Frigoribacterium Faeni Gen. Nov., Sp. Nov., a Novel Psychrophilic Genus of the Family Microbacteriaceae

Total Page:16

File Type:pdf, Size:1020Kb

Frigoribacterium Faeni Gen. Nov., Sp. Nov., a Novel Psychrophilic Genus of the Family Microbacteriaceae International Journal of Systematic and Evolutionary Microbiology (2000), 50, 355–363 Printed in Great Britain Frigoribacterium faeni gen. nov., sp. nov., a novel psychrophilic genus of the family Microbacteriaceae P. Ka$ mpfer,1 F. A. Rainey,2,6 M. A. Andersson,3 E.-L. Nurmiaho Lassila,4 U. Ulrych,5 H.-J. Busse,5 N. Weiss,6 R. Mikkola3 and M. Salkinoja-Salonen3 Author for correspondence: P. Ka$ mpfer. Tel: ­49 641 99 37352. Fax: ­49 641 99 37359. e-mail: peter.kaempfer!agrar.uni-giessen.de 1 Institut fu$ r Angewandte The taxonomic position of five actinobacterial strains isolated from dust, an Mikrobiologie, Justus- animal shed, the air inside a museum and soil was investigated using a Liebig Universita$ t, Senckenbergstr. 3, D-35390 polyphasic approach. The growth characteristics were unusual for Giessen, Germany actinomycetes. Optimal growth was at temperatures ranging from 2 to 10 SC. 2 Department of Biological After small-step adaptation (5 SC steps) to higher temperatures, the strains Sciences, 508 Life Sciences were also able to grow at 20 SC. Cell wall analyses revealed that the organisms Building, Louisiana State showed a hitherto undescribed, new group B-type peptidoglycan [type B2β University, Baton Rouge, LA 70803, USA according to Schleifer & Kandler (1972), but with lysine instead of ornithine]. All strains contained menaquinone MK-9. Mycolic acids were not detected. 3 Department of Applied Chemistry and Diphosphatidylglycerol, phosphatidylglycerol and an unknown glycolipid were Microbiology, PO Box 56 detected in the polar lipid extracts. The main fatty acids were 12-methyl- (Biocentre) 00014 tetradecanoic acid (15:0anteiso), 12-methyl-tetradecenoic acid (15:1anteiso), University of Helsinki, Finland 14-methyl-pentadecanoic acid (16:0iso) and 14-methyl-hexadecanoic acid (17:0iso), as well as an unusual compound identified as 1,1-dimethoxy-anteiso- 4 Department of Bioscience, PO Box 56 (Biocentre) pentadecane (15:0anteiso-DMA). The GMC content of DNA was approximately 00014 University of 71 mol%. The results of 16S rRNA gene sequence comparisons revealed that Helsinki, Finland the strains represent a new lineage in the suborder Micrococcineae and the 5 Institut fu$ r Bakteriologie, family Microbacteriaceae of the order Actinomycetales. On the basis of these Mykologie und Hygiene, results the new genus Frigoribacterium gen. nov. is proposed, harbouring the Veterinarmedizinische $ T T Universita$ t Wien, new species Frigoribacterium faeni sp. nov. (type strain ¯ 801 ¯ DSM 10309 ). Veterina$ rplatz 1, A-1210 Wien, Austria 6 DSMZ-Deutsche Sammlung Keywords: Frigoribacterium gen. nov., psychrophilic genus of the family von Mikroorganismen und Microbacteriaceae, 16S rDNA, chemotaxonomy Zellkulturen GmbH, D-38124 Braunschweig, Germany INTRODUCTION 1996) and Cryobacterium (Suzuki et al., 1997) were also shown to represent new branches within the The family Microbacteriaceae was proposed by Park et family Microbacteriaceae. The type genus Micro- al. (1993) to accommodate the Gram-positive genera bacterium was redefined by Takeuchi & Hatano (1998), Agromyces, Aureobacterium, Clavibacter, Curtobac- who proposed the unification of the genera Micro- terium and Microbacterium. On the basis of 16S rRNA bacterium and Aureobacterium on the basis of 16S sequence data, Stackebrandt et al. (1997) redefined the rRNA sequence data and chemotaxonomic data. A family to accommodate the above-mentioned genera common feature of the eight currently recognized