Occurrence of Rhodococcus sp. RR1 prmA and Rhodococcus jostii RHA1 prmA across microbial communities and their enumeration during 1,4-dioxane biodegradation

IF 1.7 4区 生物学 Q4 BIOCHEMICAL RESEARCH METHODS Journal of microbiological methods Pub Date : 2024-02-23 DOI:10.1016/j.mimet.2024.106908
Zohre Eshghdoostkhatami, Alison M. Cupples
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Abstract

1,4-Dioxane, a likely human carcinogen, is a co-contaminant at many chlorinated solvent contaminated sites. Conventional treatment technologies, such as carbon sorption or air stripping, are largely ineffective, and so many researchers have explored bioremediation for site clean-up. An important step towards this involves examining the occurrence of the functional genes associated with 1,4-dioxane biodegradation. The current research explored potential biomarkers for 1,4-dioxane in three mixed microbial communities (wetland sediment, agricultural soil, impacted site sediment) using monooxygenase targeted amplicon sequencing, followed by quantitative PCR (qPCR). A BLAST analysis of the sequencing data detected only two of the genes previously associated with 1,4-dioxane metabolism or co-metabolism, namely propane monooxygenase (prmA) from Rhodococcus jostii RHA1 and Rhodococcus sp. RR1. To investigate this further, qPCR primers and probes were designed, and the assays were used to enumerate prmA gene copies in the three communities. Gene copies of Rhodococcus RR1 prmA were detected in all three, while gene copies of Rhodococcus jostii RHA1 prmA were detected in two of the three sample types (except impacted site sediment). Further, there was a statistically significant increase in RR1 prmA gene copies in the microcosms inoculated with impacted site sediment following 1,4-dioxane biodegradation compared to the control microcosms (no 1,4-dioxane) or to the initial copy numbers before incubation. Overall, the results indicate the importance of Rhodococcus associated prmA, compared to other 1,4-dioxane degrading associated biomarkers, in three different microbial communities. Also, the newly designed qPCR assays provide a platform for others to investigate 1,4-dioxane biodegradation potential in mixed communities and should be of particular interest to those considering bioremediation as a potential 1,4-dioxane remediation approach.

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1,4-Dioxane 生物降解过程中微生物群落中 Rhodococcus sp.
1,4-二恶烷可能是一种人类致癌物质,是许多氯化溶剂污染场地的共污染物质。传统的处理技术,如碳吸附或空气剥离,基本上没有效果,因此许多研究人员探索了生物修复技术来清理场地。其中重要的一步就是研究与 1,4- 二恶烷生物降解相关的功能基因。目前的研究采用单氧酶定向扩增子测序法,然后进行定量 PCR(qPCR),在三个混合微生物群落(湿地沉积物、农业土壤、受影响场地沉积物)中探索 1,4-二恶烷的潜在生物标志物。对测序数据进行 BLAST 分析后发现,以前与 1,4-Dioxane 代谢或共代谢相关的基因只有两个,即来自 Rhodococcus jostii RHA1 和 Rhodococcus sp.为进一步研究这一问题,设计了 qPCR 引物和探针,并利用该检测方法统计了三个群落中的 prmA 基因拷贝数。在所有三种样本中都检测到了 Rhodococcus RR1 prmA 的基因拷贝,而在三种样本类型中的两种(受影响地点沉积物除外)中检测到了 Rhodococcus jostii RHA1 prmA 的基因拷贝。此外,与对照微生态系统(不含 1,4-二恶烷)或培养前的初始拷贝数相比,1,4-二恶烷生物降解后接种了受影响场地沉积物的微生态系统中的 RR1 prmA 基因拷贝数出现了统计学意义上的显著增加。总之,研究结果表明,与其他降解 1,4-二恶烷的相关生物标志物相比,与 Rhodococcus 相关的 prmA 在三个不同的微生物群落中具有重要意义。此外,新设计的 qPCR 检测方法为其他研究 1,4-二噁烷在混合群落中的生物降解潜力提供了一个平台,对于那些考虑将生物修复作为一种潜在的 1,4-二噁烷修复方法的人来说,应该特别感兴趣。
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来源期刊
Journal of microbiological methods
Journal of microbiological methods 生物-生化研究方法
CiteScore
4.30
自引率
4.50%
发文量
151
审稿时长
29 days
期刊介绍: The Journal of Microbiological Methods publishes scholarly and original articles, notes and review articles. These articles must include novel and/or state-of-the-art methods, or significant improvements to existing methods. Novel and innovative applications of current methods that are validated and useful will also be published. JMM strives for scholarship, innovation and excellence. This demands scientific rigour, the best available methods and technologies, correctly replicated experiments/tests, the inclusion of proper controls, calibrations, and the correct statistical analysis. The presentation of the data must support the interpretation of the method/approach. All aspects of microbiology are covered, except virology. These include agricultural microbiology, applied and environmental microbiology, bioassays, bioinformatics, biotechnology, biochemical microbiology, clinical microbiology, diagnostics, food monitoring and quality control microbiology, microbial genetics and genomics, geomicrobiology, microbiome methods regardless of habitat, high through-put sequencing methods and analysis, microbial pathogenesis and host responses, metabolomics, metagenomics, metaproteomics, microbial ecology and diversity, microbial physiology, microbial ultra-structure, microscopic and imaging methods, molecular microbiology, mycology, novel mathematical microbiology and modelling, parasitology, plant-microbe interactions, protein markers/profiles, proteomics, pyrosequencing, public health microbiology, radioisotopes applied to microbiology, robotics applied to microbiological methods,rumen microbiology, microbiological methods for space missions and extreme environments, sampling methods and samplers, soil and sediment microbiology, transcriptomics, veterinary microbiology, sero-diagnostics and typing/identification.
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