Coffin R B, Velinsky D J, Devereux R, Price W A, Cifuentes L A
Technical Resources, Inc., U.S. Environmental Protection Agency, Sabine Island, Gulf Breeze, Florida 32561.
Appl Environ Microbiol. 1990 Jul;56(7):2012-20. doi: 10.1128/aem.56.7.2012-2020.1990.
The natural abundance of stable carbon isotopes measured in bacterial nucleic acids extracted from estuarine bacterial concentrates was used to trace sources of organic matter for bacteria in aquatic environments. The stable carbon isotope ratios of Pseudomonas aeruginosa and nucleic acids extracted from cultures resembled those of the carbon source on which bacteria were grown. The carbon isotope discrimination between the substrate and total cell carbon from bacterial cultures averaged 2.3% +/- 0.6% (n = 13). Furthermore, the isotope discrimination between the substrate and nucleic acids extracted from bacterial cultures was 2.4% +/- 0.4% (n = 10), not significantly different from the discrimination between bacteria and the substrate. Estuarine water samples were prefiltered through 1-micron-pore-size cartridge filters. Bacterium-sized particles in the filtrates were concentrated with tangential-flow filtration and centrifugation, and nucleic acids were then extracted from these concentrates. Hybridization with 16S rRNA probes showed that approximately 90% of the nucleic acids extracted on two sample dates were of eubacterial origin. Bacteria and nucleic acids from incubation experiments using estuarine water samples enriched with dissolved organic matter from Spartina alterniflora and Cyclotella caspia had stable carbon isotope values similar to those of the substrate sources. In a survey that compared diverse estuarine environments, stable carbon isotopes of bacteria grown in incubation experiments ranged from -31.9 to -20.5%. The range in isotope values of nucleic acids extracted from indigenous bacteria from the same waters was similar, -27.9 to -20.2%. Generally, the lack of isotope discrimination between bacteria and nucleic acids that was noted in the laboratory was observed in the field.(ABSTRACT TRUNCATED AT 250 WORDS)
通过测量从河口细菌浓缩物中提取的细菌核酸中稳定碳同位素的自然丰度,来追踪水生环境中细菌的有机物质来源。铜绿假单胞菌及其培养物中提取的核酸的稳定碳同位素比率,与细菌生长所依赖的碳源的比率相似。细菌培养物中底物与总细胞碳之间的碳同位素分馏平均为2.3%±0.6%(n = 13)。此外,底物与细菌培养物中提取的核酸之间的同位素分馏为2.4%±0.4%(n = 10),与细菌和底物之间的分馏没有显著差异。河口水样先通过孔径为1微米的筒式过滤器进行预过滤。滤液中细菌大小的颗粒通过切向流过滤和离心进行浓缩,然后从这些浓缩物中提取核酸。与16S rRNA探针杂交显示,在两个采样日期提取的核酸中,约90%源自真细菌。使用富含互花米草和里海圆筛藻溶解有机物的河口水样进行培养实验,所得细菌和核酸的稳定碳同位素值与底物来源的相似。在一项比较不同河口环境的调查中,培养实验中生长的细菌的稳定碳同位素范围为-31.9%至-20.5%。从同一水域的本地细菌中提取的核酸的同位素值范围相似,为-27.9%至-20.2%。一般来说,在野外也观察到了实验室中所发现的细菌与核酸之间缺乏同位素分馏的现象。(摘要截短于250字)