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Identification and functional expression of a new xylose isomerase from the goat rumen microbiome in Saccharomyces cerevisiae
Authors:Gabriel de Souza Colombo  Isis Viana Mendes  Betúlia de Morais Souto  Cristine Chaves Barreto  Luana Assis Serra  Eliane Ferreira Noronha  Nádia Skorupa Parachin  João Ricardo Moreira de Almeida  Betania Ferraz Quirino
Institution:1. Genetics and Biotechnology Laboratory, Embrapa-Agroenergy, Brasília, DF, Brazil

Genomic Sciences and Biotechnology Program, Universidade Católica de Brasília, Brasília, DF, Brazil;2. Genomic Sciences and Biotechnology Program, Universidade Católica de Brasília, Brasília, DF, Brazil;3. Genetics and Biotechnology Laboratory, Embrapa-Agroenergy, Brasília, DF, Brazil;4. Departmentof Cellular Biology, Universidade de Brasília, Brasília, DF, Brazil

Abstract:The current climate crisis demands replacement of fossil energy sources with sustainable alternatives. In this scenario, second-generation bioethanol, a product of lignocellulosic biomass fermentation, represents a more sustainable alternative. However, Saccharomyces cerevisiae cannot metabolize pentoses, such as xylose, present as a major component of lignocellulosic biomass. Xylose isomerase (XI) is an enzyme that allows xylose consumption by yeasts, because it converts xylose into xylulose, which is further converted to ethanol by the pentose-phosphate pathway. Only a few XI were successfully expressed in S. cerevisiae strains. This work presents a new bacterial XI, named GR-XI 1, obtained from a Brazilian goat rumen metagenomic library. Phylogenetic analysis confirmed the bacterial origin of the gene, which is related to Firmicutes XIs. After codon optimization, this enzyme, renamed XySC1, was functionally expressed in S. cerevisiae, allowing growth in media with xylose as sole carbon source. Overexpression of XySC1 in S. cerevisiae allowed the recombinant strain to efficiently consume and metabolize xylose under aerobic conditions.
Keywords:yeast  Saccharomyces cerevisiae  metagenomics  xylose  xylose isomerase
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