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理性工程改造天然聚羟基烷酸酯生产微生物以提高合成和回收效率。

Rational engineering of natural polyhydroxyalkanoates producing microorganisms for improved synthesis and recovery.

机构信息

Departamento de Microbiología, Facultad de Biología, Universidad de Sevilla, Sevilla, Spain.

Biosystems Engineering Laboratory, Department of Chemical and Bioprocess Engineering, Universidad de Santiago de Chile (USACH), Santiago, Chile.

出版信息

Microb Biotechnol. 2023 Feb;16(2):262-285. doi: 10.1111/1751-7915.14109. Epub 2022 Jul 6.

DOI:10.1111/1751-7915.14109
PMID:35792877
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9871526/
Abstract

Microbial production of biopolymers derived from renewable substrates and waste streams reduces our heavy reliance on petrochemical plastics. One of the most important biodegradable polymers is the family of polyhydroxyalkanoates (PHAs), naturally occurring intracellular polyoxoesters produced for decades by bacterial fermentation of sugars and fatty acids at the industrial scale. Despite the advances, PHA production still suffers from heavy costs associated with carbon substrates and downstream processing to recover the intracellular product, thus restricting market positioning. In recent years, model-aided metabolic engineering and novel synthetic biology approaches have spurred our understanding of carbon flux partitioning through competing pathways and cellular resource allocation during PHA synthesis, enabling the rational design of superior biopolymer producers and programmable cellular lytic systems. This review describes these attempts to rationally engineering the cellular operation of several microbes to elevate PHA production on specific substrates and waste products. We also delve into genome reduction, morphology, and redox cofactor engineering to boost PHA biosynthesis. Besides, we critically evaluate engineered bacterial strains in various fermentation modes in terms of PHA productivity and the period required for product recovery.

摘要

微生物利用可再生底物和废物流生产的生物聚合物减少了我们对石化塑料的严重依赖。最重要的可生物降解聚合物之一是聚羟基烷酸酯(PHA)家族,几十年来,这些天然存在的细胞内聚氧酯一直通过细菌发酵糖和脂肪酸在工业规模上生产。尽管取得了这些进展,但 PHA 的生产仍然受到与碳底物相关的高成本和下游加工的限制,以回收细胞内产物,从而限制了市场定位。近年来,模型辅助代谢工程和新的合成生物学方法推动了我们对碳通量通过竞争途径和 PHA 合成过程中的细胞资源分配进行分区的理解,从而能够合理设计出更优越的生物聚合物生产菌和可编程的细胞裂解系统。这篇综述描述了这些尝试,旨在合理设计几种微生物的细胞操作,以提高特定底物和废物上的 PHA 生产。我们还深入探讨了基因组减少、形态和氧化还原辅因子工程,以促进 PHA 生物合成。此外,我们还从 PHA 生产力和产品回收所需的时间两方面,对不同发酵模式下的工程菌进行了批判性评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fadb/9871526/63308344a8f1/MBT2-16-262-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fadb/9871526/53dab445c809/MBT2-16-262-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fadb/9871526/4bfd2f0e8811/MBT2-16-262-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fadb/9871526/950ea1ebfa06/MBT2-16-262-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fadb/9871526/47a91c7f284e/MBT2-16-262-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fadb/9871526/63308344a8f1/MBT2-16-262-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fadb/9871526/53dab445c809/MBT2-16-262-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fadb/9871526/4bfd2f0e8811/MBT2-16-262-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fadb/9871526/950ea1ebfa06/MBT2-16-262-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fadb/9871526/47a91c7f284e/MBT2-16-262-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fadb/9871526/63308344a8f1/MBT2-16-262-g005.jpg

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