{"title":"开发用于生物乙醇生产的淀粉发酵 Zymomonas mobilis 菌株。","authors":"Yingchi Wei, Jia Li, Changhui Wang, Jiangke Yang, Wei Shen","doi":"10.1186/s12934-024-02539-2","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Biorefinery using microorganisms to produce biofuels and value-added biochemicals derived from renewable biomass offers a promising alternative to meet our sustainable energy and environmental goals. The ethanologenic strain Zymomonas mobilis is considered as an excellent chassis for constructing microbial cell factories for diverse biochemicals due to its outstanding industrial characteristics in ethanol production, high specific productivity, and Generally Recognized as Safe (GRAS) status. Nonetheless, the restricted substrate range constrains its application.</p><p><strong>Results: </strong>The truncated ice nucleation protein InaK from Pseudomonas syringae was used as an autotransporter passenger, and α-amylase was fused to the C- terminal of InaK to equip the ethanol-producing bacterium with the capability to ferment renewable biomass. Western blot and flow cytometry analysis confirmed that the amylase was situated on the outer membrane. Whole-cell activity assays demonstrated that the amylase maintained its activity on the cell surface. The recombinant Z. mobilis facilitated the hydrolysis of starch into oligosaccharides and enabled the streamlining of simultaneous saccharification and fermentation (SSF) processes. In a 5% starch medium under SSF, recombinant strains containing P<sub>eno</sub> reached a maximum titer of 13.61 ± 0.12 g/L within 48 h. This represents an increase of 111.0% compared to the control strain's titer of titer of 6.45 ± 0.25 g/L.</p><p><strong>Conclusions: </strong>By fusing the truncated ice nucleation protein InaK with α-amylase, we achieved efficient expression and surface display of the enzyme on Z. mobilis. This fusion protein exhibited remarkable enzymatic activity. Its presence enabled a cost-effective bioproduction process using starch as the sole carbon source, and it significantly reduced the required cycle time for SSF. This study not only provides an excellent Z. mobilis chassis for sustainable bioproduction from starch but also highlights the potential of Z. mobilis to function as an effective cellular factory for producing high-value products from renewable biomass.</p>","PeriodicalId":18582,"journal":{"name":"Microbial Cell Factories","volume":"23 1","pages":"301"},"PeriodicalIF":4.3000,"publicationDate":"2024-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11552318/pdf/","citationCount":"0","resultStr":"{\"title\":\"Development of a starch-fermenting Zymomonas mobilis strain for bioethanol production.\",\"authors\":\"Yingchi Wei, Jia Li, Changhui Wang, Jiangke Yang, Wei Shen\",\"doi\":\"10.1186/s12934-024-02539-2\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Biorefinery using microorganisms to produce biofuels and value-added biochemicals derived from renewable biomass offers a promising alternative to meet our sustainable energy and environmental goals. The ethanologenic strain Zymomonas mobilis is considered as an excellent chassis for constructing microbial cell factories for diverse biochemicals due to its outstanding industrial characteristics in ethanol production, high specific productivity, and Generally Recognized as Safe (GRAS) status. Nonetheless, the restricted substrate range constrains its application.</p><p><strong>Results: </strong>The truncated ice nucleation protein InaK from Pseudomonas syringae was used as an autotransporter passenger, and α-amylase was fused to the C- terminal of InaK to equip the ethanol-producing bacterium with the capability to ferment renewable biomass. Western blot and flow cytometry analysis confirmed that the amylase was situated on the outer membrane. Whole-cell activity assays demonstrated that the amylase maintained its activity on the cell surface. The recombinant Z. mobilis facilitated the hydrolysis of starch into oligosaccharides and enabled the streamlining of simultaneous saccharification and fermentation (SSF) processes. In a 5% starch medium under SSF, recombinant strains containing P<sub>eno</sub> reached a maximum titer of 13.61 ± 0.12 g/L within 48 h. This represents an increase of 111.0% compared to the control strain's titer of titer of 6.45 ± 0.25 g/L.</p><p><strong>Conclusions: </strong>By fusing the truncated ice nucleation protein InaK with α-amylase, we achieved efficient expression and surface display of the enzyme on Z. mobilis. This fusion protein exhibited remarkable enzymatic activity. Its presence enabled a cost-effective bioproduction process using starch as the sole carbon source, and it significantly reduced the required cycle time for SSF. 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引用次数: 0
