The puzzle of two tandem acyl-CoA ligases of Pseudomonas putida F1.

IF 3.9 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Applied and Environmental Microbiology Pub Date : 2024-11-20 Epub Date: 2024-10-15 DOI:10.1128/aem.01267-24
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 ∆fadD1fadD2 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 ∆fabAdesA unsaturated fatty acid auxotrophic strain carrying a deletion of either ∆fadD1 or ∆fadD2 were constructed. Growth of the ∆fabAdesAfadD1 strain was very weak, whereas the ∆fabAdesAfadD2 strain grew as well as the ∆fabAdesA parent strain. Overexpression of either fadD1 or fadD2 restored growth of the ∆fabAdesAfadD1 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.

假单胞菌 F1 的两种串联酰基-CoA 连接酶之谜。
假单胞菌 F1 基因组和许多其他假单胞菌的基因组都含有两个串联基因,分别编码酰基-CoA 连接酶 Pput_1340 (fadD1) 和 Pput_1339 (fadD2),其中 Pput_1339 (fadD2) 是上游基因。当发现这两个基因能补充以油酸为唯一碳源的大肠杆菌酰基-CoA 合成酶 fadD 缺失菌株的生长时,就指定了这两个基因为 fadD。定点突变显示,大肠杆菌 FadD 功能所需的 ATP/AMP 结构域残基对于 FadD1 和 FadD2 的完全功能也是必不可少的。在以不同链长脂肪酸为唯一碳源的最小培养基中测试了构建的 ∆fadD1、∆fadD2 和 ∆fadD1∆fadD2 菌株的生长情况。缺乏 FadD1 会明显延缓不同链长脂肪酸的生长,而同时缺乏 FadD1 和 FadD2 则会进一步延缓生长。构建了缺失 ∆fadD1 或 ∆fadD2 的 ∆fabA∆desA 不饱和脂肪酸辅助菌株的衍生物。∆fabA∆desA∆fadD1 菌株的生长非常弱,而 ∆fabA∆desA∆fadD2 菌株的生长与 ∆fabA∆desA 母株一样好。过量表达 fadD1 或 fadD2 能恢复 ∆fabA∆desA∆fadD1 菌株的生长,其中过量表达 fadD2 比过量表达 fadD1 的效果更好。虽然 fadD1 的表达水平远高于 fadD2,但 ∆fadD1 或 ∆fadD2 基因是共转录的。这归因于位于 FadD2 编码序列上游的 fadD1 启动子:假单胞菌表现出极大的新陈代谢多样性,因此定植于广泛的生态位。这些细菌的一个特征是有一对串联基因被注释为参与脂肪酸降解的酰基-CoA 连接酶。据注释,假单胞菌 F1 基因组至少有 9 个编码酰基-CoA 连接酶的基因,除了这对串联基因外,其他基因散布在染色体周围。由于在其他假单胞菌中也发现了类似的串联对,我们构建了串联连接酶的缺失突变体并对其进行了鉴定。我们报告说,编码的蛋白质是参与脂肪酸降解的真正的酰基-CoA 连接酶。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
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.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信