본 연구는 스노우베리 추출물과 발효 추출물을 대상으로 피부 상재균인 Staphylococcus aureus, Staphylococcus epidermidis, Escherichia coli, Pseudomonas aeruginosa, Candida albicans를 이 용하여 천연화장품 소재로서의 항균 활성을 비교 평가하였다. 이를 위한 스노우베리 추출물의 항균 활성은 10-200mg/mL 농도에서 생육저해환(paper disc diffusion method)과 최소저해농도(Minimum inhibitory concentration)를 평가하였다. 스노우베리 추출물과 발효 추출물의 생육저해환을 확인하였을 때, 스노우베 리 추출물의 경우 뿌리 추출물에서만 100mg/mL, 200mg/mL의 농도에서 항균력을 나타내었고, 발효 추출 물의 경우 200mg/mL에서 항균력을 나타내는 것을 확인하였다. 그러나 스노우베리 추출물과 발효 추출물 의 4종의 세균에 대한 항균력은 확인할 수 있었으나, 진균인 Candida albicans에서는 항균력을 확인할 수 없었다. MIC 결과 스노우베리 잎, 뿌리 추출물에서 발효의 경우 줄기 추출물에서 각 균에 대한 최소저해 농도가 100mg/mL, 200mg/mL로 확인되었다. 이러한 결과는 스노우베리가 피부 개선을 위한 항균 소재 및 방부제로서의 활용 가치가 있다고 사료된다.

Hesperetin은 Hesperidin에서 유도되는 강한 항산화 기능의 플라보노이드 비당체이다. 본 연구 에서는 Hesperetin과 이의 Cyclodextrin 포접 복합체에 대하여 항산화, 항염증 및 항균 활성을 비교하였다. Hesperetin은 Hesperidin에 효소처리하여 제조되었으며, Hesperetin/Cyclodextrin 포접체는 용매 증류법에 의해 β-Cyclodextrin 및 Hydroxypropyl-β-Cyclodextrin을 사용하여 제조되었다. Hesperetin에 비해 Hesperetin/Hydroxypropyl-β-Cyclodextrin 포접체의 용해도는 93.5배 증가하였고, Hesperetin/β -Cyclodextrin 포접체의 용해도는 22.5배 증가하였다. 항산화 분석에서 Hydroxypropyl-β-Cyclodextrin 포접체는 Hesperetin과 유사한 라디칼 소거 활성능을 보인 반면, β-Cyclodextrin 포접체는 Hesperetin 보 다 약간 낮은 활성을 나타내었다. RAW 264.7 세포에 대한 세포독성은 Hydroxypropyl-β-Cyclodextrin 포접체, β-Cyclodextrin 포접체, Hesperetin의 순으로 세포독성이 낮았다. Hesperetin과 Cyclodextrin 포 접체는 모두 세포내 산화질소(NO), 종양괴사인자-α(TNF-α) 및 인터루킨-6(IL-6)과 같은 염증 매개체 를 감소시켰다. Hesperetin 및 Hydroxypropyl-β-Cyclodextrin 포접체는 상대적으로 β-Cyclodextrin 포접체 보다 더 효과적이었다. 피부 유해성 세균인 황색 포도상구균과 녹농균에 대해 억제 효과를 시험한 결과, 황색 포도상구균에 대해서는 Hesperetin = Hydroxypropyl-β-Cyclodextrin 포접체 > β -Cyclodextrin 포접체의 순서로 항균 효과를 나타내었으나, 녹농균에 대해서는 뚜렷한 억제효과를 나타내 지 않았다. 결론적으로, Hesperidin의 비당체 형태인 Hesperetin과 이의 Cyclodextrin 포접체는 다양한 생 물학적 활성을 보여주었으며, 용해도가 높은 Hydroxypropyl-β-Cyclodextrin 포접체가 β-Cyclodextrin 포접체에 비해 상대적으로 더 높은 활성을 나타내었다.

Makgeolli’s fermentation characteristics and antioxidant and antimicrobial activities were investigated to examine the effect of Prunus mume extract addition. Makgeolli, with the addition of various levels (0, 1, 3, and 5%) of Prunus mume extract (PME), was brewed with fermenting agents, Ipguk and Nuruk. The alcohol content of all samples remarkably increased during the initial 3 days and then gradually increased up to over 18% by the end of fermentation (7 days for Nuruk and 15 days for Ipguk). Although the alcohol content was slightly reduced and acidity was increased with the concentration of PME, there was no other negative effect of PME on the fermentation of Makgeolli. The contents of total phenols and flavonoids for Ipguk samples were higher than those for Nuruk samples, and these values significantly increased at over 3% PME addition. As the PME content increased, the antioxidant activity increased for both Nuruk and Ipguk samples. Only Makgeolli with Ipguk had vigorous antimicrobial activity against E. coli and S. aureus at over 3% addition of PME. These results indicate that PME can be an effective natural additive for enhancing Makgeolli’s antioxidant and antimicrobial activities.

