Pub Date : 2025-01-31DOI: 10.1016/j.margen.2025.101178
Liyan Liu , Hai Shi , Zihua Guo , Xiaotong Zhang , Xueqi Li , Xiao-Hua Zhang , Yunhui Zhang
Dimethylsulfide (DMS) is a volatile organic compound that influences climate change and plays a key role in the global sulfur cycle and chemotaxis. Marine bacteria can produce DMS from dimethylsulfoniopropionate (DMSP) and other sulfur precursors. A highly efficient DMS-producing strain, Marinobacter flavimaris ZYH30, was isolated from the surface sediment of the South China Sea, but the key genes involved in DMS production in its genome remain unknown. Here, we reported the complete genome sequence of M. flavimaris ZYH30 and its genomic potential in DMS cycling. The genome of M. flavimaris ZYH30 consists of a circular chromosome with a length of 4,631,282 bp and its GC content is 57.26 %. Genomic analysis showed that strain ZYH30 possesses a set of genes involved in DMS cycling, including a DMSP lyase DddL. In addition, M. flavimaris ZYH30 contained a mddH gene involved in hydrogen sulfide (H2S) and methanethiol (MeSH) dependent DMS production pathways. This study provides genetic insights into the DMS production processes and sulfur cycling in marine sediment bacteria.
{"title":"Genomic analysis of Marinobacter flavimaris ZYH30 reveals its role in marine dimethylsulfide cycling","authors":"Liyan Liu , Hai Shi , Zihua Guo , Xiaotong Zhang , Xueqi Li , Xiao-Hua Zhang , Yunhui Zhang","doi":"10.1016/j.margen.2025.101178","DOIUrl":"10.1016/j.margen.2025.101178","url":null,"abstract":"<div><div>Dimethylsulfide (DMS) is a volatile organic compound that influences climate change and plays a key role in the global sulfur cycle and chemotaxis. Marine bacteria can produce DMS from dimethylsulfoniopropionate (DMSP) and other sulfur precursors. A highly efficient DMS-producing strain, <em>Marinobacter flavimaris</em> ZYH30, was isolated from the surface sediment of the South China Sea, but the key genes involved in DMS production in its genome remain unknown. Here, we reported the complete genome sequence of <em>M. flavimaris</em> ZYH30 and its genomic potential in DMS cycling. The genome of <em>M. flavimaris</em> ZYH30 consists of a circular chromosome with a length of 4,631,282 bp and its GC content is 57.26 %. Genomic analysis showed that strain ZYH30 possesses a set of genes involved in DMS cycling, including a DMSP lyase DddL. In addition, <em>M. flavimaris</em> ZYH30 contained a <em>mddH</em> gene involved in hydrogen sulfide (H<sub>2</sub>S) and methanethiol (MeSH) dependent DMS production pathways. This study provides genetic insights into the DMS production processes and sulfur cycling in marine sediment bacteria.</div></div>","PeriodicalId":18321,"journal":{"name":"Marine genomics","volume":"80 ","pages":"Article 101178"},"PeriodicalIF":1.3,"publicationDate":"2025-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143158637","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-25DOI: 10.1016/j.margen.2025.101168
Shi-Ning Cai , Hai-Xia Zhu , Zhi-Gang Tang , Xue-Yun Geng , Mei-Ling Sun
As a consequence of marine eutrophication, there has been an exponential growth of Ulva prolifera, culminating in the yearly emergence of a massive green tide along the shores of Qingdao. This phenomenon exerts a detrimental impact on the marine ecosystem. As reported, the expression level of Alteromonas enzymes involved in U. prolifera polysaccharides degradation is increased during the green tide outbreak period, potentially accelerating the breakdown of U. prolifera biomass. This enhanced degradation could facilitate the transition to the waning phase of the green tide event. In this study, strain Alteromonas marina OM2201 was isolated from seawater samples taken during an U. prolifera bloom in the coastal waters of Qingdao. Its genome contains a ring chromosome and two plasmids. The length of the circular chromosome was 4,489,073 bp with GC content of 44.21 mol%, and the length of plasmid 1 was 233,636 bp with GC content of 42.24 mol%, and the length of plasmid 2 was 5594 bp with GC content of 39.61 mol%. Genomic analysis showed that Alteromonas marina OM2201 contained a variety of ulvan lyase genes, indicating that it could promote the degradation of U. prolifera polysaccharides. This genetic makeup potentially enables the strain to expedite the decomposition of U. prolifera biomass. Therefore, this study broadens our understanding of the Alteromonas bacteria that can degrade U. prolifera polysaccharides during the outbreak period.
