국내 유통되는 반려동물 사료의 살모넬라 분석시 증균 배양법, 효소면역기법에 의한 분석, 종 특이 primer를 활 용한 PCR 방법을 활용하여 비교 평가하였다. 시료 175점 Salmonella spp. 검출 결과 증균배양법 및 종 특이 primer를 활용한 PCR 방법에 의한 검출 방법에서 2점의 시료(육포, 옥수수 글루텐)가 양성으로 확인되었고, 효소면역기법에 의한 검출방법에서는 1점의 시료(옥수수 글루텐)가 양성 으로 확인되었다. 증균배양법 및 효소면역기법에 의한 검 출방법에 비해 종 특이 primer를 활용한 PCR 방법을 적 용 할 경우 시료에서 분리된 균주의 종(species) 판별이 가 능하였다.

The purpose of this study was to develop an indirect enzyme-linked immunosorbent assay (indirect ELISA) based on a monoclonal antibody (MAb) that is specific to mackerel thermal stable-soluble protein (TSSP), that can be used for the rapid detection of mackerel in processed marine foods. Among the four MAbs (3A5-1, 2, 9, and 12) developed in previous studies, the 3A5-2 MAb that showed high specificity and sensitivity were selected and used to develop the indirect ELISA method. The detection range of the indirect ELISA was 0.02%-0.001% and the detection limit of 0.001% was shown. No cross-reaction to other marine products and food ingredients was observed by the indirect ELISA. Processed marine foods containing mackerel with ≥ 0.3 O.D. value at 405 nm were estimated as positive samples by the indirect ELISA. Therefore, the indirect ELISA can be used as a rapid and sensitive method to identify mackerel authenticity and adulteration in processed marine foods.

α-Amylase 및 protease 활성을 동시에 가지는 1-B-12 균주를 된장으로부터 분리하였다. 16S rRNA 유전자 염기서열 분석결과, Bacillus licheniformis로 동정되어 B. licheniformis 1-B-12 균주로 명명하였다. 효소활성 측면에서 현미(50%), 미강(30%) 및 대두(20%)의 조합이 최적의 기질 조합 조건으로 확인되었다. 기능성이 부가된 효소식품을 제조하기 위하여 Lactobacillus casei GW140 균주를 도입하였는데, B. licheniformis 1-B-12 균주와의 혼합배양 조건은 2단발효(B. licheniformis 1-B-12 접종 > 24 h 발효 > L. casei GW140 접종 > 12 h 추가 발효)가 적합한 것으로 나타났다. 이러한 최적 조건으로 생산된 효소식품을 동결건조하여 25℃에서 보관하였을 때 시험 마지막 날인 45일까지 효소의 활성이 유지되었다.

Waste activated sludge (WAS) and food waste (FW) are available year round at low cost and have the potential to promote synergism in anaerobic digestion (AD). The goal of this study was to clarify the synergism in co-digestion of WAS and FW. A slight amount of FW at various ratios was added to WAS as an auxiliary substrate, and anaerobic batch tests were performed under mesophilic conditions. By adding FW, total CH₄ produced was increased, where most of them were come from WAS, clearly suggesting synergism. Also, lag period was shortened and CH₄ production rate was increased by FW addition. It was hypothesized that enhanced performance was owing to the facilitated hydrolysis of WAS by FW addition, which was revealed by the increased activities of hydrolytic α-amylase and protease.