Lactic acid bacteria as probiotics are intensively used in human and animal species. These probiotic properties of LABs were variable according to bacterial strain and species. However, there was limited information on probiotic properties of monkey origin LABs. In this study, we investigated the antibacterial activity of monkey and human origin LABs against monkey origin enteric bacteria by the agar disc diffusion test and broth culture inhibition assay. All LABs represented enough tolerance to pepsin (0.3%) and bile acid (pH = 2). To 50% of Clostridium perfringens and 20% of Escherichia coli, monkey origin LABs showed statistically higher antibacterial activity compared to human origin LABs (p < 0.05). Also, distinct antibacterial activity was verified among some bacteria species and strains. Higher antibacterial activity against enteric bacteria except for C. perfringens was verified in Lactobacillus johnsonii strains compared to Lactobacillus reuteri and Lactobacillus salivarius. Statistically different antibacterial activity against C. perfringens was verified among strains within L. reuteri and L. johnsonii. In conclusion, we prove the higher probiotic properties of monkey origin LABs against homogenous enteric bacteria although humans and monkeys were phylogenetically similar species. For non-human primates, homogenous LABs should be used as probiotics, not human origin LABs. Furthermore, it was confirmed among monkey origin LABs, L. johnsonii showed a high antibacterial activity on various enteric pathogenic bacteria and was an appropriate lactic acid strain for inhibiting C. perfringens.

The purpose of this study was to introduce a new in vitro method for evaluating the antimicrobial activity of toothpaste, reflecting the actual toothbrushing time and the dilution of toothpaste by salivation. We designed three experimental groups and one negative control group. The experimental groups were (1) 90 μL of toothpaste + 10 μL 1X phosphate-buffered saline (PBS, 9/10 dilution group), (2) 50 μL of toothpaste + 40 μL 1X PBS (1/2 dilution group), and (3) 25 μL of toothpaste + 65 μL 1X PBS (1/4 dilution group). During toothbrushing, saliva is continuously secreted into the oral cavity and the toothpaste concentration is diluted over time during toothbrushing. Therefore, the 1/2 and 1/4 dilution experimental groups were added. The negative control group was toothpaste diluted 20,000-fold with 1X PBS. Miracle Fresh Doctor toothpaste and Streptococcus mitis KCOM 1350, Prevotella intermedia KCOM 1107, Fusobacterium nucleatum subsp. polymorphum KCOM 1322, and Aggregatibacter actinomycetemcomitans KCOM 1306 were used as the toothpaste and target bacterial strains, respectively. The number of bacterial cells plated on agar plates in the negative control group was 1,000 CFU. If the number of colonies on the experimental group plate was less than one, the treatment was considered to have > 99.9% bactericidal activity. These results suggest that this new in vitro method for antimicrobial evaluation could be used as the standard method for testing the antimicrobial activity of toothpaste.

This study was conducted in order to investigate the antioxidant and antimicrobial activity of Solanum nigrum L. fruit powder after undergoing different extraction solvent processes. The total phenolic content of Solanum nigrum L. fruit powder measured a 14.66 GAE mg/g after undergoing ethanol extraction, and the total flavonoid content measured at 201.23 mg CE/g when undergoing ethanol extraction. The ABTS radical scavenging activity was 160.38~209.53 TEAC umol/g, and the DPPH radical scavenging activity was 53.99~90.76 TEAC umol/g, which indicated a higher level of antioxidant power in the ethanol extract as opposed to in the water extract. The FRAP (ferric reducing antioxidant power) of Solanum nigrum L. fruit powder was 115.58~194.58 TEAC umol/g, and B. subtilis KCTC 2189 showed greater antimicrobial activity in the ethanol extract (concentration 200 ug/uL) as opposed to the water extract. Solanum nigrum L. fruit powder revealed differences in antioxidant and antimicrobial activity between the different extraction solvents. In particular, ethanol extract had higher antioxidant and antibacterial activity, meaning it is more favorable for usage as a functional food material.

