• 제목/요약/키워드: Ethanol fermentation

검색결과 907건 처리시간 0.029초

Pichia stipitis에 의한 Xylose 발효의 최적조건 결정 (Determination of Optimum Conditions for Xylose Fermentation by Pichia stipitis)

  • 권순효;유연우서진호
    • KSBB Journal
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    • 제8권5호
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    • pp.452-456
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    • 1993
  • Pichia stipitis CBS 5776에 의한 xylose의 최적 알코올 발효조건에 대한 연구를 수행하였다. 최적 세포성장 및 최대 ethanol 생성은 초가 pH가 5.0인 100 g/l 의 xylose배지를 이용하여 $30^{\circ}C$에서 0.05VVM으로 통기하고 300rpm으로 교반하는 발효 조건에셔 얻을 수 있었다. 이러한 최적 발효조건 서의 최대 비성장속도와 최대 세포농도는 각각 $0.14hr^{-1}$$1.3\times109$ cells/ml이였다. 또한 최대 etha­n nol 농도는 72시간 발효시에 100 g/l 의 xylose 중 에셔 96%을 이용하여 40.2 g/l 을 얻었으며, 이때 의 단위부피당 ethanol 생산성은 0.56 g/l-hr이고 ethanol 수율은 0.42g-ethanol/g-xylose로서 이론수율의 82%였다.

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Electrochemical and Biochemical Analysis of Ethanol Fermentation of Zymomonas mobilis KCCM11336

  • Jeon, Bo-Young;Hwang, Tae-Sik;Park, Doo-Hyun
    • Journal of Microbiology and Biotechnology
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    • 제19권7호
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    • pp.666-674
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    • 2009
  • An electrochemical bioreactor (ECB) composed of a cathode compartment and an air anode was used in this study to characterize the ethanol fermentation of Zymomonas mobilis. The cathode and air anode were constructed of modified graphite felt with neutral red (NR) and a modified porous carbon plate with cellulose acetate and porous ceramic membrane, respectively. The air anode operates as a catalyst to generate protons and electrons from water. The growth and ethanol production of Z. mobilis were 50% higher in the ECB than were observed under anoxic nitrogen conditions. Ethanol production by growing cells and the crude enzyme of Z. mobilis were significantly lower under aerobic conditions than under other conditions. The growing cells and crude enzyme of Z. mobilis did not catalyze ethanol production from pyruvate and acetaldehyde. The membrane fraction of crude enzyme catalyzed ethanol production from glucose, but the soluble fraction did not. NADH was oxidized to $NAD^+$in association with $H_2O_2$reduction, via the catalysis of crude enzyme. Our results suggested that NADH/$NAD^+$balance may be a critical factor for ethanol production from glucose in the metabolism of Z. mobilis, and that the metabolic activity of both growing cells and crude enzyme for ethanol fermentation may be induced in the presence of glucose.

돼지감자 분말을 이용한 고정화 Kluyveromyces marxianus sp.의 에탄올 연속발효 (Continuous Ethanol Fermentation by Immobilized Kluyveromyces marxianus F043 Using Jerusalem Arichoke Powder)

  • 신지현;최언호
    • 한국미생물·생명공학회지
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    • 제23권3호
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    • pp.346-351
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    • 1995
  • To produce ethanol from Jerusalem artichoke powder efficiently, Kluyveromyces marxianus F043 cells were encapsulated in 2% sodium alginate and were cultured in a countinuous reactor to investigate the fermentation properties. Immobilized K. marxianus F043 cells were activated for 48 hours in a fermentor for continuous ethanol production. The culture in a CSTR using a Jerusalem artichoke substrate treated with 2% cellulase showed a decrease in ethanol concentration and an increase in residual saccharide concentration with a increasing dilution rate. Optimum conditions for high ethanol productivity and low residual saccharide output were clarified to be given at a dilution rate of 0.2 h$^{-1}$ and a Jerusalem artichoke medium concentration of 75 g/l. Ethanol productivity of 3.1 g/l-h and saccharide utilization of 62.6% were obtained under the optimum condition. When the fermentation was performed for 3 weeks under these conditions, the effluent medium showed stable ethanol concentrations of 16.3 - 17.9 g/l and viable cells of 6.60-7.16 log cells/ml without contamination. Trace amounts of methyl, n-propyl, iso-butyl, isoamyl alcohols besides ethanol were detected.

