High-throughput and genome-guided optimization of exopolysaccharide production in marine bacteria for sustainable biotechnology

Marine bacteria are an untapped resource for exopolysaccharides (EPS) with broad potential applications in biomedicine, bioremediation, and food industries. However, industrial utilization remains limited due to low yields and strain-specific variability. This study explores seven novel marine bacterial strains (<i>Limnobacter alexandrii</i> LZ-4, <i>Nioella ostreopsis</i> Z7-4, <i>Mesorhizobium alexandrii</i> Z1-4, <i>Marinobacter shengliensis subsp. Alexandrii</i> LZ-6, <i>Marinobacter alexandrii</i> LZ-8, <i>Memelialla alexandrii</i> LZ-28, and <i>Sulfitobacter alexandrii</i> AM1-D1) isolated from marine dinoflagellate microbiota. A genome-guided, high-throughput fermentation strategy was employed to optimize EPS production. Genomic analysis identified distinct EPS biosynthesis pathways (e.g., alginate and cellulose synthesis) and key genes (<i>algA/C/D, bcsB,</i> and <i>epsE/H/J</i>) involved in both the polymerization and the secretion of EPS. High-throughput screening under 50 fermentation conditions revealed sucrose and fructose as optimal carbon sources, with alkaline pH (7-9) significantly enhancing EPS yields (up to 159.6 µg/mL). Strain-specific optimization demonstrated that LZ-4 and Z7-4 achieved maximal EPS production at 28°C, whereas LZ-8 exhibited a high EPS production at 37°C. The study underscores the synergy between genomic insights and systematic screening, offering a scalable framework for rapid strain optimization. These findings pave the way for sustainable EPS bioproduction, reducing reliance on synthetic polymers and advancing industrial biotechnology in alignment with circular bioeconomy goals.IMPORTANCEThis study integrates genomic analysis with high-throughput fermentation to optimize exopolysaccharide (EPS) production in seven novel marine bacterial strains. By identifying key EPS biosynthesis genes and pathways, we tailored fermentation conditions using sucrose and alkaline pH, achieving yields up to 159.6 µg/mL. Strain-specific optimizations revealed significant enhancements in EPS production, highlighting the potential for sustainable industrial applications. This work bridges ecological insights with bioprocessing, offering a scalable framework for efficient EPS production that reduces reliance on synthetic polymers, advancing circular bioeconomy goals. The findings underscore the importance of marine microbial resources in biotechnology.

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Publication Details

Journal
Applied and Environmental Microbiology
Published
2025-10-21
DOI
https://doi.org/10.1128/aem.00837-25
Citations
1
Primary Topic
Enzyme Production and Characterization
Type
article
Field-Weighted Citation Impact
1.23
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article

High-throughput and genome-guided optimization of exopolysaccharide production in marine bacteria for sustainable biotechnology

Min Qi, Hongbo Yi, Yajun Wei, Qiao Yang et al.
1 citations
Applied and Environmental Microbiology
Enzyme Production and Characterization
1.23
article

High-throughput and genome-guided optimization of exopolysaccharide production in marine bacteria for sustainable biotechnology

Min Qi, Hongbo Yi, Yajun Wei, Qiao Yang, Fang Zhou, Rong Xiang, Z. Vivian Feng, Xi Yang
article en
1 citations

Abstract

Marine bacteria are an untapped resource for exopolysaccharides (EPS) with broad potential applications in biomedicine, bioremediation, and food industries. However, industrial utilization remains limited due to low yields and strain-specific variability. This study explores seven novel marine bacterial strains (<i>Limnobacter alexandrii</i> LZ-4, <i>Nioella ostreopsis</i> Z7-4, <i>Mesorhizobium alexandrii</i> Z1-4, <i>Marinobacter shengliensis subsp. Alexandrii</i> LZ-6, <i>Marinobacter alexandrii</i> LZ-8, <i>Memelialla alexandrii</i> LZ-28, and <i>Sulfitobacter alexandrii</i> AM1-D1) isolated from marine dinoflagellate microbiota. A genome-guided, high-throughput fermentation strategy was employed to optimize EPS production. Genomic analysis identified distinct EPS biosynthesis pathways (e.g., alginate and cellulose synthesis) and key genes (<i>algA/C/D, bcsB,</i> and <i>epsE/H/J</i>) involved in both the polymerization and the secretion of EPS. High-throughput screening under 50 fermentation conditions revealed sucrose and fructose as optimal carbon sources, with alkaline pH (7-9) significantly enhancing EPS yields (up to 159.6 µg/mL). Strain-specific optimization demonstrated that LZ-4 and Z7-4 achieved maximal EPS production at 28°C, whereas LZ-8 exhibited a high EPS production at 37°C. The study underscores the synergy between genomic insights and systematic screening, offering a scalable framework for rapid strain optimization. These findings pave the way for sustainable EPS bioproduction, reducing reliance on synthetic polymers and advancing industrial biotechnology in alignment with circular bioeconomy goals.IMPORTANCEThis study integrates genomic analysis with high-throughput fermentation to optimize exopolysaccharide (EPS) production in seven novel marine bacterial strains. By identifying key EPS biosynthesis genes and pathways, we tailored fermentation conditions using sucrose and alkaline pH, achieving yields up to 159.6 µg/mL. Strain-specific optimizations revealed significant enhancements in EPS production, highlighting the potential for sustainable industrial applications. This work bridges ecological insights with bioprocessing, offering a scalable framework for efficient EPS production that reduces reliance on synthetic polymers, advancing circular bioeconomy goals. The findings underscore the importance of marine microbial resources in biotechnology.

Applied and Environmental MicrobiologyVol. 91(11)
University of Science and Technology (YE), Zhejiang Ocean University (CN), Guangdong Academy of Agricultural Sciences (CN), Ministry of Agriculture (ID), Ministry of Agriculture and Rural Affairs (CN), Fujian University of Technology (CN), Korea University of Science and Technology (KR)
Openalex Percentile: Top 17%
Enzyme Production and Characterization
1.23
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