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Duck-Chul Oh 6 Articles
Lysinibacillus jejuensis sp. nov., Isolated from Swinery Waste
Ji-Young Kim , So-Hyun Park , Duck-Chul Oh , Young-Ju Kim
J. Microbiol. 2013;51(6):872-876.   Published online December 19, 2013
DOI: https://doi.org/10.1007/s12275-013-2500-7
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AbstractAbstract PDF
A Gram-positive, endospore-forming, rod-shaped bacterium, designated strain N2-5T, was isolated from swinery waste collected in Jeju, Republic of Korea. A phylogenetic analysis based on 16S rRNA gene sequences demonstrated that strain N2-5T formed a phyletic group within the phylum Firmicutes with less than 97.0% similarities to members of the genus Lysinibacillus, its nearest phylogenetic neighbors. The highest levels of sequence similarity to the isolate were observed against Lysinibacillus xylanilyticus XDB9T (96.8%), Lysinibacillus macroides LMG 18474T (95.6%), and Lysinibacillus parviboronicapiens BAM-582 T (95.6%). The organism grew optimally at 30°C and pH 7 and in the presence of 1–3% (w/v) NaCl. Strain N2-5T was chemotaxonomically characterized by possessing menaquinone-7 (MK-7) as the major menaquinone, and iso-C15:0 (54.9%), iso-C17:1ω10c (12.0%), and C16:1ω7c alcohol (11.8%) as the predominant fatty acids. The genomic DNA G+C content of the novel strain was 43.3 mol% and the cell-wall peptidoglycan was type A4α. The major polar lipids were diphosphatidylglycerol, phosphatidylglycerol, and phosphatidylethanolamine. Based on its phenotypic properties and phylogenetic data, strain N2-5T (=DSM 28310T =KCTC13837 T) represents a novel species in the genus Lysinibacillus, for which the name Lysinibacillus jejuensis sp. nov. is proposed.

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  • Distribution and Characterization of Quaternary Ammonium Biocides Resistant Bacteria in Different Soils, in South-Western China
    Ziyi Guo, Cunli Qin, Lilan Zhang
    Microorganisms.2024; 12(8): 1742.     CrossRef
  • Ureibacillus aquaedulcis sp. nov., isolated from freshwater well and reclassification of Lysinibacillus yapensis and Lysinibacillus antri as Ureibacillus yapensis comb. nov. and Ureibacillus antri comb. nov.
    Amit Yadav, Ruchi Teware, Agrima Bhatt, Yash Bhavsar, Akanksha Maurya, Vipool Thorat, Venkata Ramana Vemuluri, Kiran Kirdat
    Archives of Microbiology.2024;[Epub]     CrossRef
  • Lysinibacillus cavernae sp. nov., isolated from cave soil
    Yu Kan, Xue-Ke Niu, Manik Prabhu Narsing Rao, Zhou-Yan Dong, Yuan-Guo Xie, Ying-Qian Kang, Wen-Jun Li
    Archives of Microbiology.2020; 202(6): 1529.     CrossRef
  • Robust Demarcation of the Family Caryophanaceae (Planococcaceae) and Its Different Genera Including Three Novel Genera Based on Phylogenomics and Highly Specific Molecular Signatures
    Radhey S. Gupta, Sudip Patel
    Frontiers in Microbiology.2020;[Epub]     CrossRef
  • Isolation and characterization of a novel piezotolerant bacterium Lysinibacillus yapensis sp. nov., from deep-sea sediment of the Yap Trench, Pacific Ocean
    Libo Yu, Xixiang Tang, Shiping Wei, Yinkun Qiu, Xiashutong Xu, Guangxin Xu, Qilin Wang, Qian Yang