摘要
背景:利用微生物生产生物燃料和从可再生生物质中提取的增值生物化学品的生物精炼厂,为实现可持续能源和环境目标提供了一种前景广阔的替代方法。乙醇菌株 Zymomonas mobilis 因其在乙醇生产方面的突出工业特性、高特定生产率和公认安全(GRAS)状态,被认为是构建微生物细胞工厂以生产多种生物化学品的极佳底盘。然而,底物范围的限制制约了它的应用:结果:利用丁香假单胞菌(Pseudomonas syringae)的截短冰核蛋白 InaK 作为自转运载体,并将α-淀粉酶融合到 InaK 的 C 端,使乙醇生产菌具有发酵可再生生物质的能力。Western 印迹和流式细胞仪分析证实,淀粉酶位于外膜上。全细胞活性测定表明,淀粉酶在细胞表面保持活性。重组的 Z. mobilis 能促进淀粉水解成低聚糖,并简化同步糖化和发酵(SSF)过程。在 SSF 条件下的 5% 淀粉培养基中,含有 Peno 的重组菌株在 48 小时内达到 13.61 ± 0.12 g/L 的最大滴度,与对照菌株 6.45 ± 0.25 g/L 的滴度相比,增加了 111.0%:通过将截短的冰核化蛋白 InaK 与 α 淀粉酶融合,我们实现了该酶在 Z. mobilis 上的高效表达和表面展示。这种融合蛋白具有显著的酶活性。它的存在使以淀粉为唯一碳源的生物生产过程具有成本效益,并大大缩短了 SSF 所需的周期时间。这项研究不仅为淀粉的可持续生物生产提供了一个极好的Z. mobilis底盘,而且突出了Z. mobilis作为一个有效的细胞工厂,利用可再生生物质生产高价值产品的潜力。
Development of a starch-fermenting Zymomonas mobilis strain for bioethanol production.
Background: Biorefinery using microorganisms to produce biofuels and value-added biochemicals derived from renewable biomass offers a promising alternative to meet our sustainable energy and environmental goals. The ethanologenic strain Zymomonas mobilis is considered as an excellent chassis for constructing microbial cell factories for diverse biochemicals due to its outstanding industrial characteristics in ethanol production, high specific productivity, and Generally Recognized as Safe (GRAS) status. Nonetheless, the restricted substrate range constrains its application.
Results: The truncated ice nucleation protein InaK from Pseudomonas syringae was used as an autotransporter passenger, and α-amylase was fused to the C- terminal of InaK to equip the ethanol-producing bacterium with the capability to ferment renewable biomass. Western blot and flow cytometry analysis confirmed that the amylase was situated on the outer membrane. Whole-cell activity assays demonstrated that the amylase maintained its activity on the cell surface. The recombinant Z. mobilis facilitated the hydrolysis of starch into oligosaccharides and enabled the streamlining of simultaneous saccharification and fermentation (SSF) processes. In a 5% starch medium under SSF, recombinant strains containing Peno reached a maximum titer of 13.61 ± 0.12 g/L within 48 h. This represents an increase of 111.0% compared to the control strain's titer of titer of 6.45 ± 0.25 g/L.
Conclusions: By fusing the truncated ice nucleation protein InaK with α-amylase, we achieved efficient expression and surface display of the enzyme on Z. mobilis. This fusion protein exhibited remarkable enzymatic activity. Its presence enabled a cost-effective bioproduction process using starch as the sole carbon source, and it significantly reduced the required cycle time for SSF. This study not only provides an excellent Z. mobilis chassis for sustainable bioproduction from starch but also highlights the potential of Z. mobilis to function as an effective cellular factory for producing high-value products from renewable biomass.
期刊介绍:
Microbial Cell Factories is an open access peer-reviewed journal that covers any topic related to the development, use and investigation of microbial cells as producers of recombinant proteins and natural products, or as catalyzers of biological transformations of industrial interest. Microbial Cell Factories is the world leading, primary research journal fully focusing on Applied Microbiology.
The journal is divided into the following editorial sections:
-Metabolic engineering
-Synthetic biology
-Whole-cell biocatalysis
-Microbial regulations
-Recombinant protein production/bioprocessing
-Production of natural compounds
-Systems biology of cell factories
-Microbial production processes
-Cell-free systems