• 제목/요약/키워드: cell separating enzymes

검색결과 3건 처리시간 0.015초

식물세포분리효소를 이용한 채소류의 단세포화 (Enzymatic Maceration of Vegetables with Cell Separating Enzymes)

  • 박용곤;강윤한
    • 한국식품저장유통학회지
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    • 제7권2호
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    • pp.184-188
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    • 2000
  • This study was conducted to investigate enzymatic maceration of radish, cabbage, soybean sprout and carrot with cell separating enzymes in order to obtain individual cells. We studied the macerating properties of Macerozyme R-200, Macerozyme R-10 and Sumyzyme MC on vegetables. Degree of enzymatic maceration was decreasing order of radish, carrot, cabbage and soybean sprout. The degree of enzymatic maceration among macerating enzymes was decreasing order of Macerozyme R-200, Macerozyme R-10 and Sumyzyme MC. The degrees of enzymatic maceration of radish, carrot, soybean sprout and cabbage treated with Macerozyme R-200 for 2hr were 91.0, 80.6, 62.5 and 35.1%, respectively. Total pectin, color and viscosity of carrot macerates increased as the maceration rate increased.

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식물세포분리효소를 이용한 수박과 참외의 단세포 함유 반응물 특성 (Characteristics of Suspension Containing Single Cells from Watermelon and Muskmelon Treated with Cell Separating Enzymes)

  • 박용곤;강윤한
    • 한국식품과학회지
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    • 제36권1호
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    • pp.58-63
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    • 2004
  • 수박과 참외의 황용도 증진을 위하여 조직을 개개의 세포로 분리할 수 있는 단세포화 기술을 적용하였다. 그 결과 이들을 시판 식물세포분리효소인 Macerozyme A와 Sumyzyme MC로 30분에서 120분간 반응시간별 단세포 함유 반응물의 특성을 조사하였다. 단세포화로 얻을 수 있는 수율, 반응률, 단세포 함유 반응물의 색도, 점도, 총당, 총펙틴, 총폴리페놀, 무기질, 유리 아미노산 함량을 조사하였으며 또한 분리된 단세포의 형태변화를 입도분포로 조사하였다. 전반적으로 효소반응시간이 경과 할수록 반응물의 성분 함량은 증가하였으나 세포벽에 의하여 내부 구성성분이 보호를 받아 안정하게 유지되는 것으로 나타났다. 수박과 참외의 무기질 함량은 주스보다는 단세포 함유 반응물에서 상대적으로 함량이 높게 나타났다. 참외의 경우 무기질인 K의 함량은 효소반응물과 주스에서 각각 240.8 mg%, 172.7 mg%였다. 본 연구 결과는 수박과 참외로부터 효소반응 물의을 이용하여 새로운 형태의 음료 개발을 위한 기초자료로 활용 가능할 것으로 판단되었다.

토양으로부터 genomic DNA의 효과적인 분리 (Improved Genomic DNA Isolation from Soil)

  • 강주형;김보혜;이선이;김영진;이준원;박영민;안순철
    • 생명과학회지
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    • 제15권6호
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    • pp.851-856
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    • 2005
  • Although valuable microbes have been isolated from the soil for the various productions of useful components, the microbes which can be cultivated in the laboratory are only $0.1-1\%$ of all microbes. To solve this problem, the study has recently been tried for making the valuable components from the environment by directly separating unculturable micrbial DNA in the soil. But it is known that humic acid originated from the soil interrupts various restriction enzymes and molecular biological process. Thus, in order to prevent these problems, this study modified the method separated soil DNA with phenol, CTAB and PEG. In order to compare the degree of purity for each DNA and the molecular biological application process, $A_{260}/A_{280}$ ratio, restriction enzymes, and PCR were performed. In case of DNA by the modified method, total yield of DNA was lower but $A_{260}/A_{280}$ ratio was higher than the previously reported methods. It was confirmed that the degree of purity is improved by the modified method. But it was not cut off by all kinds of tested restriction enzymes because of the operation of a very small amount of interrupting substances. When PCR was operated with each diluted DNA in different concentrations and GAPDH primer, the DNA by the modified method could be processed for PCR in the concentration of 100 times higher than by the previously reported separation method. Therefore, this experiment can find out the possibility of utilization for the unknown substances by effectively removing the harmful materials including humic acid and help establishing metagenomic DNA library from the soil DNA having the high degree of purity.