthesis and the accumulation of PHB in the "post-exponential phase," when the supply of nitrite was completely exhausted. Cell suspensons of N. agilis assimilated acetate in the absence of bicarbonate and even in the absence of nitrite. However, the addition of nitrite increased the rate of acetate assimilation by cell suspensions. The distribution of (14)C-acetate incorporated by cell suspensions was qualitatively similar to that found with growing cultures. Cell suspensions of N. agilis slowly oxidized acetate to CO(2). Addition of nitrite suppressed CO(2) production from acetate but increased the assimilation of acetate carbon into cell material. N. agilis contained all the enzymes of the tricarboxylic acid cycle. Growth of N. agilis in the presence of acetate did not significantly affect the levels of the enzymes of the tricarboxylic acid cycle, but did result in a 100-fold increase in the specific activity of isocitratase. In contrast, carboxydismutase was partially repressed. N. agilis was grown heterotrophically through seven transfers on a medium containing acetate and casein hydrolysate. The addition of nitrite increased the rate of heterotrophic growth. Heterotrophically grown organisms still retained their ability to grow autotrophically with nitrite. However, these organisms oxidized nitrite at a slower rate. Organisms from autotrophic and heterotrophic cultures were analyzed to determine the mean guanine plus cytosine content of their deoxyribonucleic acid; in both cases this mean was 61.2 +/- 1%. We concluded that N. agilis is not an obligate autotroph; it appears to be a facultative autotroph which resembles the novel facultative autotroph, Thiobacillus intermedius, very closely.
乙酸盐(1至10毫摩尔)对敏捷硝化杆菌的亚硝酸盐氧化速率或指数生长没有影响。然而,乙酸盐 -1-(14)C和 -2-(14)C都被生长中的培养物同化,并且乙酸盐碳占新合成细胞碳的33%至39%。来自乙酸盐的碳被纳入所有主要的细胞成分,包括细胞蛋白质的大部分氨基酸和聚-β-羟基丁酸酯(PHB)。在乙酸盐存在下生长的培养物浊度显著增加,部分归因于蛋白质合成以及在亚硝酸盐供应完全耗尽的“指数后期”PHB的积累。敏捷硝化杆菌的细胞悬液在没有碳酸氢盐甚至没有亚硝酸盐的情况下也能同化乙酸盐。然而,添加亚硝酸盐会提高细胞悬液对乙酸盐的同化速率。细胞悬液掺入的(14)C - 乙酸盐的分布在质量上与在生长培养物中发现的相似。敏捷硝化杆菌的细胞悬液将乙酸盐缓慢氧化为CO(2)。添加亚硝酸盐会抑制乙酸盐产生CO(2),但会增加乙酸盐碳向细胞物质中的同化。敏捷硝化杆菌含有三羧酸循环的所有酶。在乙酸盐存在下敏捷硝化杆菌的生长并没有显著影响三羧酸循环中酶的水平,但确实导致异柠檬酸酶的比活性增加了100倍。相比之下,羧化歧化酶受到部分抑制。敏捷硝化杆菌在含有乙酸盐和酪蛋白水解物的培养基上进行了七次异养传代培养。添加亚硝酸盐提高了异养生长速率。异养生长的生物体仍然保留了利用亚硝酸盐进行自养生长的能力。然而,这些生物体氧化亚硝酸盐的速率较慢。对来自自养和异养培养物的生物体进行分析,以确定其脱氧核糖核酸中鸟嘌呤加胞嘧啶的平均含量;在这两种情况下,该平均值均为61.2±1%。我们得出结论,敏捷硝化杆菌不是专性自养菌;它似乎是一种兼性自养菌,与新型兼性自养菌中间硫杆菌非常相似。