• 제목/요약/키워드: optimum medium

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Halomonas sp. ES 10에 의한 alkaline protease의 생산 (Production of alkaline protease by the moderate halophile, Halomonas sp. ES 10)

  • 김찬조;김교창;오만진;최성현
    • Applied Biological Chemistry
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    • 제34권4호
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    • pp.307-311
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    • 1991
  • 무염조건에서는 생육할 수 없고 2 M의 NaCl 존재하에서 가장 잘 생육하는 중도 호염성균이며 alkaline protease를 생산하는 ES 10균주를 멸치젓에서 분리하여 Halomonas속 균으로 동정하였다. 이 균은 합성배지인 TSM배지에 DL-alanine의 첨가로 생육이 촉진되고 L-proline의 첨가로 생육이 저해되었다. 이 균의 세포내 $Na^+$함량은 Bacillus subtilis나 E. coli보다 5배 정도 많았으며 $K^+$함량은 25배, $Mg^{2+}$함량은 38배 정도 많았다. 이 균의 Protease 생산은 NaCl 1 M첨가된 Norberg와 Hofsten배지에서 $20^{\circ}C$로 배양했을 때 가장 양호하였다.

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정치배양에서 Acetobacter sp. A9에 의한 셀룰로오스 생산특성 (Characteristics of Cellulose Production by Acetobacter sp. A9 in Static Culture)

  • 손홍주;이오미;김용균;박연규;이상준
    • KSBB Journal
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    • 제15권6호
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    • pp.573-577
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    • 2000
  • 부패된 사과로부터 새롭게 분리된 Acetobacte sp. A9에 의 한 Be 생산조건을 정치배양에 의하여 검토하였다. 본 균주는 2 $25-30^{\circ}C$에서 BC를 생산할 수 있었으며, $30^{\circ}C$에서 최대 생산 능을 나타내었다. 또한 본 균주는 배지의 초기 pH 6.5-8.0에 서 BC를 생산할 수 있었으며, pH 6.5에서 최대 생산능을 나타내었다. BC 생산올 위한 최적 배지조건은 glucose 1.0%, y yeast extract 1.0%, polypeptone 0.7%, acetic acid 0.15% 및 succinic acid 0.02 %였다. Acetobacter sp. A9에 의한 BC 생산 은 "growth-associated type"이었다. 최적 배양조건하에서 배양 6일만에 최대 $24.1 g/m^2$ 의 BC가 생산되어 기본배지보다 약 2배의 생산성 향상이 이루어졌다.. BC 생산능은 배지의 표면 적보다는 배지량과 배지의 깊이에 크게 영향올 받았다.

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Penicillium verruculosum의 Xylan분해활성도의 생성에 대한 Xylan의 영향 (Effect of Xylan on Production of Xylanolytic Activity from Penicillium verruculosum)

  • 조남철;정두례;유영균
    • 한국식품영양과학회지
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    • 제21권4호
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    • pp.423-427
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    • 1992
  • Penicillium verruculosum을 xylan을 함유한 액체배지에서 26일간 배양하면서 xylan 분해활성도를 비롯한 몇 가지 변화를 관찰하였다. Xylan과 PNPX 분해활성도는 단백질량의 증가와 함께 배양 8일까지 급격히 증가하였으나 배양액 중의 환원당의 변화와는 비례하지 않았다. 배양 12일째의 배양상징 액을 탄소원으로서 cell-obiose octaacetate를 가한 배양상징액과 함께 전기영동하였을때 서로 다른 단백질 분포양상을 보였으며 본 배양상징액에 있어 섬유소 성분들에 대한 분해활성도는 거의 나타나지 않은 반면 xylan에 대해서는 매우 높은 활성도를 나타냈다. 배양 상징 액에 xylan을 가했을 때 반응 생성물로서 xylose와 xylobiose를 비롯하여 소당류들이 생성됨으로서 endo-type의 분해활성도로 추정 되었으며 이 때 xylobiose가 가장 많은 비율을 차지했다. Xylan과 PNPX분해 활성도에 대한 배양 상징액의 최적온도는 각각 50~6$0^{\circ}C$와 60~7$0^{\circ}C$였으며 최적pH는 각각 3.0-4.0과 4.0-5.0이었다.

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Methanol 자화성 세균 Pseudomonas sp. ILS-003에 의한 $poly-{\beta}-hydroxybutyric$ acid의 생산 (Production of $poly-{\beta}-hydroxybutyric$ acid by methanol assimilating bacterium, Pseudomonas sp. ILS-003)

  • 이일석;방원기
    • Applied Biological Chemistry
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    • 제34권3호
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    • pp.273-278
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    • 1991
  • Methanol 자화성 세균 Pseudomonas sp. ILS-003 균주를 이용하여 methanol로부터 PHB생산의 최적조건을 검토하였다. PHB 생산에 있어서 초기 pH 6.4, 온도 $30^{\circ}C$ 및 methanol 농도가 1.0(v/v)일 때 최적이었으며, 질소원으로는 $(NH_4)_2SO_4$가 최적이었으며 농도는 0.8g/l로서 C/N비가 17.4이었다. 또한 2가 금속이온의 결핍은 PHB축적효과를 나타내었다. Fed-batch culture에서 methanol 첨가의 효과는 0.25%(v/v)씩 첨가했을 때 가장 좋았다. 상기의 최적조건하에서 96시간 배양시 균체량은 2.78g/l였고 PHB의 양은 1.94g/l로서 건조균체량의 69.8%이었다.

