从受污染土壤和沉积物中富集多环芳烃 (PAH) 降解严格厌氧硫酸盐还原培养物。

Kartik Dhar, Kadiyala Venkateswarlu, Mallavarapu Megharaj
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引用次数: 0

摘要

硫酸盐还原菌(SRB)在全球生物地球化学循环中发挥着重要作用,其中一些还参与了有机污染物的厌氧生物降解,包括难降解和有害的多环芳烃(PAHs)。为实验室获得能降解多环芳烃的 SRB 培养物,对于发展多环芳烃厌氧生物降解这一年轻领域至关重要。SRB 在多环芳烃基质上生长异常缓慢,而且对氧气高度敏感。因此,多环芳烃降解 SRB 培养物的富集和维护以及生物降解过程的表征仍然是一项繁琐而艰巨的任务,尤其是对于新研究人员而言。为了解决这些技术上的限制,我们开发了稳健有效的方案来获取和鉴定多环芳烃降解 SRB 培养物。在这套方案中,我们将逐步介绍从受污染的土壤或沉积物中制备接种体、制备缺氧培养基、在完全厌氧的硫酸盐还原条件下建立以多环芳烃为底物的富集培养物、连续培养转移以获得高富集培养物等步骤、在缓慢生长的培养物中快速验证 SRB 的活力,通过使用有机溶剂提取残留物评估 PAH 的降解情况,随后使用气相色谱-质谱法进行分析,以及以微型化、中等通量的形式分光光度法测定硫酸盐和硫化物。这些方案有望成为获取和鉴定多环芳烃降解硫酸盐还原培养物的综合手册。© 2024 作者。当前协议》由 Wiley Periodicals LLC 出版。基本规程 1:从受污染土壤和沉积物中获得可降解 PAH 的严格厌氧硫酸盐还原富集培养物 支持规程 1:厌氧工作站的操作和维护 支持规程 2:设置气体吹扫系统以制备缺氧溶液 支持规程 3:验证生长缓慢的 SRB 富集培养物的存活率 支持规程 4:从低浓度硫酸盐还原培养物中提取基因组 DNA 支持规程 5:从受污染土壤和沉积物中获得可降解 PAH 的严格厌氧硫酸盐还原富集培养物从低生物量培养物中提取基因组 DNA 基本规程 2:从液体培养物中提取残留多环芳烃并通过气相色谱-质谱进行分析 基本规程 3:用分光光度法测定 SRB 培养物中的硫酸盐浓度 基本规程 4:用亚甲基蓝法用分光光度法测定 SRB 培养物中的硫化物浓度 替代规程:用分光光度法测定 SRB 培养物中的硫化物浓度用胶体硫化铜法用分光光度法测定 SRB 培养物中的硫化物浓度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Enrichment of Polycyclic Aromatic Hydrocarbon (PAH)–Degrading Strictly Anaerobic Sulfate-Reducing Cultures from Contaminated Soil and Sediment

Sulfate-reducing bacteria (SRB) are crucial players in global biogeochemical cycling and some have been implicated in the anaerobic biodegradation of organic pollutants, including recalcitrant and hazardous polycyclic aromatic hydrocarbons (PAHs). Obtaining PAH-degrading SRB cultures for laboratories is of paramount importance in the development of the young field of anaerobic biodegradation of PAHs. SRB grow exceptionally slowly on PAH substrates and are highly sensitive to oxygen. Consequently, enrichment and maintenance of PAH-degrading SRB cultures and characterization of the biodegradation process remain a tedious and formidable task, especially for new researchers. To address these technical constraints, we have developed robust and effective protocols for obtaining and characterizing PAH-degrading SRB cultures. In this set of protocols, we describe step-by-step procedures for preparing inocula from contaminated soil or sediment, preparing anoxic medium, establishing enrichment cultures with PAHs as substrates under completely anaerobic sulfate-reducing conditions, successive culture transfers to obtain highly enriched cultures, rapid verification of the viability of SRB in slow-growing cultures, assessment of PAH degradation by extracting residuals using organic solvent and subsequent analysis by gas chromatography–mass spectrometry, and spectrophotometric determination of sulfate and sulfide in miniaturized, medium-throughput format. These protocols are expected to serve as a comprehensive manual for obtaining and characterizing PAH-degrading sulfate-reducing cultures. © 2024 The Author(s). Current Protocols published by Wiley Periodicals LLC.

Basic Protocol 1: Obtaining PAH-degrading strictly anaerobic sulfate-reducing enrichment cultures from contaminated soil and sediment

Support Protocol 1: Operation and maintenance of an anaerobic workstation

Support Protocol 2: Setup of gas purging systems for preparing anoxic solutions

Support Protocol 3: Verification of viability in slow-growing SRB enrichment cultures

Support Protocol 4: Extraction of genomic DNA from low-biomass cultures

Basic Protocol 2: Extraction of residual PAH from liquid culture and analysis by GC-MS

Basic Protocol 3: Spectrophotometric determination of sulfate concentration in SRB cultures

Basic Protocol 4: Spectrophotometric determination of sulfide concentrations in SRB cultures by the methylene blue method

Alternate Protocol: Spectrophotometric determination of sulfide concentrations in SRB cultures by the colloidal copper sulfide method

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