Suppr超能文献

瘤胃产甲烷菌瘤胃短杆菌M1菌株对抑制剂月桂酸的转录组反应

The transcriptome response of the ruminal methanogen Methanobrevibacter ruminantium strain M1 to the inhibitor lauric acid.

作者信息

Zhou Xuan, Stevens Marc J A, Neuenschwander Stefan, Schwarm Angela, Kreuzer Michael, Bratus-Neuenschwander Anna, Zeitz Johanna O

机构信息

Institute of Agricultural Sciences, ETH Zurich, Universitätstrasse 2, 8092, Zurich, Switzerland.

Laboratory of Food Biotechnology, Institute of Food, Nutrition and Health, ETH Zurich, Schmelzbergstrasse 7, 8092, Zurich, Switzerland.

出版信息

BMC Res Notes. 2018 Feb 17;11(1):135. doi: 10.1186/s13104-018-3242-8.

Abstract

OBJECTIVE

Lauric acid (C) is a medium-chain fatty acid that inhibits growth and production of the greenhouse gas methane by rumen methanogens such as Methanobrevibacter ruminantium. To understand the inhibitory mechanism of C, a transcriptome analysis was performed in M. ruminantium strain M1 (DSM 1093) using RNA-Seq.

RESULTS

Pure cell cultures in the exponential growth phase were treated with 0.4 mg/ml C, dissolved in dimethyl sulfoxide (DMSO), for 1 h and transcriptomic changes were compared to DMSO-only treated cells (final DMSO concentration 0.2%). Exposure to C resulted in differential expression of 163 of the 2280 genes in the M1 genome (maximum log-fold change 6.6). Remarkably, C hardly affected the expression of genes involved in methanogenesis. Instead, most affected genes encode cell-surface associated proteins (adhesion-like proteins, membrane-associated transporters and hydrogenases), and proteins involved in detoxification or DNA-repair processes. Enrichment analysis on the genes regulated in the C-treated group showed a significant enrichment for categories 'cell surface' and 'mobile elements' (activated by C), and for the categories 'regulation' and 'protein fate' (represssed). These results are useful to generate and test specific hypotheses on the mechanism how C affects rumen methanogens.

摘要

目的

月桂酸(C)是一种中链脂肪酸,可抑制瘤胃产甲烷菌(如反刍兽甲烷短杆菌)产生温室气体甲烷以及其生长。为了解C的抑制机制,使用RNA测序技术对反刍兽甲烷短杆菌菌株M1(DSM 1093)进行了转录组分析。

结果

处于指数生长期的纯细胞培养物用溶解于二甲基亚砜(DMSO)中的0.4mg/ml C处理1小时,并将转录组变化与仅用DMSO处理的细胞(最终DMSO浓度0.2%)进行比较。暴露于C导致M1基因组中2280个基因中的163个基因差异表达(最大对数倍数变化为6.6)。值得注意的是,C几乎不影响参与甲烷生成的基因的表达。相反,受影响最大的基因编码细胞表面相关蛋白(粘附样蛋白、膜相关转运蛋白和氢化酶),以及参与解毒或DNA修复过程的蛋白。对C处理组中调控的基因进行的富集分析表明,“细胞表面”和“移动元件”类别(被C激活)以及“调控”和“蛋白质命运”类别(被抑制)有显著富集。这些结果有助于生成和测试关于C如何影响瘤胃产甲烷菌机制的具体假设。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb69/5816558/6f2cf6183e58/13104_2018_3242_Fig1_HTML.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验