Ashley N Hall, Benjamin W Hall, Kyle J Kinney, Gabby G Olsen, Amy B Banta, Daniel R Noguera, Timothy J Donohue, Jason M Peters
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Genetic manipulation of these bacteria is needed to introduce engineered pathways and modulate expression of native genes with the goal of enhancing bioproduct output. Although recent work has expanded the genetic toolkit for <i>Z. mobilis</i>, <i>N. aromaticivorans</i> and <i>R. sphaeroides</i> still need facile, reliable approaches to deliver genetic payloads to the genome and to control gene expression. Here, we expand the platform of genetic tools for <i>N. aromaticivorans</i> and <i>R. sphaeroides</i> to address these issues. We demonstrate that Tn<i>7</i> transposition is an effective approach for introducing engineered DNA into the chromosome of <i>N. aromaticivorans</i> and <i>R. sphaeroides</i>. We screen a synthetic promoter library to identify isopropyl β-D-1-thiogalactopyranoside-inducible promoters with regulated activity in both organisms (up to ~15-fold induction in <i>N. aromaticivorans</i> and ~5-fold induction in <i>R. sphaeroides</i>). Combining Tn<i>7</i> integration with promoters from our library, we establish CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) interference systems for <i>N. aromaticivorans</i> and <i>R. sphaeroides</i> (up to ~10-fold knockdown in <i>N. aromaticivorans</i> and <i>R. sphaeroides</i>) that can target essential genes and modulate engineered pathways. We anticipate that these systems will greatly facilitate both genetic engineering and gene function discovery efforts in these species and other Alphaproteobacteria.IMPORTANCEIt is important to increase our understanding of the microbial world to improve health, agriculture, the environment, and biotechnology. For example, building a sustainable bioeconomy depends on the efficient conversion of plant material to valuable biofuels and bioproducts by microbes. One limitation in this conversion process is that microbes with otherwise promising properties for conversion are challenging to genetically engineer. Here we report genetic tools for <i>Novosphingobium aromaticivorans</i> and <i>Rhodobacter sphaeroides</i> that add to the burgeoning set of tools available for genome engineering and gene expression in Alphaproteobacteria. Our approaches allow straightforward insertion of engineered pathways into the <i>N. aromaticivorans</i> or <i>R. sphaeroides</i> genome and control of gene expression by inducing genes with synthetic promoters or repressing genes using CRISPR interference. These tools can be used in future work to gain additional insight into these and other Alphaproteobacteria and to aid in optimizing yield of biofuels and bioproducts.</p>","PeriodicalId":8002,"journal":{"name":"Applied and Environmental Microbiology","volume":" ","pages":"e0034824"},"PeriodicalIF":3.9000,"publicationDate":"2024-10-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11497788/pdf/","citationCount":"0","resultStr":"{\"title\":\"Tools for genetic engineering and gene expression control in <i>Novosphingobium aromaticivorans</i> and <i>Rhodobacter sphaeroides</i>.\",\"authors\":\"Ashley N Hall, Benjamin W Hall, Kyle J Kinney, Gabby G Olsen, Amy B Banta, Daniel R Noguera, Timothy J Donohue, Jason M Peters\",\"doi\":\"10.1128/aem.00348-24\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Alphaproteobacteria have a variety of cellular and metabolic features that provide important insights into biological systems and enable biotechnologies. 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We demonstrate that Tn<i>7</i> transposition is an effective approach for introducing engineered DNA into the chromosome of <i>N. aromaticivorans</i> and <i>R. sphaeroides</i>. We screen a synthetic promoter library to identify isopropyl β-D-1-thiogalactopyranoside-inducible promoters with regulated activity in both organisms (up to ~15-fold induction in <i>N. aromaticivorans</i> and ~5-fold induction in <i>R. sphaeroides</i>). Combining Tn<i>7</i> integration with promoters from our library, we establish CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) interference systems for <i>N. aromaticivorans</i> and <i>R. sphaeroides</i> (up to ~10-fold knockdown in <i>N. aromaticivorans</i> and <i>R. sphaeroides</i>) that can target essential genes and modulate engineered pathways. We anticipate that these systems will greatly facilitate both genetic engineering and gene function discovery efforts in these species and other Alphaproteobacteria.IMPORTANCEIt is important to increase our understanding of the microbial world to improve health, agriculture, the environment, and biotechnology. For example, building a sustainable bioeconomy depends on the efficient conversion of plant material to valuable biofuels and bioproducts by microbes. One limitation in this conversion process is that microbes with otherwise promising properties for conversion are challenging to genetically engineer. Here we report genetic tools for <i>Novosphingobium aromaticivorans</i> and <i>Rhodobacter sphaeroides</i> that add to the burgeoning set of tools available for genome engineering and gene expression in Alphaproteobacteria. Our approaches allow straightforward insertion of engineered pathways into the <i>N. aromaticivorans</i> or <i>R. sphaeroides</i> genome and control of gene expression by inducing genes with synthetic promoters or repressing genes using CRISPR interference. 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引用次数: 0
