• Title/Summary/Keyword: 효모배양

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Measurement of Galactose and Cell Concentrations in Fermentation Process by Near-infrared Spectroscopy (근적외선 분광분석법을 이용한 발효과정 중 갈락토즈 및 미생물 농도의 측정에 관한 연구)

  • 김학성;노상하;김기복;서진호;김명동
    • Proceedings of the Korean Society for Agricultural Machinery Conference
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    • 2003.02a
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    • pp.455-460
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    • 2003
  • 발효공정에 있어 배양법으로는 회분식 배양법, 연속식 배양법과 유가식(fed-batch) 배양법이 있다. 이것은 발효 과정 중 기질과 균류 등의 추가 투입 및 추출에 따른 분류로서 특히, 유가식 배양의 경우 배양액의 농도가 너무 높거나 낮으면 에탄올의 생산이 많아지거나 효모의 성장 속도가 늦어지게 된다 유가식 공정은 항생제, 비타민, 아미노산, 효소 및 재조합 단백질 등의 생산에 주로 이용된다. (중략)

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Studies on the Preservation of Soybean Paste (Part 1) Inhibition of the Growth of Film-forming Yeast (된장의 변질방지에 관한 연구 (제1보) 산막효모의 발육억제)

  • 차원섭
    • Microbiology and Biotechnology Letters
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    • v.6 no.2
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    • pp.81-84
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    • 1978
  • Film-forming yeasts were isolated from deteriolated soybean paste and after identification factors affected on the growth of the organisms were studied to provide information on the protection of the product from deteriolation. The isolated yeasts were identified as Pichia membranaefaciens. The yeasts could grow within the temperature limit of 10$^{\circ}C$ and 68$^{\circ}C$ with optimum at 25$^{\circ}C$. The optimum pH was 6.0 and the growth was reduced in order at 7.0, 5.0, 8.0 and 4.0. The maximum concentration of sodium chloride in Hayduck solution was 15% above which the yeasts ceased to grow.

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Optimization of Environmental Conditions for Hirudin Production from Recombinant Saccharomyces cerevisiae (재조합 효모를 이용한 Hirudin 발효생산조건의 최적화)

  • 이동훈;서진호
    • KSBB Journal
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    • v.9 no.1
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    • pp.8-15
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    • 1994
  • The research has been carried out to optimize a recombinant S. cerevisine fermentation process for the production of an anticoagulant hirudin. The structural gene coding for hirudin was combined with the GAL10 promoter for controlled expression, the MFal signal sequence for hirudin secretion, and the GAL7 terminator for transcriptional termination. Growth medium composition and environmental conditions were optimized for maximizing cell growth and final hirudin concentration. The optimized conditions included yeast extract 40g/$\ell$, casamino acid 5g/$\ell$, g1ucose 20g/$\ell$, galactose 30g/$\ell$, DO 50% and temperature $30^{\circ}C$. These conditions yielded the specific cell growth rate of $0.13hr^{-1}$, the final cell density of 30g cell/$\ell$ and the final hirudin concentration of 64mg/$\ell$ in the batch fermentation with a 2.5$\ell$ jar fermentor.

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Effect of Ginseng Residue Extract on Yeast Growth (효모생육에 미치는 홍삼박의 영향)

  • 김상달;도재호
    • Journal of Ginseng Research
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    • v.10 no.1
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    • pp.1-10
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    • 1986
  • To evaluate the possible utilization of ginseng by-products, chemical components of ginseng residue, reducing ability of DPPH, effect of residue extract on the yeast growth, amino acid contents of yeast cell, increase of residue extract yield by enzyme treatment were studied. Alcohol and water extract residue contained 43-46% total reducing sugar and 14-15% crude protein, while alcohol extract residue had 0.18% n-BuOH extract. Water extract of alcohol extract residue had about 45% reducing ability of DPPH in comparison with that of alcohol extract from ginseng roots. Essential nutrients for the yeast growth were found in extract when Saccharomyces cerevisiae was cultured in Czapeck medium, a compound medium, with the residue. The addition of residue extract to malt medium, a natural medium, enhanced 30-40% yeast growth. And content of each amino acid in yeast cell cultured on malt medium with ginseng residue extract was much more than that of the cell cultured without ginseng extract, but amino acid composition of yeast cell did not differ from one another. The treatment of alcohol extract residue with cellulase increased 250% yield of residue extract.

