• 제목/요약/키워드: extracellular wall polysaccharides

검색결과 5건 처리시간 0.022초

Dental Plaque Streptococci가 생산하는 세포외 다당류에 관한 연구 (STUDIES ON THE EXTRACELLULAR POLYSACCHARIDES PRODUCED BY ISOLATED DENTAL PLAQUE STREPTOCOCCI)

  • 정태영
    • 대한치과의사협회지
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    • 제9권12호
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    • pp.819-822
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    • 1971
  • For this investigation, author isolated Streptococcus mitis strain SD-9 from the bacterial flora in the human dental plaque, which was incubated in brain-heart infusion media containing 5% sucrose at 37℃ for 24 hours. For the cytochemical demonstration of polysaccharide produced by this strain, a modified thiosemicarbazide osmium method (Critchley et al., 1967) was used. After fixation with this reagent, the harvested cells was suspended in 1% agar for the higher concentration of cells(Kellenberger et al., 1964). And they were dehydrated in the various concentration of ethanol, and embedded in Epon 812(Luft, 1961). Sectioning was done with the Sorvall MT-2 Porter Blum ultramicrotome by means of a glass knife, and the sections were stained with saturated uranyl acetate and lead citrate (Raynolds, 1963). All preparations were examined in a electron microscope, Hitachi HU-ll E-1 type. The morphological features of extracellular polysaccharide produced by Streptococcus mitis strain SD-9 were appeared in 3 structurally different forms, those are, electron dense fibrillar material linearly arranged adjacent to the outer surface of cell wall, highly electron dense globular material adjacent to the outer surface of cell wall, and strutureless fluffy meshwork of possible very fine filament.

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Lactococcus lactis subsp. cremoris ATCC 11602-A1의 세포벽 구성분과 Phage 내성과의 관련성에 관한 연구 (The Relationship between the Cell Wall Components of Lactococcus lactis subsp.cremoris ATCC 11602-A1 and Its Bacteriophage Resistance)

  • 이춘화;배인휴;강국희
    • 한국미생물·생명공학회지
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    • 제22권3호
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    • pp.240-245
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    • 1994
  • Relation the phage defense mechanism of phage resistant Lactococcus lactis subsp. cremoris ATCC 11602-A1 to its cell wall components was investigated. To determine whether teichoic acid which is known to be one of the phage receptor site present on the cell wall, phage adsorption was examined after treatment 5% TCA(60%$\CIRC $C) and concanavalin A to the cell wall of A1 and parent strain. However, the adsorption rate of two strains did not change. Total amount of phosphate after TCA treatment did not change in both strains, but a difference between the two strains was observed. Ribitol and glycerol, components of teichoic acid, could not be detected in the cell walls of two strains by GC analysis. These results suggest that although teichoic acid was not present in the cell walls of both strains, the composition of cell wall of two strains was not identical. Measurement of amount of protein and SDS-polyacryamide gel electrophoresis were carried out to examine the involvement of cell wall protein in phage resistance, showing that protein is nothing to do with phage adsorption of parent strain, but phage resistance of A1 is related to protein. Cell wall carbohydrates of A1 contained rhamnose, glucose, and galactose. Total amount of carbohydrate of 1% SDS-treated A1 cell wall was reduced to the level of parent strain. The results suggest that phage resistance of A1 was due to the presence of a higher level of carbohydrates then parent strain, and to interaction of carbohydrate and protein.

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미생물 다당류의 구조와 세포생리학적 기능 (Structures and functions of microbial extracellular or wall polysaccharides in the physiology of producer organisms)

  • 박용일
    • 미생물과산업
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    • 제26권1호
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    • pp.18-30
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    • 2000
  • 질소 고정능이 있는 Nostoc pruniforme를 재료로, 3종의 유기물, glucose, oxalic, 및 ethanol을 N-free medium과 NO$^{[-993]}$ riched medium에 처리해 주었을 때 다음과 같은 효과를 얻었다. 1)N-free medium과 NO$^{[-993]}$ riched medium에서 위의 유기물 모두가 질소 고정과정의 energy원으로서 또는 substrate로서의 유효한 결과를 얻었다. 3)oxalic acid를 처리한 실험에서는NO$^{[-993]}$ richedmedium의 경우 고농도 처리구에서 질소고정량이 많았고 N-free medium은 그 반대의 결과였다. 4)비교구인 control의 질소 고정량은 일예를 제회하고는 전반적으로 고농도 처리구와 저농도 처리구의 중간에 위치했다.

