- Mucibacter soli gen. nov., sp. nov., a new member of the family Chitinophagaceae producing mucin
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Min-Kyeong Kim , Sewook Park , Tae-Su Kim , Yochan Joung , Ji-Hye Han , Seung Bum Kim
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J. Microbiol. 2019;57(5):356-361. Published online February 22, 2019
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DOI: https://doi.org/10.1007/s12275-019-8512-1
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A Gram-stain-negative, mucus-forming, motile by gliding,
non-spore-forming and short rod-shaped bacterial strain
designated R1-15T was isolated from soil and its taxonomic
position was evaluated using a polyphasic approach. Strain
R1-15T grew at 15–37°C (optimum, 30°C), at pH 6–7 (optimum,
pH 6) and in the presence of 0–1% (w/v) NaCl (optimum,
0%) on 0.1X TSA. On the basis of 16S rRNA gene sequence
similarity, the novel strain was assigned to the family
Chitinophagaceae of the phylum Bacteroidetes, and its closest
related taxa were species of the genera Taibaiella (88.76–
90.02% sequence similarity), Lacibacter (89.24–90.00%), Chitinophaga
(88.61–89.76%), and Terrimonas (89.04%). Flexirubin-
type pigments were produced. The only isoprenoid
quinone was MK-7, and the major polar lipid was phosphatidylethanolamine.
Based on whole genome comparisons
between the strain R1-15T and the type strains of relatives,
the orthologous average nucleotide identity values were 66.9–
67.0%. The DNA G+C content of strain R1-15T was 43.8
mol%. The combination of phylogenetic, chemotaxonomic
and phenotypic data clearly supported separation of strain
R1-15T from related taxa, and thus the name Mucibacter
soli gen. nov., sp. nov. is proposed. The type strain is R1-15T
(= KCTC 62274T = JCM 31190T).
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- Simplicispira sedimenti sp. nov., isolated from a sediment of drainage ditch in winery
Xing Chen, Yuan-Dong Li, Xiu-Ming Liu, Li Gao, Xing-Kui Zhou, Li-Min Dong, Gang Du, Neeli Habib, Wen-Jun Li, Yan-Qing Duan Antonie van Leeuwenhoek.2024;[Epub] CrossRef - Saline soil improvement promotes the transformation of microbial salt tolerance mechanisms and microbial-plant-animal ecological interactions
Keyu Yao, Guanghao Wang, Wen Zhang, Qiang Liu, Jian Hu, Mao Ye, Xin Jiang Journal of Environmental Management.2024; 372: 123360. CrossRef - Cast from the Past? Microbial Diversity of a Neolithic Stone Circle
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International Journal of Systematic and Evolutionary Microbiology
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- Diversity and Physiological Properties of Root Endophytic Actinobacteria in Native Herbaceous Plants of Korea
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Tae-Ui Kim , Sung-Heun Cho , Ji-Hye Han , Young Min Shin , Hyang Burm Lee , Seung Bum Kim
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J. Microbiol. 2012;50(1):50-57. Published online February 27, 2012
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DOI: https://doi.org/10.1007/s12275-012-1417-x
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950
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Endophytic actinobacterial diversity in the native herbaceous
plant species of Korea was analyzed using a culturebased
approach. Sixty one actinobacterial strains were isolated,
and assigned to 15 genera based on 16S rRNA gene
analysis. The members of the genus Streptomyces comprised
45.9% of the total isolates, followed by Micromonospora
(18.8%), Rhodococcus (6.6%), Microbispora (4.9%), and
Micrococcus (4.9%). Other minor constituents included
members of Microbacterium, Streptacidiphilus, Arthrobacter,
Dietzia, Kitasatospora, Herbiconiux, Mycobacterium, Nocardia,
Rathayibacter, and Tsukamurella. Among the isolates, 65.6%
exhibited at least one hydrolytic enzyme activity out of four,
and 45.9% exhibited antagonistic activity against at least
one fungal pathogen out of five, thus demonstrating that
endophytic actinobacteria can be an important source of
bioactive compounds. Notably, most strains of Streptomyces
proved active for both enzymatic and antagonistic activities.
