Literature DB >> 33479827

Genomic analysis of a novel species Halomonas shambharensis isolated from hypersaline lake in Northwest India.

Kapilesh Jadhav1, Bijayendra Kushwaha2, Indrani Jadhav2, Prem Shankar3, Anjali Geethadevi4, Gaurav Kumar5, Sonam Mittal6, Guru Prasad Sharma7, Madhuri Parashar2,8, Deepak Parashar9,10.   

Abstract

Genome analysis of Halomonas shambharensis, a novel species, was performed to understand the osmoprotectant strategies used by the strain to overcome the salinity stress and to explore the prospective industrial uses. It will also help to better understand the ecological roles of Halomonas species in hypersaline habitats. Ultrastructure of the cell was determined by using transmission electron microscopy. Standard microbiological methods were used to find out growth parameters and heterotrophic mode of nutrition. For Genome analysis, complete bacterial genome sequencing was performed using the Oxford Nanopore MinION DNA Sequencer. Assembly, annotation and finishing of the obtained sequence were done by using a Prokaryotic Genome Annotation Pipeline (PGAP) (SPAdes v. 3.10.1). Predicted Coading sequences (CDSs) obtained through the PGAP were used for functional annotation using Clusters of Orthologous Groups and Kyoto Encyclopedia of Genes and Genomes (KEGG) platforms. The H. shambharensis was found to be a Gram-stain-negative, rod-shaped bacterium, motile with a peritrichous flagella. The H. shambharensis bacterium can grow in a wide range of temperature (from 25 to 65 °C), pH (pH 4 to pH 12.0) and salt concentration (5.0% NaCl to 30.0% NaCl). After annotation and assembly, the total genome size obtained was 1,533,947 bp, which revealed 146 subsystems, 3847 coding sequences, and 19RNAs with G+C content of 63.6%. Gene annotation identified the genes related to various metabolic pathways, including carbohydrate metabolism, fatty acid metabolism and stress tolerance. The genomic dataset of H. shambharensis will be useful for analysis of protein-coding gene families and how these coding genes are significant for the survival and metabolism among the different species of Halomonas. The complete genome sequence presented here will help to unravel the biotechnological potential of H. shambharensis for production of the high-value products such as betaine, or as a source of gene-mining for individual enzymes.

Entities:  

Keywords:  Genome analysis; Genome annotation; Halomonas shambharensis; Oxford Nanopore Technology; Sambhar Salt Lake

Mesh:

Substances:

Year:  2021        PMID: 33479827     DOI: 10.1007/s11033-020-06131-w

Source DB:  PubMed          Journal:  Mol Biol Rep        ISSN: 0301-4851            Impact factor:   2.316


  12 in total

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Authors:  R L Tatusov; M Y Galperin; D A Natale; E V Koonin
Journal:  Nucleic Acids Res       Date:  2000-01-01       Impact factor: 16.971

2.  Halomonas sambharensis sp. nov., a Moderately Halophilic Bacterium Isolated from the Saltern Crystallizer Ponds of the Sambhar Salt Lake in India.

Authors:  Bijayendra Kushwaha; Indrani Jadhav; Kapilesh Jadhav
Journal:  Curr Microbiol       Date:  2020-01-30       Impact factor: 2.188

Review 3.  Why do bacteria use so many enzymes to scavenge hydrogen peroxide?

Authors:  Surabhi Mishra; James Imlay
Journal:  Arch Biochem Biophys       Date:  2012-05-16       Impact factor: 4.013

Review 4.  Osmoadaptation in bacteria.

Authors:  E A Galinski
Journal:  Adv Microb Physiol       Date:  1995       Impact factor: 3.517

5.  RASTtk: a modular and extensible implementation of the RAST algorithm for building custom annotation pipelines and annotating batches of genomes.

Authors:  Thomas Brettin; James J Davis; Terry Disz; Robert A Edwards; Svetlana Gerdes; Gary J Olsen; Robert Olson; Ross Overbeek; Bruce Parrello; Gordon D Pusch; Maulik Shukla; James A Thomason; Rick Stevens; Veronika Vonstein; Alice R Wattam; Fangfang Xia
Journal:  Sci Rep       Date:  2015-02-10       Impact factor: 4.379

6.  Draft genome sequence of Halomonas lutea strain YIM 91125(T) (DSM 23508(T)) isolated from the alkaline Lake Ebinur in Northwest China.

Authors:  Xiao-Yang Gao; Xiao-Yang Zhi; Hong-Wei Li; Yu Zhou; Alla Lapidus; James Han; Matthew Haynes; Elizabeth Lobos; Marcel Huntemann; Amrita Pati; Natalia N Ivanova; Konstantinos Mavromatis; Brian J Tindall; Victor Markowitz; Tanja Woyke; Hans-Peter Klenk; Nikos C Kyrpides; Wen-Jun Li
Journal:  Stand Genomic Sci       Date:  2015-01-20

7.  The RAST Server: rapid annotations using subsystems technology.

Authors:  Ramy K Aziz; Daniela Bartels; Aaron A Best; Matthew DeJongh; Terrence Disz; Robert A Edwards; Kevin Formsma; Svetlana Gerdes; Elizabeth M Glass; Michael Kubal; Folker Meyer; Gary J Olsen; Robert Olson; Andrei L Osterman; Ross A Overbeek; Leslie K McNeil; Daniel Paarmann; Tobias Paczian; Bruce Parrello; Gordon D Pusch; Claudia Reich; Rick Stevens; Olga Vassieva; Veronika Vonstein; Andreas Wilke; Olga Zagnitko
Journal:  BMC Genomics       Date:  2008-02-08       Impact factor: 3.969

8.  The SEED and the Rapid Annotation of microbial genomes using Subsystems Technology (RAST).

Authors:  Ross Overbeek; Robert Olson; Gordon D Pusch; Gary J Olsen; James J Davis; Terry Disz; Robert A Edwards; Svetlana Gerdes; Bruce Parrello; Maulik Shukla; Veronika Vonstein; Alice R Wattam; Fangfang Xia; Rick Stevens
Journal:  Nucleic Acids Res       Date:  2013-11-29       Impact factor: 16.971

9.  NCBI prokaryotic genome annotation pipeline.

Authors:  Tatiana Tatusova; Michael DiCuccio; Azat Badretdin; Vyacheslav Chetvernin; Eric P Nawrocki; Leonid Zaslavsky; Alexandre Lomsadze; Kim D Pruitt; Mark Borodovsky; James Ostell
Journal:  Nucleic Acids Res       Date:  2016-06-24       Impact factor: 16.971

10.  Complete genome sequence of Halomonas sp. R5-57.

Authors:  Adele Williamson; Concetta De Santi; Bjørn Altermark; Christian Karlsen; Erik Hjerde
Journal:  Stand Genomic Sci       Date:  2016-09-07
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