Department of Microbiology, University of New Hampshire, Durham, New Hampshire 03824.
Appl Environ Microbiol. 1986 Oct;52(4):696-9. doi: 10.1128/aem.52.4.696-699.1986.
One host (Rana catesbiana)-associated and two free-living mesophilic strains of bacteria with violet pigmentation and biochemical characteristics of Chromobacterium violaceum were isolated from freshwater habitats. Cells of each freshly isolated strain and of strain ATCC 12472 (the neotype strain) grew anaerobically with glucose as the sole carbon and energy source. The major fermentation products of cells grown in Trypticase soy broth (BBL Microbiology Systems, Cockeysville, Md.) supplemented with glucose included acetate, small amounts of propionate, lactate, and pyruvate. The final cell yield and culture growth rate of each strain cultured anaerobically in this medium increased approximately twofold with the addition of 2 mM NaNO(3). Final growth yields increased in direct proportion to the quantity of added NaNO(3) over the range of 0.5 to 5 mM. Each strain reduced NO(3), producing NO(2), NO, and N(2)O. NO(2) accumulated transiently. With 2 mM NaNO(3) in the medium, N(2)O made up 85 to 98% of the N product recovered with each strain. N-oxides were recovered in the same quantity and distribution whether 0.01 atm (ca. 1 kPa) of C(2)H(2) (added to block N(2)O reduction) was present or not. Neither N(2) production nor gas accumulation was detected during NO(3) reduction by growing cells. Cell growth in media containing 0.5 to 5 mM NaNO(2) in lieu of NaNO(3) was delayed, and although N(2)O was produced by the end of growth, NO(2) -containing media did not support growth to an extent greater than did medium lacking NO(3) or NO(2). The data indicate that C. violaceum cells ferment glucose or denitrify, terminating denitrification with the production of N(2)O, and that NO(2) reduction to N(2)O is not coupled to growth but may serve as a detoxification mechanism. No strain detectably fixed N(2) (reduced C(2)H(2)).
从淡水生境中分离到一种与虹彩蟾(Rana catesbiana)相关的兼性嗜温和两种自由生活的嗜中温细菌菌株,它们具有紫色色素和粘质沙雷氏菌的生化特征。每个新分离菌株的细胞和 ATCC 12472 菌株(新典型菌株)的细胞在以葡萄糖为唯一碳源和能源的情况下进行厌氧生长。在添加葡萄糖的胰蛋白酶大豆肉汤(BBL Microbiology Systems,Cockeysville,MD)中生长的细胞的主要发酵产物包括乙酸盐、少量丙酸盐、乳酸盐和丙酮酸。在该培养基中进行厌氧培养时,每个菌株的最终细胞产量和培养物生长速率约增加两倍,添加 2 mM NaNO(3)。在 0.5 至 5 mM 的范围内,添加的 NaNO(3)量与最终生长产量成正比。每个菌株还原 NO(3),产生 NO(2)、NO 和 N(2)O。NO(2)短暂积累。在培养基中添加 2 mM NaNO(3)时,每个菌株产生的 N 产物中 N(2)O 占 85%至 98%。无论培养基中是否存在 0.01 大气压(约 1 kPa)的 C(2)H(2)(添加以阻止 N(2)O 还原),都以相同的数量和分布回收 N-氧化物。在 NO(3)还原过程中,生长细胞既不产生 N(2)也不积累气体。在含有 0.5 至 5 mM NaNO(2)的培养基中细胞生长延迟,尽管在生长结束时产生了 N(2)O,但含 NO(2)的培养基的生长程度并不大于缺乏 NO(3)或 NO(2)的培养基。数据表明,粘质沙雷氏菌细胞发酵葡萄糖或反硝化,以产生 N(2)O 来终止反硝化,并且 NO(2)还原为 N(2)O 与生长无关,但可能作为一种解毒机制。没有菌株可检测到固定 N(2)(还原 C(2)H(2))。