Genome Sequence of Oceanobacillus Picturae Strain S1, an Halophilic
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
BMC Genomics Biomed Central
CORE Metadata, citation and similar papers at core.ac.uk Provided by PubMed Central BMC Genomics BioMed Central Research article Open Access A novel firmicute protein family related to the actinobacterial resuscitation-promoting factors by non-orthologous domain displacement Adriana Ravagnani†, Christopher L Finan† and Michael Young* Address: Institute of Biological Sciences, University of Wales, Aberystwyth, Ceredigion SY23 3DD, UK Email: Adriana Ravagnani - [email protected]; Christopher L Finan - [email protected]; Michael Young* - [email protected] * Corresponding author †Equal contributors Published: 17 March 2005 Received: 21 September 2004 Accepted: 17 March 2005 BMC Genomics 2005, 6:39 doi:10.1186/1471-2164-6-39 This article is available from: http://www.biomedcentral.com/1471-2164/6/39 © 2005 Ravagnani et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Abstract Background: In Micrococcus luteus growth and resuscitation from starvation-induced dormancy is controlled by the production of a secreted growth factor. This autocrine resuscitation-promoting factor (Rpf) is the founder member of a family of proteins found throughout and confined to the actinobacteria (high G + C Gram-positive bacteria). The aim of this work was to search for and characterise a cognate gene family in the firmicutes (low G + C Gram-positive bacteria) and obtain information about how they may control bacterial growth and resuscitation. Results: In silico analysis of the accessory domains of the Rpf proteins permitted their classification into several subfamilies. -
Characterisation of Novel Isosaccharinic Acid Degrading Bacteria and Communities
University of Huddersfield Repository Kyeremeh, Isaac Ampaabeng Characterisation of Novel Isosaccharinic Acid Degrading Bacteria and Communities Original Citation Kyeremeh, Isaac Ampaabeng (2018) Characterisation of Novel Isosaccharinic Acid Degrading Bacteria and Communities. Doctoral thesis, University of Huddersfield. This version is available at http://eprints.hud.ac.uk/id/eprint/34509/ The University Repository is a digital collection of the research output of the University, available on Open Access. Copyright and Moral Rights for the items on this site are retained by the individual author and/or other copyright owners. Users may access full items free of charge; copies of full text items generally can be reproduced, displayed or performed and given to third parties in any format or medium for personal research or study, educational or not-for-profit purposes without prior permission or charge, provided: • The authors, title and full bibliographic details is credited in any copy; • A hyperlink and/or URL is included for the original metadata page; and • The content is not changed in any way. For more information, including our policy and submission procedure, please contact the Repository Team at: [email protected]. http://eprints.hud.ac.uk/ Characterisation of Novel Isosaccharinic Acid Degrading Bacteria and Communities Isaac Ampaabeng Kyeremeh, MSc (Hons) A thesis submitted to the University of Huddersfield in partial fulfilment of the requirements for the degree of Doctor of Philosophy Department of Biological Sciences September 2017 i Acknowledgement Firstly, I would like to thank Almighty God for His countenance and grace all these years. ‘I could do all things through Christ who strengthens me’ (Philippians 4:1) Secondly, my heartfelt gratitude and appreciation go to my main supervisor Professor Paul N. -
Table S5. the Information of the Bacteria Annotated in the Soil Community at Species Level