    Journal of Microbiology.2019; 57(7): 562.     CrossRef
  • Lysinibacillus alkalisoli sp. nov., isolated from saline–alkaline soil
    Ji-Quan Sun, Lian Xu, Xiao-Lei Wu
    International Journal of Systematic and Evolutionary Microbiology .2017; 67(1): 67.     CrossRef
  • Lysinibacillus acetophenoni sp. nov., a solvent-tolerant bacterium isolated from acetophenone
    M. Azmatunnisa, K. Rahul, K. V. N. S. Lakshmi, Ch. Sasikala, Ch. V. Ramana
    International Journal of Systematic and Evolutionary Microbiology .2015; 65(Pt_6): 1741.     CrossRef
  • Lysinibacillus fluoroglycofenilyticus sp. nov., a bacterium isolated from fluoroglycofen contaminated soil
    Minggen Cheng, Hao Zhang, Jing Zhang, Gang Hu, Jun Zhang, Jian He, Xing Huang
    Antonie van Leeuwenhoek.2015; 107(1): 157.     CrossRef
Winogradskyella jejuensis sp. nov., a Marine Bacterium Isolated from a Brown Alga Carpopeltis affinis
Ji-Young Kim , Duck-Chul Oh
J. Microbiol. 2012;50(5):888-892.   Published online November 4, 2012
DOI: https://doi.org/10.1007/s12275-012-2447-0
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AbstractAbstract PDF
A Gram-negative, orange-pigmented, rod-shaped bacterium, designated strain CP32T was isolated from a brown alga Carpopeltis affinis collected on the coast of Jeju Island, Republic of Korea. The isolate grew at 10–37°C (optimum 25°C) and at pH 6.5–9.5 (optimum pH 7.0). The 16S rRNA gene sequence of the isolate showed much similarity with the type strains of recognized species of the genus Winogradskyella (94.0–96.6%). The most closely related species were Winogradskyella echinorum KMM 6211T, Winogradskyella ulvae KMM 6390T, Winogradskyella thalassocola KMM 3907T, Winogradskyella poriferorum UST030701-295T, and Winogradskyella eximia KMM 3944T. The major respiratory quinone was menaquinone-6 (MK-6) and the predominant cellular fatty acids were iso-C15:1 G (24.8%), iso-C15:0 (23.4%), and iso-C17:0 3-OH (11.6 %). The DNA G+C content was 33.3 mol%. The polar lipid profile was composed of phosphatidylethanolamine, two aminolipids, and five unknown lipids. On the basis of phenotypic features, and the result of 16S rRNA gene sequence analysis, strain CP32T (=KCTC 23835T =JCM 18454T) represents a novel species of the genus Winogradskyella, for which the name Winogradskyella jejuensis sp. nov. is proposed.

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  • Light and carbon sources addition alter microbial community in biofloc-based Litopenaeus vannamei culture systems
    Wenwen Jiang, Wenjing Ren, Li Li, Shuanglin Dong, Xiangli Tian
    Aquaculture.2020; 515: 734572.     CrossRef
  • Taxonomic study of nine new Winogradskyella species occurring in the shallow waters of Helgoland Roads, North Sea. Proposal of Winogradskyella schleiferi sp. nov., Winogradskyella costae sp. nov., Winogradskyella helgolandensis sp. nov., Winogradskyella v
    Carlota Alejandre-Colomo, Tomeu Viver, Mercedes Urdiain, Ben Francis, Jens Harder, Peter Kämpfer, Rudolf Amann, Ramon Rosselló-Móra
    Systematic and Applied Microbiology.2020; 43(6): 126128.     CrossRef
  • Winogradskyella algae sp. nov., a marine bacterium isolated from the brown alga