in addition to the genera Agrococcus and Rathayi- genera within the family Microbacteriaceae is the bacter. The new genera Leucobacter (Takeuchi et al., group B-type peptidoglycan. In this type the di- carboxyl amino acid (in most cases -glutamate or - ................................................................................................................................................. hydroxyglutamate) at position 2 is linked with the Abbreviations: DMA, dimethyl acetal; ECL, equivalent chain length; FAME, fatty acid methyl ester. amino acid at position 4 (-alanine) via an interpep- The EMBL accession numbers for the 16S rRNA gene sequences of strains tide bridge containing a -amino acid. Very recently, 801, NS 4, 227, 301 and 312 are Y18807, AJ243012, AF157478, AF157479 the occurrence of psychrophilic organisms within and AF157480, respectively. the family Microbacteriaceae has been shown with the 01194 # 2000 IUMS 355 P. Ka$ mpfer and others description of the genus Cryobacterium (Suzuki et al., microtitre plates were done as described earlier (Ka$ mpfer et 1997). In an extensive study of bacteria collected from al., 1991, 1997). Tests were read after 7 d at 20 mC. dust samples and animal sheds (Andersson et al., 1999) Chemotaxonomy. Preparation of cell walls and determi- four isolates were obtained which revealed atypical nation of peptidoglycan structure were carried out by the growth characteristics. This was also found for a strain methods described by Schleifer & Kandler (1972) with the isolated from the Sainsbury Center for Visual Arts in modification that TLC on cellulose sheets was used instead Norwich, UK. All of them showed initially good of paper chromatography. Briefly, 1 mg freeze-dried cell growth at 2–10 mC but only moderate growth at walls were hydrolysed in 0±2 ml 4 M HCl at 100 mC for 16 h 25 mC. A detailed study of the cell wall type revealed an (total hydrolysate) or 45 min (partial hydrolysate). Di- interesting hitherto undescribed B-type. amino acids were identified from total hydrolysate by one- dimensional chromatography in the solvent system meth- In this paper we describe the morphological, physio- anol}pyridine}water}10 M HCl (320:40:70:10 by vol.). logical, chemotaxonomic and phylogenetic charac- Amino acids and peptides from partial hydrolysate were teristics of these organisms. On the basis of our results identified after two-dimensional chromatography in the and the unique taxonomic properties of the organisms, systems described by Schleifer & Kandler (1972) by their it can be concluded that they represent a new genus for mobilities and staining characteristics with ninhydrin spray. The resulting ‘fingerprints’ could be compared with known which we propose the genus name Frigoribacterium peptidoglycan structures. The configuration of lysine was gen. nov. and the new species Frigoribacterium faeni determined by using -lysine decarboxylase (Sigma; L 0882). sp. nov. Cell wall acyl type was determined by the method of Uchida & Aida (1977). METHODS Extraction and analysis of isoprenoid quinones and polar lipids. T Menaquinones were extracted and analysed as de- Sampling and isolation. Strains 301, 312 and 801 were scribed by Tindall (1990). Polar lipids were extracted and isolated from airborne dust in a cattle barn in Southern analysed by TLC according to Ventosa et al. (1993). Finland. Dusts aerosolized during the distribution and handling of feed and bedding were collected on nuclepore Preparation and analysis of fatty acids and fatty acetals. filters as described by Palmgren et al. (1986). The cow barn Fatty acid methyl esters (FAMEs) were determined ac- aerosols were collected for 10 min on nuclepore filters with cording to Ka$ mpfer et