» Articles » PMID: 28078050

Complete Genome Sequence of LP1 Isolated from an Arctic Deep-sea Hydrothermal Vent System

Overview
Publisher Biomed Central
Specialty Genetics
Date 2017 Jan 13
PMID 28078050
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

LP1 within the family was isolated from a biofilm growing on the surface of a black smoker chimney at the Loki's Castle vent field, located on the Arctic Mid-Ocean Ridge. The complete genome of LP1 is the first genome to be published within the genus LP1 consists of a single 2,966,978 bp circular chromosome with a GC content of 29.8%. The genome comprises 2,537 protein-coding genes, 40 tRNA species and 2 rRNA operons. The microaerophilic, organotrophic isolate contains genes for all central carbohydrate metabolic pathways. However, genes for the oxidative branch of the pentose-phosphate-pathway, the glyoxylate shunt of the tricarboxylic acid cycle and the ATP citrate lyase for reverse TCA are not present. LP1 utilizes starch, sucrose and diverse proteinous carbon sources. In accordance, the genome harbours 130 proteases and 104 carbohydrate-active enzymes, indicating a specialization in degrading organic matter. Among a small arsenal of 24 glycosyl hydrolases, which offer the possibility to hydrolyse diverse poly- and oligosaccharides, a starch utilization cluster was identified. Furthermore, a variety of enzymes may be secreted via T9SS and contribute to the hydrolytic variety of the microorganism. Genes for gliding motility are present, which may enable the bacteria to move within the biofilm. A substantial number of genes encoding for extracellular polysaccharide synthesis pathways, curli fibres and attachment to surfaces could mediate adhesion in the biofilm and may contribute to the biofilm formation. In addition to aerobic respiration, the complete denitrification pathway and genes for sulphide oxidation e.g. sulphide:quinone reductase are present in the genome. sulphide:quinone reductase and denitrification may serve as detoxification systems allowing LP1 to thrive in a sulphide and nitrate enriched environment. The information gained from the genome gives a greater insight in the functional role of LP1 in the biofilm and its adaption strategy in an extreme environment.

Citing Articles

In silico prediction of potential indigenous microbial biomarkers in Penaeus vannamei identified through meta-analysis and genome-scale metabolic modelling.

Devika N, Katneni V, Jangam A, Suganya P, Shekhar M, Jithendran K Environ Microbiome. 2023; 18(1):2.

PMID: 36631881 PMC: 9835370. DOI: 10.1186/s40793-022-00458-6.


Machine Learning Predicts Biogeochemistry from Microbial Community Structure in a Complex Model System.

Dutta A, Goldman T, Keating J, Burke E, Williamson N, Dirmeier R Microbiol Spectr. 2022; 10(1):e0190921.

PMID: 35138192 PMC: 8826735. DOI: 10.1128/spectrum.01909-21.


Genomic insights into diverse bacterial taxa that degrade extracellular DNA in marine sediments.

Wasmund K, Pelikan C, Schintlmeister A, Wagner M, Watzka M, Richter A Nat Microbiol. 2021; 6(7):885-898.

PMID: 34127845 PMC: 8289736. DOI: 10.1038/s41564-021-00917-9.


Characterization and Diversity Analysis of the Extracellular Proteases of Thermophilic 1A02591 From Deep-Sea Hydrothermal Vent Sediment.

Cheng J, Wang Y, Zhang X, Sun M, Zhang X, Song X Front Microbiol. 2021; 12:643508.

PMID: 33796092 PMC: 8007923. DOI: 10.3389/fmicb.2021.643508.


Comparison of Alginate Utilization Pathways in Culturable Bacteria Isolated From Arctic and Antarctic Marine Environments.

Cha Q, Wang X, Ren X, Li D, Wang P, Li P Front Microbiol. 2021; 12:609393.

PMID: 33584613 PMC: 7874173. DOI: 10.3389/fmicb.2021.609393.


References
1.
Hugo C, Segers P, Hoste B, Vancanneyt M, Kersters K . Chryseobacterium joostei sp. nov., isolated from the dairy environment. Int J Syst Evol Microbiol. 2003; 53(Pt 3):771-777. DOI: 10.1099/ijs.0.02232-0. View

2.
Berne C, Ducret A, Hardy G, Brun Y . Adhesins Involved in Attachment to Abiotic Surfaces by Gram-Negative Bacteria. Microbiol Spectr. 2015; 3(4). PMC: 4566860. DOI: 10.1128/microbiolspec.MB-0018-2015. View

3.
Shoji M, Sato K, Yukitake H, Kondo Y, Narita Y, Kadowaki T . Por secretion system-dependent secretion and glycosylation of Porphyromonas gingivalis hemin-binding protein 35. PLoS One. 2011; 6(6):e21372. PMC: 3120885. DOI: 10.1371/journal.pone.0021372. View

4.
Stokke R, Dahle H, Roalkvam I, Wissuwa J, Daae F, Tooming-Klunderud A . Functional interactions among filamentous Epsilonproteobacteria and Bacteroidetes in a deep-sea hydrothermal vent biofilm. Environ Microbiol. 2015; 17(10):4063-77. DOI: 10.1111/1462-2920.12970. View

5.
Chen Y, Zhang Z, Fu Y, Wang Y, Wang Y, Jiao N . Altuibacter lentus gen. nov., sp. nov., a novel member of family Flavobacteriaceae isolated from deep seawater of the South China Sea. Antonie Van Leeuwenhoek. 2013; 104(6):1151-7. DOI: 10.1007/s10482-013-0037-8. View