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Medium Optimization for Pediocin SA131 Production by Pediococcus pentosaceus SA131 against Bovine Mastitis Using Response Surface Methodology

  • Park, Yeo-Lang;Lee, Na-Kyoung;Park, Keun-Kyu;Park, Yong-Ho;Kim, Jong-Man;Nam, Hyang-Mi;Jung, Suk-Chan;Paik, Hyun-Dong
    • 한국축산식품학회지
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    • 제30권1호
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    • pp.66-72
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    • 2010
  • Pediococcus pentosaceus SA131 was isolated from jeotgal, is the bacteriocin producer against bovine mastitis pathogens, Streptococcus uberis E290, Enterococcus gallinarum E362, and Staphylococcus epidermidis ATCC 12228. The medium composition for pediocin SA131 production by P. pentosaceus SA131 was optimized using response surface methodology. Component of medium was studied as carbon source (glucose, fructose, lactose, glycerol, sucrose, maltose, and mannitol), nitrogen source (beef extract, yeast extract, peptone, malt extract, and tryptone), mineral and surfactant ($MgSO_4$, $KH_2PO_4$, $(NH_4)_2SO_4$, $MnSO_4$, NaCl, sodium acetate, and Tween 80). Through one factor-at-a-time experiment, glucose, fructose, yeast extract, malt extract, NaCl, $MgSO_4$, and Tween 80 were determined as the good ingredient. The effects of major factors for pediocin SA131 production were investigated by two-level fractional factorial designs (FFD). By a $2^4$ FFD, fructose, yeast extract, and $MnSO_4$ were found to be the important factors for the bacteriocin production. Subsequently, a $2^3$ central composite design (CCD) was adopted to derive a statistical model for optimizing the composition of the fermentation medium. The estimated optimum composition for the production of pediocin SA131 by P. pentosaceus SA131 was as follows; 0.13% fructose, 1% glucose, 1.8% yeast extract, 2.58% $MnSO_4$, 0.2% NaCl, and 0.2% Tween 80. The pediocin production under optimized medium was increased to 1,000 AU/mL, compared to the 400 AU/mL in MRS medium.

병재배 배지살균 시 배지내부의 실시간 온도측정 방법 (Methods of temperature measurement of medium in bottle during sterilization)

  • 정종천;전창성;이찬중;오진아;신평균
    • 한국버섯학회지
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    • 제9권2호
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    • pp.74-79
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    • 2011
  • 본 시험은 버섯 배지를 살균할 때 배지의 내부에 삽입하여 실시간으로 온도 측정값을 저장할 수 있고 고온고압에 견디는 기기(iButton Temperature Data Logger DS-1922T)를 사용하였다. 이 온도측정기는 살균기의 종류, 배지의 종류와 용량, 살균방법별로 일정한 시간 간격에 따라 살균기 및 배지 내부의 온도변화와 살균온도 유지시간의 측정이 가능하였다. 이 실험에 사용한 방법과 결과는 버섯 재배현장에서 응용함으로써 알맞은 배지 살균으로 버섯의 안정생산에 기여할 것으로 기대된다.

배지조성이 Gluconacetobacter hansenii PJK의 Bacterial Cellulose의 교반 생산에 미치는 영향 (Medium Composition Affecting Production of Bacterial Cellulose by Gluconacetobacter hansenii PJK in an Agitated Culture)

  • 정재용;장호남;박중곤
    • KSBB Journal
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    • 제19권6호
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    • pp.451-456
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    • 2004
  • 교반배양시 배지에 첨가되는 에탄올의 농도가 증가할수록 $Cel^-$ mutant의 발생율이 증가하므로 $1.5\%$ 에탄올이 첨가된 배지의 경우 500 rpm보다 높은 교반속도를 유지해야 효과적으로 $Cel^-$ mutant의 발생이 억제되고 BC 생산량을 증가시킬 수 있다. 교반 배양과 같은 강한 shear stress의 배양환경 하에서는 진탕배양의 경우와 달리 $1.0\%$ 에탄올을 분할공급하더라도 BC 생산의 효율성을 높일 수 없었다. Phosphate ion이 첨가된 배지보다 첨가되지 않은 배지에서 BC 생산량이 더 높았다. 배지조성 중 아세트산의 농도를 $1.0\%$로 증가시키면 균체의 건조중량은 변화가 없었으나 BC 생산량이 감소되었다. 배양액의 pH 제어는 BC의 생산에는 영향을 미치지 않았으나 균체의 성장과 WSPS의 생산을 향상시켰다.

