首页> 外文期刊>Reaction Chemistry & Engineering >Efficient biotransformation of 5-hydroxymethylfurfural to 5-hydroxymethyl-2-furancarboxylic acid by a new whole-cell biocatalyst Pseudomonas aeruginosa PC-1
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Efficient biotransformation of 5-hydroxymethylfurfural to 5-hydroxymethyl-2-furancarboxylic acid by a new whole-cell biocatalyst Pseudomonas aeruginosa PC-1

机译:通过新的全细胞生物催化剂假单胞菌PC-1高效地将5-羟甲基糠醛与5-羟甲基-2- FurancarBoxic甲酸的生物转化。

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摘要

5-Hydroxymethyl-2-furancarboxylic acid (HMFCA) is a significant added-value intermediate derivatized from the bio-based platform chemical 5-hydroxymethylfurfuraldehyde (HMF). In the HMFCA biosynthesis process, the catalytic performance of the biocatalyst always decreases due to the presence of HMF toxicity, which is not conducive to achieving high product accumulation. Herein, we successfully obtained a new whole-cell biocatalyst from Pseudomonas aeruginosa PC~(-1), which was first reported to produce HMFCA from HMF. After optimization, 90.1% yield of HMFCA was attained within 6 h using a 100 mM substrate. Importantly, a much lower cell dosage was needed in the process. In order to achieve higher HMFCA accumulation, a fed-batch strategy was developed by using the growing cells from P. aeruginosa PC~(-1). Consequently, a total concentration of 721 mM HMFCA was obtained from 800 mM HMF within 58 h after 8 cycles of fed-batch, which is the highest concentration to date. The efficient HMFCA production made P. aeruginosa PC~(-1) a promising whole-cell biocatalyst for selective, large scale biotransformation of HMF.
机译:5-羟甲基-2-呋喃羧酸(HMFCA)是从生物基平台化学5-羟甲基糠醛(HMF)的显着添加值中间体。在HMFCA生物合成过程中,生物催化剂的催化性能始终由于HMF毒性的存在而降低,这不利于实现高产品积累。在此,我们成功地从铜绿假单胞菌PC〜(-1)中获得了新的全细胞生物催化剂,首先报道了从HMF产生HMFCA。优化后,使用100mM基质在6小时内达到90.1%HMFCA。重要的是,在该过程中需要一种更低的细胞剂量。为了实现更高的HMFCA积累,通过使用来自P.铜绿假单胞菌PC〜(-1)的生长细胞来开发FED批量策略。因此,在8次循环的批量循环之后,在58小时内从800mM HMF的总浓度从90mM HMF中获得,其是迄今为止最高的浓度。高效的HMFCA生产P.铜绿假单胞菌PC〜(-1)一种有前途的全细胞生物催化剂,用于选择性,大规模的HMF的生物转化。

著录项

  • 来源
    《Reaction Chemistry & Engineering》 |2020年第8期|共8页
  • 作者

    Xin Pan; Sihua Wu; Deshan Yao;

  • 作者单位

    Department of Cardiology Affiliated Hospital of Yangzhou University Yangzhou University Yangzhou Jiangsu 225000 China;

    Department of Cardiology Affiliated Hospital of Yangzhou University Yangzhou University Yangzhou Jiangsu 225000 China;

    Department of Cardiology Affiliated Hospital of Yangzhou University Yangzhou University Yangzhou Jiangsu 225000 China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 物理化学(理论化学)、化学物理学;
  • 关键词

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