Genome Analysis of a Potential Novel Vibrio Species Secreting pH- and Thermo-Stable Alginate Lyase and Its Application in Producing Alginate Oligosaccharides

Alginate lyase is an attractive biocatalyst that can specifically degrade alginate to produce oligosaccharides, showing great potential for industrial and medicinal applications. Herein, an alginate-degrading strain HB236076 was isolated from <i>Sargassum</i> sp. in Qionghai, Hainan, China. The low 16S rRNA gene sequence identity (<98.4%), ANI value (<71.9%), and dDDH value (<23.9%) clearly indicated that the isolate represented a potential novel species of the genus <i>Vibrio</i>. The genome contained two chromosomes with lengths of 3,007,948 bp and 874,895 bp, respectively, totaling 3,882,843 bp with a G+C content of 46.5%. Among 3482 genes, 3332 protein-coding genes, 116 tRNA, and 34 rRNA sequences were predicted. Analysis of the amino acid sequences showed that the strain encoded 73 carbohydrate-active enzymes (CAZymes), predicting seven PL7 (Alg1-7) and two PL17 family (Alg8, 9) alginate lyases. The extracellular alginate lyase from strain HB236076 showed the maximum activity at 50 °C and pH 7.0, with over 90% activity measured in the range of 30-60 °C and pH 6.0-10.0, exhibiting a wide range of temperature and pH activities. The enzyme also remained at more than 90% of the original activity at a wide pH range (3.0-9.0) and temperature below 50 °C for more than 2 h, demonstrating significant thermal and pH stabilities. Fe<sup>2+</sup> had a good promoting effect on the alginate lyase activity at 10 mM, increasing by 3.5 times. Thin layer chromatography (TLC) and electrospray ionization mass spectrometry (ESI-MS) analyses suggested that alginate lyase in fermentation broth could catalyze sodium alginate to produce disaccharides and trisaccharides, which showed antimicrobial activity against <i>Shigella dysenteriae</i>, <i>Aeromonas hydrophila</i>, <i>Staphylococcus aureus</i>, <i>Streptococcus agalactiae</i>, and <i>Escherichia coli</i>. This research provided extended insights into the production mechanism of alginate lyase from <i>Vibrio</i> sp. HB236076, which was beneficial for further application in the preparation of pH-stable and thermo-stable alginate lyase and alginate oligosaccharides.

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Journal
Marine Drugs
Published
2024-09-10
DOI
https://doi.org/10.3390/md22090414
Citations
1
Primary Topic
Aquaculture disease management and microbiota
Type
article
Field-Weighted Citation Impact
0.24

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article

Genome Analysis of a Potential Novel Vibrio Species Secreting pH- and Thermo-Stable Alginate Lyase and Its Application in Producing Alginate Oligosaccharides

Ke Bao, Huiqin Huang, Miao Yang, Kaishan Zhang et al.
1 citations
Marine Drugs
Aquaculture disease management and microbiota
0.24
article

Genome Analysis of a Potential Novel Vibrio Species Secreting pH- and Thermo-Stable Alginate Lyase and Its Application in Producing Alginate Oligosaccharides

Ke Bao, Huiqin Huang, Miao Yang, Kaishan Zhang, Qianhuan Sun
article en
1 citations

Abstract

Alginate lyase is an attractive biocatalyst that can specifically degrade alginate to produce oligosaccharides, showing great potential for industrial and medicinal applications. Herein, an alginate-degrading strain HB236076 was isolated from <i>Sargassum</i> sp. in Qionghai, Hainan, China. The low 16S rRNA gene sequence identity (<98.4%), ANI value (<71.9%), and dDDH value (<23.9%) clearly indicated that the isolate represented a potential novel species of the genus <i>Vibrio</i>. The genome contained two chromosomes with lengths of 3,007,948 bp and 874,895 bp, respectively, totaling 3,882,843 bp with a G+C content of 46.5%. Among 3482 genes, 3332 protein-coding genes, 116 tRNA, and 34 rRNA sequences were predicted. Analysis of the amino acid sequences showed that the strain encoded 73 carbohydrate-active enzymes (CAZymes), predicting seven PL7 (Alg1-7) and two PL17 family (Alg8, 9) alginate lyases. The extracellular alginate lyase from strain HB236076 showed the maximum activity at 50 °C and pH 7.0, with over 90% activity measured in the range of 30-60 °C and pH 6.0-10.0, exhibiting a wide range of temperature and pH activities. The enzyme also remained at more than 90% of the original activity at a wide pH range (3.0-9.0) and temperature below 50 °C for more than 2 h, demonstrating significant thermal and pH stabilities. Fe<sup>2+</sup> had a good promoting effect on the alginate lyase activity at 10 mM, increasing by 3.5 times. Thin layer chromatography (TLC) and electrospray ionization mass spectrometry (ESI-MS) analyses suggested that alginate lyase in fermentation broth could catalyze sodium alginate to produce disaccharides and trisaccharides, which showed antimicrobial activity against <i>Shigella dysenteriae</i>, <i>Aeromonas hydrophila</i>, <i>Staphylococcus aureus</i>, <i>Streptococcus agalactiae</i>, and <i>Escherichia coli</i>. This research provided extended insights into the production mechanism of alginate lyase from <i>Vibrio</i> sp. HB236076, which was beneficial for further application in the preparation of pH-stable and thermo-stable alginate lyase and alginate oligosaccharides.

Marine DrugsVol. 22(9)
Chinese Academy of Tropical Agricultural Sciences (CN), Huazhong Agricultural University (CN), Hangzhou DAC Biotech (China) (CN)
National Natural Science Foundation of China, Ministry of Agriculture of the People's Republic of China, Ministry of Science and Technology, Taiwan, Hainan Provincial Department of Science and Technology, Key Research and Development Project of Hainan Province, National Key Research and Development Program of China
Openalex Percentile: Top 42%
Aquaculture disease management and microbiota
0.24
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