• Title/Summary/Keyword: Lactococcus lactis subsp

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Lactococcus lactis subsp. cremoris FC에 대한 Lactoferrin과 Transferrin의 생장촉진효과 (Effects of Lactoferrin and Transferrin on the Growth of Lactococcus lactis subsp. cremoris FC)

  • 김완섭
    • Journal of Dairy Science and Biotechnology
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    • 제35권3호
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    • pp.196-201
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    • 2017
  • Lactococcus lactis subsp. cremoris FC는 카스피해 요구르트의 명칭으로 강한 점성을 가지는 것을 특징으로 하는 코카커스 지방 유래의 발효유로부터 분리된 균주로 있다. 본 연구는 Lc. lactis subsp. cremoris FC의 생장에 대한 lactoferrin group(native-lactoferrin, apo-lactoferrin, 그리고 holo-lactoferrin)과 transferrin (apo-transferrin과 holo-transferrin)의 첨가가 생장에 미치는 영향을 알아보기 위하여 수행하였다. Lc. lactis subsp. cremoris FC의 생장에 lactoferrin과 transferrin의 첨가효과는 0.5 또는 1 mg/mL의 농도로 첨가하는 것이 생장 촉진에 좋은 효과를 나타내는 것으로 조사되었다.

Lactococcus lactis subsp. lactis ATCC 7962의 nisin 저항성 유전자를 포함하는 plasmid pCS100의 특성규명 (Characteristics of the Plasmid pCS100 Containing Nisin Resistant Gene from Lactococcus lactis subsp. lactis ATCC7962.)

  • 송종효;이형주;김정환;정대균
    • 한국미생물·생명공학회지
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    • 제26권6호
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    • pp.562-565
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    • 1998
  • Nisin-producing and nisin resistant L. lactis subsp. lactis ATCC7962 harbored six plasmids. To find a plasmid containing a nisin resistant gene, these plasmids were transformed into L lactis LM0230 of plasmid-free and nisin sensitive strain. After screening on nisin selection media containing nisin (150 $\mu\textrm{g}$/$m\ell$), several nisin resistant transformants were obtained and the level of nisin resistance was very similar to that of wild type L lactis subsp. lactis ATCC7962. A 26.5 kb plasmid, named as pCS100, which confers resistance to nisin, was identified in transformants. The pCS100 was digested with EcoRI and Southern blot hybridization was done with nisI probe to localize the nisin resistant gene. A 4 kb EcoRI fragment showed a strong positive signal, and it was cloned into pBluescript for the potential selection marker.

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10-Hydroxyoctadecanoic Acid Produced by Lactococcus lactis subsp. lactis as a Part of Flocculent Aggregate

  • Park, Hee-Jun;Lim, Yoong-Ho;Kim, Youn-Soon;Kyung, Kyu-Hang
    • Journal of Microbiology and Biotechnology
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    • 제9권1호
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    • pp.39-43
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    • 1999
  • A flocculent aggregate produced by Lactococcus lactis subsp. lactis in broths containing Tween 80, including MRS broth, had a microscopic structure of intertwined thread-like filaments. The filamentous structure was not elongated bacterial cells, but consisted of an organic solvent-soluble portion and an insoluble solid. L. lactis subsp. lactis grown at $25^{\circ}C$ for 15 days in tryptic soy broth with 0.1% Tween 80 and 1.0% malt extract produced 13 mg/l of flocculent aggregate, which contained 0.84 g/g of organic solvent-soluble component. The organic solvent-soluble part was identified as 10-hydroxyoctadecanoic acid.

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김치유산균인 Lactococcus lactis subsp. lactis YH-10가 생산하는 박테리오신의 특성 (Characterization of Bacteriocin, lacticin YH-10, Produced by Lactococcus lactis subsp. lactis YH-10 Isolated from Kimchi)