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Shruti Agrawal, Arun Bhatt Current Microbiology.2023;[Epub] CrossRef - The characteristics of actinomyces strptomyces griseorubiginosus 83 – the effective biosorbent of silver
Nigora Bekmukhamedova, Khurshida Khamidova, A. Muratov, S. Khasanov E3S Web of Conferences.2023; 371: 01038. CrossRef - Endophytic bacteria of wheat and the potential to improve microelement composition of grain
O. O. Makar, N. D. Romanyuk Studia Biologica.2022; 16(3): 101. CrossRef - Isolation and identification of endophytic actinobacteria from Citrullus colocynthis (L.) Schrad and their antibacterial properties
Aram R. Ali, Yadollah Bahrami, Elham Kakaei, Sara Mohammadzadeh, Sasan Bouk, Nastaran Jalilian Microbial Cell Factories.2022;[Epub] CrossRef - Comparative Secretome Analyses of Toxigenic and AtoxigenicRathayibacterSpecies
Matthew A. Tancos, Michael B. McMahon, Wesley M. Garrett, Douglas G. Luster, Elizabeth E. Rogers Phytopathology®.2021; 111(9): 1530. CrossRef - Evaluation of Rpf protein of Micrococcus luteus for cultivation of soil actinobacteria
Yuhui Wang, Jiangli Shi, Lingjie Tang, Yufan Zhang, Yujia Zhang, Xinyu Wang, Xiumin Zhang Systematic and Applied Microbiology.2021; 44(5): 126234. CrossRef - Diversity and function of culturable actinobacteria in the root-associated of Salvia miltiorrhiza Bunge
Yu-Rui Wu, Cui-Bai Li, Yan-Hong Wu, Lan Li, Bo Li, Wen-Bo Li, Bu-Jin Ma, Zhu-Yun Yan PeerJ.2021; 9: e11749. CrossRef - Diversity and Antimicrobial Potential of Cultivable Endophytic Actinobacteria Associated With the Medicinal Plant Thymus roseus
Zulpiya Musa, Jinbiao Ma, Dilfuza Egamberdieva, Osama Abdalla Abdelshafy Mohamad, Gulsumay Abaydulla, Yonghong Liu, Wen-Jun Li, Li Li Frontiers in Microbiology.2020;[Epub] CrossRef - Seasonal Variation Influence Endophytic Actinobacterial Communities of Medicinal Plants from Tropical Deciduous Forest of Meghalaya and Characterization of Their Plant Growth-Promoting Potentials
Dina Barman, Mamtaj S. Dkhar Current Microbiology.2020; 77(8): 1689. CrossRef - Molecular and biotechnological aspects of secondary metabolites in actinobacteria
Richa Salwan, Vivek Sharma Microbiological Research.2020; 231: 126374. CrossRef - Isolation and screening of actinomycetes producing cellulase and xylanase from Mamasa soil, West Sulawesi
A L Putri, R Setiawan IOP Conference Series: Earth and Environmental Science.2019; 308(1): 012035. CrossRef - Plant Growth-Promoting Potential of Endophytic Bacteria Isolated from Costus speciosus in Tropical Deciduous Forest of Eastern Himalaya
Dina Barman, Mamtaj S. Dkhar Proceedings of the National Academy of Sciences, India Section B: Biological Sciences.2019; 89(3): 841. CrossRef - Endophyte: Understanding the Microbes and its Applications
Raymond Oriebe Anyasi, Harrison Ifeanyichuk Atagana Pakistan Journal of Biological Sciences.2019; 22(4): 154. CrossRef - Inter- and intracellular colonization of Arabidopsis roots by endophytic actinobacteria and the impact of plant hormones on their antimicrobial activity
Anne van der Meij, Joost Willemse, Martinus A. Schneijderberg, René Geurts, Jos M. Raaijmakers, Gilles P. van Wezel Antonie van Leeuwenhoek.2018; 111(5): 679. CrossRef - Bioprospection of actinobacteria derived from freshwater sediments for their potential to produce antimicrobial compounds
Zothanpuia, Ajit Kumar Passari, Vincent Vineeth Leo, Preeti Chandra, Brijesh Kumar, Chandra Nayak, Abeer Hashem, Elsayed Fathi Abd_Allah, Abdulaziz A. Alqarawi, Bhim Pratap Singh Microbial Cell Factories.2018;[Epub] CrossRef - Endophytic actinobacteria: Diversity, secondary metabolism and mechanisms to unsilence biosynthetic gene clusters
