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作 者:王婷 刘婵婵 任娟 荆蓉蓉 钱卫东 WANG Ting;LIU Chanchan;REN Juan;JING Rongrong;QIAN Weidong(School of Food and Biological Engineering,Shaanxi University of Science&Technology,Xi’an 710021,China;Xi’an Medical College,Xi’an 710032,China)
机构地区:[1]陕西科技大学食品与生物工程学院,陕西西安710021 [2]西安医学高等专科学校,陕西西安710032
出 处:《食品科学》2021年第6期193-199,共7页Food Science
基 金:中国富硒产业研究院富硒专项科技计划项目(2018FXZX03-15);陕西省教育厅产业化服务地方专项(18JC006);陕西省教育厅专项科研计划项目(18JK0097);西安市未央区科技计划项目(201824)。
摘 要:为解析Na_(2)SeO_(3)诱导多形汉逊酵母DL-1(Hansenula polymorpha DL-1,HP-DL-1)生物合成谷胱甘肽(glutathione,GSH)的分子机制。通过DTNB法以及Illumina测序平台对比分析不同浓度Na_(2)SeO_(3)对HP-DL-1合成GSH产量的影响及Na_(2)SeO_(3)诱导下GSH高产菌株与出发菌株转录组差异。结果表明:以60μmol/L Na_(2)SeO_(3)诱导HPDL-1发酵48 h,酵母总GSH产量达(530.22±9.6)mg/L;与对照组相比,Na_(2)SeO_(3)诱导组共有1254个显著性差异表达基因(differentially expressed genes,DEGs),其中630个DEGs表达上调,624个DEGs表达下调;依据基因本体(Gene Ontology,GO)和KEGG(Kyoto Encyclopedia of Genes and Genomes)富集,这些差异基因主要集中在细胞周期、有丝分裂、氨基酸生物合成、糖酵解、核糖体组分、甲烷、脂肪、核酸、GSH等多条代谢通路。本研究为分子改造构建高产GSH的酵母工程菌株提供一定参考。To elucidate the mechanism of glutathione(GSH)biosynthesis by Hansenula polymorpha DL-1(HP-DL-1)exposed to Na_(2)SeO_(3),we examined the differentially expressed genes(DEGs)in yeast cells treated and not treated with Na_(2)SeO_(3) using a combination of transcriptomic sequencing and bioinformatic methods.The results showed that 60μmol/L Na_(2)SeO_(3) was found to be able to increase the GSH yield of yeast cells up to(530.22±9.6)mg/L after 48 h fermentation.A total of 1254 DEGs was identified in the Na_(2)SeO_(3)-induced group,of which 630 genes were up-regulated,whereas the remaining 624 genes were down-regulated.The Gene Ontology(GO)and Kyoto Encyclopedia of Genes and Genomes(KEGG)pathway enrichment analyses indicated that these DEGs were involved in the cell cycle,mitosis,amino acid biosynthesis,glycolysis,ribosome components and methane,fat,nucleic acid,GSH metabolism pathways.This study provides adequate information for a better understanding of the physiological mechanism of GSH biosynthesis by H.polymorpha,which will provide theoretical support for subsequent molecular improvement for over-production of GSH by engineered strains.
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