• 제목/요약/키워드: Bifidobacterium bifidum

검색결과 112건 처리시간 0.018초

인간 진피섬유아세포에서 Bifidobacterium bifidum 배양액 및 추출액의 자외선B에 대한 보호 효능 (Protective Effects of Bifidobacterium bifidum Culture Supernatants and Intracellular Cell-Free Extracts on Human Dermal Fibroblasts against UV-B Irradiation)

  • 권기영;박귀근
    • 한국식품영양과학회지
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    • 제46권7호
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    • pp.801-808
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    • 2017
  • 본 연구는 장내세균 Bifidobacterium bifidum 배양액과 추출액을 사용하여 자외선B를 조사한 인간 진피섬유아세포에서 세포생존율과 세포 노화 및 세포주기의 변화를 살펴봄으로써 자외선B에 의한 세포 보호 효능을 평가하였다. 우선 자외선B를 조사한 결과 광량에 비례하여 HDFs의 생존율이 감소하였으며 $100mJ/cm^2$ 조사 시 67.3%로 떨어졌으나 B. bifidum 배양액과 추출액 처리 후 세포생존율을 증가시켜 자외선B에 대한 보호 효능이 있었다. 그리고 $SA-{\beta}-gal$ activity 변화를 측정한 결과에서 세포 노화율을 감소시켰음을 확인하였다. 또한, propidium iodide staining을 통하여 세포주기상 Sub-G1기 세포 수가 감소하였으므로 apoptosis를 억제하였고 이는 세포주기를 정상화하는 데 긍정적인 영향을 미쳤다. B. bifidum 배양액과 추출액 처리한 결과 세포 내 활성산소종이 감소함에 따라 p53과 p21의 발현을 감소시켰으며, 따라서 이에 본 연구에서 B. bifidum 배양액과 추출액은 UV-B로 인한 손상을 보호하는 효과가 있음을 규명하였다.

RAW 264.7 대식세포에서의 유산균에 의한 Nitric Oxide와 $TNF-{\alpha}$의 생성 증가 효과 (Effect of Lactic Acid Bacteria (Lactobacillus acidophilus, Streptococcus thermophilus, Bsfidobacterium bifidum) on the Enhancement of the Production of Nitric Oxide and TNF-$\alpha$ in RAW 264.7 Macrophage Cell)

  • 박소희;정명준;김수동;백대헌;강병용;하남주
    • 약학회지
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    • 제49권6호
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    • pp.459-464
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    • 2005
  • The immune reinforcement of the probiotic lactic acid bacteria Lactobacillus acidophilus, Streptococcus thermophilus and Bifidobacterium bifidum was studied in RAW 264.7 cell line treated with diluted solution (dilution to $2^{5}$) of the supernatnats of lactic acid bacteria. RAW 264.7 cell line was used as a macrophage model to assess the effects of lactic acid bacteria on the production of nitric oxide (NO) and cytokine tumor necrosis factor (TNF)-$\alpha$ and cell morphological changes. The production of NO and TNF-$\alpha$ were largely affected by lactic acid bacteria in dose-dependent manner in 24 or 48 hr cultures and cell morphological changes were also largely affected by lactic acid bacteria. Especially Bifidobacterium bifidum differentially stimulated the production of NO and TNF-$\alpha$. NO production was increased by Bifidobacterium bifidum 25 $\mu$l/ml more than LPS (20 ng/ml) control, and TW-$\alpha$ by Bifidobacterium bifidum 6.25 $\mu$l/ml more than LPS (10 ng/ml) control. The in vitro approaches employed here should be useful in further characterization of the effects of lactic acid bacteria on systemic immunity.

High Expression of β-Glucosidase in Bifidobacterium bifidum BGN4 and Application in Conversion of Isoflavone Glucosides During Fermentation of Soy Milk