Table S5. The information of the bacteria annotated in the soil community at species level No. Phylum Class Order Family Genus Species The number of contigs Abundance(%) 1 Firmicutes Bacilli Bacillales Bacillaceae Bacillus Bacillus cereus 1749 5.145782459 2 Bacteroidetes Cytophagia Cytophagales Hymenobacteraceae Hymenobacter Hymenobacter sedentarius 1538 4.52499338 3 Gemmatimonadetes Gemmatimonadetes Gemmatimonadales Gemmatimonadaceae Gemmatirosa Gemmatirosa kalamazoonesis 1020 3.000970902 4 Proteobacteria Alphaproteobacteria Sphingomonadales Sphingomonadaceae Sphingomonas Sphingomonas indica 797 2.344876284 5 Firmicutes Bacilli Lactobacillales Streptococcaceae Lactococcus Lactococcus piscium 542 1.594633558 6 Actinobacteria Thermoleophilia Solirubrobacterales Conexibacteraceae Conexibacter Conexibacter woesei 471 1.385742446 7 Proteobacteria Alphaproteobacteria Sphingomonadales Sphingomonadaceae Sphingomonas Sphingomonas taxi 430 1.265115184 8 Proteobacteria Alphaproteobacteria Sphingomonadales Sphingomonadaceae Sphingomonas Sphingomonas wittichii 388 1.141545794 9 Proteobacteria Alphaproteobacteria Sphingomonadales Sphingomonadaceae Sphingomonas Sphingomonas sp. FARSPH 298 0.876754244 10 Proteobacteria Alphaproteobacteria Sphingomonadales Sphingomonadaceae Sphingomonas Sorangium cellulosum 260 0.764953367 11 Proteobacteria Deltaproteobacteria Myxococcales Polyangiaceae Sorangium Sphingomonas sp. Cra20 260 0.764953367 12 Proteobacteria Alphaproteobacteria Sphingomonadales Sphingomonadaceae Sphingomonas Sphingomonas panacis 252 0.741416341 -
Enzymes from Deep-Sea Microorganisms - Takami, Hideto
EXTREMOPHILES – Vol. III - Enzymes from Deep-Sea Microorganisms - Takami, Hideto ENZYMES FROM DEEP-SEA MICROORGANISMS Takami, Hideto Microbial Genome Research Group, Japan Marine Science and Technology Center, 2- 15 Natsushima, Yokosuka, 237-0061 Japan Keywords: Mariana Trench, Challenger Deep, Deep-sea environments, Microbial flora, Bacteria, Actinomycetes, Yeast, Fungi, Extremophiles, Halophiles, 16S rDNA, Phylogenetic tree, Psychrophiles, Thermophiles, Alkaliphiles, Amylase, α- maltotetraohydrase (G4-amylase), Protease, Pseudomonas strain MS300, Hydrostatic pressure, Shinkai 2000, Shinkai 6500, Kaiko Contents 1. Introduction 2. Collection of Deep-sea Mud 3. Isolation of Microorganisms from Deep-sea Mud 3.1. Bacteria From The Mariana Trench 3.2. Bacteria From Other Deep-Sea Sites Located Off Southern Japan 4. 16S rDNA Sequences of Deep-sea Isolates 5. Exploring Unique Enzyme Producers Among Deep-sea Isolates 5.1. Screening for Amylase Producers 5.2. Purification of Amylase Produced By Pseudomonas Strain MS300 5.3. Enzyme Profiles Acknowledgments Glossary Bibliography Biographical Sketch Summary In an attempt to characterize the microbial flora on the deep-sea floor, we isolated thousands of microbes from samples collected at various deep-sea (1 050–10 897 m) sites located in the Mariana Trench and off southern Japan. Various types of bacteria, such as alkaliphiles, thermophiles, psychrophiles, and halophiles were recovered on agar platesUNESCO at atmospheric pressure at a –frequency EOLSS of 0.8 x 102–2.3 x 104/g of dry sea mud. No acidophiles were recovered. Similarly, non extremophilic bacteria were recovered at a frequency of 8.1 x 102–2.3 x 105. These deep-sea isolates were widely distributed and detectedSAMPLE at each deep-sea site , andCHAPTERS the frequency of isolation of microbes from the deep-sea mud was not directly influenced by the depth of the sampling site. -
The Natural Product Biosynthetic Potential of Red Sea Nudibranch Microbiomes
The natural product biosynthetic potential of Red Sea nudibranch microbiomes Samar M. Abdelrahman1,2, Nastassia V. Patin3,4, Amro Hanora5, Akram Aboseidah2, Shimaa Desoky2, Salha G. Desoky2, Frank J. Stewart3,4,6 and Nicole B. Lopanik1,3 1 School of Earth and Atmospheric Sciences, Georgia Institute of Technology, Atlanta, GA, USA 2 Faculty of Science, Suez University, Suez, Egypt 3 School of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, USA 4 Center for Microbial Dynamics and Infection, Georgia Institute of Technology, Atlanta, GA, USA 5 Faculty of Pharmacy, Suez Canal University, Ismailia, Egypt 6 Department of Microbiology and Immunology, Montana State University, Bozeman, MT, USA ABSTRACT Background: Antibiotic resistance is a growing problem that can be ameliorated by the discovery of novel drug candidates. Bacterial associates are often the source of pharmaceutically active natural products isolated from marine invertebrates, and thus, important targets for drug discovery. While the microbiomes of many marine organisms have been extensively studied, microbial communities from chemically-rich nudibranchs, marine invertebrates that often possess chemical defences, are relatively unknown. Methods: We applied both culture-dependent and independent approaches