{"title":"探索发酵Dyadobacter发酵JDP9的生物表面活性剂生产:来自基因组测序和分析的见解","authors":"Jyoti Solanki , Dhaval Patel , Suresh Mesara , M. Nataraj","doi":"10.1016/j.microb.2025.100345","DOIUrl":null,"url":null,"abstract":"<div><div>The present study examines the comprehensive analysis of the whole genome shotgun sequencing of <em>Dyadobacter fermentans</em> JDP9. The <em>Dyadobacter</em> genus is recognized for its synthesis of flexirubin; however, its capacity for biosurfactant (BS) production, particularly glycoprotein BS, has not been reported yet. A potential BS-producing <em>D. fermentans</em> JDP9 strain was isolated from hydrocarbon-contaminated soil. The BS was primarily characterized as a glycoprotein. The utilization of the Illumina platform for whole genome shotgun sequencing resulted in 2,469,724 high-quality reads assembled into 27 scaffolds, revealing a genome size of 7,979,294, GC content of 50.3 %, a Scaffold L50 value of 5, and a Scaffold N50 value of 522,766. The NCBI Prokaryotic Genome Annotation Pipeline identified 6,602 genes and 6,557 CDS. The systematic examination carried out by AntiSMASH, identified a total of 9 clusters, specifically the non-ribosomal peptide synthetase gene cluster. Herein, we proposed that the glycoprotein BS production is facilitated by enzymes involved in the dTDP-L-rhamnose biosynthetic pathway, including glucose-1-phosphate thymidylyltransferase, dTDP-glucose 4,6-dehydratase, and dTDP-4-dehydrorhamnose reductase present in the JDP9 strain genome. These enzymes contribute to generating dTDP-L-rhamnose, a crucial sugar moiety for glycosylation reactions. This study establishes a foundation for prospective investigations into glycoprotein BS production, presenting potential biotechnology implications.</div></div>","PeriodicalId":101246,"journal":{"name":"The Microbe","volume":"7 ","pages":"Article 100345"},"PeriodicalIF":0.0000,"publicationDate":"2025-04-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Exploring biosurfactant production in Dyadobacter fermentans JDP9: Insights from genome sequencing and analysis\",\"authors\":\"Jyoti Solanki , Dhaval Patel , Suresh Mesara , M. Nataraj\",\"doi\":\"10.1016/j.microb.2025.100345\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The present study examines the comprehensive analysis of the whole genome shotgun sequencing of <em>Dyadobacter fermentans</em> JDP9. The <em>Dyadobacter</em> genus is recognized for its synthesis of flexirubin; however, its capacity for biosurfactant (BS) production, particularly glycoprotein BS, has not been reported yet. A potential BS-producing <em>D. fermentans</em> JDP9 strain was isolated from hydrocarbon-contaminated soil. The BS was primarily characterized as a glycoprotein. The utilization of the Illumina platform for whole genome shotgun sequencing resulted in 2,469,724 high-quality reads assembled into 27 scaffolds, revealing a genome size of 7,979,294, GC content of 50.3 %, a Scaffold L50 value of 5, and a Scaffold N50 value of 522,766. The NCBI Prokaryotic Genome Annotation Pipeline identified 6,602 genes and 6,557 CDS. The systematic examination carried out by AntiSMASH, identified a total of 9 clusters, specifically the non-ribosomal peptide synthetase gene cluster. Herein, we proposed that the glycoprotein BS production is facilitated by enzymes involved in the dTDP-L-rhamnose biosynthetic pathway, including glucose-1-phosphate thymidylyltransferase, dTDP-glucose 4,6-dehydratase, and dTDP-4-dehydrorhamnose reductase present in the JDP9 strain genome. These enzymes contribute to generating dTDP-L-rhamnose, a crucial sugar moiety for glycosylation reactions. This study establishes a foundation for prospective investigations into glycoprotein BS production, presenting potential biotechnology implications.</div></div>\",\"PeriodicalId\":101246,\"journal\":{\"name\":\"The Microbe\",\"volume\":\"7 \",\"pages\":\"Article 100345\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-04-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Microbe\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S295019462500113X\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Microbe","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S295019462500113X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
本研究对发酵Dyadobacter发酵JDP9的全基因组进行了鸟枪法测序。Dyadobacter属以其合成柔红素而闻名;然而,其生产生物表面活性剂(BS),特别是糖蛋白BS的能力尚未见报道。从烃污染土壤中分离到一株具有产bs潜力的发酵D.发酵菌JDP9。BS的主要特征是糖蛋白。利用Illumina平台进行全基因组鸟枪测序,将2469724条高质量reads组装成27个Scaffold,基因组大小为7979294,GC含量为50.3 %,Scaffold L50值为5,Scaffold N50值为522766。NCBI原核基因组注释管道共鉴定出6602个基因和6557个CDS。AntiSMASH进行系统检查,共鉴定出9个簇,特别是非核糖体肽合成酶基因簇。在此,我们提出糖蛋白BS的产生是由参与dtdp - l -鼠李糖生物合成途径的酶促进的,包括JDP9菌株基因组中存在的葡萄糖-1-磷酸胸苷基转移酶、dtdp -葡萄糖4,6-脱水酶和dtdp -4-脱水鼠李糖还原酶。这些酶有助于生成dtdp - l -鼠李糖,这是糖基化反应的关键糖段。该研究为糖蛋白BS生产的前瞻性研究奠定了基础,并提出了潜在的生物技术意义。
Exploring biosurfactant production in Dyadobacter fermentans JDP9: Insights from genome sequencing and analysis
The present study examines the comprehensive analysis of the whole genome shotgun sequencing of Dyadobacter fermentans JDP9. The Dyadobacter genus is recognized for its synthesis of flexirubin; however, its capacity for biosurfactant (BS) production, particularly glycoprotein BS, has not been reported yet. A potential BS-producing D. fermentans JDP9 strain was isolated from hydrocarbon-contaminated soil. The BS was primarily characterized as a glycoprotein. The utilization of the Illumina platform for whole genome shotgun sequencing resulted in 2,469,724 high-quality reads assembled into 27 scaffolds, revealing a genome size of 7,979,294, GC content of 50.3 %, a Scaffold L50 value of 5, and a Scaffold N50 value of 522,766. The NCBI Prokaryotic Genome Annotation Pipeline identified 6,602 genes and 6,557 CDS. The systematic examination carried out by AntiSMASH, identified a total of 9 clusters, specifically the non-ribosomal peptide synthetase gene cluster. Herein, we proposed that the glycoprotein BS production is facilitated by enzymes involved in the dTDP-L-rhamnose biosynthetic pathway, including glucose-1-phosphate thymidylyltransferase, dTDP-glucose 4,6-dehydratase, and dTDP-4-dehydrorhamnose reductase present in the JDP9 strain genome. These enzymes contribute to generating dTDP-L-rhamnose, a crucial sugar moiety for glycosylation reactions. This study establishes a foundation for prospective investigations into glycoprotein BS production, presenting potential biotechnology implications.