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A novel method to prepare L-Arabinose from xylose mother liquor by yeast-mediated biopurification

BACKGROUND: L-arabinose is an important intermediate for anti-virus drug synthesis and has also been used in food additives for diets-controlling in recent years. Commercial production of L-arabinose is a complex progress consisting of acid hydrolysis of gum arabic, followed by multiple procedures o...

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Autores principales: Cheng, Hairong, Wang, Hengwei, Lv, Jiyang, Jiang, Mingguo, Lin, Shuangjun, Deng, Zixin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3125199/
https://www.ncbi.nlm.nih.gov/pubmed/21649890
http://dx.doi.org/10.1186/1475-2859-10-43
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author Cheng, Hairong
Wang, Hengwei
Lv, Jiyang
Jiang, Mingguo
Lin, Shuangjun
Deng, Zixin
author_facet Cheng, Hairong
Wang, Hengwei
Lv, Jiyang
Jiang, Mingguo
Lin, Shuangjun
Deng, Zixin
author_sort Cheng, Hairong
collection PubMed
description BACKGROUND: L-arabinose is an important intermediate for anti-virus drug synthesis and has also been used in food additives for diets-controlling in recent years. Commercial production of L-arabinose is a complex progress consisting of acid hydrolysis of gum arabic, followed by multiple procedures of purification, thus making high production cost. Therefore, there is a biotechnological and commercial interest in the development of new cost-effective and high-performance methods for obtaining high purity grade L-arabinose. RESULTS: An alternative, economical method for purifying L-arabinose from xylose mother liquor was developed in this study. After screening 306 yeast strains, a strain of Pichia anomala Y161 was selected as it could effectively metabolize other sugars but not L-arabinose. Fermentation in a medium containing xylose mother liquor permitted enrichment of L-arabinose by a significant depletion of other sugars. Biochemical analysis of this yeast strain confirmed that its poor capacity for utilizing L-arabinose was due to low activities of the enzymes required for the metabolism of this sugar. Response surface methodology was employed for optimization the fermentation conditions in shake flask cultures. The optimum conditions were: 75 h fermentation time, at 32.5°C, in a medium containing 21% (v/v) xylose mother liquor. Under these conditions, the highest purity of L-arabinose reached was 86.1% of total sugar, facilitating recovery of white crystalline L-arabinose from the fermentation medium by simple methods. CONCLUSION: Yeast-mediated biopurification provides a dynamic method to prepare high purity of L-arabinose from the feedstock solution xylose mother liqour, with cost-effective and high-performance properties.
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spelling pubmed-31251992011-06-29 A novel method to prepare L-Arabinose from xylose mother liquor by yeast-mediated biopurification Cheng, Hairong Wang, Hengwei Lv, Jiyang Jiang, Mingguo Lin, Shuangjun Deng, Zixin Microb Cell Fact Research BACKGROUND: L-arabinose is an important intermediate for anti-virus drug synthesis and has also been used in food additives for diets-controlling in recent years. Commercial production of L-arabinose is a complex progress consisting of acid hydrolysis of gum arabic, followed by multiple procedures of purification, thus making high production cost. Therefore, there is a biotechnological and commercial interest in the development of new cost-effective and high-performance methods for obtaining high purity grade L-arabinose. RESULTS: An alternative, economical method for purifying L-arabinose from xylose mother liquor was developed in this study. After screening 306 yeast strains, a strain of Pichia anomala Y161 was selected as it could effectively metabolize other sugars but not L-arabinose. Fermentation in a medium containing xylose mother liquor permitted enrichment of L-arabinose by a significant depletion of other sugars. Biochemical analysis of this yeast strain confirmed that its poor capacity for utilizing L-arabinose was due to low activities of the enzymes required for the metabolism of this sugar. Response surface methodology was employed for optimization the fermentation conditions in shake flask cultures. The optimum conditions were: 75 h fermentation time, at 32.5°C, in a medium containing 21% (v/v) xylose mother liquor. Under these conditions, the highest purity of L-arabinose reached was 86.1% of total sugar, facilitating recovery of white crystalline L-arabinose from the fermentation medium by simple methods. CONCLUSION: Yeast-mediated biopurification provides a dynamic method to prepare high purity of L-arabinose from the feedstock solution xylose mother liqour, with cost-effective and high-performance properties. BioMed Central 2011-06-07 /pmc/articles/PMC3125199/ /pubmed/21649890 http://dx.doi.org/10.1186/1475-2859-10-43 Text en Copyright ©2011 Cheng et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Cheng, Hairong
Wang, Hengwei
Lv, Jiyang
Jiang, Mingguo
Lin, Shuangjun
Deng, Zixin
A novel method to prepare L-Arabinose from xylose mother liquor by yeast-mediated biopurification
title A novel method to prepare L-Arabinose from xylose mother liquor by yeast-mediated biopurification
title_full A novel method to prepare L-Arabinose from xylose mother liquor by yeast-mediated biopurification
title_fullStr A novel method to prepare L-Arabinose from xylose mother liquor by yeast-mediated biopurification
title_full_unstemmed A novel method to prepare L-Arabinose from xylose mother liquor by yeast-mediated biopurification
title_short A novel method to prepare L-Arabinose from xylose mother liquor by yeast-mediated biopurification
title_sort novel method to prepare l-arabinose from xylose mother liquor by yeast-mediated biopurification
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3125199/
https://www.ncbi.nlm.nih.gov/pubmed/21649890
http://dx.doi.org/10.1186/1475-2859-10-43
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