• 제목/요약/키워드: optimization of culture conditions

검색결과 316건 처리시간 0.022초

Burkholderia sp. OS17의 항균활성 증진을 위한 배양최적화 (Antimicrobial activities of Burkholderia sp. strains and optimization of culture conditions)

  • 남영호;최아영;황병수;정유진
    • 미생물학회지
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    • 제54권4호
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    • pp.428-435
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    • 2018
  • 본 연구는 담수환경에서 항균활성을 보유한 미생물을 발굴하고, 활성 증진을 위해 배양조건을 최적화하는 것이다. 상주시 중동면 오상저수지에서 시료를 채취하여 38종의 미생물을 순수분리하였다. 16S rRNA 염기서열 분석에 근거하여 Proteobacteria강(22종), Actinobacteria강(7종), Bacteroidetes강(6종), Firmicutes강(3종)으로 구성되어있는 것을 확인하였다. 메티실린내성 황색포도상구군 등 10종의 유해미생물에 대한 항균활성을 보유한 Burkholderia sp. OS17 균주를 선발하였다. 항균활성 증진을 위한 상용배지, 온도, 초기 pH별 생육 및 항균활성 비교실험을 수행하였다. OS17 균주는 YPD 배지, $35^{\circ}C$, pH 6.5로 배양했을 때 가장 활성이 높았다. LB, NB, TSB, R2A 배지와 $20^{\circ}C$, $25^{\circ}C$ 배양했을 때는 생장은 가능하나 항균활성이 전혀 없었다. 이전결과를 바탕으로 YPD 배지, $35^{\circ}C$에서 배양하면서 5 L fermenter를 이용하여 생육, 항균활성, pH 확인을 통해 배양 48시간을 최적 배양시간으로 선정하였다. 항균활성을 보유한 미생물의 배양 최적화는 항균물질 생산에 영향을 미치고, 이는 상업적 응용에 이점으로 작용할 수 있다.

Strain Selection and Optimization of Mixed Culture Conditions for Lactobacillus pentosus K1-23 with Antibacterial Activity and Aureobasidium pullulans NRRL 58012 Producing Immune-Enhancing β-Glucan

  • Sekar, Ashokkumar;Kim, Myoungjin;Jeong, Hyeong Chul;Kim, Keun
    • Journal of Microbiology and Biotechnology
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    • 제28권5호
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    • pp.697-706
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    • 2018
  • Lactobacillus pentosus K1-23 was selected from among 25 lactic acid bacterial strains owing to its high inhibitory activity against several pathogenic bacteria, including Escherichia coli, Salmonella typhimurium, S. gallinarum, Staphylococcus aureus, Pseudomonas aeruginosa, Clostridium perfringens, and Listeria monocytogenes. Additionally, among 13 strains of Aureobasidium spp., A. pullulans NRRL 58012 was shown to produce the highest amount of ${\beta}$-glucan ($15.45{\pm}0.07%$) and was selected. Next, the optimal conditions for a solid-phase mixed culture with these two different microorganisms (one bacterium and one yeast) were determined. The optimal inoculum sizes for L. pentosus and A. pullulans were 1% and 5%, respectively. The appropriate inoculation time for L. pentosus K1-23 was 3 days after the inoculation of A. pullulans to initiate fermentation. The addition of 0.5% corn steep powder and 0.1% $FeSO_4$ to the basal medium resulted in the increased production of lactic acid bacterial cells and ${\beta}$-glucan. The following optimal conditions for solid-phase mixed culture were also statistically determined by using the response surface method: $37.84^{\circ}C$, pH 5.25, moisture content of 60.82%, and culture time of 6.08 days for L. pentosus; and $24.11^{\circ}C$, pH 5.65, moisture content of 60.08%, and culture time of 5.71 days for A. pullulans. Using the predicted optimal conditions, the experimental production values of L. pentosus cells and ${\beta}$-glucan were $3.15{\pm}0.10{\times}10^8CFU/g$ and $13.41{\pm}0.04%$, respectively. This mixed culture may function as a highly efficient antibiotic substitute based on the combined action of its anti-pathogenic bacterial and immune-enhancing activities.