  • You, Hyun Ju;Ahn, Hyung Jin;Kim, Jin Yong;Wu, Qian Qian;Ji, Geun Eog
    • Journal of Microbiology and Biotechnology
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    • 제25권4호
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    • pp.469-478
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    • 2015
  • In spite of the reported probiotic effects, Bifidobacterium bifidum BGN4 (BGN4) showed no βglucosidase activity and failed to biotransform isoflavone glucosides into the more bioactive aglycones during soy milk fermentation. To develop an isoflavone-biotransforming BGN4, we constructed the recombinant B. bifidum BGN4 strain (B919G) by cloning the structural β-glucosidase gene from B. lactis AD011 (AD011) using the expression vector with the constitutively active promoter 919 from BGN4. As a result, B919G highly expressed β-glucosidase and showed higher β-glucosidase activity and heat stability than the source strain of the β-glucosidase gene, AD011. The biotransformation of daidzin and genistin compounds using the crude enzyme extract from B919G was completed within 4 h, and the bioconversion of daidzin and genistin in soy milk during fermentation with B919G also occurred within 6 h, which was much faster and higher than with AD011. The incorporation of this β-glucosidase-producing Bifidobacterium strain in soy milk could lead to the production of fermented soy milk with an elevated amount of bioavailable forms of isoflavones as well as to the indigenous probiotic effects of the Bifidobacterium strain.

Bifidobacterium에 의한 당근발효 (Fermentation of Carrot Juice by Bifidobacterium)

  • 박소영;고영태;이주연;목철균;박종현;지근억
    • 한국식품과학회지
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    • 제29권3호
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    • pp.571-575
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    • 1997
  • 본 연구에서는 당근을 원료로 하여 Bifidobacterium을 배양하여 발효하며 Bifidobacterium의 배양특성을 살펴보았다. Bifidobacterium의 다양한 균주를 $10^6\;CFU/mL$ 수준으로 접종하여 배양하였을 때 B. longum, B. adolescentis, B. infantis 균주들은 $10^8\;CFU/mL$ 이상으로 자랐고 B. bifidum 균주들은 약간 성장이 저조하여 $10^8\;CFU/mL$ 이하 수준으로 자랐다. 당근 이외의 다른 원료로서 포도, 사과, 오렌지, 복숭아, 배추, 오이 등에 배양하였을 때 복숭아, 오렌지 등에서는 배양이 양호하였으나 포도에서는 Bifidobacterium의 성장이 일어나지 않았다. L. acidophilus와 혼합 배양시 Bifidobacterium 단독 배양시보다 균의 증식이 저하되었고 배양 24시간 후부터 Bifidobacterium의 사멸이 현저하게 일어났다. Bifidobacterium 배양에 의하여 당근의 산미가 증가되며 관능성이 개선되는 것으로 나타났다. 따라서 Bifidobacterium을 이용한 당근 발효식품 개발은 Bifidobacterium균주의 증식에 의한 기능성 증가와 당근의 관능성 개선에 도움이 될 것으로 생각된다.

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Rapid Identification of Lactobacillus and Bifidobacterium in Probiotic Products Using Multiplex PCR

  • Sul, Su-Yeon;Kim, Hyun-Joong;Kim, Tae-Woon;Kim, Hae-Yeong
    • Journal of Microbiology and Biotechnology
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    • 제17권3호
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    • pp.490-495
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    • 2007
  • Lactic acid bacteria (LAB) are beneficial for the gastrointestinal tract and reinforce immunity in human health. Recently, many functional products using the lactic acid bacteria have been developed. Among these LAB, Lactobacillus acidophilus, Lactobacillus rhamnosus, Bifidobacterium longum, and Bifidobacterium bifidum are frequently used for probiotic products. In order to monitor these LAB in commercial probiotic products, a multiplex PCR method was developed. We designed four species-specific primer pairs for multiplex PCR from the 16S rRNA, 16S-23S rRNA intergenic spacer region, and 23S rRNA genes in Lactobacillus acidophilus, Lactobacillus rhamnosus, Bifidobacterium longum, and Bifidobacterium bifidum. Using these primer pairs, 4 different LAB were detected with high specificity in functional foods. We suggest that the multiplex PCR method developed in this study would be an efficient tool for simple, rapid, and reliable identification of LAB used as probiotic strains.