al. (1997), except that the cells were a nominal pore size of 0 2 µm, using a low flow personal grown at 28 mC. DMAs (dimethyl acetals) were preliminarily ± " sampling pump precalibrated to a flow of 2 l min− . Sam- identified from the extracts prepared for FAME analysis pling was carried out at a distance of 0±4 m from the bales of using the MIDI anaerobic library (BHIBLA, Version 3.8). hay and straw opened while the air contained clouds of The identity of the DMA in Frigoribacterium strains was visible dust. Strain 227 was isolated from settled dust. Settled confirmed by GC-MS analysis using an HP 5MS capillary dusts were collected from horizontal surfaces in the animal column, an HP 6890 gas chromatograph and an HP 6890 sheds " 2 m above the floor. Strain NS 4 was isolated during mass selective detector set at the ionization energy of 70 eV. The temperature was increased from 170 to 270 mC at a rate a sampling campaign for airborne bacteria in the Sainsbury −" Center for Visual Arts in Norwich, UK. It was cultivated on of 5 mC min ; the inlet temperature was 250 mC. The Wiley casein minimal medium (CAS MM; Altenburger et al., 138K and NIST}EPA}NIH mass spectral libraries were 1996) supplemented with cycloheximide and incubated at used for reference. room temperature. Subcultivation was done on PYES Base composition of DNA and DNA–DNA reassociation medium (Altenburger et al., 1996). studies. DNA was isolated by chromatography on hydroxy- Bacteria in settled and airborne dusts were resuscitated by a apatite by the procedure of Cashion et al. (1977). The base method described previously (Andersson et al., 1999) and composition of DNA and the calculation of the G­C ratio cultured on tryptic soy agar at 13–16 mC. The medium and was determined as described by Mesbah et al. (1989) and diluent for serial plating were obtained from Difco unless Tamaoka & Komagata (1984). DNA–DNA reassociation otherwise stated. experiments were performed as described by De Ley et al. (1970), with the modifications described by Huss et al. Morphological characteristics. Cell morphology was ex- (1983), by using a Gilford System model 2600 spectro- amined by phase-contrast microscopy with a light micro- photometer equipped with a model 2527-R thermo- scope (Leitz). Motility was studied by the hanging drop programmer and plotter (Gilford Instruments).
Recommended publications
  • WO 2015/066625 Al 7 May 2015 (07.05.2015) P O P C T
    (12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (10) International Publication Number (43) International Publication Date WO 2015/066625 Al 7 May 2015 (07.05.2015) P O P C T (51) International Patent Classification: (81) Designated States (unless otherwise indicated, for every C12Q 1/04 (2006.01) G01N 33/15 (2006.01) kind of national protection available): AE, AG, AL, AM, AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, (21) International Application Number: BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DK, DM, PCT/US2014/06371 1 DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, (22) International Filing Date: HN, HR, HU, ID, IL, IN, IR, IS, JP, KE, KG, KN, KP, KR, 3 November 20 14 (03 .11.20 14) KZ, LA, LC, LK, LR, LS, LU, LY, MA, MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, OM, (25) Filing Language: English PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, SC, (26) Publication Language: English SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. (30) Priority Data: 61/898,938 1 November 2013 (01. 11.2013) (84) Designated States (unless otherwise indicated, for every kind of regional protection available): ARIPO (BW, GH, (71) Applicant: WASHINGTON UNIVERSITY [US/US] GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, One Brookings Drive, St.
