首页|汉氏葡糖醋杆菌Komagataeibacter hansenii HDM1-3不同发酵时间的转录组测序分析

汉氏葡糖醋杆菌Komagataeibacter hansenii HDM1-3不同发酵时间的转录组测序分析

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为了探究汉氏葡糖醋杆菌HDM1-3(Komagataeibacter hansenii HDM1-3)在不同发酵时间的差异基因表达水平,挖掘差异表达基因在细菌纤维素(Bacterial cellulose,BC)生物合成代谢相关基因中的功能,利用Illumina HiSeq平台对发酵前期(18 h)和发酵后期(36 h)的Komagataeibacter hansenii HDM1-3菌株进行转录组测序分析,通过荧光定量PCR验证转录组测序结果的准确性,通过GO富集和KEGG富集分析差异表达基因.转录组测序共获得3 154个CDS序列,其中57个未被注释,注释率达98.22%.差异表达基因分析表明,菌株HDM1-3发酵36 h相比于发酵18 h,共有684个显著性差异表达基因,其中上调基因369个(53.9%),下调基因315个(46.1%).GO功能富集分析结果表明,发酵后期碳水化合物代谢相关功能基因下调,而细胞膜相关功能基因上调.KEGG富集分析结果表明,主要的能量代谢途径,包括糖酵解途径、磷酸戊糖途径和柠檬酸循环都显著下调,两个BC合成酶基因显著上调.这些结果为进一步分析HDM1-3菌株BC合成相关基因、提高BC产量的研究提供理论参考.
Transcriptome sequencing analysis of Komagataeibacter hansenii HDM1-3 at different fermentation time
To investigate the differential gene expression levels of Komagataeibacter hansenii HDM1-3 at different fermentation times,and explore the function of differentially expressed genes in bacterial cellulose(BC)bioanabolic genes,Illumina HiSeq platform was used to analyze the transcriptome sequencing of Komagataeibacter hansenii HDM1-3 strain at the early stage(18 h)and the late stage(36 h)of fermentation,and fluorescence quantitative PCR was used to verify the accuracy of transcriptome sequencing results.Differentially expressed genes were analyzed by GO enrichment and KEGG enrichment.A total of 3154 CDS sequences are obtained by transcript sequencing,among which 57 sequences are not annotated,with an annotation rate of 98.22%.Differentially expressed genes analysis shows that there are 684 differentially expressed genes in strain HDM1-3 after 36 h fermentation compared with 18 h fermentation,among which 369(53.9%)genes are up-regulated and 315(46.1%)genes are down-regulated.GO functional enrichment analysis shows that the functional genes related to carbohydrate metabolism are down-regulated,while the functional genes related to cell membrane are up-regulated in the late fermentation stage.KEGG enrichment analysis shows that major energy metabolism pathways,including glycolysis pathway,pentose phosphate pathway and citric acid cycle,are significantly down-regulated,and two BC synthase genes are significantly up-regulated.These results provide theoretical reference for further analysis of BC synthesis-related genes in HDM1-3 strain to improve BC yield.

Komagataeibacter hansenii HDM1-3differentially expressed genesfluorescence quantitative PCRbacterial cellulose

邱永杰、李元敬、郭丹、雷虹、李文辉

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黑龙江大学农业微生物技术教育部工程研究中心,哈尔滨 150500

黑龙江大学生命科学学院黑龙江省寒地生态修复与资源利用重点实验室,哈尔滨 150080

华南师范大学汕尾校区材料与新能源学院,汕尾 516600

汉氏葡糖醋杆菌HDM1-3 差异表达基因 荧光定量PCR 细菌纤维素

黑龙江省自然科学基金资助项目

C2015023

2024

黑龙江大学自然科学学报
黑龙江大学

黑龙江大学自然科学学报

CSTPCD
影响因子:0.27
ISSN:1001-7011
年,卷(期):2024.41(3)
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