Sepwin Nosten Sitompul, Laura Andrea Diaz Garcia, Joseph Price, Kang Lan Tee, Tuck Seng Wong
{"title":"二价金属阳离子对Cupriavidus necator H16的快速适应性实验室进化。","authors":"Sepwin Nosten Sitompul, Laura Andrea Diaz Garcia, Joseph Price, Kang Lan Tee, Tuck Seng Wong","doi":"10.1002/biot.202300577","DOIUrl":null,"url":null,"abstract":"<p>Microbial strain improvement through adaptive laboratory evolution (ALE) has been a key strategy in biotechnology for enhancing desired phenotypic traits. In this Biotech Method paper, we present an accelerated ALE (aALE) workflow and its successful implementation in evolving <i>Cupriavidus necator</i> H16 for enhanced tolerance toward elevated glycerol concentrations. The method involves the deliberate induction of genetic diversity through controlled exposure to divalent metal cations, enabling the rapid identification of improved variants. Through this approach, we observed the emergence of robust variants capable of growing in high glycerol concentration environments, demonstrating the efficacy of our aALE workflow. When cultivated in 10% v/v glycerol, the adapted variant Mn-C2-B11, selected through aALE, achieved a final OD<sub>600</sub> value of 56.0 and a dry cell weight of 15.2 g L<sup>−1</sup>, compared to the wild type (WT) strain's final OD<sub>600</sub> of 39.1 and dry cell weight of 8.4 g L<sup>−1</sup>. At an even higher glycerol concentration of 15% v/v, Mn-C2-B11 reached a final OD<sub>600</sub> of 48.9 and a dry cell weight of 12.7 g L<sup>−1</sup>, in contrast to the WT strain's final OD<sub>600</sub> of 9.0 and dry cell weight of 3.1 g L<sup>−1</sup>. Higher glycerol consumption by Mn-C2-B11 was also confirmed by high-performance liquid chromatography (HPLC) analysis. This adapted variant consumed 34.5 times more glycerol compared to the WT strain at 10% v/v glycerol. Our method offers several advantages over other reported ALE approaches, including its independence from genetically modified strains, specialized genetic tools, and potentially carcinogenic DNA-modifying agents. By utilizing divalent metal cations as mutagens, we offer a safer, more efficient, and cost-effective alternative for expansion of genetic diversity. With its ability to foster rapid microbial evolution, aALE serves as a valuable addition to the ALE toolbox, holding significant promise for the advancement of microbial strain engineering and bioprocess optimization.</p>","PeriodicalId":134,"journal":{"name":"Biotechnology Journal","volume":"19 7","pages":""},"PeriodicalIF":3.2000,"publicationDate":"2024-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/biot.202300577","citationCount":"0","resultStr":"{\"title\":\"Fast-track adaptive laboratory evolution of Cupriavidus necator H16 with divalent metal cations\",\"authors\":\"Sepwin Nosten Sitompul, Laura Andrea Diaz Garcia, Joseph Price, Kang Lan Tee, Tuck Seng Wong\",\"doi\":\"10.1002/biot.202300577\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Microbial strain improvement through adaptive laboratory evolution (ALE) has been a key strategy in biotechnology for enhancing desired phenotypic traits. In this Biotech Method paper, we present an accelerated ALE (aALE) workflow and its successful implementation in evolving <i>Cupriavidus necator</i> H16 for enhanced tolerance toward elevated glycerol concentrations. The method involves the deliberate induction of genetic diversity through controlled exposure to divalent metal cations, enabling the rapid identification of improved variants. Through this approach, we observed the emergence of robust variants capable of growing in high glycerol concentration environments, demonstrating the efficacy of our aALE workflow. When cultivated in 10% v/v glycerol, the adapted variant Mn-C2-B11, selected through aALE, achieved a final OD<sub>600</sub> value of 56.0 and a dry cell weight of 15.2 g L<sup>−1</sup>, compared to the wild type (WT) strain's final OD<sub>600</sub> of 39.1 and dry cell weight of 8.4 g L<sup>−1</sup>. At an even higher glycerol concentration of 15% v/v, Mn-C2-B11 reached a final OD<sub>600</sub> of 48.9 and a dry cell weight of 12.7 g L<sup>−1</sup>, in contrast to the WT strain's final OD<sub>600</sub> of 9.0 and dry cell weight of 3.1 g L<sup>−1</sup>. Higher glycerol consumption by Mn-C2-B11 was also confirmed by high-performance liquid chromatography (HPLC) analysis. This adapted variant consumed 34.5 times more glycerol compared to the WT strain at 10% v/v glycerol. Our method offers several advantages over other reported ALE approaches, including its independence from genetically modified strains, specialized genetic tools, and potentially carcinogenic DNA-modifying agents. By utilizing divalent metal cations as mutagens, we offer a safer, more efficient, and cost-effective alternative for expansion of genetic diversity. With its ability to foster rapid microbial evolution, aALE serves as a valuable addition to the ALE toolbox, holding significant promise for the advancement of microbial strain engineering and bioprocess optimization.