• Title/Summary/Keyword: Marine Bacterium

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Antioxidant Activity of a Chitin-degrading Bacterium Bacillus idriensis (CGH18) (키틴분해 박테리아 Bacillus idriensis (CGH18)의 항산화 활성)

  • Jung, Myoung Eun;Hong, Joo Wan;Lee, Jeong-Im;Kwak, Myoung Kuk;Kim, Hojun;Sohn, Jae Hak;Song, Young-Sun;Oh, Kwang-Suk;Seo, Youngwan
    • KSBB Journal
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    • v.28 no.4
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    • pp.217-224
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    • 2013
  • A bacterium CGH18 exhibiting antioxidizing and chitin-degrading activities in the colloidal chitin culture medium was isolated from salt-fermented crab. This strain was identified as Bacillus idriensis based on 16S rDNA sequence homology search. Its crude extract was partitioned between n-BuOH and $H_2O$. The organic layer was further partitioned between $CH_2$ $Cl_2$ and $H_2O$. Antioxidant activities of crude extract and its solvent fractions were evaluated using five different bioassay methods, including the degree of occurrence of intracellular reactive oxygen species (ROS), peroxynitrite scavenging (ONOO), and oxidative damage of genomic DNA. All fractions exhibited significant antioxidant activity in bioassay systems used.

$H_2$ Production by a Purple Sulfur Bacterium Blooming in Lake Kaiike (카이이케호에서 농밀하게 분포하는 Purple Sulfur Bacterium의 수소생산)

  • Matsuyama, Michiro;Moon, Sang-Wook
    • Applied Biological Chemistry
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    • v.40 no.1
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    • pp.58-64
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    • 1997
  • $H_2$ production by Chromatium sp., a large purple sulfur bacterium blooming in lake Kaiike, under various environmental conditions was examined. Chromatium sp. produced $H_2$ only in the presence of light and $H_2$. Maximum $H_2$ production ($0.01\;{\mu}mol/hr/(mg\;dry\;cell\;weight)$) was obtained in the solution of 20 mg $H_2S-S/l$ under low light intensity (1000 lux) at $30^{\circ}C$. $H_2$ production was severely inhibited by the presence of $N_2\;or\;NH_4^+$. The rate observed for Chromatium sp. was relatively low compared to that of other phototrophic bacteria. Chromatium sp. is probably a most potent Ha producing species in lake Kaiike, since the bacterium readily produced $H_2$ photoautotrophically even at low light intensities by the application of suboptimal $H_2$ concentrations. Based on the photoautotrophic characteristics of bacterial $H_2$ production, it is suggested that Chromatium sp. can be an economic and practical species for biological $H_2$ production system, particularly in temperate region.

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Extracellular polymeric substances produced by a marine bacterium, Hahella chejuensis

  • Lee, Hong-Kum
    • 한국생물공학회:학술대회논문집
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    • 2000.11a
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    • pp.135-136
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    • 2000
  • A bacterial strain producing a large amount of EPS was isolated from marine sediment sample collected from the Cheju Island, Republic of Korea. In the present study, the isolation and identification of this isolate, which is named Hahella chejuensis gen. nov., sp. nov., the effects of nutrients on the production of EPS, and some properties of this EPS are reported.

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Enhanced Carboxymethylcellulase Production by a Newly Isolated Marine Bacterium, Cellulophaga lytica LBH-14, Using Rice Bran

  • Gao, Wa;Lee, Eun-Jung;Lee, Sang-Un;Li, Jianhong;Chung, Chung-Han;Lee, Jin-Woo
    • Journal of Microbiology and Biotechnology
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    • v.22 no.10
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    • pp.1412-1422
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    • 2012
  • The aim of this work was to establish the optimal conditions for production of carboxymethylcellulase (CMCase) by a newly isolated marine bacterium using response surface methodology (RSM). A microorganism producing CMCase, isolated from seawater, was identified as Cellulophaga lytica based 16S rDNA sequencing and the neighborjoining method. The optimal conditions of rice bran, ammonium chloride, and initial pH of the medium for cell growth were 100.0 g/l, 5.00 g/l, and 7.0, respectively, whereas those for production of CMCase were 79.9 g/l, 8.52 g/l, and 6.1. The optimal concentrations of $K_2HPO_4$, NaCl, $MgSO_4{\cdot}7H_2O$, and $(NH_4)_2SO_4$ for cell growth were 6.25, 0.62, 0.28, and 0.42 g/l, respectively, whereas those for production of CMCase were 3.72, 0.54, 0.70, and 0.34 g/l. The optimal temperature for cell growth and the CMCase production by C. lytica LBH-14 were $35^{\circ}C$ and $25^{\circ}C$, respectively. The maximal production of CMCase under optimized condition for 3 days was 110.8 U/ml, which was 5.3 times higher than that before optimization. In this study, rice bran and ammonium chloride were developed as carbon and nitrogen sources for the production of CMCase by C. lytica LBH-14. The time for production of CMCase by a newly isolated marine bacterium with submerged fermentations reduced to 3 days, which resulted in enhanced productivity of CMCase and a decrease in its production cost.

Inhibitory Activity of Marine Bacterium on the Growth of Vibrio anguillarum (Vibrio anguillarum에 대한 항균성 세균의 분리(Vibriostatic activity of marine bacteria))

  • Byon, Ju-Yong;Kim, Eun-Heui
    • Journal of fish pathology
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    • v.13 no.1
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    • pp.1-6
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    • 2000
  • The antibacterial activity of marine bacterium(Pseudomonas aeruginosa JYMB1-3) was assayed against Vibrio anguillarum with the aim of evaluating the possible use for biocontrolling fish disease as probiotic strain. Inhibition test on the solid medium showed that vibrios were especially sensitive to the JYMB1-3. Edwardsiella tarda, Streptococcus sp. and Staphylococcus epidermidis were also sensitive to that strain, however the antibacterial abilities were varied to the pathogens. The vibriostatic activity of antibacterial substance produced from $10^7$ cells of the strain for 24 hours was equivalent to $2.5{\mu}g$ of chloramphenicol.

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Purification and Characterization of Agarase from Marine Bacterium, Algibacter lectus AS-3 (해양 미생물Algibacter lectus AS-3으로부터 agarase의 분리 및 특성)

  • Jung, Il Sun;Choi, Young Ju
    • Journal of Marine Bioscience and Biotechnology
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    • v.2 no.3
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    • pp.142-148
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    • 2007
  • An agar-degrading marine bacterium, strain AS-3 was isolated from the seawater. The strain AS-3 was identified as Algibacter lectus AS-3 by 16S rDNA sequence. The optimum medium for agarase activity of the isolated strain was determined to be marine medium, marine broth 2216 containing 0.1% agar as carbon source. An extracellular agarase was purified 6.9-fold from the culture supernatant by ammonium sulfate precipitation, ion exchange chromatography and gel filtration methods. The optimum pH and temperature for this enzyme were 7.0 and $40-50^{\circ}C$, respectively. Antioxidative activity of the strain AS-3 was 62.4% in the supernatant cultured for 12 h.

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