    [Show full text]
  • Table S1. Bacterial Otus from 16S Rrna
    Table S1. Bacterial OTUs from 16S rRNA sequencing analysis including only taxa which were identified to genus level (those OTUs identified as Ambiguous taxa, uncultured bacteria or without genus-level identifications were omitted). OTUs with only a single representative across all samples were also omitted. Taxa are listed from most to least abundant. Pitcher Plant Sample Class Order Family Genus CB1p1 CB1p2 CB1p3 CB1p4 CB5p234 Sp3p2 Sp3p4 Sp3p5 Sp5p23 Sp9p234 sum Gammaproteobacteria Legionellales Coxiellaceae Rickettsiella 1 2 0 1 2 3 60194 497 1038 2 61740 Alphaproteobacteria Rhodospirillales Rhodospirillaceae Azospirillum 686 527 10513 485 11 3 2 7 16494 8201 36929 Sphingobacteriia Sphingobacteriales Sphingobacteriaceae Pedobacter 455 302 873 103 16 19242 279 55 760 1077 23162 Betaproteobacteria Burkholderiales Oxalobacteraceae Duganella 9060 5734 2660 40 1357 280 117 29 129 35 19441 Gammaproteobacteria Pseudomonadales Pseudomonadaceae Pseudomonas 3336 1991 3475 1309 2819 233 1335 1666 3046 218 19428 Betaproteobacteria Burkholderiales Burkholderiaceae Paraburkholderia 0 1 0 1 16051 98 41 140 23 17 16372 Sphingobacteriia Sphingobacteriales Sphingobacteriaceae Mucilaginibacter 77 39 3123 20 2006 324 982 5764 408 21 12764 Gammaproteobacteria Pseudomonadales Moraxellaceae Alkanindiges 9 10 14 7 9632 6 79 518 1183 65 11523 Betaproteobacteria Neisseriales Neisseriaceae Aquitalea 0 0 0 0 1 1577 5715 1471 2141 177 11082 Flavobacteriia Flavobacteriales Flavobacteriaceae Flavobacterium 324 219 8432 533 24 123 7 15 111 324 10112 Alphaproteobacteria
    [Show full text]
  • Corynebacterium Sp.|NML98-0116
    1 Limnochorda_pilosa~GCF_001544015.1@NZ_AP014924=Bacteria-Firmicutes-Limnochordia-Limnochordales-Limnochordaceae-Limnochorda-Limnochorda_pilosa 0,9635 Ammonifex_degensii|KC4~GCF_000024605.1@NC_013385=Bacteria-Firmicutes-Clostridia-Thermoanaerobacterales-Thermoanaerobacteraceae-Ammonifex-Ammonifex_degensii 0,985 Symbiobacterium_thermophilum|IAM14863~GCF_000009905.1@NC_006177=Bacteria-Firmicutes-Clostridia-Clostridiales-Symbiobacteriaceae-Symbiobacterium-Symbiobacterium_thermophilum Varibaculum_timonense~GCF_900169515.1@NZ_LT827020=Bacteria-Actinobacteria-Actinobacteria-Actinomycetales-Actinomycetaceae-Varibaculum-Varibaculum_timonense 1 Rubrobacter_aplysinae~GCF_001029505.1@NZ_LEKH01000003=Bacteria-Actinobacteria-Rubrobacteria-Rubrobacterales-Rubrobacteraceae-Rubrobacter-Rubrobacter_aplysinae 0,975 Rubrobacter_xylanophilus|DSM9941~GCF_000014185.1@NC_008148=Bacteria-Actinobacteria-Rubrobacteria-Rubrobacterales-Rubrobacteraceae-Rubrobacter-Rubrobacter_xylanophilus 1 Rubrobacter_radiotolerans~GCF_000661895.1@NZ_CP007514=Bacteria-Actinobacteria-Rubrobacteria-Rubrobacterales-Rubrobacteraceae-Rubrobacter-Rubrobacter_radiotolerans Actinobacteria_bacterium_rbg_16_64_13~GCA_001768675.1@MELN01000053=Bacteria-Actinobacteria-unknown_class-unknown_order-unknown_family-unknown_genus-Actinobacteria_bacterium_rbg_16_64_13 1 Actinobacteria_bacterium_13_2_20cm_68_14~GCA_001914705.1@MNDB01000040=Bacteria-Actinobacteria-unknown_class-unknown_order-unknown_family-unknown_genus-Actinobacteria_bacterium_13_2_20cm_68_14 1 0,9803 Thermoleophilum_album~GCF_900108055.1@NZ_FNWJ01000001=Bacteria-Actinobacteria-Thermoleophilia-Thermoleophilales-Thermoleophilaceae-Thermoleophilum-Thermoleophilum_album
    [Show full text]
  • Stress-Tolerance and Taxonomy of Culturable Bacterial Communities Isolated from a Central Mojave Desert Soil Sample