</p>\",\"PeriodicalId\":134,\"journal\":{\"name\":\"Biotechnology Journal\",\"volume\":\"19 7\",\"pages\":\"\"},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2024-07-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/biot.202300577\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biotechnology Journal\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/biot.202300577\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMICAL RESEARCH METHODS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biotechnology Journal","FirstCategoryId":"5","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/biot.202300577","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0
摘要
通过实验室适应性进化(ALE)进行微生物菌株改良一直是生物技术中提高所需表型性状的关键策略。在这篇《生物技术方法》(Biotech Method)论文中,我们介绍了一种加速适应性进化(aALE)工作流程,并介绍了该流程在进化Cupriavidus necator H16以增强其对甘油浓度升高的耐受性方面的成功应用。该方法包括通过控制暴露于二价金属阳离子来有意诱导遗传多样性,从而快速鉴定出改良变体。通过这种方法,我们观察到了能够在高甘油浓度环境中生长的强健变种的出现,证明了我们的 AALE 工作流程的有效性。在 10% v/v 甘油中培养时,通过 aALE 筛选出的适应变体 Mn-C2-B11 的最终 OD600 值为 56.0,干细胞重量为 15.2 g L-1,而野生型(WT)菌株的最终 OD600 值为 39.1,干细胞重量为 8.4 g L-1。在更高的甘油浓度(15% v/v)下,Mn-C2-B11 的最终 OD600 为 48.9,干细胞重量为 12.7 g L-1,而 WT 菌株的最终 OD600 为 9.0,干细胞重量为 3.1 g L-1。高效液相色谱(HPLC)分析也证实,Mn-C2-B11 消耗的甘油更多。与 WT 菌株相比,在 10% v/v 甘油条件下,该适应变体的甘油消耗量增加了 34.5 倍。与其他已报道的 ALE 方法相比,我们的方法具有多项优势,包括不受转基因菌株、专业基因工具和潜在致癌 DNA 修饰剂的影响。通过利用二价金属阳离子作为诱变剂,我们为扩大遗传多样性提供了一种更安全、更高效、更具成本效益的替代方法。aALE 具有促进微生物快速进化的能力,是 ALE 工具箱的重要补充,为微生物菌种工程和生物过程优化带来了巨大的发展前景。
Fast-track adaptive laboratory evolution of Cupriavidus necator H16 with divalent metal cations
Microbial strain improvement through adaptive laboratory evolution (ALE) has been a key strategy in biotechnology for enhancing desired phenotypic traits. In this Biotech Method paper, we present an accelerated ALE (aALE) workflow and its successful implementation in evolving Cupriavidus necator H16 for enhanced tolerance toward elevated glycerol concentrations. The method involves the deliberate induction of genetic diversity through controlled exposure to divalent metal cations, enabling the rapid identification of improved variants. Through this approach, we observed the emergence of robust variants capable of growing in high glycerol concentration environments, demonstrating the efficacy of our aALE workflow. When cultivated in 10% v/v glycerol, the adapted variant Mn-C2-B11, selected through aALE, achieved a final OD600 value of 56.0 and a dry cell weight of 15.2 g L−1, compared to the wild type (WT) strain's final OD600 of 39.1 and dry cell weight of 8.4 g L−1. At an even higher glycerol concentration of 15% v/v, Mn-C2-B11 reached a final OD600 of 48.9 and a dry cell weight of 12.7 g L−1, in contrast to the WT strain's final OD600 of 9.0 and dry cell weight of 3.1 g L−1. Higher glycerol consumption by Mn-C2-B11 was also confirmed by high-performance liquid chromatography (HPLC) analysis. This adapted variant consumed 34.5 times more glycerol compared to the WT strain at 10% v/v glycerol. Our method offers several advantages over other reported ALE approaches, including its independence from genetically modified strains, specialized genetic tools, and potentially carcinogenic DNA-modifying agents. By utilizing divalent metal cations as mutagens, we offer a safer, more efficient, and cost-effective alternative for expansion of genetic diversity. With its ability to foster rapid microbial evolution, aALE serves as a valuable addition to the ALE toolbox, holding significant promise for the advancement of microbial strain engineering and bioprocess optimization.
Biotechnology JournalBiochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
8.90
自引率
2.10%
发文量
123
审稿时长
1.5 months
期刊介绍:
Biotechnology Journal (2019 Journal Citation Reports: 3.543) is fully comprehensive in its scope and publishes strictly peer-reviewed papers covering novel aspects and methods in all areas of biotechnology. Some issues are devoted to a special topic, providing the latest information on the most crucial areas of research and technological advances.
In addition to these special issues, the journal welcomes unsolicited submissions for primary research articles, such as Research Articles, Rapid Communications and Biotech Methods. BTJ also welcomes proposals of Review Articles - please send in a brief outline of the article and the senior author''s CV to the editorial office.
BTJ promotes a special emphasis on:
Systems Biotechnology
Synthetic Biology and Metabolic Engineering
Nanobiotechnology and Biomaterials
Tissue engineering, Regenerative Medicine and Stem cells
Gene Editing, Gene therapy and Immunotherapy
Omics technologies
Industrial Biotechnology, Biopharmaceuticals and Biocatalysis
Bioprocess engineering and Downstream processing
Plant Biotechnology
Biosafety, Biotech Ethics, Science Communication
Methods and Advances.