• 제목/요약/키워드: Microbial Culture

검색결과 876건 처리시간 0.033초

Characterization of Interphase Microbial Community in Luzhou-Flavored Liquor Manufacturing Pits of Various Ages by Polyphasic Detection Methods

  • Li, Hui;Huang, Jun;Liu, Xinping;Zhou, Rongqing;Ding, Xiaofei;Xiang, Qianyin;Zhang, Liqiang;Wu, Chongde
    • Journal of Microbiology and Biotechnology
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    • 제27권1호
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    • pp.130-140
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    • 2017
  • It is vital to understand the changing characteristics of interphase microbial communities and interspecies synergism during the fermentation of Chinese liquors. In this study, microbial communities in the three indispensable phases (pit mud, zaopei, and huangshui) of Luzhou-flavored liquor manufacturing pits and their shifts during cellars use were first investigated by polyphasic culture-independent approaches. The archaeal and eubacterial communities in the three phases were quantitatively assessed by combined phospholipid ether lipids/phospholipid fatty acid analysis and fluorescence in situ hybridization. In addition, qualitative information regarding the microbial community was analyzed by PCR-denaturing gradient gel electrophoresis. Results suggested that the interphase microbial community profiles were quite different, and the proportions of specific microbial groups evolved gradually. Anaerobic bacteria and gram-positive bacteria were dominant and their numbers were higher in pit mud ($10^9$ cells/g) than in huangshui ($10^7$ cells/ml) and zaopei ($10^7$ cells/g). Hydrogenotrophic methanogenic archaea were the dominant archaea, and their proportions were virtually unchanged in pit mud (around 65%), whereas they first increased and then decreased in zaopei (59%-82%-47%) and increased with pit age in huangshui (82%-92%). Interactions between microbial communities, especially between eubacteria and methanogens, played a key role in the formation of favorable niches for liquor fermentation. Furthermore, daqu (an essential saccharifying and fermentative agent) and metabolic regulation parameters greatly affected the microbial community.

용존산소 농도 조절이 미생물유래 Transglutaminase 생산에 미치는 영향 (The Effect of Dissolved Oxygen on Microbial Transglutaminase production by Streptoverticillium morbaraense)

  • 유재수;전계택;정용섭
    • KSBB Journal
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    • 제18권2호
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    • pp.155-160
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    • 2003
  • Streptoverticillium morbaraene로부터 미생물 유래 transglutaminase 생산을 위하여 최적의 용존산소 농도를 구명하였다. 용존산소는 용존산소 농도 자동 조절 시스템에 의해 조절되었다. 발효 중 용존산소 농도 조절을 위하여 통기속도는 0.3-3.9 L/min, 교반속도는 260-360 rpm으로 각각 범위를 설정하였다. 용존산소 농도를 조절한 다양한 회분식 배양에서 용존산소가 20%일 때 최대 미생물유래 transgiutaminase 생산이 가능하였다. 최분배양에서 용존산소 농도를 20%로 조절한 경우 미생물유래 transglutaminase 생산은 2.12 U/mL이었고, 용존산소를 조절하지 않은 회분식 배양의 미생물유래 transglutaminase 생산보다 1.1배 향상되었다. 역시 가장 높은 미생물유래 transglutaminase 생산은 용존산소를 20%로 조절한 유가식 배양에서 가능하였으며, 용존산소를 조절하지 않은 회분식 배양의 미생물유래 transglutaminase 생산에 비교해서 1.3배 증가하였다. 최대 건조균체량과 미생물유래 transglutaminase 생산은 각각 13.2 g/L와 2.6 U/mL이었다. 용존산소를 20%로 용존산소 농도 자동 조절 시스템에 의해 조절한 유가식 배양은 미생물유래 transgiutaminase 생산에 적절하였으며 다른 미생물 배양에도 적용할 수 있을 것으로 판단된다.

Purification and Characterization of Caseinolytic Extracellular pretense from Bacillus amyloliquefaciens S94

  • Son, Eui-Sun;Kim, Jong-Il
    • Journal of Microbiology
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    • 제40권1호
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    • pp.26-32
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    • 2002
  • From the culture supernatant of the psychrotrophic strain of Bacillus amyloliquefaciens an extracellular serine protease was purified to apparent homogeneity by successive purification steps using QAE-Sephadex, SP-Sephadex and Sephacryl S-100 column chromatography. The pretense is monomeric, with a relative molecular mass of 23,000. It is inhibited by the serine protease inhibitor phenylmethylsulfonyl fluoride, but not by EDTA. The enzyme is most active at pH 9-10 and at $45^{\circ}C$, although it is unstable at $60^{\circ}C$.

Isolation of Microorganisms for Biotechnological Application

  • Franco, Christopher-M.M.;Mcclure, Nicholas-C.
    • Journal of Microbiology and Biotechnology
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    • 제8권2호
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    • pp.101-110
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    • 1998
  • The extent of biological diversity being revealed by molecular techniques accentuates the need to develop methods to isolate and culture the large numbers of microorganisms that remain to be studied. The discovery and characterization of novel microorganisms will provide information useful in understanding microbial ecosystems and have the potential to lead to new products for the biotechnology industry. In this review, the use of innovative techniques and exploration of unusual ecosystems, that have begun to address the challenge of isolating the "uncultured" members of the microbial population, are examined.