{"title":"Complete genome sequence of Alteromonas marina OM2201, a marine bacterium degrading Ulva prolifera polysaccharides isolated from surface of the Yellow Sea","authors":"Shi-Ning Cai , Hai-Xia Zhu , Zhi-Gang Tang , Xue-Yun Geng , Mei-Ling Sun","doi":"10.1016/j.margen.2025.101168","DOIUrl":"10.1016/j.margen.2025.101168","url":null,"abstract":"<div><div>As a consequence of marine eutrophication, there has been an exponential growth of <em>Ulva prolifera</em>, culminating in the yearly emergence of a massive green tide along the shores of Qingdao. This phenomenon exerts a detrimental impact on the marine ecosystem. As reported, the expression level of <em>Alteromonas</em> enzymes involved in <em>U. prolifera</em> polysaccharides degradation is increased during the green tide outbreak period, potentially accelerating the breakdown of <em>U. prolifera</em> biomass. This enhanced degradation could facilitate the transition to the waning phase of the green tide event. In this study, strain <em>Alteromonas marina</em> OM2201 was isolated from seawater samples taken during an <em>U. prolifera</em> bloom in the coastal waters of Qingdao. Its genome contains a ring chromosome and two plasmids. The length of the circular chromosome was 4,489,073 bp with GC content of 44.21 mol%, and the length of plasmid 1 was 233,636 bp with GC content of 42.24 mol%, and the length of plasmid 2 was 5594 bp with GC content of 39.61 mol%. Genomic analysis showed that <em>Alteromonas marina</em> OM2201 contained a variety of ulvan lyase genes, indicating that it could promote the degradation of <em>U. prolifera</em> polysaccharides. This genetic makeup potentially enables the strain to expedite the decomposition of <em>U. prolifera</em> biomass. Therefore, this study broadens our understanding of the <em>Alteromonas</em> bacteria that can degrade <em>U. prolifera</em> polysaccharides during the outbreak period.</div></div>","PeriodicalId":18321,"journal":{"name":"Marine genomics","volume":"80 ","pages":"Article 101168"},"PeriodicalIF":1.3,"publicationDate":"2025-01-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143158638","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-23DOI: 10.1016/j.margen.2025.101166
Liyun Liang , Songyang Li , Zengpeng Li , Mingliang Chen
We isolated a novel bacterial strain Acinetobacter sp. P1332 from the pufferfish Takifugu oblongus in the southeastern coast of Fujian Province, China. This strain has been identified as a potent producer of the neurotoxin tetrodotoxin (TTX). In this study, we present the complete genome sequence of Acinetobacter sp. P1332, which is a crucial advancement in identifying the genetic factors involved in TTX biosynthesis. The genome spans 4,017,868 base pairs and has a mean G + C content of 41.3 %. It encodes 3944 genes, along with 90 tRNAs and 21 rRNAs. This detailed genomic information provides an essential resource for further research into the biosynthetic pathways of TTX and its applications in biotechnology and toxinology.
{"title":"The complete genome sequence of Acinetobacter sp. P1332, a tetrodotoxin-producing bacteria","authors":"Liyun Liang , Songyang Li , Zengpeng Li , Mingliang Chen","doi":"10.1016/j.margen.2025.101166","DOIUrl":"10.1016/j.margen.2025.101166","url":null,"abstract":"<div><div>We isolated a novel bacterial strain <em>Acinetobacter</em> sp. P1332 from the pufferfish <em>Takifugu oblongus</em> in the southeastern coast of Fujian Province, China. This strain has been identified as a potent producer of the neurotoxin tetrodotoxin (TTX). In this study, we present the complete genome sequence of <em>Acinetobacter</em> sp. P1332, which is a crucial advancement in identifying the genetic factors involved in TTX biosynthesis. The genome spans 4,017,868 base pairs and has a mean G + C content of 41.3 %. It encodes 3944 genes, along with 90 tRNAs and 21 rRNAs. This detailed genomic information provides an essential resource for further research into the biosynthetic pathways of TTX and its applications in biotechnology and toxinology.</div></div>","PeriodicalId":18321,"journal":{"name":"Marine genomics","volume":"80 ","pages":"Article 101166"},"PeriodicalIF":1.3,"publicationDate":"2025-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143158640","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-22DOI: 10.1016/j.margen.2025.101167
Jun Li , Ya Ma , Ronghua Zhang , Nan Zhang
Betaine is a zwitterionic compatible compound, which is widely distributed in nature and can be found in a variety of microorganisms. It plays key roles in osmotic protection and one‑carbon metabolism. Sulfitobacter sp. PM12, a Gram-negative and aerobic bacterium, was isolated from the deep-sea samples collected from the Mariana Trench. Here, we report the complete genome sequence of strain PM12 and its genomic characteristics to synthesize and catabolize betaine. The genome of strain PM12 contains one circular chromosome (3,009,717 bp) and seven circular plasmids. Genomic analysis showed that strain PM12 contained a set of genes involved in betaine biosynthesis and biodegradation, indicating that it possesses the ability to metabolize betaine. This study enlarges our understanding of the betaine metabolism driven by bacteria in the ocean, and reveals the potential strategy of the strain PM12 to adapt the extreme environments of the Mariana Trench.