    Valeriya V. Kurilenko, Lyudmila A. Romanenko, Marina P. Isaeva, Vassilii I. Svetashev, Valery V. Mikhailov
    Antonie van Leeuwenhoek.2019; 112(5): 731.     CrossRef
  • Ulvibacterium marinum gen. nov., sp. nov., a novel marine bacterium of the family Flavobacteriaceae, isolated from a culture of the green alga Ulva prolifera
    Zenghu Zhang, Zhenzhen Hu, Lili Tang, Zengmeng Wang, Yongyu Zhang
    Antonie van Leeuwenhoek.2019; 112(7): 1077.     CrossRef
  • Analysis of 1,000 Type-Strain Genomes Improves Taxonomic Classification of Bacteroidetes
    Marina García-López, Jan P. Meier-Kolthoff, Brian J. Tindall, Sabine Gronow, Tanja Woyke, Nikos C. Kyrpides, Richard L. Hahnke, Markus Göker
    Frontiers in Microbiology.2019;[Epub]     CrossRef
  • Isolation and genome analysis of Winogradskyella algicola sp. nov., the dominant bacterial species associated with the green alga Dunaliella tertiolecta
    Jaeho Song, Yeonjung Lim, Hye-Jin Jang, Yochan Joung, Ilnam Kang, Seong-Joo Hong, Choul-Gyun Lee, Jang-Cheon Cho
    Journal of Microbiology.2019; 57(11): 982.     CrossRef
  • Winogradskyella haliclonae sp. nov., isolated from a marine sponge of the genus Haliclona
    Johannes Schellenberg, Hans-Jürgen Busse, Martin Hardt, Patrick Schubert, Thomas Wilke, Peter Kämpfer, Stefanie P. Glaeser
    International Journal of Systematic and Evolutionary Microbiology .2017; 67(12): 4902.     CrossRef
  • Maripseudobacter aurantiacus gen. nov., sp. nov., a novel member of the family Flavobacteriaceae isolated from a sedimentation basin
    Can Chen, Yue Su, Tianyi Tao, Geyi Fu, Chongya Zhang, Cong Sun, Xinqi Zhang, Min Wu
    International Journal of Systematic and Evolutionary Microbiology.2017; 67(4): 778.     CrossRef
  • Winogradskyella aurantia sp. nov., isolated from a marine solar saltern
    Yue Sun, Bi-Yao Chen, Zong-Jun Du
    Antonie van Leeuwenhoek.2017; 110(11): 1445.     CrossRef
  • Taeania maliponensis gen. nov., sp. nov., a member of the family Flavobacteriaceae isolated from seawater
    Yong-Taek Jung, Sun Young Yoon, Jung-Sook Lee, Jung-Hoon Yoon
    International Journal of Systematic and Evolutionary Microbiology.2016; 66(9): 3552.     CrossRef
  • Winogradskyella crassostreae sp. nov., isolated from an oyster (Crassostrea gigas)
    Sooyeon Park, Ji-Min Park, Sung-Min Won, Jung-Hoon Yoon
    International Journal of Systematic and Evolutionary Microbiology .2015; 65(Pt_9): 2890.     CrossRef
  • Winogradskyella eckloniae sp. nov., a marine bacterium isolated from the brown alga Ecklonia cava
    Ji-Young Kim, So-Hyun Park, Ga-Young Seo, Young-Ju Kim, Duck-Chul Oh
    International Journal of Systematic and Evolutionary Microbiology .2015; 65(Pt_9): 2791.     CrossRef
  • List of new names and new combinations previously effectively, but not validly, published
    Aharon Oren, George M. Garrity
    International Journal of Systematic and Evolutionary Microbiology .2015; 65(Pt_1): 1.     CrossRef
Aquimarina litoralis sp. nov., Isolated from a Coastal Seawater
You-Sung Oh , Hyung-Yeel Kahng , Young Sun Lee , Byoung-Jun Yoon , Sang-Bin Lim , Jae Sung Jung , Duck-Chul Oh , Dong-Heon Lee
J. Microbiol. 2010;48(4):433-437.   Published online August 20, 2010