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유기염소계 난분해성 산업폐수의 처리를 위한 미생물제제의 개발 (Development of Microbial Augmentation for the Treatment of Recalcitrant Industrial Wastewater Containing Chlorinated Organic Compounds)

  • 이현돈;임성원;서현효
    • 생명과학회지
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    • 제24권8호
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    • pp.887-894
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    • 2014
  • 유기염소계 난분해성 산업폐수처리에 효과적인 미생물제제 개발을 위하여 PCP (pentachlorophenol)와 TCE (trichloroethylene) 등과 같은 유기계 염소화합물이 오염되어있는 토양 및 산업폐수로부터 PCP 분해활성이 높은 GP5, GP19와 TCE 분해활성이 높은 GA6, GA15를 분리하였다. 이들 분리균주 GP5, GP19, GA6, GA15등은 Acetobactor sp., Pseudomonas sp., Arthrobacer sp., Xanthomonas sp.과 유사한 것으로 나타나 최종적으로 Acetobacter sp. GP5, Pseudomonas sp. GP19, Arthrobacer sp. GA6, Xanthomoas sp. GA15로 명명하였다. 유기염소계 산업폐수의 처리를 위한 복합미생물제제 OC17은 PCP와 TCE를 분해하는 4개의 분리 분리균주와 방향족화합물 분해균주인 Acinetobacter sp. KN11, Neisseria sp. GN13의 배양액을 혼합하여 제조하였다. 복합미생물제제 OC17은 $2.8{\times}10^9CFU/g$의 균체수를 갖고 있으며, 밀도는 $0.299g/cm^3$, 수분함량은 26.8%를 나타내었다. 복합미생물 제제 OC17은 PCP 500 mg/l가 포함되어있는 인공폐수를 이용한 실험에서 배양 65시간에 87%의 분해효율을 나타내었고, TCE (300 uM)의 분해효율은 배양 50시간에 90%의 분해효율을 나타내었다. 복합미생물제제 OC17을 이용한 유기 염소계 산업폐수의 처리효율 시험을 위한 연속배양 실험 에서 10일간 처리 하였을 때 91%의 COD 제거효율을 나타내었다.

음이온계 합성세제의 미생물분해 (Microbial Degradation of Anionic Synthetic Detergents)

  • 김영배;이수래
    • 한국미생물·생명공학회지
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    • 제4권3호
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    • pp.117-121
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    • 1976
  • 음이온계 합성세제인 ABS (alkyl benzene sulfonate)의 분해능이 우수한 균주를 자연계에서 분리하여 Pseudomonas caryophylli로 동정하였다. ABS 10 ppm을 함유한 인공폐수에서 분리균주를 배양시 ABS는 40% 이상, BOD는 89%, COD는 71% 감소되었으며 ABS분해능은 자연미생물군에 의한 혼합배양시의 2배 이상이었다. 분리균주에 의한 시판 합성세제의 분해율은 Hiti 46.2%, Kleenup 37.5%, No.1 29%, OK 27.8%이었다.

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Fermentation of MR-387A and B, Novel Aminopeptidase M Inhibitors by Streptomyces sp. SL-387: Phosphate Repression of Inhibitor Formation

  • YUNG-HEE KHO;CHUNG, MYUNG-CHUL;HYO-KON CHUN;HO-JAE LEE;CHOONG-HWAN LEE,;SU-IL KIM
    • Journal of Microbiology and Biotechnology
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    • 제5권4호
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    • pp.213-217
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    • 1995
  • The effect of inorganic phosphate on the fermentative production of aminopeptidase M inhibitors MR-387A and B by Streptomyces sp. SL-387 has been studied. With inorganic phosphate concentrations higher than 0.78 mM, an inverse correlation was found between the maximum inhibitor production and the initial phosphate concentration added. Growth sensitivity of this actinomycete to arsenate, a phosphate analogue, and the use of magnesium carbonate, a phosphate-trapping agent, suggested that the inhibitor formation was under phosphate repression. Exogenous ATP further increased the degree of phosphate interference in both phosphate-repressed and non repressed culture conditions. The use of a phosphate analogue and a protein synthesis inhibitor also suggested that the phosphate itself repressed inhibitor formation.

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Application of Recent DNA/RNA-based Techniques in Rumen Ecology

  • McSweeney, C.S.;Denman, S.E.;Wright, A.-D.G.;Yu, Z.
    • Asian-Australasian Journal of Animal Sciences
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    • 제20권2호
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    • pp.283-294
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    • 2007
  • Conventional culture-based methods of enumerating rumen microorganisms (bacteria, archaea, protozoa, and fungi) are being rapidly replaced by nucleic acid-based techniques which can be used to characterise complex microbial communities without incubation. The foundation of these techniques is 16S/18S rDNA sequence analysis which has provided a phylogenetically based classification scheme for enumeration and identification of microbial community members. While these analyses are very informative for determining the composition of the microbial community and monitoring changes in population size, they can only infer function based on these observations. The next step in functional analysis of the ecosystem is to measure how specific and, or, predominant members of the ecosystem are operating and interacting with other groups. It is also apparent that techniques which optimise the analysis of complex microbial communities rather than the detection of single organisms will need to address the issues of high throughput analysis using many primers/probes in a single sample. Nearly all the molecular ecological techniques are dependant upon the efficient extraction of high quality DNA/RNA representing the diversity of ruminal microbial communities. Recent reviews and technical manuals written on the subject of molecular microbial ecology of animals provide a broad perspective of the variety of techniques available and their potential application in the field of animal science which is beyond the scope of this treatise. This paper will focus on nucleic acid based molecular methods which have recently been developed for studying major functional groups (cellulolytic bacteria, protozoa, fungi and methanogens) of microorganisms that are important in nutritional studies, as well as, novel methods for studying microbial diversity and function from a genomics perspective.