  • Park, Eun-Min;Kim, Young-Hwa;Park, So-Jin;Kim, Yun-Im;Ha, Yu-Mi;Kim, Sung-Koo
    • 생명과학회지
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    • 제14권4호
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    • pp.683-688
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    • 2004
  • API test를 통해서 김치에서 분리한 유산균이 Lactococcus lactis subsp. lactis의 한 종임 을 확인하고 Lactococcus lactis subsp. lactis YH-10이라 명명하고, 생산된 박테리오신을 lacticin YH-10으로 명명하였다. Lactococcus lactis subsp. lactis YH-10을 $25^{\circ}C$, 3$0^{\circ}C$와 37$^{\circ}C$에서 배양한 결과 $25^{\circ}C$에서 박테리오신을 생성하였다. Lacticin YH-10은 여러 가지 단백질 분해효소에 의해 항균활성을 소실하였으므로, 단백질로된 박테리오신임을 확인하였다. 또한 $\alpha$-amylase, $\beta$-amylase, glucoamylase의 처리에도 활성을 일부 소실하였으므로 박테리오신의 분류 중 classIV에 속함을 알 수 있었다 Ammonium sulfate정제한 후 SDS-PAGE를 통해 박테리오신의 분자량이 대략 14kDa임이 확인되었다. Lacticin YH-10은 단백질계 물질로서 인체 내에서 분해가 가능하기 때문에 일반 화학 보존제 보다 인체에 안정함을 알 수 있다. Lacticin YH-10은 낮은 pH와 높은 온도에서 항균활성을 가지고 있기 때문에 식품보존제로서 이용할 수 있다.

Purification and Characterization of Bacteriocin J105 Produced by Lactococcus latis subsp. lactis J105 Isolated from Kimchi

  • Kwak, Gyu-Suk;Kim, Sung-Koo;Jun, Hong-Ki
    • Journal of Microbiology and Biotechnology
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    • 제11권2호
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    • pp.275-280
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    • 2001
  • Bacteriocin J105 is a proteinaceous inhibitory substance produced by Latococcus latis subsp. lactis j105 isolated from Kimchi. Bacteriocin J105 was purified to homogeneity by the pH-dependent adsorption-desorption method and reverse-phase HPLC from the culture broth of Lactococcus lactis subsp. lactis J105. Purification of bacteriocin J105 resulted in a 1.47-fold increase in the specific activity and the recovery was 1.5%. Its molecular mass measured by the electrophoretic pattern in the sodium, dodecyl sulfate polyacrylamide gel was about 3.4 kDa. It was stable at $121^{\circ}C$ for 15 min at pH between 2 and 4. However, at pH above 5, bacteriocin was rapidly inactivated. Twenty-one residues from the N-terminal portion of bacteriocin J105 were sequenced using sequence analysis of lantibiotics. Bacteriocin J105 showed significant homology with known nisin A from lactic acid bacteria.

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Molecular Cloning of a $\beta$-D-Galactosidase Gene from Lactococcus lactis subsp. lactis 7962

  • CHANG, HAE-CHOON;YANG-DO CHOI;HYONG-JOO LEE
    • Journal of Microbiology and Biotechnology
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    • 제6권6호
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    • pp.386-390
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    • 1996
  • The ${\beta}$-galactosidase gene from Lactococcus lactis subsp. lactis ATCC 7962 was cloned and its enzymatic properties were characterized, with a view to assessing its potential use as a selection marker in the food-grade cloning vector. Chromosomal DNA from L. lactis subsp. lactis 7962 was cleaved with PstI and ligated into pBR322 for transformation into Escherichia coli TGl. Transformants showing ${\beta}$-galactosidase activity possessed the pBR322 plasmid containing a 10 kilobase (kb) PstI fragment and this plasmid was named pCKL11. The cloned ${\beta}$-galactosidase gene came from the chromosomal DNA of L. lactis subsp. lactis 7962 was confirmed by Southern hybridization. A restriction map of pCKL11 was constructed from the cleavage of both pCKL11 and the purified 10kb insert fraqment. The. optimum pH of the ${\beta}$-galactosidase determined with the E. coli harboring the pCKL11 was 7.0. The optimum temperature was $50^{\circ}C$, while the pI of the enzyme was 7.4. These values were the same as those of the enzyme from the parent strain.

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A Plasmid of Lactococcus lactis subsp. lactis ML8 Linked with Lactose Metabolism and Extracellular Proteinase

  • LEE, JONG-HOON;HYONG JOO LEE
    • Journal of Microbiology and Biotechnology
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    • 제6권6호
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    • pp.381-385
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    • 1996
  • Three distinct plasmids, with approximate molecular weights of 1, 4.5, and 33 megadaltons, were found in Lactococcus lactis subsp. lactis (L. lactis) ML8. Slow acid-producing mutants of L. lactis ML8, isolated by plasmid curing with acriflavine treatment, lacked the 33-megadalton plasmids. The plasmid-cured mutant showed lactose-negative (Lac) characteristics and the alteration of extracellular proteinase pattern. The possible involvement of extracellular proteinase with the 33-megadalton plasmid is highlighted in this research.

