The glucose/xylose facilitator Gxf1 from Candida intermedia expressed in a xylose-fermenting industrial strain of Saccharomyces cerevisiae increases xylose uptake in SSCF of wheat straw

被引:31
作者
Fonseca, Cesar [3 ,4 ]
Olofsson, Kim [1 ]
Ferreira, Carla [3 ]
Runquist, David [2 ]
Fonseca, Luis L. [4 ]
Hahn-Hagerdal, Barbel [2 ]
Liden, Gunnar [1 ]
机构
[1] Lund Univ, Dept Chem Engn, SE-22100 Lund, Sweden
[2] Lund Univ, Dept Appl Microbiol, SE-22100 Lund, Sweden
[3] Univ Nova Lisboa, Fac Ciencias & Tecnol, Dept Ciencias Vida, Ctr Recursos Microbiol CREM, P-2829516 Caparica, Portugal
[4] Univ Nova Lisboa, ITQB, P-2780156 Oeiras, Portugal
关键词
Xylose transport; Industrial Saccharomyces cerevisiae; Simultaneous saccharification and co-fermentation; Bioethanol; Gxf1; SIMULTANEOUS SACCHARIFICATION; CO-FERMENTATION; HEXOSE TRANSPORTERS; GENE-EXPRESSION; RECOMBINANT; YEAST; PERFORMANCE; ETHANOL; CONVERSION; VECTORS;
D O I
10.1016/j.enzmictec.2011.02.010
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
Ethanolic fermentation of lignocellulose raw materials requires industrial xylose-fermenting strains capable of complete and efficient D-xylose consumption. A central question in xylose fermentation by Saccharomyces cerevisiae engineered for xylose fermentation is to improve the xylose uptake. In the current study, the glucose/xylose facilitator Gxf1 from Candida intermedia, was expressed in three different xylose-fermenting S. cerevisiae strains of industrial origin. The in vivo effect on aerobic xylose growth and the initial xylose uptake rate were assessed. The expression of Gxf1 resulted in enhanced aerobic xylose growth only for the TMB3400 based strain. It displayed more than a 2-fold higher affinity for D-xylose than the parental strain and approximately 2-fold higher initial specific growth rate at 4 g/L D-xylose. Enhanced xylose consumption was furthermore observed when the GXF1-strain was assessed in simultaneous saccharification and co-fermentation (SSCF) of pretreated wheat straw. However, the ethanol yield remained unchanged due to increased by-product formation. Metabolic flux analysis suggested that the expression of the Gxf1 transporter had shifted the control of xylose catabolism from transport to the NAD(+) dependent oxidation of xylitol to xylulose. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:518 / 525
页数:8
相关论文
共 45 条
  • [1] Influence of strain and cultivation procedure on the performance of simultaneous saccharification and fermentation of steam pretreated spruce
    Alkasrawi, M
    Rudolf, A
    Lidén, G
    Zacchi, G
    [J]. ENZYME AND MICROBIAL TECHNOLOGY, 2006, 38 (1-2) : 279 - 286
  • [2] [Anonymous], 1989, Molecular Cloning: A Laboratory
  • [3] Modeling simultaneous glucose and xylose uptake in Saccharomyces cerevisiae from kinetics and gene expression of sugar transporters
    Bertilsson, Magnus
    Andersson, Jonas
    Liden, Gunnar
    [J]. BIOPROCESS AND BIOSYSTEMS ENGINEERING, 2008, 31 (04) : 369 - 377
  • [4] Prefermentation improves xylose utilization in simultaneous saccharification and co-fermentation of pretreated spruce
    Bertilsson, Magnus
    Olofsson, Kim
    Liden, Gunnar
    [J]. BIOTECHNOLOGY FOR BIOFUELS, 2009, 2
  • [5] FONSECA C, 2004, C BOOK 11 INT C YEAS, P71
  • [6] L-Arabinose transport and catabolism in yeast
    Fonseca, Cesar
    Romao, Rute
    de Sousa, Helena Rodrigues
    Hahn-Hagerdal, Barbel
    Spencer-Martins, Isabel
    [J]. FEBS JOURNAL, 2007, 274 (14) : 3589 - 3600
  • [7] Control of xylose consumption by xylose transport in recombinant Saccharomyces cerevisiae
    Gárdonyi, M
    Jeppsson, M
    Lidén, G
    Gorwa-Grausland, MF
    Hahn-Hägerdal, B
    [J]. BIOTECHNOLOGY AND BIOENGINEERING, 2003, 82 (07) : 818 - 824
  • [8] Gárdonyi M, 2003, FEMS YEAST RES, V3, P45, DOI 10.1111/j.1567-1364.2003.tb00137.x
  • [9] Gietz RD, 2002, METHOD ENZYMOL, V350, P87
  • [10] NEW YEAST-ESCHERICHIA-COLI SHUTTLE VECTORS CONSTRUCTED WITH INVITRO MUTAGENIZED YEAST GENES LACKING 6-BASE PAIR RESTRICTION SITES
    GIETZ, RD
    SUGINO, A
    [J]. GENE, 1988, 74 (02) : 527 - 534