to better understand the biochemical potential of microbial communities associated with nudibranchs. Gram-positive microorganisms isolated from nudibranchs collected in the Red Sea were screened for antibacterial and antitumor activity. To assess their biochemical potential, the isolates were screened for the presence of natural product biosynthetic gene clusters, including polyketide synthase (PKS) and Submitted 6 August 2020 non-ribosomal peptide synthetase (NRPS) genes, using PCR. The microbiomes of Accepted 18 November 2020 the nudibranchs were investigated by high-throughput sequencing of 16S rRNA Published 4 February 2021 amplicons. -
Genome Diversity of Spore-Forming Firmicutes MICHAEL Y
Genome Diversity of Spore-Forming Firmicutes MICHAEL Y. GALPERIN National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD 20894 ABSTRACT Formation of heat-resistant endospores is a specific Vibrio subtilis (and also Vibrio bacillus), Ferdinand Cohn property of the members of the phylum Firmicutes (low-G+C assigned it to the genus Bacillus and family Bacillaceae, Gram-positive bacteria). It is found in representatives of four specifically noting the existence of heat-sensitive vegeta- different classes of Firmicutes, Bacilli, Clostridia, Erysipelotrichia, tive cells and heat-resistant endospores (see reference 1). and Negativicutes, which all encode similar sets of core sporulation fi proteins. Each of these classes also includes non-spore-forming Soon after that, Robert Koch identi ed Bacillus anthracis organisms that sometimes belong to the same genus or even as the causative agent of anthrax in cattle and the species as their spore-forming relatives. This chapter reviews the endospores as a means of the propagation of this orga- diversity of the members of phylum Firmicutes, its current taxon- nism among its hosts. In subsequent studies, the ability to omy, and the status of genome-sequencing projects for various form endospores, the specific purple staining by crystal subgroups within the phylum. It also discusses the evolution of the violet-iodine (Gram-positive staining, reflecting the pres- Firmicutes from their apparently spore-forming common ancestor ence of a thick peptidoglycan layer and the absence of and the independent loss of sporulation genes in several different lineages (staphylococci, streptococci, listeria, lactobacilli, an outer membrane), and the relatively low (typically ruminococci) in the course of their adaptation to the saprophytic less than 50%) molar fraction of guanine and cytosine lifestyle in a nutrient-rich environment. -
Complete Genome Sequence and Function Gene Identify of Prometryne-Degrading Strain Pseudomonas Sp
microorganisms Article Complete Genome Sequence and Function Gene Identify of Prometryne-Degrading Strain Pseudomonas sp. DY-1 Dong Liang 1,† , Changyixin Xiao 1,† , Fuping Song 2, Haitao Li 1 , Rongmei Liu 1,* and Jiguo Gao 1,* 1 College of Life Science, Northeast Agricultural University, Harbin 150038, China; [email protected] (D.L.); [email protected] (C.X.); [email protected] (H.L.) 2 State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing 100193, China; [email protected] * Correspondence: [email protected] (R.L.); [email protected] (J.G.); Tel.: +86-133-5999-0992 (J.G.) † These authors contributed equally to this work. Abstract: The genus Pseudomonas is widely recognized for its potential for environmental reme- diation and plant growth promotion. Pseudomonas sp. DY-1 was isolated from the agricultural soil contaminated five years by prometryne, it manifested an outstanding prometryne degradation efficiency and an untapped potential for plant resistance improvement. Thus, it is meaningful to comprehend the genetic background for strain DY-1. The whole genome sequence of this strain revealed a series of environment adaptive and plant beneficial genes which involved in environmen- tal stress response, heavy metal or metalloid resistance, nitrate dissimilatory reduction, riboflavin synthesis, and iron acquisition. Detailed analyses presented the potential of strain DY-1 for degrad- ing various organic compounds via a homogenized pathway or the protocatechuate and catechol branches of the β-ketoadipate pathway. In addition, heterologous expression, and high efficiency Citation: Liang, D.; Xiao, C.; Song, F.; liquid chromatography (HPLC) confirmed that prometryne could be oxidized by a Baeyer-Villiger Li, H.; Liu, R.; Gao, J. -