DOI: https://doi.org/10.1007/s12275-010-0088-8
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AbstractAbstract PDF
A strictly aerobic, red-pigmented, non-motile, catalase- and oxidase-positive, Gram-staining-negative bacterium, designated strain CNURIC011T, was isolated from seawater off the coast of Jeju Island in Korea. A phylogenetic analysis based on 16S rRNA gene sequences showed that strain CNURIC011T belongs to the genus Aquimarina in the family Flavobacteriaceae. 16S rRNA gene sequence analysis revealed that the close relatives of the novel strain are Aquimarina latercula ATCC 23177T, Aquimarina marcrocephali JAMB N27T, Aquimarina intermedia KMM 6258T, Aquimarina muelleri KMM 6020T, and Aquimarina brevivitae SMK-19T, with sequence similarities of 97.6, 96.6, 96.0, 95.6, and 94.2%, respectively. DNA-DNA hybridization revealed that the level of relatedness between strain CNURIC011T and Aquimarina latercula ATCC 23177T (=KCTC 2912T) was 4.9%. The DNA G+C content was 35.8 mol% and the major respiratory quinone was MK-6. The major fatty acids were iso-C15:0 (14.9%), C15:0 (13.9%), iso-C17:0 3-OH (12.6%), iso-C15:1 G (7.3%), and iso-C17:1 ω9c (7.2%). On the basis of phenotypic, phylogenetic, and genotypic data, strain CNURIC011T represents a novel species within the genus Aquimarina, for which the name Aquimarina litoralis sp. nov. is proposed. The type strain is CNURIC011T (=KCTC 22614T =JCM 15974T).

Citations

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  • Aquimarina ulvae sp. nov. and Polaribacter litoreus sp. nov., isolated from the green alga Ulva prolifera
    Sylvia Kristyanto, Jiyoung Woo, Keun-Hyung Choi
    International Journal of Systematic and Evolutionary Microbiology .2026;[Epub]     CrossRef
  • Validation List no. 222. Valid publication of new names and new combinations effectively published outside the IJSEM
    Aharon Oren, Markus Göker
    International Journal of Systematic and Evolutionary Microbiology .2025;[Epub]     CrossRef
  • Insights into the Antimicrobial Activities and Metabolomes of Aquimarina (Flavobacteriaceae, Bacteroidetes) Species from the Rare Marine Biosphere
    Sandra Godinho Silva, Patrícia Paula, José Paulo da Silva, Dalila Mil-Homens, Miguel Cacho Teixeira, Arsénio Mendes Fialho, Rodrigo Costa, Tina Keller-Costa
    Marine Drugs.2022; 20(7): 423.     CrossRef
  • Insights into the genomic repertoire of Aquimarina litoralis CCMR20, a symbiont of coral Mussismilia braziliensis
    Tooba Varasteh, Diogo Tschoeke, Gizele Garcia, Arthur Silva Lima, Ana Paula B. Moreira, Cristiane Thompson, Fabiano Thompson
    Archives of Microbiology.2021; 203(5): 2743.     CrossRef
  • Aquimarina sp. Associated With a Cuticular Disease of Cultured Larval Palinurid and Scyllarid Lobsters
    Mei C. Ooi, Evan F. Goulden, Andrew J. Trotter, Gregory G. Smith, Andrew R. Bridle
    Frontiers in Microbiology.2020;[Epub]     CrossRef
  • Comparative genome analysis provides novel insight into the interaction of Aquimarina sp. AD1, BL5 and AD10 with their macroalgal host
    Jennifer Hudson, Vipra Kumar, Suhelen Egan
    Marine Genomics.2019; 46: 8.     CrossRef