Growth-inhibiting Effects of Brazilian and Oriental Medicinal Plants on Human Intestinal Bacteria

  • Kim, Moo-Key;Lee, Sung-Eun;Lee, Hoi-Seon
    • Journal of Applied Biological Chemistry
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    • 제43권1호
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    • pp.54-58
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    • 2000
  • Methanol extracts of 27 Brazilian plant samples and 10 oriental medicinal plant samples (27 families), using spectrophotometric and paper disc agar diffusion methods under anaerobic conditions, were tested in vitro for their growth-inhibiting activities against Bifidobacterium longum, Bifidobacterium bifidum, Bifidobacterium adolescentis, Clostridium perfringens, and Bacteroides fragilis. The responses varied with bacterial strains, plant species, and tissues sampled. In a test with B. longum and B. bifidum(20 mg/disc), extracts of Acanthopanax sessilifolinus stem bark and Ampelozizyphus amazonicus leaves strongly inhibited the growth of B. longum, whereas other plant samples did not inhibit any intestinal bacteria tested. At 5 mg/disc, adding extracts of Aralia eleta, Euterpe oleracea, and Syzygium guineense to the media strongly inhibited the growth of C. perfringens and B. fragilis without growth inhibition of B. adolescentis, B. longum, and B. bifidum. Extracts of Jacaranda mimosifolia and Ulmus paraifolia significantly inhibited the growth of C. perfringens and B. fragilis as well as B. adolescentis. These results may be indications of at least one of the pharmacological actions of the five Brazilian plants but not oriental medicinal plants tested.

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Rapid Identification of Bifidobacteria in Dairy Products by Gene-targeted Species-specific PCR Technique and DGGE

  • Hong, Wei-Shung;Chen, Ming-Ju
    • Asian-Australasian Journal of Animal Sciences
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    • 제20권12호
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    • pp.1887-1894
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    • 2007
  • In this paper, a rapid and reliable gene-targeted species-specific polymerase chain reaction (PCR) technique based on a two-step process was established to identify bifidobacteria in dairy products. The first step was the PCR assay for genus Bifidobacterium with genus specific primers followed by the second step, which identified the species level with species-specific primer mixtures. Ten specific primer pairs, designed from nucleotide sequences of the 16-23S rRNA region, were developed for the Bifidobacterium species including B. angulatum, B. animalis, B. bifidum, B. breve, B. catenulatum, B. infantis, B. longum, B. minimum, B. subtile, and B. thermophilum. This technique was applied to the identification of Bifidobacterium species isolated from 6 probiotic products, and four different Bifidobacterium spp. (B. bifidum, B. longum, B. infantis, and B. breve) were identified. The findings indicated that the 16S-23S rDNA gene-targeted species-specific PCR technique is a simple and reliable method for identification of bifidobacteria in probiotic products. PCR combined with Denaturing Gradient Gel Electrophoresis (DGGE) for identification of the bifidobacteria was also evaluated and compared with the gene-targeted species-specific technique. Results indicated that for fermented milk products consistency was found for both species-specific PCR and PCR-DGGE in detecting species. However, in some lyophilized products, the bands corresponding to these species were not visualized in the DGGE profile but the specific PCR gave a positive result.

Lactobacillus spp., Bifidobacterium spp. 및 Bacillus coagulans의 과산화수소 저항성과 과산화수소 생성 능력 (Resistant Activity to Hydrogen Peroxide of Lactobacillus spp., Bifidobacterium spp., Bacillus coagulans and Hydrogen Peroxide Generation Capability of Lactobacillus spp.)

  • 이종혁;윤영호
    • Journal of Dairy Science and Biotechnology
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    • 제22권2호
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    • pp.107-112
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    • 2004
  • 과산화수소 형태의 반응성 산소에 대한 Lactobacillus Spp., Bifidobacterium spp. 및 Bacillus coagulans의 저항성과 세포 내에서 생성능력을 측정하기 위하여 본 연구가 수행되었다. Lactobacillus spp. 중에서 높은 과산화수소 저항성을 나타낸 균주는 L. acidophilus CU4111와 L. casei Cu4114인 것으로 나타났고 가장 낮은 저항성을 보인 균주는 L. brevis Cu4206이었다. Bifidobacterium longum CU4131은 높은 수준의 저항성을 나타내며 Bacillus coagulans를 포함하는 포자형성유산균주들은 전반적으로 과산화수소에 대한 저항성 이 높은 것으로 나타났다. 세포질 추출액 중의 과산화수소 함유 농도는 Bifidobacterium bifidum CU 4134가 가장 높고 Lactobacilli spp.의 세포질 추출액 중의 과산화수소 함유 농도는 L. casei CU 4114가 가장 높은 것으로 나타났다.