{"title":"Genomic analysis of Sulfitobacter sp. PM12 reveals its role in betaine metabolism","authors":"Jun Li , Ya Ma , Ronghua Zhang , Nan Zhang","doi":"10.1016/j.margen.2025.101167","DOIUrl":"10.1016/j.margen.2025.101167","url":null,"abstract":"<div><div>Betaine is a zwitterionic compatible compound, which is widely distributed in nature and can be found in a variety of microorganisms. It plays key roles in osmotic protection and one‑carbon metabolism. <em>Sulfitobacter</em> sp. PM12, a Gram-negative and aerobic bacterium, was isolated from the deep-sea samples collected from the Mariana Trench. Here, we report the complete genome sequence of strain PM12 and its genomic characteristics to synthesize and catabolize betaine. The genome of strain PM12 contains one circular chromosome (3,009,717 bp) and seven circular plasmids. Genomic analysis showed that strain PM12 contained a set of genes involved in betaine biosynthesis and biodegradation, indicating that it possesses the ability to metabolize betaine. This study enlarges our understanding of the betaine metabolism driven by bacteria in the ocean, and reveals the potential strategy of the strain PM12 to adapt the extreme environments of the Mariana Trench.</div></div>","PeriodicalId":18321,"journal":{"name":"Marine genomics","volume":"80 ","pages":"Article 101167"},"PeriodicalIF":1.3,"publicationDate":"2025-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143158639","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-16DOI: 10.1016/j.margen.2025.101165
Yu-Qi Zhang , Qi Yuan , Ji-Qing Liu , Xiao-Chen Liang , Jing-Ping Wang , Wen-Xin Jiang , Ping-Yi Li
Marine bacteria play important roles in the degradation and recycling of algal polysaccharides. However, the marine bacteria involved in fucoidan degradation and their degradation pathways remain poorly understood. Here, we report the complete genome sequence of Isoptericola halotolerans SM2308, isolated from a brown algal sample collected from an intertidal zone of the Yellow Sea in China. The genome of strain SM2308 consists of a single circular chromosome of 4,011,455 bp with a high GC content of 72.70 %. Strain SM2308 exhibited rapid growth on fucoidan as the sole carbon source, indicating its capacity to degrade fucoidan. Gene annotation and metabolic pathway analyses showed that strain SM2308 possesses a complete pathway for utilizing fucoidan, including the extracellular breakdown of polymeric fucoidan into smaller fucooligosaccharides/fucose by fucoidanases, the transmembrane transport of fucooligosaccharides/fucose into the cytoplasm by an ABC transporter, and the intracellular fucose catabolism via a non-phosphorylative pathway. This represents the first genome of an actinobacterium from the order Micrococcales with fucoidan-degrading ability. The genome of Isoptericola halotolerans SM2308 provides insights into the role of actinobacteria in the biogeochemical cycling of fucoidan in marine ecosystems.
