Analysis of ethanol fermentation mechanism of ethanol producing white-rot fungus Phlebia sp MG-60 by RNA-seq

被引:14
|
作者
Wang, Jianqiao [1 ]
Suzuki, Tomohiro [2 ]
Dohra, Hideo [3 ,4 ]
Takigami, Shoko [1 ]
Kako, Hiroko [1 ]
Soga, Ayumi [1 ]
Kamei, Ichiro [5 ]
Mori, Toshio [1 ]
Kawagishi, Hirokazu [1 ,4 ,6 ]
Hirai, Hirofumi [1 ,4 ]
机构
[1] Shizuoka Univ, Fac Agr, Suruga Ku, 836 Ohya, Shizuoka 4228529, Japan
[2] Utsunomiya Univ, Ctr Biosci Res & Educ, 350 Mine Machi, Utsunomiya, Tochigi 3218505, Japan
[3] Shizuoka Univ, Inst Genet Res & Biotechnol, Suruga Ku, 836 Ohya, Shizuoka 4228529, Japan
[4] Shizuoka Univ, Res Inst Green Sci & Technol, Suruga Ku, 836 Ohya, Shizuoka 4228529, Japan
[5] Miyazaki Univ, Fac Agr, 1-1 Gakuen Kibanadai Nishi, Miyazaki 8892192, Japan
[6] Shizuoka Univ, Grad Sch Sci & Technol, Suruga Ku, 836 Ohya, Shizuoka 4228529, Japan
来源
BMC GENOMICS | 2016年 / 17卷
关键词
RNA-seq; Ethanol fermentation mechanism; Phlebia sp MG-60; White-rot fungi; PYRUVATE DECARBOXYLASE; RECOMBINANT EXPRESSION; LIPID-COMPOSITION; DNA-SEQUENCES; DEHYDROGENASE; IMPROVEMENT; XYLOSE; GENE; SACCHARIFICATION; DELIGNIFICATION;
D O I
10.1186/s12864-016-2977-7
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: The white-rot fungus Phlebia sp. MG-60 shows valuable properties such as high ethanol yield from several lignocellulosic materials, although white-rot fungi commonly degrade woody components to CO2 and H2O. In order to identify genes involved in ethanol production by Phlebia sp. MG-60, we compared genes differentially expressed by the ethanol producing fungus Phlebia sp. MG-60 and the model white-rot fungus Phanerochaete chrysosporium under ethanol fermenting and non-fermenting conditions using next-generation sequencing technologies. Results: mRNAs from mycelia of Phlebia sp. MG-60 and P. chrysosporium under fermenting and non-fermenting conditions were sequenced using the MiSeq system. To detect differentially expressed genes, expression levels were measured in fragments per kilobase of exon per million mapped reads (FPKM). Differentially expressed genes were annotated using BLAST searches, Gene Ontology classifications, and KEGG pathway analysis. Functional analyses of differentially expressed genes revealed that genes involved in glucose uptake, glycolysis, and ethanol synthesis were widely upregulated in Phlebia sp. MG-60 under fermenting conditions. Conclusions: In this study, we provided novel transcriptomic information on Phlebia sp. MG-60, and these RNA-seq data were useful in targeting genes involved in ethanol production for future genetic engineering.
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页数:11
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