Optimization of submerged culture conditions for the mycelial growth and exo-biopolymer production by Cordyceps millitaris

  • 박종필;;송치현;윤종원
    • 한국생물공학회:학술대회논문집
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    • 한국생물공학회 2000년도 추계학술발표대회 및 bio-venture fair
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    • pp.317-320
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    • 2000
  • The optimal temperature and pH for both mycelial growth and exe-biopolymer production by Cordyceps millitaris in shake flask culture were found to be $20^{\circ}C$ and 6.0, respectively. Sucrose (4%) and corn steep powder (1%) were the most suitable carbon and nitrogen source for mycelial growth and exo-biopolymer production. The maximum specific growth rate $(0.142h^{-1})$ was achieved when sucrose was used as the sole carbon source. Exo-biopolymer production was increased with the increase in C/N molar ratio concentration, probably due to the facilitated carbon uptake. Under the optimal culture conditions, the maximum mycelial growth exe-biopolymer concentration were reached to around 13.3 g dry cell weigh/l and 3.33 g/l, respectively.

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Bacillus subtilis JK-1의 생물계면활성제 생산을 위한 배양 특성 (Characteristics of Culture Conditions for the Production of Crude Biosurfactant by Bacillus subtilis JK-1)

  • 김지연
    • Journal of Applied Biological Chemistry
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    • 제54권3호
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    • pp.153-158
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    • 2011
  • 본 연구에서는 Bacillus subtilis JK-1의 생물계면활성제 생산을 위한 배양 특성을 조사하기 위하여 다양한 배양 온도와 배지의 pH, NaCl 농도에 따른 균주의 생장과 배양액의 pH, crude 생물계면활성제의 표면장력을 배양 시간대별로 측정하였다. B. subtilis JK-1은 $15-45^{\circ}C$와 pH 6-10, 0-10% (w/v) NaCl 농도의 환경에서 생장과 생물계면활성제 생산이 가능하였으며, 배양액의 pH는 중성 또는 약알칼리성으로 점차 변화 하였다. 생물계면활성제 생산은 pH 7.0의 초기 배지에서 $35^{\circ}C$, 48시간 동안 배양했을 때 최대였으며, 이 때의 표면장력은 24.0mN/m이었다. 그리고 배지 내 NaCl 농도가 0% (w/v)에서 10% (w/v)로 증가할수록 균주 생육도는 감소하였고, 최종 배양액의 pH는 약알칼리성에서 산성으로 변화하였으며, 표면장력 값은 증가하였다.

키토산분해효소 생산을 위한 Bacillus sp. P16 배양조건의 최적화 (Optimization of Culture Conditions of Chitosanase-producing Bacillus sp. P16)

  • 정미라;조유영;지연태;박노동
    • Applied Biological Chemistry
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    • 제42권3호
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    • pp.193-198
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    • 1999
  • 키토산분해효소를 분비하는 세균 Bacillus sp. P16의 최적배양조건을 조사하였다. 키토산분해효소 생산을 위한 최적 탄소원은 0.5%분말 키토산이었으며, 최적 질소원은 1% tryptone이었다. 최적온도는 $37^{\circ}C$였으며, 최적 초기 pH는 7.0이었다. 이 조건에서 $60{\sim}$72시간 배양하였을 때 효소 생산이 최고에 도달하였으며, 효소활성은 약 30% 증가하였다. 이를 발효조에서 배양하면 $6{\sim}$12시간 배양으로 최대활성에 도달하였으며, 효소 생산은 약 100% 증가하였다.

