Korean Journal of Microbiology (미생물학회지)

The Microbiological Society of Korea (한국미생물학회)
권호 표지

Isolation and Identification of Wild Yeast and Its Use for the Production of Grapewine

야생 효모의 분리.동정 및 이를 이용한 포도주 제조

  • Published : 2007.09.30
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Abstract

The domestic cultured Campbell's Early and Geubong grapes were fermented far the production of red wines with the isolated wild yeast Saccharomyces cerevisiae IJ850. For the isolation of wild yeast, Geubong and Campbell's Early grapejuices were naturally fermented at room temperature for 6 days without adding stater culture. The strain isolated from Geubong which has 1.8 times higher fermentative ability than the strains isolated Campbell Early was selected. The selected strain was identified by using 26S rDNA sequencing. The strain showed 99.7% of similarity with Saccharomyces cerevisiae and thus identified as Saccharomyces cerevisiae IJ850. It was investigated the fermentative ability as the start culture. For the production of grapewine, the final sugar concentrations of grapejuices were adjusted to the $25^{\circ}Brix$ with anhydrous glucose. The grapejuices were fermented at room temperature for 10 days in the air-locked bottles filled with $CO_2$ gas. The final yield and alcohol concentration of Campbell's Early and Geubong grapewines fermented with the isolated wild yeast were 80.8%, 11.0% and 87.8%, 13.0%, respectively. Between the isolated wild yeast S. cerevisiae IJ850 and the commercial yeast S. cerevisiae EC1118, total acidities of grapewines produced with wild yeast were lower than those produced with the commercial yeast. The pH values and the values of color analysis of grapewines produced with both strains were similar. The total phenol contents of campbell's Early and Geubong wines produced with the isolated yeast and the commercial yeast were obtained in the range of 75 to 125mg/L. In conclusion, S. cerevesiae IJ850 isolated from the domestic cultured Geubong grape is able to use to produce grapewines as stater culture.

거봉 포도로부터 분리하여 동정한 야생효모 Saccharomyces cerevisiae IJ850을 이용, 국내산 캠벨얼리와 거봉포도를 발효시켜 적포도주를 제조하고, 이의 발효특성을 분석함으로서 포도주제조용 발효균주로서의 가능성을 알아보고자 하였다. 야생발효균주의 분리를 위하여 안성지역 거봉포도와 캠벨얼리 포도즙을 실온에서 6일 동안 스타터의 첨가없이 자연발효시켜 우세균주를 분리하였다. 거봉에서 분리된 효모의 발효능이 캠벨얼리에서 분리된 효모보다 1.8배정도 높았다. 거봉에서 분리한 발효균주를 분자 생물학적 인 방법 인 26S rDNA 염기서열에 근거하여 동정한 결과, Saccharomyces cerevisiae와 99.7%의 유사성을 나타내어 Saccharomyces cerevisiae IJ850으로 동정되었다. 분리균주를 이용한 포도주의 제조에서는 캠벨얼리와 거봉포도즙의 최종 당도를 $25^{\circ}Brix$로 포도당을 이용하여 보당하고, 이산화탄소를 발효조에 채우고, 실온에서 10일간 발효시켰다. 포도주의 수율은 캠벨얼리가 75%, 거봉이 85%였고 최종 알코올 도수는 캠벨얼리가 11.0%, 거봉이 13.0%이었다. 산업용발효균주인 S. cerevisiae EC-1118과 비교한 결과 총산도는 캠벨얼리와 거봉포도주 모두에서 산업용 발효균주인 EC-1118에 비하여 분리한 S. cerevisiae IJ850에서 낮은 수치를 보였다. 포도주의 pH와 색도 분석에서는 S. cerevisiae IJ850과 S. cerevisiae EC-1118로 제조한 포도주모두에서 비슷한 수치를 보여주었으나, 페놀 성분분석에서는 S. cerevisiae EC-1118로 제조한 캠벨얼리 포도주에서 125 mg/L의 함량을, S. cerevisiae IJ850으로 제조한 거봉포도주에서 75 mg/L의 함량을 나타내었다. 따라서 국내 거봉포도로부터 분리한 S. cerevesiae IJ850는 포도주 생산에 사용될 수 있는 균주로써 그 가능성을 보여주었다.

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