Influences of Cultural Medium Component on the Production of Poly($\gamma$-glutamic acid) by Bacillus sp. RKY3

  • Jung Duk-Yeon;Jung Sunok;Yun Jong-Sun;Kim Jin-Nam;Wee Young-Jung;Jang Hong-Gi;Ryu Hwa-Won
    • Biotechnology and Bioprocess Engineering:BBE
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    • 제10권4호
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    • pp.289-295
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    • 2005
  • In this study, the cultural medium used for the efficient production of $\gamma$-PGA with a newly isolated Bacillus sp. RKY3 was optimized. It was necessary to supplement the culture medium with L-glutamic acid and an additional carbon source in order to induce the effective production of $\gamma$-PGA. The amount of $\gamma$-PGA increased with the addition of L-glutamic acid to the medium. The addition of 90 g/L L-glutamic acid to the medium resulted in the maximal yield of $\gamma$-PGA (83.2 g/L). The optimum nitrogen source was determined to be peptone, but corn steep liquor, a cheap nutrient, was also found to be effective for $\gamma$-PGA production. Both the $\gamma$-PGA production and cell growth increased rapidly with the addition of small amounts of $K_2HPO_4$ and $MgSO_4\cdot7H_{2}O$. Bacillus sp. RKY3 appears to require $Mg^{2+}$, rather than $Mn^{2+}$, for $\gamma$-PGA production, which is distinct from the production protocols associated with other, previously reported bacteria. Bacillus sp. RKY3 may also have contributed some minor $\gamma$-PGA depolymerase activity, resulting in the reduction of the molecular weight of the produced $\gamma$-PGA at the end of fermentation.

Bacillus subtilis EK11로부터 Protopectinase 생산을 위한 배지성분의 영향 (Effect of Medium Composition on Protopectinase Production from Bacillus subtilis EK11)

  • 이대희;박은경;문철환;하정욱;이승철;황용일
    • 한국미생물·생명공학회지
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    • 제27권5호
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    • pp.378-384
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    • 1999
  • Protopectinase (PPases) are heterologous group of enzymes that degrade pectin from the insoluble protopection which is constituent of the middle lamella and primary cell wall of higher plants by restricted depolymerization. From the previous report[6], enzymatically separated plant cells, which are produced from plant tissues by PPases treatment, showed well-conserved cellular components with their rigid cell wall and this characteristic is applicable to preparation of novel food material. The purpose of this study is to investigate the effect of medium composition of PPase production from Bacillus subtilis EK11 which was selected as a PPase producer. Various carbon sources and concentrations on PPase production were studied and corn starch at 0.7% was the most effective for production of PPase. Among the nitrogen sources, yeast extract was the most effective for PPase production and the effect of (NH4)2SO4 was notable as inotganic nitrogen source. Inorganic compounds such as KH2PO4, K2HPO4, Na3-citrate.2H2O and MgSO4 were optimized for PPase production. PPase activity was inhibited by the adition of Ba2+ or Zn2+. The optimal medium for PPase production was devised: 0.7% corn starch, 0.3% yeast extract, 1.4% KH2PO4, 0.6% K2HPO4, 0.1% Na3-citrate.2H2O and 0.02% MgSO4. PPase production by using the optimum medium was carried out with shaking cultivation at 37$^{\circ}C$. The maximum PPase activity of 256unit/ml could be obtained after the cultivation for 48hrs. The activity was increased about 2.2timesthan the activity, 112 unit/ml, in basal medium.

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백색부후균에 의한 크라프트 펄프 표백폐수의 탈색 (Decoorizatiion of Kraft Pulp Bleaching Effluent by White -rot Fungi)

  • 조남석;이재원;박종문;최태호;안드레레오노비치
    • 펄프종이기술
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    • 제31권4호
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    • pp.58-68
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    • 1999
  • This experiment was to investigate decoloization characteristics of E1 effluents from the bleaching plant of pulp mill with three white-rot fungi(Trametes versicolor, Ganoderma appanatum and Pleurotus ostreatus).In addition, the effect of carbon and nitrogen resources was discussed on its decolorization. The color removal of E1 effluent during shaking and stationary cultures were 72% and 80%, respectively. Stationary culture was more effective on decolorization of E1 effluent compared to the shaking culture. The optimum inoculum weight was 1.0g based on dry weight of mycelia . The decolorization medium I showed 88% of the color removal of E1 effluent with in one day cultivation of T.versicolor and P.ostreatus . Color removal was increased from 87% to 90%. T.versicolor and P.ostreatus by the addition of 0.5% glucose. By addition of nitorgen sources(ammonium sulfate and ammonium choride), medium was much higher than that of carbon source. With 0.1% ammoniumm sulfate, P.ostreatus and T.versicolor showed 94% and 92% of the color removal within one day of cultivation , respectively. On decolorization medium II, T.versicolor and P.ostretus were 94% of oclor removal with addition of carbon source. The addition of nitrogen source was much more efficient than that of carbon source. With 0.1% amminium chloride, T.versicolor and P.ostreatus showed 95% of its color removal . The decolorization medium II was higher color removal than medium I, and also MnP and laccase were produced. However, the decolorization medium I produced a little MnP and laccase activity. It could be suggested that MnP and laccase may play an important role in decolorization of E1 effluent.

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