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Detection and Capturing of 14C Radioactively-Labeled Small Subunit rRNA from Mixed Microbial Communities of a Microbial Mat Using Magnetic Beads

机译:使用磁珠从微生物垫的混合微生物群落中检测和捕获14C放射性标记的小亚基rRNA

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摘要

Carbon cycling in the hypersaline microbial mats from Chiprana Lake, Spain is primarily dependent on phototrophic microorganisms with the ability to fix CO2 into organics that can be further utilized by aerobic as well as anaerobic heterotrophic bacteria. Here, mat pieces were incubated in seawater amended with 14C sodium bicarbonate and the incorporation of the radiocarbon in the small subunit ribosomal RNA (SSU rRNA) of mat organisms was followed using scintillation counter and autoradiography. Different domains of SSU rRNA were separated from the total RNA by means of streptavidin-coated magnetic beads and biotin-labeled oligonucleotide probes. The 14C label was detected in isolated RNA by both scintillation counter and autoradiography, however the latter technique was less sensitive. Using scintillation counter, the radiolabel incorporation increased with time with a maximum rate of 0.18 Bq ng−1 detected after 25 days. The bacterial SSU rRNA could be captured using the magnetic beads, however the hybridization efficiency was around 20%. The captured RNA was radioactively labeled, which could be mainly due to the fixation of radiocarbon by phototrophic organisms. In conclusion, the incubation of microbial mats in the presence of radiolabeled bicarbonate leads to the incorporation of the 14C label into RNA molecules through photosynthesis and this label can be detected using scintillation counter. The used approach could be useful in studying the fate of fixed carbon and its uptake by other microorganisms in complex microbial mats, particularly when species-specific probes are used and the hybridization efficiency and RNA yield are further optimized.
机译:来自西班牙奇普拉纳湖的高盐微生物垫中的碳循环主要依赖于光养微生物,其能够将二氧化碳固定在有机物中,好氧和厌氧异养细菌也可以利用它们。在这里,将垫块在用 14 碳酸氢钠修正的海水中孵育,然后使用闪烁计数器和放射自显影技术,将放射性碳掺入垫生物的小亚基核糖体RNA(SSU rRNA)中。通过链霉亲和素包被的磁珠和生物素标记的寡核苷酸探针将SSU rRNA的不同结构域与总RNA分开。闪烁计数器和放射自显影技术都在分离的RNA中检测到了 14 C标记,但是后者的敏感性较低。使用闪烁计数器,放射性标记的掺入随时间增加,在25天后检测到的最大比率为0.18 Bq ng -1 。可以使用磁珠捕获细菌SSU rRNA,但是杂交效率约为20%。捕获的RNA进行了放射性标记,这可能主要是由于光养生物固定了放射性碳。总而言之,在存在放射性标记的碳酸氢盐的情况下孵育微生物垫会导致 14 C标签通过光合作用掺入RNA分子,并且可以使用闪烁计数器检测该标签。所使用的方法可能有助于研究固定碳的命运以及复杂微生物垫中其他微生物对其的吸收,特别是当使用物种特异性探针并且进一步优化杂交效率和RNA产量时。

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