Unveiling the Biosynthetic Landscape of Endophytic Streptomyces sp. PGLac3x via Growth Optimization and Whole-Genome Analysis.

IF 2.2 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Indian Journal of Microbiology Pub Date : 2026-06-01 Epub Date: 2025-12-06 DOI:10.1007/s12088-025-01532-6
C E Ezeobiora, N E Maningi, D H Amin, N H Igbokwe, C F Okpalanwa, C M Stephen, U E Mendie
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引用次数: 0

Abstract

The re-isolation of already known compounds in natural product research is a significant challenge. To address this, genome mining and optimization studies serve as dereplication strategies. This study focused on optimizing the growth and analyzing the genome of endophytic Streptomyces sp. strain PGLac3x isolated from Piper guineense. The growth optimization study assessed mycelium dry weight in mg/100 mL of media. Genomic DNA was extracted and 16S rRNA gene and whole genome sequencing (WGS) were performed via Sanger and Illumina Miseq technologies. Comprehensive genome analysis was conducted using the Bacterial and Viral Bioinformatics Resource Center (BV-BRC) database, and antibiotic and secondary metabolite analysis shell (antiSMASH) tool version 6.1.1. PGLac3x optimally grew on potato dextrose media at 32 °C, pH 7-8, and 2% salt concentration over 16 days. Based on the 16S rRNA gene blast, PGLac3x is closely related to Streptomyces sampsonii ATCC 25495 T (99.31%), Streptomyces albidoflavus NBRC 100770 T (99.30%) and Streptomyces champavatii NRRL B-5682 T (99.24%). The genome size is 6.96 Mb, with 59 biosynthetic gene clusters (BGCs) and a guanine-cytosine content of 73.46%. The genome contained 6477 coding sequences (CDS), 50 tRNAs, and 3 rRNAs, along with genes for polyketide synthases (T1PKS, T2PKS, T3PKS), terpenes, non-ribosomal peptide synthetases (NRPS), and ribosomally synthesized and post-translationally modified peptides (RiPPs). PGLac3x's phylogenetic distinctiveness and low gene similarity to the BGCs of known compounds suggests its potential to synthesize of distinct compounds. This study unveiled the biosynthetic potential, genetic diversity of secondary metabolites of Streptomyces sp. PGLac3x and provided a fresh insight for the exploration of new bioactive compounds.

Supplementary information: The online version contains supplementary material available at 10.1007/s12088-025-01532-6.

通过生长优化和全基因组分析揭示内生链霉菌PGLac3x的生物合成景观。
天然产物研究中已知化合物的再分离是一个重大挑战。为了解决这个问题,基因组挖掘和优化研究可以作为去复制策略。本研究对豚鼠内生链霉菌(Streptomyces sp.)菌株PGLac3x的生长进行了优化,并对其基因组进行了分析。生长优化研究在mg/100 mL培养基中评估菌丝干重。提取基因组DNA,通过Sanger和Illumina Miseq技术进行16S rRNA基因和全基因组测序(WGS)。使用细菌和病毒生物信息学资源中心(BV-BRC)数据库和抗生素和次级代谢物分析shell (antiSMASH)工具6.1.1版进行全面的基因组分析。PGLac3x在32°C、pH 7-8、2%盐浓度的马铃薯葡萄糖培养基上生长16天。基于16S rRNA基因blast, PGLac3x与sampsonii链霉菌ATCC 25495 T(99.31%)、Streptomyces albidoflavus NBRC 100770 T(99.30%)和champavatii链霉菌NRRL B-5682 T(99.24%)亲缘关系密切。基因组大小为6.96 Mb,有59个生物合成基因簇(BGCs),鸟嘌呤-胞嘧啶含量为73.46%。该基因组包含6477个编码序列(CDS)、50个trna和3个rrna,以及多酮合成酶(T1PKS、T2PKS、T3PKS)、萜烯、非核糖体肽合成酶(NRPS)、核糖体合成和翻译后修饰肽(RiPPs)的基因。PGLac3x的系统发育独特性和与已知化合物bgc的低基因相似性表明它具有合成独特化合物的潜力。本研究揭示了链霉菌(Streptomyces sp. PGLac3x)次生代谢产物的生物合成潜力和遗传多样性,为探索新的生物活性化合物提供了新的思路。补充资料:在线版本包含补充资料,下载地址:10.1007/s12088-025-01532-6。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Indian Journal of Microbiology
Indian Journal of Microbiology BIOTECHNOLOGY & APPLIED MICROBIOLOGY-MICROBIOLOGY
CiteScore
6.00
自引率
10.00%
发文量
51
审稿时长
1 months
期刊介绍: Indian Journal of Microbiology is the official organ of the Association of Microbiologists of India (AMI). It publishes full-length papers, short communication reviews and mini reviews on all aspects of microbiological research, published quarterly (March, June, September and December). Areas of special interest include agricultural, food, environmental, industrial, medical, pharmaceutical, veterinary and molecular microbiology.
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