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Isolation of Wild Killer Yeast from Traditional Meju and Production of Killer Toxin (재래식 메주로부터 야생 Killer 효모의 분리 및 Killer Toxin의 생산)

  • Lee, Jong-Su;Lee, Seong-Hun;Kim, Jae-Ho;Yu, Jin-Yeong
    • KSBB Journal
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    • v.14 no.4
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    • pp.434-439
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    • 1999
  • A wild yeast S-13 which has excellent killer toxin activity to gas-producing yeast of traditional Doenjang and Kochujang was selected among forty seven strains of Meju yeasts and identified as Hansenular capsulata S-13 by investigation of the morphological, cultural and physiological properties. The optimal conditions for the production of killer toxin were investigated. H. capsulata s-13 showed the higest killer toxin activities when it was cultured up to the late-log phase of 36 hr in YEPD medium (pH4.5) at $25^{\circ}C$ H. capsultara S-13 showed killer toxin activities to seven strains of industrial yeasts such as S. cerevisiae, C. veratilis and P. membranaefacieus.

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옥수수 전분박을 이용한 식사료효모생산에 관한 연구

  • 성낙계;김명찬;윤미경;김종규;윤한대
    • Proceedings of the Korean Society for Applied Microbiology Conference
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    • 1976.10a
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    • pp.187.1-187
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    • 1976
  • 우리나라의 전분원료는 74년 이후 옥수수를 주로 사용함에 따라 부산물로써 폐기되는 전분박은 전국적으로 약 2,000M/T으로 추산된다. 이 전분박을 산당화처리하여 식전 및 가축, 양어사료제조를 목적으로 효모를 배양하는 실험을 하였다.(중략)

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어분함량이 다른 배합사료에 Kluyveromyces fragilis, Candida utilis 및 맥주효모가 조피볼락 (Sebastes Schlegili)의 성장 및 체성분에 미치는 효과

  • 김동주;김중균;임한규;이상민
    • Proceedings of the Korean Society of Fisheries Technology Conference
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    • 2000.05a
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    • pp.255-256
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    • 2000
  • 효모는 크기가 매우 작고 영양성분이 풍부하기 때문에 양식 시 먹이생물로 이용되는 동물성 플랑크톤의 먹이나 배합사료의 첨가제로 많이 사용되고 있다. 효모의 종류는 수 없이 많은데 이러한 효모들 중에서 Kluyeromyces fragilis 와 Candida utilis 는 대량배양이 가능하며 병원성 균주가 아닌 먹이생물로서 개발가능성이 높은 것으로 보고되어 있다 (Epifanio, 1979). 또한 Lee et al (1999)은 영양성분을 분석하여 사료첨가제로 이용가능성을 타진한 바 있다. 본 연구는 양식 생산량이 증가하고 있는 조피볼락을 대상으로 경제적인 측면을 고려하여 어분 함량을 달리 첨가한 배합사료에 K. fragilis, C. utilis 및 맥주효모를 각각 3%씩 첨가한 사료를 제조, 공급하여 이들 효모첨가가 조피볼락의 성장과 체성분에 미치는 영향을 조사하였다. (중략)

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고온성방면균에 의한 효모생성에 판한 연구 (제이) 고온성방면균이 생산하는 $\alpha$-amylase의 효모학적 성질

  • 최용진;조홍항;양한철
    • Proceedings of the Korean Society for Applied Microbiology Conference
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    • 1976.04a
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    • pp.184.1-184
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    • 1976
  • 고온성방면균의 이용가능성을 검토할 목적으로 전보에서는 내열성 $\alpha-amylase$ 생산능이 극히 우수한 균주를 전국토양시료로 부터 분리하여 균주의 형태학적성질과 아울러 $\alpha-amylase$ 생산을 위한 배양조건을 검토하였으며 본보에서는 생산된 $\alpha-amylase의$ 효모학적 기본성질을 조사하여 그 결과를 보고코져 한다.

