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从农业土壤和根际中摄取 4-氯-2-甲基苯氧乙酸的消费者携带编码加氧酶的 cadA、r/sdpA 和 tfdA 样基因。

Consumers of 4-chloro-2-methylphenoxyacetic acid from agricultural soil and drilosphere harbor cadA, r/sdpA, and tfdA-like gene encoding oxygenases.

机构信息

Department of Ecological Microbiology, University of Bayreuth, Bayreuth, Germany; State Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China.

出版信息

FEMS Microbiol Ecol. 2013 Oct;86(1):114-29. doi: 10.1111/1574-6941.12144. Epub 2013 May 23.

DOI:10.1111/1574-6941.12144
PMID:23646893
Abstract

Microbial degradation of 2-methyl-4-chlorophenoxyacetic acid (MCPA) in soil is enhanced by earthworms and initiated by tfdA-like, cadA and r/sdpA gene encoding oxygenases. Copy numbers of such genes increased during MCPA degradation in soil, and MCPA stimulated transcription of tfdA-like and r/sdpA genes up to 4×. Transcription of cadA was detected in the presence of MCPA only. DNA stable isotope probing after consumption of 0.6-0.8 mg 13C-MCPA gdw -1 in oxic microcosms indicated diverse labeled oxygenase genes in bulk soil, burrow walls, and cast. 9, 6, and 3 operational taxonomic units of tfdA-like, cadA, and r/sdpA genes, respectively, were labeled and affiliated with group 2 Alphaproteobacteria including Bradyrhizobia and group 1 class III Betaproteobacteria. New genes encoding putative MCPA degrading oxygenases were identified. Diversity of labeled OTUs tended to be lower for cast than for bulk soil. The collective data indicate (1) hitherto unknown active MCPA degraders and/or oxygenase genes in soil; (2) that multiple oxygenases are associated with MCPA degradation in soil at the same time; (3) that earthworms impact the capability of MCPA degraders in soil to respond to MCPA; and (4) the collective data enable a more in-depth analysis of MCPA degrader communities in soil by future structural gene-based experimental strategies.

摘要

土壤中 2-甲基-4-氯苯氧乙酸(MCPA)的微生物降解受蚯蚓的促进,并由编码加氧酶的 tfdA 样、cadA 和 r/sdpA 基因引发。在土壤中 MCPA 降解过程中,这些基因的拷贝数增加,并且 MCPA 刺激 tfdA 样和 r/sdpA 基因的转录增加了 4 倍。仅在存在 MCPA 的情况下检测到 cadA 的转录。在需氧微宇宙中消耗 0.6-0.8 mg 13C-MCPA gdw -1 后进行的 DNA 稳定同位素探针分析表明,在原状土壤、洞穴壁和粪便中存在不同的标记加氧酶基因。分别有 9、6 和 3 个 tfdA 样、cadA 和 r/sdpA 基因的操作分类单元被标记,并与包括慢生根瘤菌在内的α变形菌纲第 2 群和β变形菌纲第 1 类第 3 群有关。鉴定出了编码潜在的 MCPA 降解加氧酶的新基因。标记 OTUs 的多样性对于粪便而言比原状土壤更低。综合数据表明:(1)土壤中存在迄今未知的活跃的 MCPA 降解菌和/或加氧酶基因;(2)同时有多种加氧酶与土壤中 MCPA 的降解相关;(3)蚯蚓影响土壤中 MCPA 降解菌对 MCPA 的响应能力;(4)综合数据使得通过未来基于结构基因的实验策略对土壤中的 MCPA 降解菌群落进行更深入的分析成为可能。

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