{"title":"Genomic analysis of Isoptericola halotolerans SM2308 reveals its potential involved in fucoidan degradation","authors":"Yu-Qi Zhang , Qi Yuan , Ji-Qing Liu , Xiao-Chen Liang , Jing-Ping Wang , Wen-Xin Jiang , Ping-Yi Li","doi":"10.1016/j.margen.2025.101165","DOIUrl":"10.1016/j.margen.2025.101165","url":null,"abstract":"<div><div>Marine bacteria play important roles in the degradation and recycling of algal polysaccharides. However, the marine bacteria involved in fucoidan degradation and their degradation pathways remain poorly understood. Here, we report the complete genome sequence of <em>Isoptericola halotolerans</em> SM2308, isolated from a brown algal sample collected from an intertidal zone of the Yellow Sea in China. The genome of strain SM2308 consists of a single circular chromosome of 4,011,455 bp with a high GC content of 72.70 %. Strain SM2308 exhibited rapid growth on fucoidan as the sole carbon source, indicating its capacity to degrade fucoidan. Gene annotation and metabolic pathway analyses showed that strain SM2308 possesses a complete pathway for utilizing fucoidan, including the extracellular breakdown of polymeric fucoidan into smaller fucooligosaccharides/fucose by fucoidanases, the transmembrane transport of fucooligosaccharides/fucose into the cytoplasm by an ABC transporter, and the intracellular fucose catabolism via a non-phosphorylative pathway. This represents the first genome of an actinobacterium from the order Micrococcales with fucoidan-degrading ability. The genome of <em>Isoptericola halotolerans</em> SM2308 provides insights into the role of actinobacteria in the biogeochemical cycling of fucoidan in marine ecosystems.</div></div>","PeriodicalId":18321,"journal":{"name":"Marine genomics","volume":"79 ","pages":"Article 101165"},"PeriodicalIF":1.3,"publicationDate":"2025-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143008063","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-12-11DOI: 10.1016/j.margen.2024.101164
Chen Liang , Wei Wang , Jianming Chen
This is the first report of a transcriptome assembly of a newly discovered a new Protocruzia species sampled from the under-sampled area near the Mariana Trench. We sequenced the transcriptome of P. marianaensis using the Illumina Novaseq 6000 platform. De novo assembly and analysis of the coding regions predicted 36,116 unigenes, 74.91 % of which was annotated by public databases. The transcriptome of P. marianaensis will be a valuable resource in studying the ecological and biological characteristics of this new species, which is the first Protocruzia species in deep sea. These data can also help to understand protozoa survival mechanisms in deep-sea habitats and provide essential biological material for investigating unique life phenomena and processes in the deep ocean.
{"title":"First transcriptome assembly of a new ciliate species (Protocruzia marianaensis) isolated from the Mariana Trench area","authors":"Chen Liang , Wei Wang , Jianming Chen","doi":"10.1016/j.margen.2024.101164","DOIUrl":"10.1016/j.margen.2024.101164","url":null,"abstract":"<div><div>This is the first report of a transcriptome assembly of a newly discovered a new <em>Protocruzia</em> species sampled from the under-sampled area near the Mariana Trench. We sequenced the transcriptome of <em>P. marianaensis</em> using the Illumina Novaseq 6000 platform. De novo assembly and analysis of the coding regions predicted 36,116 unigenes, 74.91 % of which was annotated by public databases. The transcriptome of <em>P. marianaensis</em> will be a valuable resource in studying the ecological and biological characteristics of this new species, which is the first <em>Protocruzia</em> species in deep sea. These data can also help to understand protozoa survival mechanisms in deep-sea habitats and provide essential biological material for investigating unique life phenomena and processes in the deep ocean.</div></div>","PeriodicalId":18321,"journal":{"name":"Marine genomics","volume":"79 ","pages":"Article 101164"},"PeriodicalIF":1.3,"publicationDate":"2024-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143039734","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Alginate is a natural marine polysaccharide and an important marine organic carbon source, which is mainly produced by marine brown algae. Marinobacter sp. M5B, a Gram-negative and aerobic bacterium, was isolated from the surface seawater samples collected from the Mariana Trench. Here, we report the complete genome sequence of strain M5B and its genomic characteristics to synthesize alginate. The genome of strain M5B contains one circular chromosome (4,415,647 bp) with the GC content of 57.14 %. Genomic analysis showed that strain M5B contained a set of genes involved in alginate synthesis, indicating that it possesses the potential ability to synthesis alginate. This study provides novel insights into alginate synthesis by marine microorganisms.
