Exploring biosurfactant production in Dyadobacter fermentans JDP9: Insights from genome sequencing and analysis

Jyoti Solanki , Dhaval Patel , Suresh Mesara , M. Nataraj
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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.
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
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。
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