Suppr超能文献

泡菜发酵过程中乳酸菌基因表达的宏转录组分析。

Metatranscriptomic analysis of lactic acid bacterial gene expression during kimchi fermentation.

机构信息

Department of Life Science, Chung-Ang University, Seoul 156-756, Republic of Korea.

出版信息

Int J Food Microbiol. 2013 May 15;163(2-3):171-9. doi: 10.1016/j.ijfoodmicro.2013.02.022. Epub 2013 Mar 6.

Abstract

Barcode-based 16S rRNA gene pyrosequencing showed that the kimchi microbiome was dominated by six lactic acid bacteria (LAB), Leuconostoc (Lc.) mesenteroides, Lactobacillus (Lb.) sakei, Weissella (W.) koreensis, Lc. gelidum, Lc. carnosum, and Lc. gasicomitatum. Therefore, we used completed genome sequences of representatives of these bacteria to investigate metatranscriptomic gene-expression profiles during kimchi fermentation. Total mRNA was extracted from kimchi samples taken at five time points during a 29 day-fermentation. Nearly all (97.7%) of the metagenome sequences that were recruited on all LAB genomes of GenBank mapped onto the six LAB strains; this high coverage rate indicated that this approach for assessing processes carried out by the kimchi microbiome was valid. Expressed mRNA sequences (as cDNA) were determined using Illumina GA IIx. Assignment of mRNA sequences to metabolic genes using MG-RAST revealed the prevalence of carbohydrate metabolism and lactic acid fermentation. The mRNA sequencing reads were mapped onto genomes of the six LAB strains, which showed that Lc. mesenteroides was most active during the early-stage fermentation, whereas gene expression by Lb. sakei and W. koreensis was high during later stages. However, gene expression by Lb. sakei decreased rapidly at 25 days of fermentation, which was possibly caused by bacteriophage infection of the Lactobacillus species. Many genes related to carbohydrate transport and hydrolysis and lactate fermentation were actively expressed, which indicated typical heterolactic acid fermentation. Mannitol dehydrogenase-encoding genes (mdh) were identified from all Leuconostoc species and especially Lc. mesenteroides, which harbored three copies (two copies on chromosome and one copy on plasmid) of mdh with different expression patterns. These results contribute to knowledge of the active populations and gene expression in the LAB community responsible for an important fermentation process.

摘要

基于条码的 16S rRNA 基因焦磷酸测序显示,泡菜微生物组主要由六种乳酸菌(LAB)组成,分别是肠膜明串珠菌(Lc. mesenteroides)、清酒乳杆菌(Lb. sakei)、朝鲜泡菜乳杆菌(W. koreensis)、嗜冷明串珠菌(Lc. gelidum)、干酪乳杆菌(Lc. carnosum)和颗粒明串珠菌(Lc. gasicomitatum)。因此,我们使用这些细菌代表的完成基因组序列来研究泡菜发酵过程中的宏转录组基因表达谱。从发酵 29 天期间五个时间点的泡菜样品中提取总 mRNA。在 GenBank 上所有 LAB 基因组上招募的几乎所有(97.7%)宏基因组序列都映射到了这六种 LAB 菌株上;这种高覆盖率表明,这种评估泡菜微生物组所进行过程的方法是有效的。使用 Illumina GA IIx 确定了表达的 mRNA 序列(作为 cDNA)。使用 MG-RAST 将 mRNA 序列分配给代谢基因,揭示了碳水化合物代谢和乳酸发酵的普遍性。将 mRNA 测序读数映射到这六种 LAB 菌株的基因组上,结果表明肠膜明串珠菌在早期发酵阶段最为活跃,而清酒乳杆菌和朝鲜泡菜乳杆菌的基因表达在后期较高。然而,清酒乳杆菌的基因表达在发酵 25 天时迅速下降,这可能是由于乳酸菌被噬菌体感染。许多与碳水化合物运输和水解以及乳酸发酵相关的基因被积极表达,这表明了典型的异型乳酸发酵。从所有肠膜明串珠菌物种中鉴定出甘露醇脱氢酶编码基因(mdh),尤其是肠膜明串珠菌,它在染色体上有两个拷贝(一个拷贝在染色体上,一个拷贝在质粒上)和一个拷贝具有不同表达模式的 mdh。这些结果有助于了解负责重要发酵过程的 LAB 群落中的活跃种群和基因表达。

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