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Effect of gene POX06509 deletion on gene expression of Penicillium oxalicum

ABSTRACT: Explore the functions of important transcription factors that regulate the expression of cellulase gene and xylanase gene

ORGANISM(S): Penicillium oxalicum

PROVIDER: GSE154642 | GEO | 2023/07/20

REPOSITORIES: GEO

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Effect of gene POX05503 deletion on gene expression of Penicillium oxalicum

Project description:Explore the functions of protein kinase that regulate the expression of cellulase gene and xylanase gene

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Effect of gene POX07948 deletion on gene expression of Penicillium oxalicum

Project description:To explore the effect of phosphokinase POX07948 on the transcription levels of cellulase-encoding genes and xylanase-encoding genes

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Effect of gene POX00158 deletion on gene expression of Penicillium oxalicum

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Effect of gene POX09752 deletion on gene expression of Penicillium oxalicum

Project description:To explore the effect of transcription factor POX09752 on the transcription levels of cellulase-encoding genes and xylanase-encoding genes

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Effect of gene POX07071 deletion on gene expression of Penicillium oxalicum

Project description:To explore the effect of G-protein POX07071 on the transcription levels of cellulase-encoding genes and xylanase-encoding genes

2023-07-20 | GSE154704 | GEO

Comparative genomic, transcriptomic and secretomic profilings of Penicillium oxalicum HP7-1 and its cellulase and xylanase hyper-producing mutant EU2106, and identification of two novel regulators for cellulase and xylanase gene expression

Project description:In this study,comparative genomic, transcriptomic and secretomic profilings of Penicillium oxalicum HP7-1 and its cellulase and xylanase hyper-producing mutant EU2106 were employed to screen for novel regulators for cellulase and xylanase gene expression.

2016-08-31 | GSE80076 | GEO

Effect of gene POX01907 deletion on gene expression of Penicillium oxalicum

Project description:Explore the functions of important transcription factors that regulate the expression of amylase genes

2023-07-20 | GSE154638 | GEO

Effects of transcription factor POX04513 on the transcription of cellulase genes and xylanase genes in Penicillium oxalicum

Project description:To investigate the effect of the transcription factor POX04513 in Penicillium oxalicum on the expression levels of cellulase and xylanase genes in solid and liquid fermentation

2023-05-06 | GSE154882 | GEO

Penicillium oxalicum

Project description:Comparative genomic, transcriptomic and secretomic profilings of Penicillium oxalicum HP7-1 and its cellulase and xylanase hyper-producing mutant EU2106, and identification of two novel regulators for cellulase and xylanase gene expression

| PRJNA317762 | ENA

Transcriptomic analysis of fungus Penicillium oxalicum and its mtr23B deletion and complemented strains

Project description:The goals of this study are to compare differential gene expressions for Penicillium oxalicum wild type strain (WT), mtr23B knockout strain (Δmtr23B) and complemented strain (Rmtr23B) on Vogel’s medium with 2% glucose (G) or 1% wheat bran and 1% cellulose (CW) as carbon resources. When cultivated in a repression medium for cellulolytic enzyme formation (G), the deletion of mtr23B upregulated genes involved in lyase activity, hydrolase activity, acyl carrier activity, monooxygenase activity, electron transfer activity, phosphopantetheine binding, heme binding, cell wall organization or biogenesis, oxidation-reduction process and extracellular region. The downregulated genes in Δmtr23B were mainly involved in transmembrane transporter activity, amino acid transmembrane transporter activity, membrane and integral component of membrane. When cultivated in an inducing medium for cellulolytic enzyme formation (CW), the downregulated genes in Δmtr23B were mainly involved in glucosidase activity, polygalacturonase activity, oxidoreductase activity, heme binding, oxidareductase activity, xylanase activity, cellulase activity, cellulose binding, oxidation-reduction process, cellulose catabolic process, xylan catabolic process and extracellular region. We find the expression levels of five secondary metabolism gene clusters (totally 28 clusters) were silenced in Δmtr23B. This study provides the information that mtr23B is required in conidiation and hydrolase activity of P. oxalicum.

2019-12-14 | GSE142001 | GEO

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