    geosciences Article Stress-Tolerance and Taxonomy of Culturable Bacterial Communities Isolated from a Central Mojave Desert Soil Sample Andrey A. Belov 1,*, Vladimir S. Cheptsov 1,2 , Elena A. Vorobyova 1,2, Natalia A. Manucharova 1 and Zakhar S. Ezhelev 1 1 Soil Science Faculty, Lomonosov Moscow State University, Moscow 119991, Russia; [email protected] (V.S.C.); [email protected] (E.A.V.); [email protected] (N.A.M.); [email protected] (Z.S.E.) 2 Space Research Institute, Russian Academy of Sciences, Moscow 119991, Russia * Correspondence: [email protected]; Tel.: +7-917-584-44-07 Received: 28 February 2019; Accepted: 8 April 2019; Published: 10 April 2019 Abstract: The arid Mojave Desert is one of the most significant terrestrial analogue objects for astrobiological research due to its genesis, mineralogy, and climate. However, the knowledge of culturable bacterial communities found in this extreme ecotope’s soil is yet insufficient. Therefore, our research has been aimed to fulfil this lack of knowledge and improve the understanding of functioning of edaphic bacterial communities of the Central Mojave Desert soil. We characterized aerobic heterotrophic soil bacterial communities of the central region of the Mojave Desert. A high total number of prokaryotic cells and a high proportion of culturable forms in the soil studied were observed. Prevalence of Actinobacteria, Proteobacteria, and Firmicutes was discovered. The dominance of pigmented strains in culturable communities and high proportion of thermotolerant and pH-tolerant bacteria were detected. Resistance to a number of salts, including the ones found in Martian regolith, as well as antibiotic resistance, were also estimated.
    [Show full text]
  • 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
    [Show full text]
  • Agrococcus Citreus Sp. Nov., Isolated from a Medieval Wall Painting of the Chapel of Castle Herberstein (Austria)
    International Journal of Systematic Bacteriology (1999), 49, 1165-1 170 Printed in Great Britain Agrococcus citreus sp. nov., isolated from a medieval wall painting of the chapel of Castle Herberstein (Austria) Monika Wieser,'t2 Peter S~humann,~Karin Martin,4 Petra AItenburger,lJ2 Jutta B~rghardt,~Werner Lubitz' and Hans-Jurgen Busse'f2 Author for correspondence: Hans-Jurgen Busse. Tel: +43 1 25077 21 19. Fax: +43 1 25077 2190. e-mail : [email protected] 1 lnstitut fur Mikrobiologie A bacterial strain, D-l/laT,isolated from a medieval wall painting of the chapel und Genetik, Universitat of Herberstein (Styria, Austria) was characterized by a polyphasic approach. Wien, A-1030 Wien, Austria Strain D-l/laTshared 981O!O 165 rRNA sequence similarity to Agrococcus jenensis. The chemotaxonomic characteristics including polar lipid pattern, 2 lnstitut fur Bakteriologie, Mykologie und Hygiene, whole cell sugars, quinone system, polyamine pattern, cell wall composition Veterinarmedizinische and fatty acid profile were in good agreement with those of Agrococcus Universitat, A-1 21 0 Wien, jenensis. The G+C content of the DNA was determined to be 74 mol%. The Austria value of 47 O/O DNA reassociation obtained after DNA-DNA hybridization DSMZ-Deutsche Sammlung between DNA of Agrococcus jenensis and strain D-l/laTas well as differences von Mikroorganismen und Zellkulturen GmbH, in the amino acid composition of the peptidoglycan and in physiological Aussenstelle Jena, characteristics demonstrate that the isolate represents a new species of the Germany genus Agrococcus. The name Agrococcus citreus sp. nov. is proposed for the Hans-Knoll-lnstitut fur new species harbouring isolate D-l/laT.The type strain is DSM 12453T.