Raghavan Dinesh, Veeraraghavan Srinivasan, Sheeja T. E., Muthuswamy Anandaraj, Hamza Srambikkal Critical Reviews in Microbiology.2017; 43(5): 546. CrossRef - RETRACTED: Production of Potent Antimicrobial Compounds from Streptomyces cyaneofuscatus Associated with Fresh Water Sediment
Zothanpuia, Ajit K. Passari, Preeti Chandra, Vincent V. Leo, Vineet K. Mishra, Brijesh Kumar, Bhim P. Singh Frontiers in Microbiology.2017;[Epub] CrossRef - Arthrobacter pokkalii sp nov, a Novel Plant Associated Actinobacterium with Plant Beneficial Properties, Isolated from Saline Tolerant Pokkali Rice, Kerala, India
Ramya Krishnan, Rahul Ravikumar Menon, Naoto Tanaka, Hans-Jürgen Busse, Srinivasan Krishnamurthi, Natarajan Rameshkumar, Pankaj Kumar Arora PLOS ONE.2016; 11(3): e0150322. CrossRef - Diversity of Culturable Plant Growth-Promoting Bacterial Endophytes Associated with Sugarcane Roots and Their Effect of Growth by Co-Inoculation of Diazotrophs and Actinomycetes
Worarat Kruasuwan, Arinthip Thamchaipenet Journal of Plant Growth Regulation.2016; 35(4): 1074. CrossRef - Distribution and Identification of Endophytic Streptomyces Species from Schima wallichii as Potential Biocontrol Agents against Fungal Plant Pathogens
AJIT KUMAR PASSARI, VINEET KUMAR MISHRA, VIJAI KUMAR GUPTA, RATUL SAIKIA, BHIM PRATAP SINGH Polish Journal of Microbiology.2016; 65(3): 319. CrossRef - Isolation and antimicrobial activities of actinobacteria closely associated with liquorice plants Glycyrrhiza glabra L. and Glycyrrhiza inflate BAT. in Xinjiang, China
Ke Zhao, Chong Zhao, Ping Liao, Qin Zhang, Yanbing Li, Maoke Liu, Xiaoling Ao, Yunfu Gu, Decong Liao, Kaiwei Xu, Xiumei Yu, Quanju Xiang, Chengyi Huang, Qiang Chen, Lili Zhang, Xiaoping Zhang, Petri Penttinen Microbiology.2016; 162(7): 1135. CrossRef - Continuing hunt for endophytic actinomycetes as a source of novel biologically active metabolites
Meeta Masand, Polpass Arul Jose, Ekta Menghani, Solomon Robinson David Jebakumar World Journal of Microbiology and Biotechnology.2015; 31(12): 1863. CrossRef - Endophytic Actinobacteria and the Interaction of Micromonospora and Nitrogen Fixing Plants
Martha E. Trujillo, Raúl Riesco, Patricia Benito, Lorena Carro Frontiers in Microbiology.2015;[Epub] CrossRef - Biodiversity and plant growth promoting traits of culturable endophytic actinobacteria associated with Jatropha curcas L. growing in Panxi dry-hot valley soil
Sheng Qin, Qian Miao, Wei-Wei Feng, Yu Wang, Xiao Zhu, Ke Xing, Ji-Hong Jiang Applied Soil Ecology.2015; 93: 47. CrossRef - Isolation, abundance and phylogenetic affiliation of endophytic actinomycetes associated with medicinal plants and screening for their in vitro antimicrobial biosynthetic potential
Ajit K. Passari, Vineet K. Mishra, Ratul Saikia, Vijai K. Gupta, Bhim P. Singh Frontiers in Microbiology.2015;[Epub] CrossRef - Microbispora sp. LGMB259 Endophytic Actinomycete Isolated from Vochysia divergens (Pantanal, Brazil) Producing β-Carbolines and Indoles with Biological Activity
Daiani C. Savi, Khaled A. Shaaban, Nathalia Vargas, Larissa V. Ponomareva, Yvelise M. Possiede, Jon S. Thorson, Chirlei Glienke, Jürgen Rohr Current Microbiology.2015; 70(3): 345. CrossRef - Endophytic microorganisms—promising applications in bioremediation of greenhouse gases
Z. Stępniewska, A. Kuźniar Applied Microbiology and Biotechnology.2013; 97(22): 9589. CrossRef - Micromonospora is a normal occupant of actinorhizal nodules
Lorena Carro, Petar Pujic, Martha E Trujillo, Philippe Normand Journal of Biosciences.2013; 38(4): 685. CrossRef
- Comparison of Bacterial Composition between Human Saliva and Dental Unit Water System
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Eun-Hyoung Jeon , Ji-Hye Han , Tae-Young Ahn
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J. Microbiol. 2007;45(1):1-5.
