Cell Sizes Matter for Industrial Bioproduction, a Case of Polyhydroxybutyrate

Most bacterial cells are 1-2 microns in size, limiting intracellular products like polyhydroxyalkanoates (PHA) accumulation. Cell size is regulated by key genes such as mreB and minCD, which encode cellular skeleton protein and control cell fission ring location, respectively. Their expression changes significantly affect microbial growth. This study successfully redesigns the ClpXP protein degradation system by deleting the sspB gene and using mutated SsrA tags with different degradation rates to control MreB degradation. Dynamic degradation of MreB allows non-model bacterium Halomonas bluephagenesis to grow normally and increase cell size simultaneously. Combined with overexpression of minCD, H. bluephagenesis with progressive MreB degradation increases the cell size further, albeit with a reduced growth rate. H. bluephagenesis CYL0307, with the PHB granule-associated protein PhaP1 deleted and phaAB<sub>Re</sub> overexpressed in the MreB-degraded strain, increases cell volume more than nine times compared to the original strain. CYL0307 produces 149 g L<sup>-1</sup> cell dry weight containing 82% PHB after 44 h in a 5000 L bioreactor, with cells containing single large PHB granules, simplifying recovery and purification. These results provide a post-translational gene regulation method in H. bluephagenesis and a strategy for enhancing PHB production via morphological engineering.

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Publication Details

Journal
Advanced Science
Published
2025-02-18
DOI
https://doi.org/10.1002/advs.202412256
Citations
9
Primary Topic
biodegradable polymer synthesis and properties
Type
article
Field-Weighted Citation Impact
5.37

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article

Cell Sizes Matter for Industrial Bioproduction, a Case of Polyhydroxybutyrate

Wei Guo, Lizhan Zhang, Yan Xu, Fuqing Wu et al.
9 citations
Advanced Science
biodegradable polymer synthesis and properties
5.37
article

Cell Sizes Matter for Industrial Bioproduction, a Case of Polyhydroxybutyrate

Wei Guo, Lizhan Zhang, Yan Xu, Fuqing Wu, Shuang Zheng, Jason H. Yang, Xu Liu, Jiale Wang, Guo‐Qiang Chen, Qiong Wu, Yi‐Ling Chen
article en
9 citations

Abstract

Most bacterial cells are 1-2 microns in size, limiting intracellular products like polyhydroxyalkanoates (PHA) accumulation. Cell size is regulated by key genes such as mreB and minCD, which encode cellular skeleton protein and control cell fission ring location, respectively. Their expression changes significantly affect microbial growth. This study successfully redesigns the ClpXP protein degradation system by deleting the sspB gene and using mutated SsrA tags with different degradation rates to control MreB degradation. Dynamic degradation of MreB allows non-model bacterium Halomonas bluephagenesis to grow normally and increase cell size simultaneously. Combined with overexpression of minCD, H. bluephagenesis with progressive MreB degradation increases the cell size further, albeit with a reduced growth rate. H. bluephagenesis CYL0307, with the PHB granule-associated protein PhaP1 deleted and phaAB<sub>Re</sub> overexpressed in the MreB-degraded strain, increases cell volume more than nine times compared to the original strain. CYL0307 produces 149 g L<sup>-1</sup> cell dry weight containing 82% PHB after 44 h in a 5000 L bioreactor, with cells containing single large PHB granules, simplifying recovery and purification. These results provide a post-translational gene regulation method in H. bluephagenesis and a strategy for enhancing PHB production via morphological engineering.

Advanced ScienceVol. 12(14)
Chinese Academy of Agricultural Sciences (CN), Center for Life Sciences (CN), Tsinghua University (CN)
National Natural Science Foundation of China, Ministry of Science and Technology of the People's Republic of China, China Postdoctoral Science Foundation, Peking University
Openalex Percentile: Top 4%
biodegradable polymer synthesis and properties
5.37
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