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利用 PCR-RFLP 技术筛选红树林沼泽中的 PAH 降解菌。

Screening of PAH-degrading bacteria in a mangrove swamp using PCR-RFLP.

机构信息

Key Laboratory of Ministry of Education for Coast and Wetland Ecosystems, School of Life Sciences, Xiamen University, Xiamen 361005, China.

出版信息

Mar Pollut Bull. 2010 Nov;60(11):2056-61. doi: 10.1016/j.marpolbul.2010.07.013. Epub 2010 Aug 16.

Abstract

There are abundant PAH-degrading bacteria in mangrove sediments, and it is very important to screen the high efficiency degraders in order to perform bioremediation of PAH polluted environments. In order to obtain the more highly efficient PAH-degrading bacteria from a mangrove swamp, we first obtained 62 strains of PAH-degrading bacteria using traditional culture methods and based on their morphological characteristics. We then used the modern molecular biological technology of PCR-RFLP, in which the 16S rDNA of these strains were digested by different enzymes. Based on differences in the PCR-RFLP profiles, we obtained five strains of phenanthrene-degrading bacteria, five strains of pyrene-degrading bacteria, four strains of fluoranthene-degrading bacteria, five strains of benzo[a]pyrene-degrading bacteria and two strains of mixed PAH-degrading bacteria (including phenanthrene, pyrene, fluoranthene and benzo[a]pyrene). Finally, a total of 14 different PAH-degrading bacteria were obtained. The 16S rDNA sequences of these strains were aligned with the BLAST program on the NCBI website and it was found that they belonged to the α-proteobacteria and γ-proteobacteria, including four strains, where the similarities were no more than 97% and which were suspected therefore to be new species. This study indicated that PCR-RFLP was a very important method to screen degrading-bacteria, and also a significant molecular biological tool for the rapid classification and accurate identification of many different strains. On the other hand, it also showed that rich bacterial resources existed in mangrove areas, and that exploring and developing the functional microorganism from these mangrove areas would have wide use in the study of bioremediation of contaminated environments in the future.

摘要

红树林沉积物中存在丰富的多环芳烃降解菌,筛选高效降解菌对于多环芳烃污染环境的生物修复非常重要。为了从红树林沼泽中获得更高效的多环芳烃降解菌,我们首先采用传统的培养方法,根据形态特征获得了 62 株多环芳烃降解菌。然后,我们利用现代分子生物学技术 PCR-RFLP,用不同的酶对这些菌株的 16S rDNA 进行酶切。根据 PCR-RFLP 图谱的差异,我们获得了 5 株菲降解菌、5 株芘降解菌、4 株荧蒽降解菌、5 株苯并[a]芘降解菌和 2 株混合多环芳烃降解菌(包括菲、芘、荧蒽和苯并[a]芘)。最终,共获得 14 株不同的多环芳烃降解菌。这些菌株的 16S rDNA 序列与 NCBI 网站上的 BLAST 程序进行比对,发现它们属于α-变形菌纲和γ-变形菌纲,其中有 4 株相似度不超过 97%,因此疑似为新种。本研究表明,PCR-RFLP 是筛选降解菌的重要方法,也是快速分类和准确鉴定许多不同菌株的重要分子生物学工具。另一方面,它还表明红树林地区存在丰富的细菌资源,从这些红树林地区探索和开发功能微生物,将在未来污染环境的生物修复研究中具有广泛的应用前景。

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