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用于鉴定和原位检测降解烃类的食烷菌菌株的特异性寡核苷酸探针的开发。

Development of specific oligonucleotide probes for the identification and in situ detection of hydrocarbon-degrading Alcanivorax strains.

作者信息

Syutsubo K, Kishira H, Harayama S

机构信息

Marine Biotechnology Institute, Kamaishi Laboratories, 3-75-1 Heita, Kamaishi, Iwate 026-0001, Japan.

出版信息

Environ Microbiol. 2001 Jun;3(6):371-9. doi: 10.1046/j.1462-2920.2001.00204.x.

Abstract

The genus Alcanivorax comprises diverse hydrocarbon-degrading marine bacteria. Novel 16S rRNA-targeted oligonucleotide DNA probes (ALV735 and ALV735-b) were developed to quantify two subgroups of the Alcanivorax/Fundibacter group by fluorescence in situ hybridization (FISH), and the conditions for the single-mismatch discrimination of the probes were optimized. The specificity of the probes was improved further using a singly mismatched oligonucleotide as a competitor. The growth of Alcanivorax cells in crude oil-contaminated sea water under the biostimulation condition was investigated by FISH with the probe ALV735, which targeted the main cluster of the Alcanivorax/Fundibacter group. The size of the Alcanivorax population increased with increasing incubation time and accounted for 91% of the 4',6-diamidino-2-phenylindole (DAPI) count after incubation for 2 weeks. The probes developed in this study are useful for detecting Alcanivorax populations in petroleum hydrocarbon-degrading microbial consortia.

摘要

食烷菌属包含多种可降解碳氢化合物的海洋细菌。开发了新型的靶向16S rRNA的寡核苷酸DNA探针(ALV735和ALV735-b),通过荧光原位杂交(FISH)对食烷菌属/深海杆菌属菌群的两个亚群进行定量分析,并优化了探针的单碱基错配鉴别条件。使用单碱基错配的寡核苷酸作为竞争物进一步提高了探针的特异性。用靶向食烷菌属/深海杆菌属菌群主要簇的探针ALV735,通过FISH研究了在生物刺激条件下原油污染海水中食烷菌细胞的生长情况。食烷菌种群大小随培养时间增加而增大,培养2周后占4',6-二脒基-2-苯基吲哚(DAPI)计数的91%。本研究中开发的探针可用于检测石油烃降解微生物群落中的食烷菌种群。

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