摘要
兼性蛋白细菌具有多种细胞和新陈代谢特征,可为生物系统提供重要的洞察力,并促进生物技术的发展。例如,一些物种能够将植物生物质转化为有价值的生物燃料和生物产品,从而有可能促进可持续生物经济的发展。在阿尔法蛋白细菌中,Novosphingobium aromaticivorans、Rhodobacter sphaeroides 和 Zymomonas mobilis 显示出作为生物体的前景,可以通过工程改造将提取的植物木质素或糖转化为生物产品和生物燃料。需要对这些细菌进行基因操作,以引入工程途径和调节本地基因的表达,从而提高生物产品的产量。虽然最近的工作扩展了 Z. mobilis 的基因工具包,但 N. aromaticivorans 和 R. sphaeroides 仍需要简便、可靠的方法将基因有效载荷传递到基因组并控制基因表达。在这里,我们扩展了 N. aromaticivorans 和 R. sphaeroides 的遗传工具平台,以解决这些问题。我们证明了 Tn7 转座是一种有效的方法,可将工程 DNA 导入 N. aromaticivorans 和 R. sphaeroides 的染色体。我们筛选了一个合成启动子文库,以确定在两种生物中都具有调节活性的异丙基β-D-1-硫代半乳糖苷诱导型启动子(在芳香链球菌中的诱导活性可达约 15 倍,在水蚤中的诱导活性可达约 5 倍)。结合 Tn7 与我们文库中的启动子,我们建立了针对 N. aromaticivorans 和 R. sphaeroides 的 CRISPR(Clustered Regularly Interspaced Short Palindromic Repeats)干扰系统(在 N. aromaticivorans 和 R. sphaeroides 中最高可敲除约 10 倍),该系统可靶向重要基因并调节工程途径。我们预计这些系统将极大地促进这些物种和其他阿尔法蛋白细菌的基因工程和基因功能发现工作。例如,建立可持续的生物经济依赖于微生物将植物材料高效转化为有价值的生物燃料和生物产品。这种转化过程中的一个限制因素是,具有良好转化特性的微生物很难进行基因工程改造。在此,我们报告了针对芳香新磷胆菌(Novosphingobium aromaticivorans)和水螅红杆菌(Rhodobacter sphaeroides)的遗传工具,这些工具为阿尔法蛋白细菌基因组工程和基因表达提供了更多工具。我们的方法可以将工程途径直接插入芳香酵母菌或水单胞菌的基因组,并通过合成启动子诱导基因或 CRISPR 干扰抑制基因来控制基因表达。这些工具可用于未来的工作中,以获得对这些和其他阿尔法蛋白细菌的更多了解,并帮助优化生物燃料和生物产品的产量。
Tools for genetic engineering and gene expression control in Novosphingobium aromaticivorans and Rhodobacter sphaeroides.
Alphaproteobacteria have a variety of cellular and metabolic features that provide important insights into biological systems and enable biotechnologies. For example, some species are capable of converting plant biomass into valuable biofuels and bioproducts that have the potential to contribute to the sustainable bioeconomy. Among the Alphaproteobacteria, Novosphingobium aromaticivorans, Rhodobacter sphaeroides, and Zymomonas mobilis show promise as organisms that can be engineered to convert extracted plant lignin or sugars into bioproducts and biofuels. Genetic manipulation of these bacteria is needed to introduce engineered pathways and modulate expression of native genes with the goal of enhancing bioproduct output. Although recent work has expanded the genetic toolkit for Z. mobilis, N. aromaticivorans and R. sphaeroides still need facile, reliable approaches to deliver genetic payloads to the genome and to control gene expression. Here, we expand the platform of genetic tools for N. aromaticivorans and R. sphaeroides to address these issues. We demonstrate that Tn7 transposition is an effective approach for introducing engineered DNA into the chromosome of N. aromaticivorans and R. sphaeroides. We screen a synthetic promoter library to identify isopropyl β-D-1-thiogalactopyranoside-inducible promoters with regulated activity in both organisms (up to ~15-fold induction in N. aromaticivorans and ~5-fold induction in R. sphaeroides). Combining Tn7 integration with promoters from our library, we establish CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) interference systems for N. aromaticivorans and R. sphaeroides (up to ~10-fold knockdown in N. aromaticivorans and R. sphaeroides) that can target essential genes and modulate engineered pathways. We anticipate that these systems will greatly facilitate both genetic engineering and gene function discovery efforts in these species and other Alphaproteobacteria.IMPORTANCEIt is important to increase our understanding of the microbial world to improve health, agriculture, the environment, and biotechnology. For example, building a sustainable bioeconomy depends on the efficient conversion of plant material to valuable biofuels and bioproducts by microbes. One limitation in this conversion process is that microbes with otherwise promising properties for conversion are challenging to genetically engineer. Here we report genetic tools for Novosphingobium aromaticivorans and Rhodobacter sphaeroides that add to the burgeoning set of tools available for genome engineering and gene expression in Alphaproteobacteria. Our approaches allow straightforward insertion of engineered pathways into the N. aromaticivorans or R. sphaeroides genome and control of gene expression by inducing genes with synthetic promoters or repressing genes using CRISPR interference. These tools can be used in future work to gain additional insight into these and other Alphaproteobacteria and to aid in optimizing yield of biofuels and bioproducts.
期刊介绍:
Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.