Hanson J R, Macalady J L, Harris D, Scow K M
Department of Land, Air and Water Resources, University of California, Davis, California 95616, USA.
Appl Environ Microbiol. 1999 Dec;65(12):5403-8. doi: 10.1128/AEM.65.12.5403-5408.1999.
Phospholipid fatty acid (PLFA) analysis of a soil microbial community was coupled with (13)C isotope tracer analysis to measure the community's response to addition of 35 microg of [(13)C]toluene ml of soil solution(-1). After 119 h of incubation with toluene, 96% of the incorporated (13)C was detected in only 16 of the total 59 PLFAs (27%) extracted from the soil. Of the total (13)C-enriched PLFAs, 85% were identical to the PLFAs contained in a toluene-metabolizing bacterium isolated from the same soil. In contrast, the majority of the soil PLFAs (91%) became labeled when the same soil was incubated with [(13)C]glucose. Our study showed that coupling (13)C tracer analysis with PLFA analysis is an effective technique for distinguishing a specific microbial population involved in metabolism of a labeled substrate in complex environments such as soil.
对土壤微生物群落进行磷脂脂肪酸(PLFA)分析,并结合¹³C同位素示踪分析,以测定该群落对每毫升土壤溶液添加35微克[¹³C]甲苯的反应。在用甲苯培养119小时后,在从土壤中提取的总共59种PLFA(占27%)中,只有16种检测到了96%的掺入¹³C。在总¹³C富集的PLFA中,85%与从同一土壤中分离出的甲苯代谢细菌所含的PLFA相同。相比之下,当同一土壤与[¹³C]葡萄糖一起培养时,大多数土壤PLFA(91%)都被标记。我们的研究表明,将¹³C示踪分析与PLFA分析相结合是一种有效的技术,可用于区分在诸如土壤等复杂环境中参与标记底物代谢的特定微生物种群。