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Studies on the Production of Intra- and Extra-cellular Lipids by the Strains in the Genus RHODOTORULA (Rhodotorula 속(屬) 균주(菌株)에 의(依)한 세포(細胞) 내외(內外) 지질생산(脂質生産)에 관(關)한 연구(硏究))

  • Park, Sung-Oh
    • Applied Biological Chemistry
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    • v.17 no.2
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    • pp.93-116
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    • 1974
  • A potent intracellular-lipid-producing yeast, Rhodotorula glutinis var. glutinis SW-17, was screened out from a variety of arable soils, compost heaps, and fodders, and two strains of excellent extracellular-lipid-producing yeasts, Rhodotorula glutinis var. glutinis SW-5 and Rhodotorula graminis SW-54, were screened out from the surface of many species of leaves. And then the intra- and extra-cellular lipid productions by those Rhodotorula yeasts were studied. The results were as follows: 1. During the shaking culture of 8 days at $24^{\circ}C$, both the intra- and extra-cellular lipid accumulation started almost at the stationary phase of growth, when the nitrogen source in the medium was a little more than half used up. The intracellular lipid production by Rhodotorula glutinis var. glutinis SW-17 reached 58.42% (w/w) of dried yeast, and the extracellular lipid production by Rhodotorula graminis SW-54 amounted to 2.62g per liter of the medium. 2. After the carbon and nitrogen sources in the medium were almost consumed, if the yeasts were shake-cultured further in a state of starvation, the yeast cells re-utilized the already produced intra- and extra-cellular lipids and the lipids completely disappeared in the medium in about 90 days. 3. The relative concentration of carbon and nitrogen sources in the media greatly influenced both the intra- and extra-cellular lipid production. When the nitrogen source in the medium was almost used up for the growth of yeast, and excess carbon sources were still available, the lipid production vigorously proceeded. As long as the nitrogen source concentration in the medium was high, the lipid production was greatly suppressed. 4. The optimum pH for both the intra- and extra-cellular lipid production by those yeasts was pH 5.0-6.0. 5. The fatty acid components of the intracellular lipid of Rhodotorula glutinis var. glutinis SW-17 were myristic, palmitic, palmitoleic, stearic, oleic, linoleic, and linolenic acids. The largest components of the fatty acids were palmitic acid equivalent to 30-45% of the whole fatty acids and oleic acid equivalent to 35-50%. 6. The fatty acid components of the extracellular lipid of Rhodotorula glutinis var. glutinis SW-5 and Rhodotorula graminis SW-54 were myristic, palmitic, stearic, oleic, linoleic, linolenic, 3-D-hydroxypalmitic, and 3-D-hydroxystearic acids. The largest components of the fatty acids were 3-D-hydroxypalmitic acid equivalent to 22-25% of the acids and 3-D-hydroxystearic acid equivalent to 13-17%. 7. The polyol component of the intracellular lipids was only glycerol, whereas the polyols of extracellular lipids were glycerol, mannitol, xylitol and arabitol.

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Production of Candida utilis Biomass on Chinese Cabbage Juice (배추즙액을 기질로 이용한 Candida utilis 균체의 생산)

  • Lee, Nam-Seok;Kyung, Kyu-Hang
    • Korean Journal of Food Science and Technology
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    • v.24 no.3
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    • pp.221-225
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    • 1992
  • The possibility of using Chinese cabbage juice as a substrate for the production of Candida utilis cell mass was explored. Dry cell weight production and cell yield coefficient were 1.35-1.45 g/100 ml undiluted juice and 47-50%, respectively, when C. utilis was grown by shake flask culture at $30^{\circ}C$ for 24 hr on more than three-fold diluted Chinese cabbage juice to make the final sugar content be equal to or less than 1.0%. Supplementation of glucose(2%), $KH_2PO_4(0.2%)$ and $(NH_4)_2SO_4(0.2%)$ to three-fold diluted Chinese cabbage juice did not enhance the dry cell weight yield or the protein content of the yeast cell, while supplementation of yeast extract(0.2%) and peptone(0.2%) increased dry cell weight production and protein content but not as much as the amount of each nutrient added. It was found that Chinese cabbage juice was an excellent substrate for the cultivation of C. utilis.

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