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고정화 Zymomonas mobilis 균체로부터 에탄올 생산 (Ethanol Production Using Alginate Immobilized Cells of Zymomonas rnobilis)

  • 한면수;정동효
    • 한국미생물·생명공학회지
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    • 제20권5호
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    • pp.588-596
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    • 1992
  • Zymomonas mobilis KCTC 1534 균체를 alginate에 고정화시킨 후 기질농도의 상관성으로 회분발효와 반연속발효에서 에탄올 생산을 시도하였다. 회분발효에서 17 glucose 농도를 발효시간 25시간에서 최대 에탄올 생산성 2.91g/l.h 얻었고 이경우 비에탄올 생산속도 $29.14g/{\ell}{\cdot}h$, 비기질 소모속도 $60.24g/{\ell}{\cdot}h$, 에탄올 수율 계수 0.48g/g, 기질전환율 98.4이었다. 생산배지의 전량 교환에 변수를 준 반복발효는 교환시간 20-24 시간에서 약 30일 동안 에탄올생산성이 2.24-$2.94g/{\ell}{\cdot}h$, 에탄올 수율계수 0.42-0.51g/g, 기질전환율 95.9-99.6%로 실행할 수 있었다. 반연속 발효의 경우 생산 배지의 교환 간격을 희석속도로 이용한 유효 희석속도 $0.36h^{-1}$에서 17% glucose 농도로 최대 에탄올생산성 $15.7g/{\ell}{\cdot}h$를 얻었고 이 경우 비 에탄올 생산속도 $156.9g/{\ell}{\cdot}h$ 비기질 소모속도 $396.0g/{\ell}{\cdot}h$, 에탄올 수율계수 0.39, 기질전환율 64.7% 이었다.

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수성이상계에서 K.fragilis의 에탄올 추출발효 특성에 관한 연구 (Extractive Ethanol Fermentation Characteristics of K.fragilis in an Aqueous Two Phase System)

  • 김진한;허병기목영일
    • KSBB Journal
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    • 제9권5호
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    • pp.443-449
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    • 1994
  • 여러 가지 조성의 PEG 20000jDx로 구성한 수성 이상계를 사용한 에탄올 추출발효실험을 통하여 K. fragilis에 의한 돼지감자 주스의 발효 특성을 초기 당농도 및 생성 알코올 농도의 함수로 규명하여 다음의 결과를 얻었다. 균체의 비증식속도 빛 에탄올 비생성속도는 PEG 및 Dx 농도가 낮을수록 증가하였다. 비증식속도는 조성에 무관하게 초기 당농도 $80g/\ell$에서 최대치를 보였고, 에탄올 비생성속도는 $120g/\ell$최대치를 보였다. 생성 알코올 농도에 의한 저해 영향은 비증식속도에 대하여 지수함수형 을, 에탄올 비생성속도에 대하여 쌍곡선함수형을 나타냈다. Dx 농도가 2.5~5% 범위에셔 PEG 농도 가 낮을수록 에탄올 저해 영향은 감소하였다. 총괄 에탄올 생산성은 초기 당농도가 증가할수록 높았으 며 생산성이 최대치에 도랄하는 소요시간도 당농도가 증가함에 따라 증가하였다. 시간별 에탄올 생산 속도는 초기 당농도 $160g/\ell$ 에서 가장 높은 값을 보 였다. 총괄 에탄올 생산성은 대조실험에 비하여 수 성이상계 추출발효를 통하여 1.2배 이상 증가하였고 초기 당농도가 높을수록 이상계 추출발효가 더욱 유리한 것으로 나타났다.

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Effect of Different Pretreatment Methods on the Bioconversion of Rice Bran into Ethanol

  • Eyini, M.;Rajapandy, V.;Parani, K.;Lee, Min-Woong
    • Mycobiology
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    • 제32권4호
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    • pp.170-172
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    • 2004
  • The efficiency of acid, enzyme and microbial pretreatment of rice bran was compared based on the content of cellulose, hemicellulose, reducing sugars and xylose in the substrate. An isolate of Aspergillus niger or a strain of Trichoderma viride(MTCC 800) was employed for microbial pretreatment of rice bran in solid state. Acid pretreatment resulted in the highest amount of reducing sugars followed by enzyme and microbial pretreatment. A. niger showed a higher rate of hydrolysis than T. viride. The rice bran hydrolysate obtained from the different methods was subsequently fermented to ethanol either by Zymomonas mobilis(NCIM 806) or by Pichia stipitis(NCIM 3497). P. stipitis fermentation resulted in higher ethanol(37% higher) and biomass production($76{\sim}83%$ higher) than those of Z. mobilis. Maximum ethanol production resulted at 12h in Zymomonas fermentation, while in Pichia fermentation, it was observed at 60h. Microbial pretreatment of rice bran by A. niger followed by fermentation employing P. stipitis was more efficient but slower than the other microbial pretreatment and fermentation.

