Aeckersberg F, Rainey F A, Widdel F
Max-Planck-Institut für Marine Mikrobiologie, Bremen, Germany.
Arch Microbiol. 1998 Oct;170(5):361-9. doi: 10.1007/s002030050654.
Natural relationships, improvement of anaerobic growth on hydrocarbons, and properties that may provide clues to an understanding of oxygen-independent alkane metabolism were studied with two mesophilic sulfate-reducing bacteria, strains Hxd3 and Pnd3. Strain Hxd3 had been formerly isolated from an oil tank; strain Pnd3 was isolated from marine sediment. Strains Hxd3 and Pnd3 grew under strictly anoxic conditions on n-alkanes in the range of C12-C20 and C14-C17, respectively, reducing sulfate to sulfide. Both strains shared 90% 16 S rRNA sequence similarity and clustered with classified species of completely oxidizing, sulfate-reducing bacteria within the delta-subclass of Proteobacteria. Anaerobic growth on alkanes was stimulated by alpha-cyclodextrin, which served as a non-degradable carrier for the hydrophobic substrate. Cells of strain Hxd3 grown on hydrocarbons and alpha-cyclodextrin were used to study the composition of cellular fatty acids and in vivo activities. When strain Hxd3 was grown on hexadecane (C16H34), cellular fatty acids with C-odd chains were dominant. Vice versa, cultures grown on heptadecane (C17H36) contained mainly fatty acids with C-even chains. In contrast, during growth on 1-alkenes or fatty acids, a C-even substrate yielded C-even fatty acids, and a C-odd substrate yielded C-odd fatty acids. These results suggest that anaerobic degradation of alkanes by strain Hxd3 does not occur via a desaturation to the corresponding 1-alkenes, a hypothetical reaction formerly discussed in the literature. Rather an alteration of the carbon chain by a C-odd carbon unit is likely to occur during activation; one hypothetical reaction is a terminal addition of a C1 unit. In contrast, fatty acid analyses of strain Pnd3 after growth on alkanes did not indicate an alteration of the carbon chain by a C-odd carbon unit, suggesting that the initial reaction differed from that in strain Hxd3. When hexadecane-grown cells of strain Hxd3 were resuspended in medium with 1-hexadecene, an adaptation period of 2 days was observed. Also this result is not in favor of an anaerobic alkane degradation via the corresponding 1-alkene.
利用两株嗜温性硫酸盐还原菌Hxd3和Pnd3,研究了它们的自然关系、在烃类上厌氧生长的改善情况以及可能为理解不依赖氧气的烷烃代谢提供线索的特性。菌株Hxd3先前从一个油罐中分离得到;菌株Pnd3从海洋沉积物中分离得到。菌株Hxd3和Pnd3分别在严格缺氧条件下,以C12 - C20范围内的正构烷烃和C14 - C17范围内的正构烷烃为底物生长,将硫酸盐还原为硫化物。两株菌株的16S rRNA序列相似度为90%,并与变形菌纲δ亚类中完全氧化的硫酸盐还原细菌的已分类物种聚类在一起。α - 环糊精可刺激菌株在烷烃上的厌氧生长,它作为疏水底物的不可降解载体。以烃类和α - 环糊精为底物生长的菌株Hxd3细胞用于研究细胞脂肪酸组成和体内活性。当菌株Hxd3在十六烷(C16H34)上生长时,具有奇数碳链的细胞脂肪酸占主导。反之,在十七烷(C17H36)上生长的培养物主要含有偶数碳链的脂肪酸。相比之下,在1 - 烯烃或脂肪酸上生长时,偶数碳底物产生偶数碳脂肪酸,奇数碳底物产生奇数碳脂肪酸。这些结果表明,菌株Hxd3对烷烃的厌氧降解不是通过去饱和生成相应的1 - 烯烃来进行的,这是文献中先前讨论过的一个假设反应。相反,在激活过程中很可能发生由奇数碳单元引起的碳链改变;一个假设反应是末端添加一个C1单元。相比之下,菌株Pnd3在烷烃上生长后进行的脂肪酸分析并未表明存在由奇数碳单元引起的碳链改变,这表明其初始反应与菌株Hxd3不同。当将十六烷生长的菌株Hxd3细胞重悬于含有1 - 十六烯的培养基中时,观察到2天的适应期。该结果同样不支持通过相应的1 - 烯烃进行厌氧烷烃降解。