详细信息

Transcriptional regulatory networks of methanol-independent protein expression in Pichia pastoris under the AOX1 promoter with trans-acting elements engineering  ( SCI-EXPANDED收录 EI收录)  

文献类型:期刊文献

英文题名:Transcriptional regulatory networks of methanol-independent protein expression in Pichia pastoris under the AOX1 promoter with trans-acting elements engineering

作者:Shi, Lei[1];Wang, Jinjia[1];Wang, Xiaolong[1];Zhang, Yuanxing[1,2];Song, Zhiwei[3,4];Cai, Menghao[1];Zhou, Xiangshan[1]

机构:[1]East China Univ Sci & Technol, State Key Lab Bioreactor Engn, 130 Meilong Rd, Shanghai 200237, Peoples R China;[2]Shanghai Collaborat Innovat Ctr Biomfg, Shanghai 200237, Peoples R China;[3]Bioproc Technol Inst, Singapore, Singapore;[4]Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Biochem, Singapore, Singapore

年份:2020

卷号:7

期号:1

外文期刊名:BIORESOURCES AND BIOPROCESSING

收录:;EI(收录号:20224513084541);WOS:【SCI-EXPANDED(收录号:WOS:000521556300001)】;

语种:英文

外文关键词:Pichia pastoris; RNA-seq; Carbon sources; AOX1 promoter

摘要:To explore the differences in the intracellular transcriptional mechanism in carbon-derepressed and wild-type Pichia pastoris strains fed with three different carbon sources. RNA in carbon-derepressed (Delta mig1 Delta mig2 Delta nrg1-Mit1; Mut) and wild-type (WT) P. pastoris fed with three different carbon sources (dextrose, glycerol, and methanol) were sequenced. Differentially expressed genes (DEGs) associated with these carbon sources were obtained and clustered into modules using weighted gene co-expression network analysis (WGCNA). Signaling pathway enrichment analysis was performed using KEGG, and protein to protein interaction (PPI) network was also constructed. A total of 2536 DEGs were obtained from three intersections, and some of them were enriched in carbon sources and involved in carbon metabolism, secondary metabolisms, and amino acid biosynthesis. Two modules, MEgreenyellow (involved in protease, oxidative phosphorylation, endoplasmic reticulum protein processing, folate carbon pool, and glycerol phospholipid metabolism pathways) and MEmidnightblue (involved in protease, endocytosis, steroid biosynthesis, and hippo signaling pathways) were significantly correlated with the strain type. Eight hub genes and two sub-networks were obtained from PPI network. Sub-network A enriched in proteasomes pathway while sub-network B enriched in ribosome pathway. The genes involved in carbon metabolism, secondary metabolic, and amino acid biosynthesis pathways changed significantly under different carbon sources. The changes in proteasome and ribosome activities play roles in carbohydrate metabolism in the methanol-free P-AOX1 start-up Mut strain.

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