Huijuan Dong, Bo Chen, Haihong Wang, John E Cronan
{"title":"The puzzle of two tandem acyl-CoA ligases of <i>Pseudomonas putida</i> F1.","authors":"Huijuan Dong, Bo Chen, Haihong Wang, John E Cronan","doi":"10.1128/aem.01267-24","DOIUrl":null,"url":null,"abstract":"<p><p>The <i>Pseudomonas putida</i> F1 genome and those of many other pseudomonads contain two tandem genes encoding acyl-CoA ligases Pput_1340 (<i>fadD1</i>) and Pput_1339 (<i>fadD2</i>) with Pput_1339 (<i>fadD2</i>) being the upstream gene. The <i>fadD</i> designation was assigned when both genes were found to complement the growth of an <i>Escherichia coli</i> acyl-CoA synthetase <i>fadD</i> deletion strain with oleic acid as sole carbon source. Site-directed mutagenesis showed that residues of the ATP/AMP domain required for function of <i>E. coli</i> FadD were also essential for full function of FadD1 and FadD2. Growth of the constructed ∆<i>fadD1</i>, ∆<i>fadD2,</i> and ∆<i>fadD1</i>∆<i>fadD2</i> strains was tested in minimal medium with different chain length fatty acids as sole carbon sources. Lack of FadD1 significantly retarded growth with different chain length fatty acids and lack of both FadD1 and FadD2 further retarded growth. Derivatives of the ∆<i>fabA</i>∆<i>desA</i> unsaturated fatty acid auxotrophic strain carrying a deletion of either ∆<i>fadD1</i> or ∆<i>fadD2</i> were constructed. Growth of the ∆<i>fabA</i>∆<i>desA</i>∆<i>fadD1</i> strain was very weak, whereas the ∆<i>fabA</i>∆<i>desA</i>∆<i>fadD2</i> strain grew as well as the ∆<i>fabA</i>∆<i>desA</i> parent strain. Overexpression of either <i>fadD1</i> or <i>fadD2</i> restored growth of the ∆<i>fabA</i>∆<i>desA</i>∆<i>fadD1</i> strain with <i>fadD2</i> overexpression having a greater effect than <i>fadD1</i> overexpression. The ∆<i>fadD1</i> or ∆<i>fadD2</i> genes are cotranscribed although the expression level of <i>fadD1</i> is much higher than that of <i>fadD2</i>. This is attributed to a <i>fadD1</i> promoter located within the upstream FadD2 coding sequence.</p><p><strong>Importance: </strong><i>Pseudomonas</i> bacteria demonstrate a great deal of metabolic diversity and consequently colonize a wide range of ecological niches. A characteristic of these bacteria is a pair of genes in tandem annotated as acyl-CoA ligases involved in fatty acid degradation. The <i>Pseudomonas putida</i> F1 genome is annotated as having at least nine genes encoding acyl-CoA ligases which are scattered around the chromosome excepting the tandem pair. Since similar tandem pairs are found in other pseudomonads, we have constructed and characterized deletion mutants of the tandem ligases. We report that the encoded proteins are authentic acyl-CoA ligases involved in fatty acid degradation.</p>","PeriodicalId":8002,"journal":{"name":"Applied and Environmental Microbiology","volume":" ","pages":"e0126724"},"PeriodicalIF":3.9000,"publicationDate":"2024-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied and Environmental Microbiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1128/aem.01267-24","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/10/15 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
The Pseudomonas putida F1 genome and those of many other pseudomonads contain two tandem genes encoding acyl-CoA ligases Pput_1340 (fadD1) and Pput_1339 (fadD2) with Pput_1339 (fadD2) being the upstream gene. The fadD designation was assigned when both genes were found to complement the growth of an Escherichia coli acyl-CoA synthetase fadD deletion strain with oleic acid as sole carbon source. Site-directed mutagenesis showed that residues of the ATP/AMP domain required for function of E. coli FadD were also essential for full function of FadD1 and FadD2. Growth of the constructed ∆fadD1, ∆fadD2, and ∆fadD1∆fadD2 strains was tested in minimal medium with different chain length fatty acids as sole carbon sources. Lack of FadD1 significantly retarded growth with different chain length fatty acids and lack of both FadD1 and FadD2 further retarded growth. Derivatives of the ∆fabA∆desA unsaturated fatty acid auxotrophic strain carrying a deletion of either ∆fadD1 or ∆fadD2 were constructed. Growth of the ∆fabA∆desA∆fadD1 strain was very weak, whereas the ∆fabA∆desA∆fadD2 strain grew as well as the ∆fabA∆desA parent strain. Overexpression of either fadD1 or fadD2 restored growth of the ∆fabA∆desA∆fadD1 strain with fadD2 overexpression having a greater effect than fadD1 overexpression. The ∆fadD1 or ∆fadD2 genes are cotranscribed although the expression level of fadD1 is much higher than that of fadD2. This is attributed to a fadD1 promoter located within the upstream FadD2 coding sequence.
Importance: Pseudomonas bacteria demonstrate a great deal of metabolic diversity and consequently colonize a wide range of ecological niches. A characteristic of these bacteria is a pair of genes in tandem annotated as acyl-CoA ligases involved in fatty acid degradation. The Pseudomonas putida F1 genome is annotated as having at least nine genes encoding acyl-CoA ligases which are scattered around the chromosome excepting the tandem pair. Since similar tandem pairs are found in other pseudomonads, we have constructed and characterized deletion mutants of the tandem ligases. We report that the encoded proteins are authentic acyl-CoA ligases involved in fatty acid degradation.
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.