Simultaneous Saccharification and Fermentation of Ground Corn Stover for the Production of Fuel Ethanol Using Phanerochaete chrysosporium, Gloeophyllum trabeum, Saccharomyces cerevisiae, and Escherichia coli K011

  • Vincent, Micky;Pometto III, Anthony L.;Leeuwen, J. (Hans) Van
    • Journal of Microbiology and Biotechnology
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    • 제21권7호
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    • pp.703-710
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    • 2011
  • Enzymatic saccharification of corn stover using Phanerochaete chrysosporium and Gloeophyllum trabeum and subsequent fermentation of the saccharification products to ethanol by Saccharomyces cerevisiae and Escherichia coli K011 were achieved. Prior to simultaneous saccharification and fermentation (SSF) for ethanol production, solid-state fermentation was performed for four days on ground corn stover using either P. chrysosporium or G. trabeum to induce in situ cellulase production. During SSF with S. cerevisiae or E. coli, ethanol production was the highest on day 4 for all samples. For corn stover treated with P. chrysosporium, the conversion to ethanol was 2.29 g/100 g corn stover with S. cerevisiae as the fermenting organism, whereas for the sample inoculated with E. coli K011, the ethanol production was 4.14 g/100 g corn stover. Corn stover treated with G. trabeum showed a conversion 1.90 and 4.79 g/100 g corn stover with S. cerevisiae and E. coli K011 as the fermenting organisms, respectively. Other fermentation co-products, such as acetic acid and lactic acid, were also monitored. Acetic acid production ranged between 0.45 and 0.78 g/100 g corn stover, while no lactic acid production was detected throughout the 5 days of SSF. The results of our experiment suggest that it is possible to perform SSF of corn stover using P. chrysosporium, G. trabeum, S. cerevisiae and E. coli K011 for the production of fuel ethanol.

Ethanol Production from Lignocellulosic Biomass by Simultaneous Saccharification and Fermentation Employing the Reuse of Yeast and Enzyme

  • KIM, JUN-SUK;KYUNG-KEUN OH;SEUNG-WOOK KIM;YONG-SEOB JEONG;SUK-IN HONG
    • Journal of Microbiology and Biotechnology
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    • 제9권3호
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    • pp.297-302
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    • 1999
  • Simultaneous saccharification and fermentation (SSF) experiments were carried out with a lignocellulosic biomass. The effects of temperature on enzymatic saccharification and the ethanol fermentation were also investigated. The batch SSF process gave a final ethanol concentration of 10.44 g/l and equivalent glucose yield of 0.55 g/g, which was increased by 67% or higher over the saccharification at 42℃. The optimal operating condition was found to vary in several parameters, such as the transmembrane pressure, permeation rate, and separation coefficient, related to the SSF combined with membrane system (semi-batch system). When the fermentation was operated in a semi-batch mode, the efficiency of the enzymes and yeast lasted three times longer than in a batch mode.

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米糠배지에서 酵母에 의한 에탄올 발효액의 평가 (Assessment of Ethanol Fermentation with Rice Bran by Yeasts)

  • 손경현;윤종수;성용분;이강표;김재철;이재흥
    • 한국미생물·생명공학회지
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    • 제20권1호
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    • pp.85-90
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    • 1992
  • Saccharomyces속 효모를 사용하여 미강을 배지로 하여 에탄올을 발효특성을 조사하였다. 액화효소와 당화효소를 전처리한 미강에서 여러 Saccharomyces속 효모들을 배양한 결과 Saccharomyces cerevisiae IFO 2346이 높은 에탄올 생성 및 유리아미노산 함량을 나타내었다. 균체성장은 발효 24시간에 $3\times 10^8$cell/ml로 증가하였으며, 발효 72시간후 4.7의 에탄올을 생성하였다. 유리아미노산 총량은 발효과정중 1,099mg/l에서 829mg/l로 감소하였으나, glutamic acid, histidine 및 isoleucine은 오히려 각각 218%, 31%5 및 1%48로 증가하였다.

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홍조류(Eucheuma denticulatum)를 이용한 바이오에탄올 생산 (Bioethanol Production from the Red Seaweed Eucheuma denticulatum)

  • 김상원;곽승희;라채훈;김성구
    • 한국미생물·생명공학회지
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    • 제45권4호
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    • pp.316-321
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    • 2017
  • Hyperthermal acid hydrolysis pretreatment of Eucheuma denticulatum was carried out using 12% (w/v) seaweed slurry and 90 mM $H_3PO_4$ at $150^{\circ}C$ for 10 min. The use of Candida lusitaniae with adaptive evolution was evaluated for ethanol fermentation. The levels of ethanol production by separate hydrolysis and fermentation (SHF) at 72 h with non-adapted and adapted C. lusitaniae were 10.1 g/l with ethanol yield ($Y_{EtOH}$) of 0.23, and 18.1 g/l with $Y_{EtOH}$ of 0.45, respectively. Adaptive evolution was employed in this study to improve the efficiency of ethanol fermentation. Development of the SHF process could enhance the overall ethanol fermentation yields of the red seaweed E. denticulatum.