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首页> 外文期刊>Applied and Environmental Microbiology >Effect of 5-Fluoro-2′-Deoxyuridine on [3H]Thymidine Incorporation by Bacterioplankton in the Waters of Southwest Florida
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Effect of 5-Fluoro-2′-Deoxyuridine on [3H]Thymidine Incorporation by Bacterioplankton in the Waters of Southwest Florida

机译:5-氟-2'-脱氧尿苷对佛罗里达西南水域菌株菌施氮量的影响

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The effect of 5-fluoro-2′-deoxyuridine (FdUrd) on [methyl-3H] thymidine incorporation by bacterioplankton populations in subtropical freshwater, estuarine, and oceanic environments was examined. In estuarine waters, intracellular isotope dilution was inhibited by FdUrd, which enabled us to estimate both intracellular and extracellular isotope dilution. In 2 of 10 cases, extracellular isotope dilution was significant. At low concentrations of [methyl-3H]thymidine or [6-3H]thymidine, FdUrd completely inhibited incorporation of radioactivity into protein and RNA. At high concentrations of [3H]thymidine, however, FdUrd had little effect on labeling patterns. The dihydrofolate reductase inhibitors amethopterin and trimethoprim had no effect on macromolecular labeling patterns. These results suggest that thymidylate synthase is not involved in nonspecific labeling and that FdUrd inhibits nonspecific labeling by blocking some other enzyme involved in thymidine catabolism. In oligotrophic oceanic and freshwater samples, FdUrd did not inhibit intracellular isotope dilution or [3H]thymidine labeling of protein and RNA, but caused some inhibition of [3H]thymidine incorporation into DNA. The ability of FdUrd to inhibit nonspecific macromolecular labeling during [3H]thymidine incorporation was significantly correlated (r = 0.84) with total thymidine incorporation (in picomoles per liter per hour). The results are discussed in terms of applications of FdUrd to routine bacterial production measurements and the general assumptions of [3H]thymidine incorporation.
机译:研究了5-氟-2'-脱氧尿苷(FDURD)对亚热带淡水,偏毒素和海洋环境中菌株植物群的[甲基-3H]胸苷掺入的影响。在河滨水中,通过FDURD抑制细胞内同位素稀释,使我们能够估计细胞内和细胞外同位素稀释。在10例中的2例中,细胞外同位素稀释显着。在低浓度的[甲基-3H]胸苷或[6-3H]胸苷,FDURD完全抑制放射性掺入蛋白质和RNA中。然而,在高浓度的[3H]胸苷,FDURD对标签图案几乎没有影响。二羟基溶胶还原酶抑制剂Amethopterin和Trimethokim对大分子标记图案没有影响。这些结果表明,胸苷酸合成酶不参与非特异性标记,并且通过阻断胸苷分解代谢的其他酶来抑制非特异性标记。在寡营性海洋和淡水样本中,FDURD没有抑制细胞内同位素稀释或蛋白质和RNA的胸苷标记,但引起了一些抑制[3H]胸苷掺入DNA中。 FDURD在[3H]胸苷掺入期间抑制非特异性大分子标记的能力显着相关(r = 0.84),总胸苷掺入(在每小时每升皮摩尔)。在FDURD的应用方面讨论了常规细菌生产测量的结果和[3H]胸苷掺入的一般假设。

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