{"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}
引用次数: 0
Abstract
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.