Random UV-C mutagenesis ofScheffersomyces(formerlyPichia)stipitisNRRL Y-7124 to improve anaerobic growth on lignocellulosic sugars

Author:

Hughes Stephen R1,Gibbons William R2,Bang Sookie S3,Pinkelman Rebecca3,Bischoff Kenneth M1,Slininger Patricia J4,Qureshi Nasib4,Kurtzman Cletus P5,Liu Siqing1,Saha Badal C4,Jackson John S1,Cotta Michael A4,Rich Joseph O1,Javers Jeremy E6

Affiliation:

1. grid.417548.b 0000000404786311 Renewable Product Technology (RPT) Research Unit, National Center for Agricultural Utilization Research (NCAUR), Agricultural Research Service (ARS) United States Department of Agriculture (USDA) 1815 North University Street 61604 Peoria IL USA

2. grid.263791.8 000000012167853X Department of Biology and Microbiology South Dakota State University PO Box 2207B West Hall 104 57007 Brookings SD USA

3. grid.263790.9 0000000107041727 Department of Chemical and Biological Engineering South Dakota School of Mines and Technology 501 East Saint Joseph Street 57701-3995 Rapid City SD USA

4. grid.417548.b 0000000404786311 Bioenergy Research Unit, NCAUR, ARS USDA 1815 North University Street 61604 Peoria IL USA

5. grid.417548.b 0000000404786311 Bacterial Foodborne Pathogens and Mycology Research Unit, NCAUR, ARS USDA 1815 North University Street 61604 Peoria IL USA

6. ICM, Inc. 310 North First Street 67030 Colwich KS USA

Abstract

AbstractScheffersomyces (formerly Pichia) stipitis NRRL Y-7124 was mutagenized using UV-C irradiation to produce yeast strains for anaerobic conversion of lignocellulosic sugars to ethanol. UV-C irradiation potentially produces large numbers of random mutations broadly and uniformly over the whole genome to generate unique strains. Wild-type cultures of S. stipitis NRRL Y-7124 were subjected to UV-C (234 nm) irradiation targeted at approximately 40% cell survival. When surviving cells were selected in sufficient numbers via automated plating strategies and cultured anaerobically on xylose medium for 5 months at 28°C, five novel mutagenized S. stipitis strains were obtained. Variable number tandem repeat analysis revealed that mutations had occurred in the genome, which may have produced genes that allowed the anaerobic utilization of xylose. The mutagenized strains were capable of growing anaerobically on xylose/glucose substrate with higher ethanol production during 250- to 500-h growth than a Saccharomyces cerevisiae yeast strain that is the standard for industrial fuel ethanol production. The S. stipitis strains resulting from this intense multigene mutagenesis strategy have potential application in industrial fuel ethanol production from lignocellulosic hydrolysates.

Publisher

Oxford University Press (OUP)

Subject

Applied Microbiology and Biotechnology,Biotechnology,Bioengineering

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