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DOI: https://doi.org/2500 [pii]
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Abstract
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The bacterial compositions between the dental unit water system and human saliva were characterized and compared by direct sequence analysis of 16S rDNA clone libraries. Based on the species richness estimation, bacterial diversity in the dental unit water system (DUW) was more diverse than that of the human saliva (HS). The Chao1 estimates of species richness in HS and DUW samples were 12.0 and 72.4, respectively. The total numbers of OTUs observed in the combined libraries accounted for 83% (HS) and 59% (DUW) of the Chao1 diversity estimate as defined at the 80% similarity threshold. Based on the sequence analysis, the phylum Proteobacteria was the major group in both clone libraries at phylum level. DUW clone library contained 80.0% Proteobacteria, 8.0% Bacteroides, 4.0% Nitrospira, 4.0% Firmicutes, 2.0% Planctomycetes and 2.0% Acidobacteria. On the other hand, human saliva (HS) clone library contained 55.5% Proteobacteria, 36.1% Firmicutes and 8.4% Bacteroides. The majority of bacteria identified belonged to phylum Proteobacteria in both samples. In dental unit water system (DUW), Alphaproteobacteria was detected as the major group. There was no evidence of the bacterial contamination due to a dental treatment. Most sequences were related to microorganisms derived from biofilm in oligotrophic environments.
- Phylogenetic Diversity of Acidophilic Sporoactinobacteria Isolated from Various Soils
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Sung-Heun Cho , Ji-Hye Han , Chi Nam Seong , Seung Bum Kim
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J. Microbiol. 2006;44(6):600-606.
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DOI: https://doi.org/2468 [pii]
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Abstract
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Spore forming actinobacteria (sporoactinobacteria) isolated from soils with an acidic pH in Pinus thunbergii forests and coal mine waste were subjected to taxonomic characterization. For the isolation of acidophilic actinobacteria, acidified starch casein agar (pH adjusted to 4-5) was used. The numbers of actinobacteria growing in acidic media were between 3.2 × 104 and 8.0 × 106 CFU/g soil. Forty three acidophilic actinobacterial strains were isolated and their 16S rDNA sequences were determined. The isolates were divided into eight distinctive phylogenetic clusters within the variation encompassed by the family Streptomycetaceae. Four clusters among them were assigned to the genus Streptacidiphilus, whereas the remaining four were assigned to Streptomyces. The clusters belonging to either Streptomyces or Streptacidiphilus did not form monophyletic clade. The growth pH profiles indicated that the representative isolates grew best between pH 5 and 6. It is evident from this study that acidity has played a critical role in the differentiation of the family Streptomycetaceae, and also that different mechanisms might have resulted in the evolution of two groups, Streptacidiphilus (strict acidophiles) and neutrotolerant acidophilic Streptomyces. The effect of geographic separation was clearly seen among the Streptacidiphilus isolates, which may be a key factor in speciation of the genus.
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