Department of Microbiology and Plant Biology, University of Oklahoma, Norman, OK, 73019, USA,
Appl Microbiol Biotechnol. 2014 Jan;98(2):907-18. doi: 10.1007/s00253-013-4906-x. Epub 2013 May 1.
A model flow cell system was designed to investigate pitting corrosion in pipelines associated with microbial communities. A microbial inoculum producing copious amounts of H₂S was enriched from an oil pipeline biofilm sample. Reservoirs containing a nutrient solution and the microbial inoculum were pumped continuously through six flow cells containing mild steel corrosion coupons. Two cells received corrosion inhibitor "A", two received corrosion inhibitor "B", and two ("untreated") received no additional chemicals. Coupons were removed after 1 month and analyzed for corrosion profiles and biofilm microbial communities. Coupons from replicate cells showed a high degree of similarity in pitting parameters and in microbial community profiles, as determined by 16S rRNA gene sequence libraries but differed with treatment regimen, suggesting that the corrosion inhibitors differentially affected microbial species. Viable microbial biomass values were more than 10-fold higher for coupons from flow cells treated with corrosion inhibitors than for coupons from untreated flow cells. The total number of pits >10 mils diameter and maximum pitting rate were significantly correlated with each other and the total number of pits with the estimated abundance of sequences classified as Desulfomicrobium. The maximum pitting rate was significantly correlated with the sum of the estimated abundance of Desulfomicrobium plus Clostridiales, and with the sum of the estimated abundance of Desulfomicrobium plus Betaproteobacteria. The lack of significant correlation with the estimated abundance of Deltaproteobacteria suggests not all Deltaproteobacteria species contribute equally to microbiologically influenced corrosion (MIC) and that it is not sufficient to target one bacterial group when monitoring for MIC.
设计了一种模型流动池系统,以研究与微生物群落相关的管道点蚀腐蚀。从含油管道生物膜样品中富集了大量产生 H₂S 的微生物接种物。含有营养溶液和微生物接种物的储液器被连续泵入六个装有低碳钢腐蚀试片的流动池。两个池接收腐蚀抑制剂“A”,两个池接收腐蚀抑制剂“B”,两个(“未处理”)未添加其他化学物质。一个月后取出试片,分析腐蚀轮廓和生物膜微生物群落。复制细胞的试片在点蚀参数和微生物群落图谱方面具有高度相似性,这是通过 16S rRNA 基因序列文库确定的,但与处理方案不同,这表明腐蚀抑制剂对微生物物种有不同的影响。与未处理流动池的试片相比,用腐蚀抑制剂处理的流动池的试片上的可培养微生物生物量值高出 10 倍以上。>10 密耳直径的总蚀点数和最大点蚀速率彼此之间呈显著相关,总蚀点数与被分类为脱硫微生物的序列估计丰度呈显著相关。最大点蚀速率与脱硫微生物加上梭菌目之和的估计丰度显著相关,与脱硫微生物加上β变形菌门之和的估计丰度显著相关。与δ变形菌门的估计丰度没有显著相关性表明,并非所有δ变形菌门物种都对等微生物影响腐蚀(MIC)有同等贡献,并且在监测 MIC 时,针对一个细菌群是不够的。