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Xylogone sphaerospora 유래 ${\beta}$-mannanase 정제 및 Konjac Glucomannan 가수분해 올리고당의 중합도별 Bifidobacterium spp.에 대한 증식활성 (Purification of Xylogone sphaerospora ${\beta}$-mannanase and Growth Activity of Bifidobacterium spp. by Konjac Glucomannan Hydrolysates)

  • 이희정;박귀근
    • Applied Biological Chemistry
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    • 제51권3호
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    • pp.159-163
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    • 2008
  • Sephadex G-100 column chromatography에 의해 Xylogone sphaerospora 유래 ${\beta}$-mannanase의 정제를 수행하여 비활성 8.44 units/ml, 정제배율 56.27을 나타내었다. SDS-PAGE에 의한 단일밴드를 확인하였고, 분자량은 42kDa으로 결정되었다. 정제효소에 의해 konjac glucomannan을 가수분해하여 activated carbon column chromatograph)에 의해 당가수분해물을 분리 회수하여 TLC에 의해 주요 당가수분해물은 합도 3과 4의 hetero type으로 확인되었으며 D.P. 3과 4의 예상되는 구조는 본 연구실에서 확보하고 있는 standard glucomannooligosaccharides에 의한 TLC에서 나타나는 Rf value 상으로 1차적으로 확인하고, Aspergillus niger 5-16 유래 정제 ${\beta}$-mannanase를 단계적으로 처리하여 가수분해 pattern을 TLC로 해석한 결과 D.P. 3의 구조식은 비환원말단 mannose로 부터 2번째에 1분자의 glucose가 결합하고 있는 hetero type의 구조(M-G-M)로, D.P. 4의 구조식은 비환원말단 mannose로부터 3번째에 1분자의 glucose가 결합하고 있는 hetero type의 구조(M-M-G-M)로 예상하고 있다. B. longumm, B. bifidum, B. infantis, B. adolescentis, B. animalis, B. auglutum, B. breve의 생육활성에 대한 중합도 3과4의 영향을 검토하기 위하여 modified-MRS 배지 상에 탄소원으로 중합도 3과 4를 대체하여 생육활성을 비교한 결과 B. longum에서는 D.P 4 glucomannooligosaccharide를 탄소원으로 대체한 경우 표준 MRS배지와 비교하여 3.9배의, D.P. 3을 처리한 경우에도 2.7배의 상대 활성을 나타내어 가장 우수한 생육활성을 나타냈었으며, B. breve의 경우에서도 D.P 4에서 2.47배, D.P 3에서 2.08배의 활성을 나타내었으며 B. bifidum에 있어서는 D.P. 4의 경우 2.8배의 상대활성을 나타내었다. Bifidobacterium 7균주 모두에 대해서 중합도 4의 올리고당이 중합도 3의 올리고당보다 생육활성에 크게 기여하는 것으로 나타났다.

Distribution of Dominant Bifidobacteria in the Intestinal Microflora of Korean Adults and Seniors, Identified by SDS-PAGE of Whole Cell Proteins and 16S rDNA Sequence Analysis

  • KIM TAE WOON;SONG HEE SUNG;KIM HAE YEONG
    • Journal of Microbiology and Biotechnology
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    • 제15권2호
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    • pp.388-394
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    • 2005
  • In order to investigate the distribution of dominant Bifidobacterium species in intestinal microflora of Korean adults and seniors, SDS-PAGE profiles of whole cell proteins were used for the identification of bifidobacteria. To confirm the reliability of SDS-PAGE, the Bifidobacterium species identified by SDS-PAGE of whole cell proteins were validated by using 16S rDNA sequencing analysis. The results of SDS­PAGE corresponded well with those determined by the analysis of 16S rDNA sequencing. Based on the analysis of SDS-PAGE patterns on unidentified fecal strains which showed positive in fructose-6-phosphate phosphoketolase activity, B. adolescentis, B. longum, and B. bifidum were identified in the feces of adults, and B. adolescentis, B. longum, B. bifidum, B. breve, and B. dentium were identified in those of seniors. In most of the fecal samples tested, the predominant Bifidobacterium species consisted of only a few species, and differences in the distribution and numbers of Bifidobacterium species were observed between adults and seniors. B. adolescentis and B. longum were found to be the most common species in feces of adults, but not in seniors. Accordingly, the distribution and abundance of bifidobacteria in the human intestinal microflora varied depending on the age of hosts.