Fruit Wastes
IJAMBR 3 (2015) 96-103 ISSN 2053-1818 Bacterial quality of postharvest Irvingia gabonensis (Aubry-Lecomte ex O’Rorke) fruit wastes Ebimieowei Etebu* and Gloria Tungbulu Department of Biological Sciences, Niger Delta University, Wilberforce Island, Bayelsa State, Nigeria. Article History ABSTRACT Received 01 October, 2015 Irvingia gabonensis is an economically important fruit tree. Although the fungal Received in revised form 28 postharvest quality of its fruits have been studied, bacteria associated with its October, 2015 Accepted 03 November, 2015 decay are yet unknown. Hence in this research, the bacterial quality of Irvingia fruit wastes was studied during 0, 3, 6 and 9 days after harvest (DAH). The Keywords: results obtained show that postharvest I. gabonensis fruits decayed with time. Irvingia gabonensis, Fruit weight and pH were significantly (P=0.05) influenced by DAH. Mean fruit Bacterial species weight at 0, 3, 6 and 9 DAH was 31.99, 29.46, 26.56 and 23.37 g respectively. Postharvest, Mean pH value decreased from 6.42 at 0 DAH to 6.31, 6.22 and 6.17 at 3, 6 and 9 Decay, DAH respectively. Phylogenetic analysis of 16S rRNA partial gene sequences Phylogenetic analysis. showed that bacterial species related to Bacillus, Enterobacter, Oceanobacillus and Staphylococcus were obtained from I. gabonensis fruits up to 3 DAH but not beyond. Whilst recommending proper washing of fresh Irvingia fruits to avoid Article Type: food poisoning, findings of this work offer the potential use of I. gabonensis fruit Full Length Research Article wastes as substrate for antibiotics production. ©2015 BluePen Journals Ltd. All rights reserved INTRODUCTION Irvingia gabonensis (Aubry-Lecomte ex O’Rorke) is a most known uses and is therefore considered the most highly, economically important fruit tree native to most valuable component of the fruit. -
Patterns of Horizontal Gene Transfer Into the Geobacillus Clade
Imperial College London London Institute of Medical Sciences Patterns of Horizontal Gene Transfer into the Geobacillus Clade Alexander Dmitriyevich Esin September 2018 Submitted in part fulfilment of the requirements for the degree of Doctor of Philosophy of Imperial College London For my grandmother, Marina. Without you I would have never been on this path. Your unwavering strength, love, and fierce intellect inspired me from childhood and your memory will always be with me. 2 Declaration I declare that the work presented in this submission has been undertaken by me, including all analyses performed. To the best of my knowledge it contains no material previously published or presented by others, nor material which has been accepted for any other degree of any university or other institute of higher learning, except where due acknowledgement is made in the text. 3 The copyright of this thesis rests with the author and is made available under a Creative Commons Attribution Non-Commercial No Derivatives licence. Researchers are free to copy, distribute or transmit the thesis on the condition that they attribute it, that they do not use it for commercial purposes and that they do not alter, transform or build upon it. For any reuse or redistribution, researchers must make clear to others the licence terms of this work. 4 Abstract Horizontal gene transfer (HGT) is the major driver behind rapid bacterial adaptation to a host of diverse environments and conditions. Successful HGT is dependent on overcoming a number of barriers on transfer to a new host, one of which is adhering to the adaptive architecture of the recipient genome. -
Isolation and Diversity of Sediment Bacteria in The