{"title":"Genomic analysis of Marinobacter sp. M5B reveals its role in alginate biosynthesis","authors":"Xiaoyu Si, Zhenhai Liu, Shuxin Cheng, Jingyao Xi, Bingrui Zeng, Meihui Li, Liping Zhu, Shigan Yan, Nan Zhang","doi":"10.1016/j.margen.2024.101163","DOIUrl":"10.1016/j.margen.2024.101163","url":null,"abstract":"<div><div>Alginate is a natural marine polysaccharide and an important marine organic carbon source, which is mainly produced by marine brown algae. <em>Marinobacter</em> sp. M5B, a Gram-negative and aerobic bacterium, was isolated from the surface seawater samples collected from the Mariana Trench. Here, we report the complete genome sequence of strain M5B and its genomic characteristics to synthesize alginate. The genome of strain M5B contains one circular chromosome (4,415,647 bp) with the GC content of 57.14 %. Genomic analysis showed that strain M5B contained a set of genes involved in alginate synthesis, indicating that it possesses the potential ability to synthesis alginate. This study provides novel insights into alginate synthesis by marine microorganisms.</div></div>","PeriodicalId":18321,"journal":{"name":"Marine genomics","volume":"79 ","pages":"Article 101163"},"PeriodicalIF":1.3,"publicationDate":"2024-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142746576","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-11-26DOI: 10.1016/j.margen.2024.101162
Wenzhou Zhang , Minghuang Ling , Kai Zhang , Ruzhen Liu , Xiaomei Huang , Gaili Fan , Hans-Peter Grossart , Fei Peng , Zhuhua Luo
Mangroves, owing to their unique living environment, serve as an important source of natural bioactive compounds. Sarcopodium sp. QM3–1, a marine fungus isolated from mangrove sediments of Quanzhou Bay, exhibited antifungal activity against the plant pathogen Agrobacterium tumefaciens and Magnaporthe oryzae. Whole-genome sequencing of this fungal strain revealed a genome size of 58,356,150 bp with 17,960 protein-coding genes, 539 tRNA genes, and 170 rRNA genes. Functional annotation identified a series of genes involved in the biosynthesis of secondary metabolites, including several gene clusters associated with antimicrobial activity. Notably, twenty of these gene clusters were associated with the synthesis of known bioactive compounds, including terpene, polyketides (PKS), nonribosomal peptides (NRPS), β-lactones, and phosphonates. Our findings suggest that Sarcopodium sp. QM3–1 could be a promising candidate as a biocontrol agent for combating plant pathogens in agricultural fields.
{"title":"Complete genome sequence of the marine mangrove fungus Sarcopodium sp.QM3–1 confirmed its high potential for antimicrobial activity","authors":"Wenzhou Zhang , Minghuang Ling , Kai Zhang , Ruzhen Liu , Xiaomei Huang , Gaili Fan , Hans-Peter Grossart , Fei Peng , Zhuhua Luo","doi":"10.1016/j.margen.2024.101162","DOIUrl":"10.1016/j.margen.2024.101162","url":null,"abstract":"<div><div>Mangroves, owing to their unique living environment, serve as an important source of natural bioactive compounds. <em>Sarcopodium</em> sp. QM3–1, a marine fungus isolated from mangrove sediments of Quanzhou Bay, exhibited antifungal activity against the plant pathogen <em>Agrobacterium tumefaciens</em> and <em>Magnaporthe oryzae</em>. Whole-genome sequencing of this fungal strain revealed a genome size of 58,356,150 bp with 17,960 protein-coding genes, 539 tRNA genes, and 170 rRNA genes. Functional annotation identified a series of genes involved in the biosynthesis of secondary metabolites, including several gene clusters associated with antimicrobial activity. Notably, twenty of these gene clusters were associated with the synthesis of known bioactive compounds, including terpene, polyketides (PKS), nonribosomal peptides (NRPS), β-lactones, and phosphonates. Our findings suggest that <em>Sarcopodium</em> sp. QM3–1 could be a promising candidate as a biocontrol agent for combating plant pathogens in agricultural fields.</div></div>","PeriodicalId":18321,"journal":{"name":"Marine genomics","volume":"79 ","pages":"Article 101162"},"PeriodicalIF":1.3,"publicationDate":"2024-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142719761","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-11-21DOI: 10.1016/j.margen.2024.101160
Xin-Xiao Qu , Yu-Qi Zhang , Fei-Yu He , Xi-Ying Zhang , Peng Wang , Fei Xu , Yu-Qiang Zhang , Long-Sheng Zhao , Ping-Yi Li , Fang Zhao
Alginate, mainly produced by brown algae, is an important polysaccharide that supports the growth of marine bacteria. Vreelandella sp. F11 is a Gram-negative and aerobic marine bacterium, which was isolated from the brown algae sample collected from the Weihai coast, the Yellow Sea, China. Here, we present the complete genome of strain F11 and its genomic characteristics to utilize alginate. The genome of strain F11 comprises one circular chromosome with 4,840,724 bp and a GC content of 55.04 %. Strain F11 could grow with alginate as the sole carbon source. Genomic analysis revealed that strain F11 contains a gene cluster, encoding the enzymes, transporters and a regulator protein involved in utilizing alginate. Gene annotations suggested that the alginate utilization system of strain F11 is similar to those in Vibrio strains. However, strain F11 does not contain homologs of known KdgF (a key enzyme involved in the metabolism of alginate monomer) and inner membrane transporters of alginate oligomer uptake. The result indicated that strain F11 contains novel KdgF and inner membrane transporter system, which warrants further investigation. These data suggested that Vreelandella strains play a role in alginate utilization in the ocean and lay a foundation for the application of Vreelandella in the conversion of brown algae.
