생체 내 실험에서 발효 인삼꽃 추출물(FM), 발효하지 않은 인삼꽃 추출물(FD)과 대조군으로 생리식염수를 2주간 마우스 체중 ㎏ 당 100, 200 ㎎/㎏ B.W.의 농도로 마우스에 경구 투여한 후 LPS에 의해 활성화된 복강 대식세포가 분비하는 염증성 사이토카인 IL-6, TNF-α의 생성량을 측정하였다. 그 결과, IL-6는 발효 LPS로 자극한 경우, 두 가지 농도에서 모두 처리한 군에 비해 높은 증식능을 나타내었고, LPS로 자극한 결과, 특히 발효 인삼꽃 추출물 200 ㎎/㎏ B.W. 농도에서 유의적으로 낮은 IL-6 분비량을 보였다. TNF-α의 경우, 100 ㎎/㎏ B.W.와 200 ㎎/㎏ B.W. 두 농도 모두에서 LPS로 자극하지 않은 경우, 낮은 증식 효과를 보여주었고, 자극한 경우, 인삼꽃 시료를 첨가한 군이 대조군보다 낮은 TNF-α 분비량을 보였으며, FM에서 FD보다 더 TNF-α를 억제하는 효과가 큰 것을 볼 수 있었다. 이상의 결과에 따르면 FD의 사이토카인 IL-6, TNF-α 생성 효과는 200 ㎎/㎏ B.W. 농도 투여 시 효과적으로 면역 세포와 면역 기관의 주요 기능을 증진시킬 가능성이 있을 것으로 사료된다. 이러한 연구결과를 토대로 앞으로 인삼꽃 발효를 이용한 기능성 사료 개발과 더불어 산업적 측면에서 보다 긍정적인 효과를 얻을 수 있을 것으로 판단된다.

오렌지의 위생성 및 보존성을 향상시키고, 수입국의 검역 기준을 정립하기 위한 연구의 일환으로 오렌지에 0.4, 0.6, 0.8, 1, 1.5 kGy로 감마선 조사를 실시하여 3℃에서 60일 동안 저장하면서 미생물 및 이화학적 품질 특성을 조사하였다. 오렌지 1.5 kGy 조사구의 호기성세균, 효모 및 곰팡이는 각각 3.59 log CFU/g, 3.75 log CFU/g에서 1.75 log CFU/g, 2.26 log CFU/g까지 감소하여 조사선량과 저장기간에 따라 유의적인 차이를 보였다. pH는 비조사구와 조사구 사이의 유의적인 차이를 나타내지 않았고, 산도는 조사선량과 저장기간의 증가에 따라 감소하였다. Vitamin C 함량은 조사선량과 저장기간의 증가에 따라 유의적으로 감소하였다. 관능평가는 조사선량과 저장기간이 증가할수록 감소하였고, 1.5 kGy는 색깔, 신맛, 단맛, 향, 질감, 전체적인 선호도에서 가장 낮은 선호도를 보였다. 이상의 결과를 종합하여 볼 때, 감마선 조사는 미생물학적 안정성에는 효과적이지만, 1 kGy와 1.5 kGy는 물리적 특성과 관능 특성에 좋지 않은 영향을 끼치는 것으로 보고, 품질 변화를 최소화하기 위한 최적 선량은 0.4~0.6 kGy 인 것으로 사료된다.

The effect of gamma irradiation on the survival of spore bacteria was investigated in frozen cells (-18℃) with 0.1 M phosphate buffer and inoculated cells in beef. In the case of the frozen cells at log phase, the radiation D_(10) and 12D_(10) values were 0.29 kGy and 3.48 kGy in Bacillus subtilis, 0.39 kGy and 4.68 kGy in Bacillus cereus and 0.46 kGy and 5.52 kGy in Clostridium perfrigens. And inactivation factors were 6.52-10.34 and 10.87-17.24 at the dosage of 3 kGy and 5 kGy, respectively. The radiosensitivity of inoculated cells in beef showed the D_(10) value of 0.59-0.76 kGy, the 12D_(10) value of 7.08-9.12 kGy, and inactivation factors of 3.95-8.47. The radiosensitivity of the frozen cells was higher than that of inoculated cells in beef.

