• Title/Summary/Keyword: Haloarcular sp

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Isolation of Bacteriophage from Haloarcular sp, EH-1 (Haloarcular sp. EH-1에 의한 bacteriophage의 분리)

  • 정명주
    • Journal of Life Science
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    • v.13 no.4
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    • pp.505-510
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    • 2003
  • The extremely halophilic archaebacteriurn Haloarcular sp. EH-1 was isolated from solar salts. Halophages found in Haloarcular sp. EH-1 were isolated from fermented anchovy sauce. Halophages were isolated from fermented anchovy sauce using Haloarcular sp. EH-1 as a host bacterium. The isolated halophage produced 0.5∼l.0 mm in diameter clear plaques. The halophage consists of an symmetrical head, measuring 68 nm in diameter, and a contractile tail, 100 nm long and base plates were observed. Total size of phage DNA genome obtained 20 Kbp and its sequence homology was 52.87% with H. Salinarium.

Production of Poly-3-Hydroxyalkanhoate by Haloarcular sp. EH-1 (Haloarcular sp. EH-1으로부터 생분해성 Poly-3-Hydroxyalkanoate의 생산)

  • 정명주;박형숙
    • Journal of Life Science
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    • v.9 no.6
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    • pp.737-742
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    • 1999
  • The extremely halophilic archaebacterium Haloarcular sp. EH-1 was isolated from solar salts. Haloarcular sp. EH-1 accumulated poly(3-hydroxyalkanoate) (PHA) as intracellular granules. PHA production in batch culture have been studied. The PHA was identified as poly(3-hydroxybutyric acid-co-3-hydroxyvaleric acid) (PHB/HV) of 3-hydroxybutyric acid and 3-hydroxyvaleric acid by the analysis of GC, IR and NMR. The melting temperature of PHB/HV was 152.46$^{\circ}C$, viscosity was 1.25 ㎗/g, and molecular weight was $1.44 X 10^5.$

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Amylase Production from Haloarcular sp. EH-1 (고호염성 Haloarcular sp. EH-1으로 부터 amylase 생산)

  • 정명주
    • Journal of Life Science
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    • v.12 no.5
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    • pp.570-576
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    • 2002
  • The extremely halophilic archaebacterium Haloarcular sp. EH-1 was isolated from solar salts. Amylae production from Halonrcular sp. EH-1 have been studied. The results obtained were as follows. The optimal medium composition for the production of amylase from Haloarcular sp. EH-1 were soluble starch 1.5%, yeast extract 1.0%, MgSO$_4$ 7h$_2$O 2.0%, KCI 0.1%, NaCl 25% (pH 7.5). The incubation temperature, aeration rate and agitation speed were 4$0^{\circ}C$, 100 $m\ell$ medium / 500 $m\ell$ shaking flask, and 110 rpm. The cell growth and enzymatic activity was highest at 9 days of incubation. So amylase production appeared to be a growth-related phenomenon.

Purification and Characteristics of Amylase from Haloarcular sp. EH-1 (Haloarcular sp. EH-1이 생산하는 Amylase의 정제 및 특성)

  • 정명주;박형숙
    • Microbiology and Biotechnology Letters
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    • v.27 no.2
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    • pp.129-135
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    • 1999
  • EH-1 was highest at 9 days of incubation. This regrowth and enzymatic activity of Haloarcular sp. EH-1 was highest at 9 days of incubation. This amylase was purified by acetone fractionation, DEAG-Cellulose column chromatography, 1st Sephadex G-75 gel filtration, CM-Cellulose column chromatography and 2nd Sephadex G-75 gel filtration. The amylase was purified about 98.64 fold with a yield of 11.75%. The molecular weight of amylase was estimated to be about 43,000and 40,000 by gel filtration and SDS-polyacrylamide gel electrophoresis, respectively, suggesting that the enzyme was a monomer. Amylase had an optimal temperature of 4$0^{\circ}C$, and an optimum pH of 7.0, and the thermal stability was observed the above 50% at 10$0^{\circ}C$ after 1 hour, and the stable range of pH was 6.0 to 8.0. The enzymatic activity was increased in the presence of 10 mM 2-mercaptoethanol, slightly by 10 mM SnCl2.2H2O.FeCl2.4H2O.CuCl2.2H2O.HgCl2.6H2O and SDS. End products from soluble starch were glucose, maltose and maltotriose, and Km value for soluble starch was 2.5mg/ml.

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Characteristic of Carotenoid Component from Halophilic Bacteria, Haloarcular sp. EH-1 (호염세균 Haloarcular sp. EH-1으로부터 추출한 카로테노이드 색소의 특성)

  • 정영기;최병대;강석중;정성훈;이용규;김해윤;정명주
    • KSBB Journal
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    • v.15 no.6
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    • pp.673-676
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    • 2000
  • In order to identification of carotenoid pigments of Haloarcular sp. EH-1 as a food for fish were analyzed. The content of carotenoids cultured in 3 L and 5 L bioreactor were 83.1 and 82.7 mg%, respectively. Identification of each carotenoid was achieved by means of co-TLC and co-HPLC with authentic specimens, spectroscopic and instrumental analyses, and chemical treatments as usual. The main components identified were ${\beta}$-carotene(8.1%), 3-hydroxyechinenone(42.0%) and astaxanthin(25.0%).

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Effect of Pigmentation on Rainbow Trout Fed Carotenoid Diets from Halophilic Bacteria [Haloarcular sp. EH-1] (호염세균 [Haloarcular sp. EH-1] 카로테노이드 색소를 섭이한 무지개송어의 체색효과)

  • 정영기;최병대;강석중;김철우;김해윤;정명주
    • KSBB Journal
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    • v.15 no.6
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    • pp.658-663
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    • 2000
  • This study is aimed at evaluating the pigmentation of rainbow trout with carotenoid extracts from halophilic bacteria during 8 weeks feeding. Proximate composition of the sample were analyzed. Moisture content was 77% and 73% after 4 and 8 weeks feeding, respectively. Crude protein and lipid content was slowly increased after 8 weeks feeding. But minerals content were not affected with the feeding period and constituents. Muscle carotenoids content of rainbow trout was 0.0223 mg/100g tissue in control group after 4 weeks, and 0.1702 mg/100g tissue in carophyll pink group after 8 weeks. The carotenoids pigmentation content of halophilic bacteria extracts fed group was 0.1256, 0.1382 mg/100g tissue after 8 weeks. It means that the carotenoids of bacteria extracts are a good material for fish pigmentation. The main components of rainbow trout muscle and integuments with these diets were canthaxathin,, zeaxanthin, and ${\beta}$-carotene.

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Optimal Growth Conditions for Carotenoid Pigment Production from marine Microorganism (해양미생물로부터 카로테노이드 색소의 생산을 위한 최적조건)

  • 정영기;김태수;정명주;류병호;주우홍;박정욱
    • Journal of the Korean Society of Food Science and Nutrition
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    • v.28 no.6
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    • pp.1239-1243
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    • 1999
  • The optimal medium composition for the production of carotenoid pigment from Haloarcular sp. EH 1 as a dietary for fishes were 1.0% sucrose, 1.0% yeast extract, 25% sodium chloride, 0.3% sodium citrate, 0.2% potassium chloride, 2.0% magnesium sulphate, 0.002% ferric sulphate(pH 7.0). The incubation temperate, aeration rate and agitation speed were 40oC, 100ml medium/500ml vol. shaking flask, and 180 rpm/min. The carotenoid pigment production was highest after 5 days of incubation with the light.

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