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Lactococcus lactis subsp. cremoris ATCC 11602-A1의 Bacteriophage 저항성 기작에 관한 연구 (Characteristics of the Bacteriophage Resistance Mechanism of Kactococcus lactis subsp.cremoris ATCC 11602-A1)

  • 이춘화;배인휴
    • 한국미생물·생명공학회지
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    • 제22권3호
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    • pp.233-239
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    • 1994
  • The characteristics of the bacteriophage resistant Lactococcus lactis subsp. cremoris ATCC 11602-A1, the phage-resistant mutant of Lactococcus lactis subsp. cremoris ATCC 11602, was examined. Electron microscopic study of phage adsorption to A1 revealed that after 10 min. incubation of the host-phage mixture, A1 did not show phage adsorption, and after 60 min. did not show a real burst and the release of new phage particles which could be detected in the mixture of its parent strain and phage. However, the phage adsorption rate of A1 after SDS treatment increased to 98%. Moreover, when the cell walls from A1 and parent strain, and the polysaccharide(PS) and peptidoglycan(PG) of their cell wall were mixed with phage and incubated for 15 min., PS and PG from A1 did not bind phage, but only SD-treated cell wall bound phage, and the cell wall and PS of parent strain bound phage. Both A1 and parent strain treated with 0.2 N HCl-and 5% TCA(100$$C) did not bind phage. The results suggest that the phage receptor is still present in the cell wall of the A1, but a cell wall constituent hydrolyzed by SDS blocks phage adsorption by masking the phage receptor. It also suggests that the phage receptor of parent strain is associated with PS of the cell wall.

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아토피유발인자 억제효과를 증대하는 Lactococcus lactis의 배양방법 (Lactococcus lactis Culture Methods for the Enhanced Depression of Inducers in Atopic Diseases)

  • 조유란;강상모
    • 한국미생물·생명공학회지
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    • 제40권4호
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    • pp.310-318
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    • 2012
  • 유세포 형광분석에 의한 유산균의 면역증진 효과와 황색포도상구균에 대한 유산균의 항균활성을 확인하여 항아토피 기능성이 있는 유산균을 탐색하고 그 배양법을 검토하였다. T cell에서 CD4+/CD25+/foxp3+ 증가는 Lactobacillus plantarum, Lactococcus lactis subsp. lactis (Lc. lactis)의 순으로 면역증진효과를 보였고, 황색포도상구균에 대한 항균력은 Lc. lactis, Lb. plantarum의 순으로 나타냈다. Lc. lactis 배양액 첨가배지에 Lb. plantarum을 배양한 실험에서는 항균력의 증가가 없었으나 Lb. plantarum 배양액 첨가배지에 Lc. lactis를 배양한 실험에서 황색포도상구균의 항균활성 증대가 나타났다. 항균력을 증가시키는 유산균 첨가배지법의 최적조건은 Lb. plantarum 배양상층액 10%를 첨가하고 가열살균한 배지에서의 Lc. lactis 배양으로 나타났다. 이때 유산균의 항균역가는 Lc. lactis 순수배양 시보다 대수기 말기에 급격히 증가하여, 황색포도상구균의 증식 억제력이 1.29배 높아졌다.

누룩으로부터 젖산세균의 분리 및 특성 (Identification and characteristics of Lactic Acid Bacteria Isolated from Nuruk)

  • 이정훈
    • KSBB Journal
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    • 제15권4호
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    • pp.359-365
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    • 2000
  • Three lactic acid bacteria (C-1 K-3 and T-1 strain) were isolated from Nuruk and characterized subsequently. They were useful strains for production of lactic acid and their growth was inhibited at 10% ethanol pH 4 These strains were identified as lactococcus lactis subsp. lactis NR C-1 Leuconostoc mesenteroides subsp. mesenterides NR K-3 and pediococcus pentosaceus NR T-1 respectively by morphological physiological and biochemical characterization Lac lactis subsp lactis NR C-1 showed the highest lactic acid productivity. Leu measenteroides subsp mesenteroides NR K-3 showed stable lactic acid productivity and its growth was inhibited at pH 4. P pentosaceus NR T-1 had lower lactic acid productivity than the other two bacteria but it could not grow at 10% ethanol pH 4 The lactic acid productivity of these three strains in MRS broth were higher than that in Skim milk media the optimum pH and temperature for the lactic acid production of the three strains were 30-32$^{\circ}C$ and pH 6.0∼6.8 Glucose was the optimal carbon souorce for the lactic acid production. In terms of antagonism lac lactis subsp lactis NR c-1 showed somewhat inhibitory efects against some Gram positive rod and cocci such as Lactobacillus brevis and Streptococcus mitis. And Leu mesenteroides subsp mesenteroides NR K-3 showed the inhibitory effects against Streptococcus mitis but P. pentosaceus NR T-1 didn't show any inhibitory effects against tested strains.

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