  • Real-time PCR assay for Aquimarina macrocephali subsp. homaria and its distribution in shell disease lesions of Homarus americanus, Milne-Edwards, 1837, and environmental samples
    Robert A. Quinn, Suchandra Hazra, Roxanna Smolowitz, Andrei Y. Chistoserdov
    Journal of Microbiological Methods.2017; 139: 61.     CrossRef
  • Aquimarina seongsanensis sp. nov., isolated from sea water
    Yoojin Oh, Bong-geun Choi, Joon Yong Kim, Seong Woon Roh, Sung-Jae Lee
    Antonie van Leeuwenhoek.2017; 110(8): 1019.     CrossRef
  • Aquimarina aggregata sp. nov., isolated from seawater
    Yan Wang, Hong Ming, Weiyun Guo, Hongli Chen, Chenyan Zhou
    International Journal of Systematic and Evolutionary Microbiology.2016; 66(9): 3406.     CrossRef
  • Aquimarina atlantica sp. nov., isolated from surface seawater of the Atlantic Ocean
    Guizhen Li, Qiliang Lai, Fengqin Sun, Xiupian Liu, Yunbiao Xie, Yaping Du, Guangyu Li, Zongze Shao
    Antonie van Leeuwenhoek.2014; 106(2): 293.     CrossRef
  • Aquimarina amphilecti sp. nov., isolated from the sponge Amphilectus fucorum
    Jonathan Kennedy, Lekha Menon Margassery, Niall D. O’Leary, Fergal O’Gara, John Morrissey, Alan D. W. Dobson
    International Journal of Systematic and Evolutionary Microbiology .2014; 64(Pt_2): 501.     CrossRef
  • Aquimarina penaei sp. nov., isolated from intestinal tract contents of Pacific white shrimp, Penaeus vannamei
    Xiaoyi Li, Liping Wang, Hui Huang, Qiliang Lai, Zongze Shao
    Antonie van Leeuwenhoek.2014; 106(6): 1223.     CrossRef
  • Aquimarina agarilytica sp. nov., an agarolytic species isolated from a red alga
    Bokun Lin, Guoyong Lu, Yandan Zheng, Wei Xie, Shengkang Li, Zhong Hu
    International Journal of Systematic and Evolutionary Microbiology.2012; 62(Pt_4): 869.     CrossRef
Gaetbulibacter jejuensis sp. nov., Isolated from Seawater
You-Sung Oh , Sang-Bin Lim , Hyung-Yeel Kahng , Byoung-Jun Yoon , Duck-Chul Oh , Jae-Ho Joa , Dong-Heon Lee
J. Microbiol. 2010;48(3):307-311.   Published online June 23, 2010
DOI: https://doi.org/10.1007/s12275-010-9232-8
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AbstractAbstract PDF
A novel marine bacterium, designated strain CNURIC014T was isolated from coastal seawater of Jeju Island in Korea. Strain CNURIC014T formed yellow colonies on marine agar 2216 and the cells were Gram-negative, non-motile, strictly aerobic, rod-shaped. The temperature, pH and NaCl ranges for growth were 15-37°C, pH 6.0-9.0 and 1.0-7.0% NaCl. Phylogenetic analysis based on 16S rRNA gene sequences indicated that strain CNURIC014T was most closely related to Gaetbulibacter marinus and Gaetbulibacter saemankumensis, with a sequence similarity of 95.1% and 94.6%, respectively. The DNA G+C content of the strain was 33.1 mol% and the major respiratory quinone was menaquinone-6. The major cellular fatty acids were iso-C15:1 (22.8%), iso-C15:0 (18.8%), summed feature 3 (iso-C15:0 2-OH/C16:1 ω7c, 12.9%) and iso-C17:0 3-OH (11.5%). On the basis of phenotypic, phylogenetic, and genotypic data, strain CNURIC014T represents a novel species within the genus Geatbulibacter, for which the name Gaetbulibacter jejuensis sp. nov. is proposed. The type strain is CNURIC014T (=KCTC 22615T =JCM 15976T).