{"title":"Genomic analysis of Vreelandella sp. F11 reveals its role in alginate utilization","authors":"Xin-Xiao Qu , Yu-Qi Zhang , Fei-Yu He , Xi-Ying Zhang , Peng Wang , Fei Xu , Yu-Qiang Zhang , Long-Sheng Zhao , Ping-Yi Li , Fang Zhao","doi":"10.1016/j.margen.2024.101160","DOIUrl":"10.1016/j.margen.2024.101160","url":null,"abstract":"<div><div>Alginate, mainly produced by brown algae, is an important polysaccharide that supports the growth of marine bacteria. <em>Vreelandella</em> sp. F11 is a Gram-negative and aerobic marine bacterium, which was isolated from the brown algae sample collected from the Weihai coast, the Yellow Sea, China. Here, we present the complete genome of strain F11 and its genomic characteristics to utilize alginate. The genome of strain F11 comprises one circular chromosome with 4,840,724 bp and a GC content of 55.04 %. Strain F11 could grow with alginate as the sole carbon source. Genomic analysis revealed that strain F11 contains a gene cluster, encoding the enzymes, transporters and a regulator protein involved in utilizing alginate. Gene annotations suggested that the alginate utilization system of strain F11 is similar to those in <em>Vibrio</em> strains. However, strain F11 does not contain homologs of known KdgF (a key enzyme involved in the metabolism of alginate monomer) and inner membrane transporters of alginate oligomer uptake. The result indicated that strain F11 contains novel KdgF and inner membrane transporter system, which warrants further investigation. These data suggested that <em>Vreelandella</em> strains play a role in alginate utilization in the ocean and lay a foundation for the application of <em>Vreelandella</em> in the conversion of brown algae.</div></div>","PeriodicalId":18321,"journal":{"name":"Marine genomics","volume":"79 ","pages":"Article 101160"},"PeriodicalIF":1.3,"publicationDate":"2024-11-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142700542","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-11-20DOI: 10.1016/j.margen.2024.101161
Meixue Pan , Wenbin Guo , Jingjing Duan
Stenotrophomonas sp. P2112, isolated from a marine sediment sample of the Pacific Ocean, can grow in mineral medium with polyvinyl chloride (PVC) plastic as sole carbon source. Here, we present the complete genome of Stenotrophomonas sp. P2112, which will facilitate the genome mining of PVC degrading enzymes. The total length of the sequenced genome consists of 4,382,508 bases, with mean G + C content of 66.61%. A total of 4024 coding genes including 73 tRNAs and 13 rRNAs were predicted in the genome. Some potential PVC degrading enzymes including monooxygenase and peroxidases were found in this genome.
{"title":"The complete genome sequence of Stenotrophomonas sp. P2112 for genome mining of polyvinyl chloride degrading enzymes","authors":"Meixue Pan , Wenbin Guo , Jingjing Duan","doi":"10.1016/j.margen.2024.101161","DOIUrl":"10.1016/j.margen.2024.101161","url":null,"abstract":"<div><div><em>Stenotrophomonas</em> sp. P2112, isolated from a marine sediment sample of the Pacific Ocean, can grow in mineral medium with polyvinyl chloride (PVC) plastic as sole carbon source. Here, we present the complete genome of <em>Stenotrophomonas</em> sp. P2112, which will facilitate the genome mining of PVC degrading enzymes. The total length of the sequenced genome consists of 4,382,508 bases, with mean G + C content of 66.61%. A total of 4024 coding genes including 73 tRNAs and 13 rRNAs were predicted in the genome. Some potential PVC degrading enzymes including monooxygenase and peroxidases were found in this genome.</div></div>","PeriodicalId":18321,"journal":{"name":"Marine genomics","volume":"79 ","pages":"Article 101161"},"PeriodicalIF":1.3,"publicationDate":"2024-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142700541","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}