The role of peroxisomes in xylose alcoholic fermentation in the engineered Saccharomyces cerevisiae

被引:10
作者
Dzanaeva, Ljubov [1 ]
Kruk, Barbara [2 ]
Ruchala, Justyna [2 ]
Nielsen, Jens [3 ]
Sibirny, Andriy [1 ,2 ]
Dmytruk, Kostyantyn [1 ]
机构
[1] NAS Ukraine, Inst Cell Biol, Dept Mol Genet & Biotechnol, Lvov, Ukraine
[2] Univ Rzeszow, Dept Biotechnol & Microbiol, Rzeszow, Poland
[3] Chalmers Univ Technol, Dept Biol & Biol Engn, Gothenburg, Sweden
关键词
alcoholic fermentation; peroxisomes; S; cerevisiae; xylose; YEAST; BIOSYNTHESIS; BIOFUELS; ACID;
D O I
10.1002/cbin.11353
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Xylose is a second-most abounded sugar after glucose in lignocellulosic hydrolysates and should be efficiently fermented for economically viable second-generation ethanol production. Despite significant progress in metabolic and evolutionary engineering, xylose fermentation rate of recombinant Saccharomyces cerevisiae remains lower than that for glucose. Our recent study demonstrated that peroxisome-deficient cells of yeast Ogataea polymorpha showed a decrease in ethanol production from xylose. In this work, we have studied the role of peroxisomes in xylose alcoholic fermentation in the engineered xylose-utilizing strain of S. cerevisiae. It was shown that peroxisome-less pex3 Delta mutant possessed 1.5-fold decrease of ethanol production from xylose. We hypothesized that peroxisomal catalase Cta1 may have importance for hydrogen peroxide, the important component of reactive oxygen species, detoxification during xylose alcoholic fermentation. It was clearly shown that CTA1 deletion impaired ethanol production from xylose. It was found that enhancing the peroxisome population by modulation the peroxisomal biogenesis by overexpression of PEX34 activates xylose alcoholic fermentation.
引用
收藏
页码:1606 / 1615
页数:10
相关论文
共 23 条
[1]   Association of improved oxidative stress tolerance and alleviation of glucose repression with superior xylose-utilization capability by a natural isolate of Saccharomyces cerevisiae [J].
Cheng, Cheng ;
Tang, Rui-Qi ;
Xiong, Liang ;
Hector, Ronald E. ;
Bai, Feng-Wu ;
Zhao, Xin-Qing .
BIOTECHNOLOGY FOR BIOFUELS, 2018, 11
[2]  
Ferreira Raphael, 2018, Metab Eng Commun, V6, P22, DOI 10.1016/j.meteno.2018.01.002
[3]  
Gietz RD, 2002, METHOD ENZYMOL, V350, P87
[4]   Fungal catalases: Function, phylogenetic origin and structure [J].
Hansberg, Wilhelm ;
Salas-Lizana, Rodolfo ;
Dominguez, Laura .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2012, 525 (02) :170-180
[5]   The biochemistry of peroxisomal β-oxidation in the yeast Saccharomyces cerevisiae [J].
Hiltunen, JK ;
Mursula, AM ;
Rottensteiner, H ;
Wierenga, RK ;
Kastaniotis, AJ ;
Gurvitz, A .
FEMS MICROBIOLOGY REVIEWS, 2003, 27 (01) :35-64
[6]   Metabolic engineering of Saccharomyces cerevisiae: a key cell factory platform for future biorefineries [J].
Hong, Kuk-Ki ;
Nielsen, Jens .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2012, 69 (16) :2671-2690
[7]   Transcriptional reprogramming in yeast using dCas9 and combinatorial gRNA strategies [J].
Jensen, Emil D. ;
Ferreira, Raphael ;
Jakociunas, Tadas ;
Arsovska, Dushica ;
Zhang, Jie ;
Ding, Ling ;
Smith, Justin D. ;
David, Florian ;
Nielsen, Jens ;
Jensen, Michael K. ;
Keasling, Jay D. .
MICROBIAL CELL FACTORIES, 2017, 16
[8]   Rational and Evolutionary Engineering Approaches Uncover a Small Set of Genetic Changes Efficient for Rapid Xylose Fermentation in Saccharomyces cerevisiae [J].
Kim, Soo Rin ;
Skerker, Jeffrey M. ;
Kang, Wei ;
Lesmana, Anastashia ;
Wei, Na ;
Arkin, Adam P. ;
Jin, Yong-Su .
PLOS ONE, 2013, 8 (02)
[9]   Peroxisomes and peroxisomal transketolase and transaldolase enzymes are essential for xylose alcoholic fermentation by the methylotrophic thermotolerant yeast, Ogataea (Hansenula) polymorpha [J].
Kurylenko, Olena O. ;
Ruchala, Justyna ;
Vasylyshyn, Roksolana V. ;
Stasyk, Oleh V. ;
Dmytruk, Olena V. ;
Dmytruk, Kostyantyn V. ;
Sibirny, Andriy A. .
BIOTECHNOLOGY FOR BIOFUELS, 2018, 11
[10]   Production of fuels and chemicals from xylose by engineered Saccharomyces cerevisiae: a review and perspective [J].
Kwak, Suryang ;
Jin, Yong-Su .
MICROBIAL CELL FACTORIES, 2017, 16