    [Show full text]
  • Studies on Antibacterial Activity and Diversity of Cultivable Actinobacteria Isolated from Mangrove Soil in Futian and Maoweihai of China
    Hindawi Evidence-Based Complementary and Alternative Medicine Volume 2019, Article ID 3476567, 11 pages https://doi.org/10.1155/2019/3476567 Research Article Studies on Antibacterial Activity and Diversity of Cultivable Actinobacteria Isolated from Mangrove Soil in Futian and Maoweihai of China Feina Li,1 Shaowei Liu,1 Qinpei Lu,1 Hongyun Zheng,1,2 Ilya A. Osterman,3,4 Dmitry A. Lukyanov,3 Petr V. Sergiev,3,4 Olga A. Dontsova,3,4,5 Shuangshuang Liu,6 Jingjing Ye,1,2 Dalin Huang ,2 and Chenghang Sun 1 1 Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100050, China 2College of Basic Medical Sciences, Guilin Medical University, Guilin 541004, China 3Center of Life Sciences, Skolkovo Institute of Science and Technology, Moscow 143025, Russia 4Department of Chemistry, A.N. Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow 119992, Russia 5Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Te Russian Academy of Sciences, Moscow 117997, Russia 6China Pharmaceutical University, Nanjing 210009, China Correspondence should be addressed to Dalin Huang; [email protected] and Chenghang Sun; [email protected] Received 29 March 2019; Accepted 21 May 2019; Published 9 June 2019 Guest Editor: Jayanta Kumar Patra Copyright © 2019 Feina Li et al. Tis is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Mangrove is a rich and underexploited ecosystem with great microbial diversity for discovery of novel and chemically diverse antimicrobial compounds. Te goal of the study was to explore the pharmaceutical actinobacterial resources from mangrove soil and gain insight into the diversity and novelty of cultivable actinobacteria.
    [Show full text]
  • Agromyces Aurantiacus Sp. Nov., Isolated from a Chinese Primeval Forest
    中国科技论文在线 http://www.paper.edu.cn International Journal of Systematic and Evolutionary Microbiology (2003), 53, 303–307 DOI 10.1099/ijs.0.02350-0 Note Agromyces aurantiacus sp. nov., isolated from a Chinese primeval forest Wen-Jun Li,1 Li-Ping Zhang,1 Ping Xu,1 Xiao-Long Cui,1 Li-Hua Xu,1 Zhongse Zhang,1 Peter Schumann,2 Erko Stackebrandt2 and Cheng-Lin Jiang1 Correspondence 1The Key Laboratory for Microbial Resources of Ministry of Education, PR China, Yunnan Cheng-Lin Jiang Institute of Microbiology, Yunnan University, Kunming, Yunnan 650091, China [email protected] 2DSMZ – Deutsche Sammlung von Mikroorganismen und Zellkulturen, Mascheroder Weg 1b, D-38124 Braunschweig, Germany A catalase-negative actinomycete, strain YIM 21741T, was isolated from a soil sample collected from a primeval forest at Xishuangbanna, Yunnan Province, China. Analysis of 16S rDNA showed the strain to be related to members of the genus Agromyces, with which it also shares morphological characteristics, e.g. branching hyphae breaking into diphtheroid and rod-like, irregular, non-motile fragments and a peptidoglycan containing the diagnostic amino acid 2,4-diamino-n-butyric acid. Whole-cell hydrolysates of strain YIM 21741T contained rhamnose and small quantities of glucose, galactose and mannose. The major menaquinone was MK-12, while MK-13 and MK-12 were minor components. Diagnostic phospholipids were phosphatidylglycerol and diphosphatidylglycerol. The G+C content of the DNA was 72?8 mol%. Physiological and biochemical characteristics reveal strain YIM 21741T to be different from all validly described species of the genus Agromyces. As DNA–DNA similarity values between this isolate and the phylogenetically neighbouring type strains of Agromyces bracchium and Agromyces luteolus are only moderate, the novel species Agromyces aurantiacus sp.
