• Applied Biological Chemistry
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• 제13권1호
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• pp.105-109
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• 1970

탁주 양조에 사용되는 각종원료중의 Thiamin과 쌀, 소맥분 및 옥수수분을 주원료로 일반 탁주양조법에 따라 담금하여 숙성시까지 술덧중의 Thiamin의 소장을 측정하여 다음과 같은 결과를 얻었다. 1. 각원료 100g중의 Thiamin 함량 $({\gamma})$은 쌀 107.8 소맥 분 185.0 옥수수분 410.2 누룩 347.4 소맥분입곡 170.1 옥수수분입곡 257.,3 이었으며 쌀, 소맥분 및 옥수수분중의 함량은 증자에 의하여 $40{\sim}50%$ 파괴됨을 보였다. 2. 쌀, 소맥분 및 옥수수분을 주원료로 하여 각각 담금한 술덧에서 Thiamin의 소장은 각 술덧에서 같은 경향을 보여 누룩단용법의 양구에서 담금 후 1, 2일 사이에 급격히 감소하며 이후 숙성시까지 큰 변동이 없었고 입곡혼용법의 양구에서는 담금초기에 누룩단용법구들에 비하여 감소율이 훨씬 적었다. 또한 각 숙성 술덧 100ml중의 함량은 누룩단용법의 쌀구에서 약 6${\gamma}$, 소맥분구에서 7.5${\gamma}$였고 입곡혼용법의 소맥분구에서 약 $12,4{\gamma}$, 옥수수분구에 서 15.4 ${\gamma}$ 였다. 3. 각숙성 술덧으로 제성한 탁주 100ml중에는 Thiamin이 누룩단용구들에서 $2.4{\sim}3.5{\gamma}$, 입곡혼용법구들에서 약 $5{\sim}7{\gamma}$ 함유됨을 알 수 있었다. 4. 각숙성 술덧의 지게미 100g중에는 Thiamin이 누룩단용법의 쌀구에서 약 $43.7{\gamma}$, 소맥분구에서 $56.1{\gamma}$ 그리고 입곡혼용법의 소맥분구에서 약 $57.5{\gamma}$. 옥수수분구에서 $81.4{\gamma}$ 함유되었다.

• Applied Microscopy
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• 제7권1호
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• pp.21-43
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• 1977

This experiment was undertaken in order to localize the labeled dbcAMP (dibutyryl cyclic AMP) in oocytes whose development has been suppressed by cold dbcAMP for 6 or 19 hours in vitro. Mouse oocytes were obtained from the ovaries of 3-4 week old A strain female mice, by puncturing the Graafian follicles in the modified Krebs-Ringer bicarbonate salt solution under the dissecting microscope. Those oocytes which have intact germinal vesicle were cultured in the basic culture medium supplemented with 0.4% bovine serum albumin (BSA). Cultivation of the oocytes was carried out in a microtube developed by Cho (1974). The cultures were then incubated in a humidified 5% $CO_2$ incubator maintained at $37^{\circ}C$ for 6 or 19 hours (Donahue, 1968). DbcAMP was added to culture medium for a final concentration of 100ug/ml, and $^3H-dbc$ AMP (specific activity 13 Ci/mM) for a final concentration of $40{\mu}Ci/ml$ was also added to the medium. For electron microscopic autoradiography, those oocytes recovered from the culture were washed with phosphate buffer (pH 7.4), and immediately prefixed in a 2.5% glutaraldehyde overnight and postfixed for 2 hours at $4 ^{\circ}C$ in 1% osmium tetroxide in phosphate buffer with pH 7.4 (Palade, 1952). After fixation, the materials were dehydrated in graded alcohol series and embedded in Epon 812 mixture based on the standard procedures (Luft, 1961). The thin sections $600-700{\AA}$ thick were mounted on the grids of 200 meshes. The grids containing sections were coated with a nuclear emulsion Kodak NTB-3 and stored in a cold dark box (at $4^{\circ}C$) for 3 weeks. After exposure, the samples were developed with Kodak D-19 and stained with uranyl acetate and lead citrate. Routine observation was made with Hitachi HU-11E electron microsocope. The results of the observation were as followings: 1. It was found that the labeled dbcAMP penetrated the egg plasma membrane and dispersed at random in the cytoplasm. 2. It was also observed that most of the labeled dbcAMP was attached to microfibrillar lattices portion of the oocyte cytoplasm. There fore, it is presumed that the receptor of the dbcAMP is localized in the microfibrillar lattices of the oocyte. 3. It also seems that some other cell organells such as mitochondria, Golgi complex, cortical granules are not directly related to the action of the dbcAMP. 4. The labeled dbcAMP was neither observed in the membrane nor in the nucleus. Therefore, it seems that there is no relationship between the concentration of dbcAMP and the nuclear membranous permeability. 5. There was no difference in number of dbcAMP particles when oocytes were cultured for 6 hours and 19 hours. 6. However, it was observed that, in same of the oocytes suppressed in germinal vesicle by dbcAMP for 19 hours, cell organells were moved and concentrated to a small portion of the cytoplasm, and that the morphology of the organells greatly changed to an abnormal. form. Therefore, it is supposed that those oocytes were in the process of degeneration. From the above results, it is expected that dbcAMP penetrated the egg membrane and was bound to the receptor which seems to be located in the microfibrillar lattiees portion, and that this dbcAMP-receptor complex inhibited some enzyme system of the oocytes which are essential for the germinal vesicle breakdown.