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同时掺入胸腺嘧啶核苷和亮氨酸来估算海洋水中的细菌生产力。

Estimating bacterial production in marine waters from the simultaneous incorporation of thymidine and leucine.

机构信息

College of Marine Studies, University of Delaware, Lewes, Delaware 19958.

出版信息

Appl Environ Microbiol. 1988 Aug;54(8):1934-9. doi: 10.1128/aem.54.8.1934-1939.1988.

Abstract

We examined the simultaneous incorporation of [H]thymidine and [C]leucine to obtain two independent indices of bacterial production (DNA and protein syntheses) in a single incubation. Incorporation rates of leucine estimated by the dual-label method were generally higher than those obtained by the single-label method, but the differences were small (dual/single = 1.1 +/- 0.2 [mean +/- standard deviation]) and were probably due to the presence of labeled leucyl-tRNA in the cold trichloroacetic acid-insoluble fraction. There were no significant differences in thymidine incorporation between dual- and single-label incubations (dual/ single = 1.03 +/- 0.13). Addition of the two substrates in relatively large amounts (25 nM) did not apparently increase bacterial activity during short incubations (<5 h). With the dual-label method we found that thymidine and leucine incorporation rates covaried over depth profiles of the Chesapeake Bay. Estimates of bacterial production based on thymidine and leucine differed by less than 25%. Although the need for appropriate conversion factors has not been eliminated, the dual-label approach can be used to examine the variation in bacterial production while ensuring that the observed variation in incorporation rates is due to real changes in bacterial production rather than changes in conversion factors or introduction of other artifacts.

摘要

我们同时检测了 [H]胸苷和 [C]亮氨酸的掺入,以在单次孵育中获得两个独立的细菌生产力指标(DNA 和蛋白质合成)。 双重标记法估计的亮氨酸掺入率通常高于单标记法,但差异较小(双重/单一= 1.1 +/- 0.2[平均值 +/- 标准差]),可能是由于冷三氯乙酸不溶性部分中存在标记的亮氨酰-tRNA。 双重和单标记孵育之间的胸苷掺入没有显着差异(双重/单一= 1.03 +/- 0.13)。 在短孵育时间(<5 小时)内,相对大量(25 nM)添加两种底物并未明显增加细菌活性。 使用双重标记法,我们发现 Chesapeake 湾的深度剖面中胸苷和亮氨酸的掺入率存在相关性。基于胸苷和亮氨酸的细菌生产力估计值相差小于 25%。尽管仍然需要适当的转换因子,但双重标记法可用于检查细菌生产力的变化,同时确保观察到的掺入率变化是由于细菌生产力的实际变化而不是由于转换因子的变化或引入其他假象。

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