bioRxiv preprint doi: https://doi.org/10.1101/638304; this version posted May 14, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. 1 Isolation and Diversity of Sediment Bacteria in the 2 Hypersaline Aiding Lake, China 3 4 Tong-Wei Guan, Yi-Jin Lin, Meng-Ying Ou, Ke-Bao Chen 5 6 7 Institute of Microbiology, Xihua University, Chengdu 610039, P. R. China. 8 9 Author for correspondence: 10 Tong-Wei Guan 11 Tel/Fax: +86 028 87720552 12 E-mail: [email protected] 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 bioRxiv preprint doi: https://doi.org/10.1101/638304; this version posted May 14, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. 29 Abstract A total of 343 bacteria from sediment samples of Aiding Lake, China, were isolated using 30 nine different media with 5% or 15% (w/v) NaCl. The number of species and genera of bacteria recovered 31 from the different media significantly varied, indicating the need to optimize the isolation conditions. 32 The results showed an unexpected level of bacterial diversity, with four phyla (Firmicutes, 33 Actinobacteria, Proteobacteria, and Rhodothermaeota), fourteen orders (Actinopolysporales, 34 Alteromonadales, Bacillales, Balneolales, Chromatiales, Glycomycetales, Jiangellales, Micrococcales, 35 Micromonosporales, Oceanospirillales, Pseudonocardiales, Rhizobiales, Streptomycetales, and 36 Streptosporangiales), including 17 families, 41 genera, and 71 species. -
Research Article Review Jmb
J. Microbiol. Biotechnol. (2017), 27(0), 1–5 https://doi.org/10.4014/jmb.1712.12006 Research Article Review jmb Fig. S1. Circular genomic map of B. s. subtilis KCTC 3135T by CLgenomics ver. 1.55. From the outer circle to the inward circle, the circle indicates rRNA and/or tRNA, reverse CDS, forward CDS, GC skew and the GC ratio. A 2017 ⎪ Vol. 27⎪ No. 0 2Name et al. Fig. S2. OrthoANI distance Neighbor-Joining tree with 60 strains (extended OrthoANI tree). A neighbor-joining tree based on the OrthoANI distance matrix. B. subtilis with three subspecies contains 59 genomes and S. aureus subsp. aureus DSM 20231T was used as an outgroup. The scale bar indicates the sequence divergence. J. Microbiol. Biotechnol. Title 3 Fig. S3. The tarABD MLST NJ tree and heatmap with 60 strains (extended NJ tree). A) Phylogenetic tree using the tarABD Multilocus sequence analysis (MLSA) Neighbor-Joining (NJ) tree and B) heatmap based on the similarities of the tarABD from B. subtilis genome to the reference tar or tag genes. B. subtilis with three subspecies contains 59 genomes and S. aureus subsp. aureus DSM 20231T was used for outgroup. Bootstrap values (>70%) based on 1000 replicates are shown at branch nodes. The brand nodes also recovered maximum-likelihood (ML) and maximum-parsimony (MP) trees are marked by the filled black circles. The bar indicates nucleotide substitution rate in given length of the scale. The color indicated the tblastn nucleotide similarities to reference tar (red) or tag (green) genes. A 2017 ⎪ Vol. 27⎪ No. 0 4Name et al. -
Nicotinamidase from Oceanobacillus Iheyensis HTE831
Biochemical and Mutational Analysis of a Novel Nicotinamidase from Oceanobacillus iheyensis HTE831 Guiomar Sa´nchez-Carro´ n1, Marı´a Inmaculada Garcı´a-Garcı´a1,2, Rube´n Zapata-Pe´rez1, Hideto Takami3, Francisco Garcı´a-Carmona1,2,A´ lvaro Sa´nchez-Ferrer1,2* 1 Department of Biochemistry and Molecular Biology-A, Faculty of Biology, Regional Campus of International Excellence ‘‘Campus Mare Nostrum’’, University of Murcia, Campus Espinardo, Murcia, Spain, 2 Murcia Biomedical Research Institute (IMIB), Murcia, Spain, 3 Microbial Genome Research Group, Institute of Biogeosciences, Japan Agency for Marine-Earth Science and Technology (JAMSTEC), Yokosuka, Kanagawa, Japan Abstract Nicotinamidases catalyze the hydrolysis of nicotinamide to nicotinic acid and ammonia, an important reaction in the NAD+ salvage pathway. This paper reports a new nicotinamidase from the deep-sea extremely halotolerant and alkaliphilic Oceanobacillus iheyensis HTE831 (OiNIC). The enzyme was active towards nicotinamide and several analogues, including the 21 21 prodrug pyrazinamide. The enzyme was more nicotinamidase (kcat/Km = 43.5 mM s ) than pyrazinamidase (kcat/ 21 21 Km = 3.2 mM s ). Mutational analysis was carried out on seven critical amino acids, confirming for the first time the importance of Cys133 and Phe68 residues for increasing pyrazinamidase activity 2.9- and 2.5-fold, respectively. In addition, the change in the fourth residue involved in the ion metal binding (Glu65) was detrimental to pyrazinamidase activity, decreasing it 6-fold. This residue was also involved in a new distinct structural motif DAHXXXDXXHPE described in this paper for Firmicutes nicotinamidases. Phylogenetic analysis revealed that OiNIC is the first nicotinamidase described for the order Bacillales.