Nair Aswati Ravindrananthan, Kaniyala Harshitha, Vardhan Mudumbi Harsha, Pillai Padmesh
Department of Biochemistry and Molecular Biology, Central University of Kerala (CUK), Kasaragod, Kerala, India.
Department of Genomic Science, Central University of Kerala (CUK), Kasaragod, Kerala, India.
J Basic Microbiol. 2025 May;65(5):e2400582. doi: 10.1002/jobm.202400582. Epub 2024 Dec 16.
Despite several studies documenting secondary metabolite (SM) production by endophytes, their commercial use is often limited owing to the research lacunae in the underlying biosynthetic pathway and the corresponding metabolic flux. Combining epigenetic modulation with RNA-Seq analysis constitutes a promising approach for inducing regulatory gene(s) and thereby identifying their role in SM biosynthesis. Our earlier studies had identified the hypomethylating effects of prednisone in umbelliferone (UMB) (7-hydroxyl coumarin) producing endophytic Fusarium oxysporum isolate, ZzEF8 isolated from Zingiber zerumbet rhizomes. Hypomethylating effect of prednisone (300 μM) in ZzEF8 was validated in present experiments revealing decrease in 5-mC content (0.09 ± 0.01%) in prednisone treated ZzEF8 (PrZzEF8) compared to untreated control (UtZzEF8) (0.36 ± 0.01%). Subsequent RNA-Seq analysis detected transcriptional alterations in PrZzEF8 compared to UtZzEF8. Transcripts with significant differential expression (-2 ≥ fold change (FC) ≥ 2; q-value < 0.05) were detected for 64 transcripts, with 60 upregulated and four downregulated in PrZzEF8. Upregulated differentially expressed genes (DEGs) were annotated as transmembrane transporters, non-ribosomal peptide synthetase (NRPS), Type I and III polyketide synthase (PKS), phytoene dehydrogenase, bifunctional lycopene cyclase/phytoene synthase, geranylgeranyl pyrophosphate synthase and various genes involved in nutrient assimilation, transcription factors and transporters regulating metabolite export. Expression analysis of the selected DEGs were validated by qRT-PCR. Present study proposes UMB biosynthesis through acetate-malonate pathway from acetate units via a pentaketide intermediate in ZzEF8 instead of the phenylpropanoid pathway reported in plants. Study is of relevance as the insights gained into the UMB biosynthetic pathway in ZzEF8 will help in strategizing scale-up of UMB production.
尽管有多项研究记录了内生菌产生次生代谢产物(SM)的情况,但由于其潜在生物合成途径和相应代谢通量方面的研究空白,它们的商业应用往往受到限制。将表观遗传调控与RNA测序分析相结合,是诱导调控基因并确定其在SM生物合成中作用的一种有前景的方法。我们早期的研究已经确定了泼尼松对从姜黄根茎中分离出的产伞形花内酯(UMB,7-羟基香豆素)的内生尖孢镰刀菌菌株ZzEF8的去甲基化作用。在本实验中验证了泼尼松(300μM)对ZzEF8的去甲基化作用,结果显示与未处理对照(UtZzEF8)(0.36±0.01%)相比,经泼尼松处理的ZzEF8(PrZzEF8)中5-甲基胞嘧啶含量降低(0.09±0.01%)。随后的RNA测序分析检测到PrZzEF8与UtZzEF8相比存在转录改变。检测到64个转录本有显著差异表达(-2≥倍数变化(FC)≥2;q值<0.05),其中PrZzEF8中有60个上调,4个下调。上调的差异表达基因(DEG)被注释为跨膜转运蛋白、非核糖体肽合成酶(NRPS)、I型和III型聚酮合酶(PKS)、八氢番茄红素脱氢酶、双功能番茄红素环化酶/八氢番茄红素合酶、香叶基香叶基焦磷酸合酶以及参与营养同化、转录因子和调节代谢物输出的转运蛋白的各种基因。通过qRT-PCR验证了所选DEG的表达分析。本研究提出ZzEF8中UMB通过乙酸-丙二酸途径由乙酸单位经五酮中间体生物合成,而不是植物中报道的苯丙烷途径。该研究具有重要意义,因为对ZzEF8中UMB生物合成途径的深入了解将有助于制定UMB生产扩大规模的策略。