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Beauveria bassiana Bb08의 살충성 물질 생산을 위한 배양조건의 통계적 최적화 (Statistical Optimization of Culture Conditions for the Production of Aphicidal Metabolites of Beauveria bassiana Bb08)

  • 고은수;임영훈;정형철;최재필;박인서;김정준;이동진;김근
    • 한국미생물·생명공학회지
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    • 제41권4호
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    • pp.398-406
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    • 2013
  • 본 연구에서는 B. bassiana Bb08가 생산하는 진딧물 살충 대사산물의 최대 생산을 위하여 박스벤켄(Box-Behnken) 디자인과 표면반응분석을 이용한 통계적 방법을 사용하였다. 균배양을 위한 배지는 옥수수분말, 미강, 옥수수침지액분말로 구성되었다. 균배양액은 원심분리 후 상등액을 $0.45{\mu}m$ 막여과지로 여과한 후 3령의 목화진딧물에 살포하였고, 6일 동안 매일 죽은 진딧물 수를 계수하여 살충율을 계산하였다. 통계분석한 결과 최적의 배양조건은 온도 $26.2^{\circ}C$, 배지 초기 pH 5.9, 플라스크 진탕 속도 209.0 rpm, 그리고 균배양 시간은 5.9일로 나타났다. 여과액 살포 후 4, 5, 그리고 6일째 기대 살충율은 각각 76.8, 84.9, 그리고 89.4%이었다, 배양조건 4가지 모두 살충성 대사산물 생산에 유의한 영향을 미쳤고, 영향이 큰 요인 순서는 온도, pH, 배양시간, 진탕속도의 순서로 분석되었다.

표고버섯 첨가 찹쌀머핀의 최적화 및 품질특성 (Optimization of Sweet Rice Muffin Processing Prepared with Oak Mushroom (Lentinus edodes) Powder)

  • 김보람;주나미
    • 한국식생활문화학회지
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    • 제27권2호
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    • pp.202-210
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    • 2012
  • The purpose of this study was to bake sweet rice muffins with oak mushroom ($Lentinus$ $edodes$) powder. The process included substituting sweet rice flour for cake flour and adding oak mushroom powder. This study determined the optimal mixing conditions of oak mushroom muffins by adjusting the amounts of oak mushroom powder, whole eggs, and soybean oil. The mixing conditions for the oak mushroom muffins included 3 categories: oak mushroom powder (X1), whole eggs (X2), and soybean oil (X3) by Central Composite Design (CCD) which was optimized by Response Surface Methodology (RSM). Oak mushroom muffin formulation was optimized using rheology. Yellowness (p<0.001) and redness (p<0.05) displayed a linear model pattern, whereas lightness (p<0.05) was represented by a quadratic model. Among the sensory properties, variables that appeared to show significant values such as appearance (p<0.5), texture (p<0.5), and overall quality (p<0.5) were used to identify optimums. The result of mechanical properties showed significant values in gumminess (p<0.5) and chewiness (p<0.5). The numerical and graphical methods used in this study determined that the optimum formulation for oak mushroom powder sweet rice muffins was 8.75 g of oak mushroom powder, 235.95 g of whole eggs, and 19.93 g of soybean oil.

Production of Alkaline Protease by Entrapped Bacillus licheniformis Cells in Repeated Batch Process

  • Mashhadi-Karim, Mohammad;Azin, Mehrdad;Gargari, Seyyed Latif Mousavi
    • Journal of Microbiology and Biotechnology
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    • 제21권12호
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    • pp.1250-1256
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    • 2011
  • In this study, Bacillus licheniformis cells were immobilized by entrapment in calcium alginate beads and were used for production of alkaline protease by repeated batch process. In order to increase the stability of the beads, the immobilization procedure was optimized by statistical full factorial method, by which three factors including alginate type, calcium chloride concentration, and agitation speed were studied. Optimization of the enzyme production medium, by the Taguchi method, was also studied. The obtained results showed that optimization of the cell immobilization procedure and medium constituents significantly enhanced the production of alkaline protease. In comparison with the free-cell culture in pre-optimized medium, about 7.3-fold higher productivity was resulted after optimization of the overall procedure. Repeated batch mode of operation, using optimized conditions, resulted in continuous production of the alkaline protease for 13 batches in 19 days.