    [Show full text]
  • Aestuariimicrobium Ganziense Sp. Nov., a New Gram-Positive Bacterium Isolated from Soil in the Ganzi Tibetan Autonomous Prefecture, China
    Aestuariimicrobium ganziense sp. nov., a new Gram-positive bacterium isolated from soil in the Ganzi Tibetan Autonomous Prefecture, China Yu Geng Yunnan University Jiang-Yuan Zhao Yunnan University Hui-Ren Yuan Yunnan University Le-Le Li Yunnan University Meng-Liang Wen yunnan university Ming-Gang Li yunnan university Shu-Kun Tang ( [email protected] ) Yunnan Institute of Microbiology, Yunnan University https://orcid.org/0000-0001-9141-6244 Research Article Keywords: Aestuariimicrobium ganziense sp. nov., Chemotaxonomy, 16S rRNA sequence analysis Posted Date: February 11th, 2021 DOI: https://doi.org/10.21203/rs.3.rs-215613/v1 License: This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License Version of Record: A version of this preprint was published at Archives of Microbiology on March 12th, 2021. See the published version at https://doi.org/10.1007/s00203-021-02261-2. Page 1/11 Abstract A novel Gram-stain positive, oval shaped and non-agellated bacterium, designated YIM S02566T, was isolated from alpine soil in Shadui Towns, Ganzi County, Ganzi Tibetan Autonomous Prefecture, Sichuan Province, PR China. Growth occurred at 23–35°C (optimum, 30°C) in the presence of 0.5-4 % (w/v) NaCl (optimum, 1%) and at pH 7.0–8.0 (optimum, pH 7.0). The phylogenetic analysis based on 16S rRNA gene sequence revealed that strain YIM S02566T was most closely related to the genus Aestuariimicrobium, with Aestuariimicrobium kwangyangense R27T and Aestuariimicrobium soli D6T as its closest relative (sequence similarities were 96.3% and 95.4%, respectively). YIM S02566T contained LL-diaminopimelic acid in the cell wall.
    [Show full text]
  • Microbacterium Flavum Sp. Nov. and Microbacterium Lacus Sp. Nov
    Actinomycetologica (2007) 21:53–58 Copyright Ó 2007 The Society for Actinomycetes Japan VOL. 21, NO. 2 Microbacterium flavum sp. nov. and Microbacterium lacus sp. nov., isolated from marine environments. Akiko Kageyama1, Yoko Takahashi1Ã, Yoshihide Matsuo2, Kyoko Adachi2, Hiroaki Kasai2, Yoshikazu Shizuri2 and Satoshi O¯ mura1;3 1Kitasato Institute for Life Sciences, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo 108-8642, Japan. 2Marine Biotechnology Institute, 3-75-1 Heita, Kamaishi, Iwate 026-0001, Japan. 3The Kitasato Institute, 5-9-1 Shirokane, Minato-ku, Tokyo 108-8642, Japan. (Received Feb. 21, 2007 / Accepted Jul. 9, 2007 / Published Sep. 10, 2007) Strains YM18-098T and A5E-52T were both Gram-positive, aerobic, irregular rod-shaped bacteria, with lysine and ornithine as the diagnostic diamino acids of their peptidoglycans, respectively. The acyl type of the peptidoglycan in both cases was N-glycolyl. The major menaquinones were MK-11, -12 and -13. Mycolic acids were not detected. The G+C content of the DNA was 69–70 mol%. Comparative 16S rRNA studies revealed that the isolates belonged to the genus Microbacterium, that YM18-098T was closely related to the species Microbacterium lacticum and Microbacterium schleiferi, and that A5E-52T was closely related to the species Microbacterium aurum, Microbacterium aoyamense, Microbacterium deminutum and Microbacterium pumilum. DNA-DNA relatedness analysis showed that the isolated strains represented two separate genomic species. Based on both phenotypic and genotypic data, the following new species of the genus Microbacterium are proposed: Microbacterium flavum sp. nov. and Microbacterium lacus sp. nov., with the type strains YM18-098T (= MBIC08278T, DSM 18909T) and A5E-52T (= MBIC08279T, DSM 18910T), respectively.