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Citations to this article as recorded by  
  • Validation List no. 222. Valid publication of new names and new combinations effectively published outside the IJSEM
    Aharon Oren, Markus Göker
    International Journal of Systematic and Evolutionary Microbiology .2025;[Epub]     CrossRef
  • Genome sequence of Gaetbulibacter sp. PBL-D1 isolated from a Malaysian beach: insights into glycoside hydrolase repertoires
    Ummirul Mukminin Kahar, Najiha Atiqah Md Nor, Wan Nur Izrena Wan Izanni
    BMC Genomic Data.2025;[Epub]     CrossRef
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    Yong-Xie Jin, Haeng-Ryan Kim, So-Young Kim
    Korean Journal of Food Preservation.2013; 20(6): 791.     CrossRef
Purification and Characterization of a Catalase from Photosynthetic Bacterium Rhodospirillum rubrum S1 Grown under Anaerobic Conditions
Yoon-Suk Kang , Dong-Heon Lee , Byoung-Jun Yoon , Duck-Chul Oh
J. Microbiol. 2006;44(2):185-191.
DOI: https://doi.org/2366 [pii]
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AbstractAbstract PDF
The photosynthetic bacterium, Rhodospirillum rubrum S1, when grown under anaerobic conditions, generated three different types of catalases. In this study, we purified and characterized the highest molecular weight catalase from the three catalases. The total specific catalase activity of the crude cell extracts was 88 U/mg. After the completion of the final purification step, the specific activity of the purified catalase was 1,256 U/mg. The purified catalase evidenced an estimated molecular mass of 318 kDa, consisting of four identical subunits, each of 79 kDa. The purified enzyme exhibited an apparent Km value of 30.4 mM and a Vmax of 2,564 U against hydrogen peroxide. The enzyme also exhibited a broad optimal pH (5.0~9.0), and remained stable over a broad temperature range (20°C~60°C). It maintained 90% activity against organic solvents (ethanol/chloroform) known hydroperoxidase inhibitors, and exhibited no detectable peroxidase activity. The catalase activity of the purified enzyme was reduced to 19% of full activity as the result of the administration of 10 mM 3-amino-1,2,4-triazole, a heme-containing catalase inhibitor. Sodium cyanide, sodium azide, and hydroxylamine, all of which are known heme protein inhibitors, inhibited catalase activity by 50% at concentrations of 11.5 μM, 0.52 μM, and 0.11 μM, respectively. In accordance with these findings, the enzyme was identified as a type of monofunctional catalase.
Analysis of Catalases from Photosynthetic Bacterium Rhodospirillum rubrum S1
Hee-Kyoung Lim , Young-Mi Kim , Dong-Heon Lee , Hyung-Yeel Kahng , Duck-Chul Oh
J. Microbiol. 2001;39(3):168-176.
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Five different types of catalases from photosynthetic bacterium Rhodospirillum rubrum S1 grown aerobically in the dark were found in this study, and designated Cat1 (350 kDa), Cat2 (323 kDa), Cat3 (266 kDa), Cat4 (246 kDa), and Cat5 (238 kDa). Analysis of native PAGE revealed that Cat2, Cat3, and Cat4 were also produced in the cells anaerobically grown in the light. It is notable that only Cat2 was expressed much more strongly in response to the anaerobic condition. Enzyme activity staining demonstrated that Cat3 and Cat4 had bifunctional catalase-peroxidase activities, while Cat1, Cat2, and Cat5 were typical monofunctional catalases. S1 cells grown aerobically in the presence of malate as the sole source of carbon exhibited an apparent catalase Km value of 10 mM and a Vmax of about 705 U/mg protein at late stationary growth phase. The catalase activity of S1 cells grown in the anaerobic environment exhibited a much lower Vmax of about 109 U/mg protein at late logarithmic growth phase. The catalytic activity was stable in the broad range of temperatures (30 C-60 C), and pH (6.0-10.0). R. rubrum S1 was much more resistant to H_2 O_2 in the stationary growth phase than in the exponential growth phase regardless of growth conditions. Cells of stationary growth phase treated with 15 mM H 2 O 2 for 1 h showed 3-fold higher catalase activities than the untreated cells. In addition, L-glutamate induced an 80-fold increase in total catalase activity of R. rubrum S1 compared with malic acid. Through fraction analyses of S1 cells, Cat2, Cat3, Cat4 and Cat5 were found in both cytoplasm and periplasm, while Cat1 was localized only in the cytoplasm.

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