For the purpose of improving hygienic quality of dried-Angelica Keiskei Koidz powder, the effects of ozone treatment and gamma irradiation on the microbial decontamination and physicochemical properties were investigated. Gamma irradiation at 5 to 7.5 kGy resulted in sterilizing total aerobic bacteria, molds and coliforms below detective levels, while ozone treatment for 8 hours up to 18 ppm did not sufficiently eliminate the total aerobic bacteria of the sample. The physicochemical properties of the sample were not changed by gamma irradiation up to 7.5 kGy, whereas, ozone treatment caused remarkable changes in pH, TBA value, chlorophyll, carotenoid and fatty acid compositions. Therefore, this investigation demonstrated conclusively that gamma irradiation was more effective than ozone treatment for decontaminating and sterilizing the dried-Angelica Keiskei Koidz powder, with minimal effect on the physicochemical properties analyzed.

Irradiated and non-irradiated Korean medicinal herbs were extracted by water and 70% ethanol. Antimicrobial activity of these extracts were investigated against selected food hygiene microoganisms. The ethanol extracts of the non-irradiated Agrimonia pilosa ledebour japonica Nakai, Curcuma longa Linne and Angelica gigas Nakai were completely inhibited on four species of bacteria, such as Vibrio parahaemolyticus, Clostridium perfringenes, Bacillus subtilis and Staphylococcus aureus. Also, above four strains did not have antibacterial activity in the water-ethanol mixtures. Futhermore, the ethanol extracts of the non-irradiated Agrimonia pilosa ledebour Japonica Nakai, Curcuma ledoaria Roscoe, Curcuma longa Linne and Scutellaria baikalensis George were shown inhibitory effects against Aspergillus flavus and Penicillium islandicum. And the water extract of Scutellaria baikalensis George was the same effect to these molds. Essentially the same results were observed when samples irradiated at a dose of 10 kGy.

D_(10) values obtained for radiation alone in Bacillus subtilis and Clostridium perfrigenes were 0.35-0.48 kGy in vegetative cells, and 2-2.08 kGy in spores, respectively. Irradiation dose of 24 kGy completely inhibited spores. In the case of heat treatment, D_(50, 60) values ranged from 10 to 14 minutes in vegetative cells, and D_(70, 80, 90), values ranged from 10 to 140 minutes in spores. In the case of combined treatment with heat and radiation, D_(10) values ranged from 1 to 1.25 kGy in vegetative cells, and from 3.42 to 3.61 kGy in spores. Thus, resistance of cells to gamma radiation did not seem to be influenced by pre-heating.

The yields of solvent fractions of irradiated red ginseng powder were increased in the order of petroleum ether(PE)$lt;diethyl ether(DE)$lt;ethyl acetate(EA)$lt;n-butanol (BU)$lt;aqueous fraction(AQ), and did not show any changes in fraction yields by irradiation dose levels. Inhibition activities of lipid peroxide formation were increased in the order of AQ$lt;BU $lt;PE$lt;EA$lt;DE. Inhibition activities of malonaldehyde formation were increased in the order of AQ≤BU$lt;EA$lt;PE$lt;DE. AQ fraction showed little effects on the antioxidative activity and all the activities of the samples did not changed by gamma irradiation. The reverse mutation assay using Salmonella typhunurium (TA98, TA100 and TA102) demonstrated that the nonirradiated and irradiated red ginseng powder extract did not have mutagenic activity (presence of S9 mix or not). The chromosomal aberration test in mammalian animal cell (Chinese hamster lung fibroblast, CHL) showed no significant increase in incidence of structural and numerical aberrations, comparing gamma-irradiated red ginseng powder extracts to nonirradiated red ginseng powder extract in the concentration of the sample producing cytotoxicity(presence of S9 mix or not). Therefore, gamma-irradiatied red ginseng powder (upto 10 kGy) could be safe on the genotoxic point of view.