    [Show full text]
  • Lists of Names of Prokaryotic Candidatus Taxa
    NOTIFICATION LIST: CANDIDATUS LIST NO. 1 Oren et al., Int. J. Syst. Evol. Microbiol. DOI 10.1099/ijsem.0.003789 Lists of names of prokaryotic Candidatus taxa Aharon Oren1,*, George M. Garrity2,3, Charles T. Parker3, Maria Chuvochina4 and Martha E. Trujillo5 Abstract We here present annotated lists of names of Candidatus taxa of prokaryotes with ranks between subspecies and class, pro- posed between the mid- 1990s, when the provisional status of Candidatus taxa was first established, and the end of 2018. Where necessary, corrected names are proposed that comply with the current provisions of the International Code of Nomenclature of Prokaryotes and its Orthography appendix. These lists, as well as updated lists of newly published names of Candidatus taxa with additions and corrections to the current lists to be published periodically in the International Journal of Systematic and Evo- lutionary Microbiology, may serve as the basis for the valid publication of the Candidatus names if and when the current propos- als to expand the type material for naming of prokaryotes to also include gene sequences of yet-uncultivated taxa is accepted by the International Committee on Systematics of Prokaryotes. Introduction of the category called Candidatus was first pro- morphology, basis of assignment as Candidatus, habitat, posed by Murray and Schleifer in 1994 [1]. The provisional metabolism and more. However, no such lists have yet been status Candidatus was intended for putative taxa of any rank published in the journal. that could not be described in sufficient details to warrant Currently, the nomenclature of Candidatus taxa is not covered establishment of a novel taxon, usually because of the absence by the rules of the Prokaryotic Code.
    [Show full text]
  • Complete Genome Sequence of Arthrobacter Sp
    Complete genome sequence of Arthrobacter sp. PAMC25564 and comparative genome analysis for elucidating the role of CAZymes in cold adaptation So-Ra Han Sun Moon University Byeollee Kim Sun Moon University Jong Hwa Jang Dankook University Hyun Park Korea University Tae-Jin Oh ( [email protected] ) Sun Moon University Research Article Keywords: Arthrobacter species, CAZyme, cold-adapted bacteria, genetic patterns, glycogen metabolism, trehalose pathway Posted Date: December 16th, 2020 DOI: https://doi.org/10.21203/rs.3.rs-118769/v1 License: This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License Page 1/17 Abstract Background: The Arthrobacter group is a known isolate from cold areas, the species of which are highly likely to play diverse roles in low temperatures. However, their role and survival mechanisms in cold regions such as Antarctica are not yet fully understood. In this study, we compared the genomes of sixteen strains within the Arthrobacter group, including strain PAMC25564, to identify genomic features that adapt and survive life in the cold environment. Results: The genome of Arthrobacter sp. PAMC25564 comprised 4,170,970 bp with 66.74 % GC content, a predicted genomic island, and 3,829 genes. This study provides an insight into the redundancy of CAZymes for potential cold adaptation and suggests that the isolate has glycogen, trehalose, and maltodextrin pathways associated to CAZyme genes. This strain can utilize polysaccharide or carbohydrate degradation as a source of energy. Moreover, this study provides a foundation on which to understand how the Arthrobacter strain produces energy in an extreme environment, and the genetic pattern analysis of CAZymes in cold-adapted bacteria can help to determine how bacteria adapt and survive in such environments.
    [Show full text]