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Exopolysaccharide-Overproducing Lactobacillus paracasei KB28 Induces Cytokines in Mouse Peritoneal Macrophages via Modulation of NF-${\kappa}B$ and MAPKs

  • Kang, Hee;Choi, Hye-Sun;Kim, Ji-Eun;Han, Nam-Soo
    • Journal of Microbiology and Biotechnology
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    • 제21권11호
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    • pp.1174-1178
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    • 2011
  • Exopolysaccharides (EPSs) are microbial polysaccharides that are released outside of the bacterial cell wall. There have been few studies on EPS-producing lactic acid bacteria that can enhance macrophage activity and the underlying signaling mechanism for cytokine expression. In the current study, EPS-overproducing Lactobacillus (L.) paracasei KB28 was isolated from kimchi and cultivated in conditioned media containing glucose, sucrose, and lactose. The whole bacterial cells were obtained with their EPS being attached, and the cytokine-inducing activities of these cells were investigated. Gas chromatography analysis showed the presence of glucose, galactose, mannose, xylose, arabinose, and rhamnose in EPS composition. EPS-producing L. paracasei KB28 induced the expression of tumor necrosis factor (TNF)-${\alpha}$, interleukin (IL)-6, and IL-12 in mouse macrophages. This strain also caused the degradation of $I{\kappa}B{\alpha}$ and phosphorylation of the major MAPKs: Jun N-terminal kinase (JNK), p38, and extracellular signal-regulated kinase (ERK)1/2. The use of pharmacological inhibitors showed that different signaling pathways were involved in the induction of TNF-${\alpha}$, IL-6 and IL-12 by L. paracasei KB28. Our results provide information for a better understanding of the molecular mechanisms of the immunomodulatory effect of food-derived EPS-producing lactic acid bacteria.

영지의 균사체성 ${\beta}-glucan$에 의한 Raw 264.7 대식세포의 Nitric Oxide생성 (Production of Nitric Oxide in Raw 264.7 Macrophages treated with Ganoderan, the ${\beta}-Glucan$ of Ganoderma lucidum)

  • 한만덕;이은숙;김영권;이준우;정훈;윤경하
    • 한국균학회지
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    • 제26권2호통권85호
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    • pp.246-255
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    • 1998
  • 영지균사체로부터 기능적인 면역활성 물질을 얻고자, 여러 조건으로 추출된 ${\beta}-glucan$성 다당류(GAM)의 Raw 264.7 대식세포 활성 정도를 알아보았다. GAN으로 자극된 Raw 264.7 대식세포는 대조군보다 약 $2{\sim}5$배의 nitric oxide 생성을 촉진하였다. 대식세포의 활성화 정도는 GAM의 구조와 분자량 그리고 화학적 조성에 따라 NO생성에 차이를 보였다. 서당을 탄소원으로 배양된 균사체로부터 추출된 알칼리 가용성이며 수용성인 G-BUC로 활성화된 Raw 264.7세포는 $22{\mu}M$의 NO생성을 유도하였다. G-SUC(WS)는 87%의 탄수화물과 3.4%의 단백질로된 평균분자량 30 kD의 다당류이다. 탄수화물의 구성당은 48%의 포도당과 22%의 mannose등으로 구성된 glucomannan성 GAM이다. 세포분획성 GAM가운데 세포벽으로부터 추출된 알칼리 가용성(CW-AB-WS)인 ${\beta}-glucan$성 다당류가 가장 많은 NO생성을 촉진시켜 영지의 대식세포 활성 다당류로 가장 잠재력이 있는 다당류인 것으로 나타났다. NO생성에 GAN과 대식세포 활성물질(LPS 및 $IFN-{\gamma}$)의 혼합 효과는 독자적인 자극보다는 혼합하여 자극했을 때 NO의 생성이 증폭되었다. GAM으로 활성화된 대식세포의 유사분열은 대조군에 비해 현저히 억제되었으며, 활성화된 대식세포의 배양액은 in vitro에서 L1210 암세포 주에 세포독성을 나타내었다. 이와 같은 결과로 보아 영지의 ${\beta}-glucan$성 다당류(GAN)는 ${\beta}-anomeric$ glucan receptor를 갖고 있는 대식세포를 자극하여 NO를 생성하며, 이때 NO생성의 촉진하는 다당류의 조건은 어느정도의 수용성을 갖고 있는 소량의 단백질이 포함된 고분자성 ${\beta}$glucan다당류이다.

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