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针对dszB脱硫酶基因的脱硫微生物分子驱动筛选方法的开发。

Development of molecular driven screening for desulfurizing microorganisms targeting the dszB desulfinase gene.

作者信息

Duval Emmanuel, Cravo-Laureau Cristiana, Poinel Line, Duran Robert

机构信息

Université de Pau et des Pays de l'Adour, E2S UPPA, IPREM UMR, CNRS 5254, Bat. IBEAS, Pau, France; Segula Technologies, 71 rue Henri Gautier, 44550, Montoir de Bretagne, France.

Université de Pau et des Pays de l'Adour, E2S UPPA, IPREM UMR, CNRS 5254, Bat. IBEAS, Pau, France.

出版信息

Res Microbiol. 2021 Sep-Oct;172(6):103872. doi: 10.1016/j.resmic.2021.103872. Epub 2021 Aug 8.

Abstract

COnsensus DEgenerate Hybrid Oligonucleotide Primers (CODEHOP) were developed for the detection of the dszB desulfinase gene (2'-hydroxybiphenyl-2-sulfinate desulfinase; EC 3.13.1.3) by polymerase chain reaction (PCR), which allow to reveal larger diversity than traditional primers. The new developed primers were used as molecular monitoring tool to drive a procedure for the isolation of desulfurizing microorganisms. The primers revealed a large dszB gene diversity in environmental samples, particularly in diesel-contaminated soil that served as inoculum for enrichment cultures. The isolation procedure using the dibenzothiophene sulfone (DBTO) as sole sulfur source reduced drastically the dszB gene diversity. A dszB gene closely related to that carried by Gordonia species was selected. The desulfurization activity was confirmed by the production of desulfurized 2-hydroxybiphenyl (2-HBP). Metagenomic 16S rRNA gene sequencing showed that the Gordonia genus was represented at low abundance in the initial bacterial community. Such observation highlighted that the culture medium and conditions represent the bottleneck for isolating novel desulfurizing microorganisms. The new developed primers constitute useful tool for the development of appropriate cultural-dependent procedures, including medium and culture conditions, to access novel desulfurizing microorganisms useful for the petroleum industry.

摘要

为通过聚合酶链反应(PCR)检测dszB脱硫酶基因(2'-羟基联苯-2-亚磺酸盐脱硫酶;EC 3.13.1.3)而开发了一致性简并杂交寡核苷酸引物(CODEHOP),与传统引物相比,它能揭示更大的多样性。新开发的引物被用作分子监测工具,以推动脱硫微生物的分离程序。这些引物揭示了环境样品中dszB基因的高度多样性,特别是在用作富集培养接种物的柴油污染土壤中。使用二苯并噻吩砜(DBTO)作为唯一硫源的分离程序极大地降低了dszB基因的多样性。选择了一个与戈登氏菌属携带的基因密切相关的dszB基因。通过脱硫2-羟基联苯(2-HBP)的产生证实了脱硫活性。宏基因组16S rRNA基因测序表明,戈登氏菌属在初始细菌群落中的丰度较低。这一观察结果突出表明,培养基和条件是分离新型脱硫微生物的瓶颈。新开发的引物构成了有用的工具,可用于开发适当的依赖培养的程序,包括培养基和培养条件,以获取对石油工业有用的新型脱硫微生物。

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