치아우식증 치료물질을 개발하기 위하여 한국에서 전통적으로 널리 사용되어왔던 20종류의 약용식물로부터 추출물을 분리하였다. 이를 이용하여 치아우식증 원인균인 Streptococcus sobrinus KCOM 1157에 대한 항균 활성을 나타내는 약용식물들을 조사하였다. 감초, 고삼, 황련, 박하, 송절, 부평초 등의 추출물들이 S. sobrinus KCOM 1157에 대해서 항균 활성을 보여주었다. 이 중 송절, 고삼, 황련 등의 천연 물들은 높은 항균 활성을 나타내었다. 이 결과들은 송절, 고삼, 황련의 천연물들이 S. sobrinus 를 포함한 구강질환 세균들에 대한 항우식증 치료제로서의 가능성이 있음을 의미한다.

본 연구는 귀리의 겨, 겉껍질 및 잎을 에탄올로 추출한 후 항산화 및 항균활성을 조사하였으며, 추출물을 유화형 돈육 소시지에 적용하였을 때 품질 및 저장성에 미치는 영향을 알아보기 위하여 수행하였다. 귀리의 잎 추출물(OLE)의 총 페놀함량(145.99ug CAE/mg), ABTS 라디칼 소거 활성(35.07%) 및 FRAP 활성(32.77ug Fe2+/mg)은 다른 부위에 비해 유의적으로 높게 나타났다(p<0.05). 항균 활성 측정결과 모든 부위의 추출물에서 Staphylococcus aureus, Streptococcus pneumonia과 Escherichia coli에 대해서 활성을 보이지 않았으나, OLE 및 귀리 겨 추출물은 Klebsiella pneumonia에 대해서는 120μg/disk이상에서 활성을 보였으며, OLE가 귀리 겨 추출물보다 동일 농도에서 유의적으로 높은 활성을 나타내었다(p<0.05). OLE를 유화형 돈육 소시지에 첨가하였을 때, 0.025% 첨가구에서 pH, 조직감 및 관능적 특성에 유의적인 영향을 미치지 않았다. 하지만 저장 14일차에 모든 첨가구에서 지방산화(TBARS), volatile basic nitrogen (VBN), 총균수가 대조구보다 유의적으로 낮게 측정되었다(p<0.05). 본 실험결과 OLE는 높은 항산화 활성을 보였으며, 유화형 돈육 소시지 제품에 적용하였을 때 지방산화를 지연시켰고, 총균수의 저하를 가져왔기 때문에 천연 보존제로서 좋은 첨가제로 사료된다.

본 연구에서는 붉나무 열매 Ethanol extract(ET)과 Ethyl acetate fraction(EA) 및 Butanol fraction(BT)을 천연보존제로서의 활용 가능성을 평가하기 위하여 항균활성을 측정 하였다. 항균활성은 Staphylococcus aureus(S. aureus), Staphylococcus epidermidis(S. epidermidis), Escherichia coli(E. coli), Pseudomonas aeruginosa(P. aeruginosa), Candida Albicans(Candida. A)에 대하여 Paper disc법으로 생육 저해환과 최소저해농도(MIC)를 평가하였다. Paper disc법으로 생육저해환을 측정한 결과 ET, EA, BT 모든 시료에서 S. aureus, S. epidermidis, E. coli, P. aeruginosa 균주에서 생육저해환이 관찰되었고 BT에서는 Candida. A 균주에 대한 생육저해환이 추가로 관찰 되었다. MIC 측정결과 EA 시료가 S. aureus, S. epidermidis, E. coli, P. aeruginosa 대하여 가장 낮은 농도를 보였다. 따라서 본 연구의 결과는 붉나무 열매 추출물이 다양한 항균스펙트럼을 가지고 있어 화장품에서 천연보존제로 활용 가능성이 높다고 사료 된다.

The purpose of this study was to investigate the antimicrobial activity of the ethanol extract of Garcinia mangostana L. (mangosteen) against Cutibacterium acnes (6 strains) and Staphylococcus aureus (6 strains). The antimicrobial activity of the mangosteen extract was evaluated based on its minimal bactericidal concentration. Cytotoxicity of the mangosteen extract against human embryonic kidney 293 (HEK 293) cells was determined using the cell counting method. The data showed that the mangosteen extract was not toxic to HEK 293 cells at a concentration of up to 16 μg/mL and killed 87.0% and 99.9% of C. acnes and S. aureus after 10 minutes and 1 hour of treatment, respectively. These results suggest that ethanol extract of mangosteen can be used as an anti-acne agent.

Onion vinegar, which has an undesirable flavor and taste formed through alcohol and acetic acid fermentation, possesses additives that can improve sensory quality. Thus, the objective of this study was to present an optimized blending ratio using response surface methods for an onion vinegar beverage by adding Omija extracts. This study was performed to formulate an Omija-onion vinegar beverage (OOVB) and investigate its antioxidant properties and antimicrobiological effects. The experimental design was conducted using an optimal mixture model of response surface methodology which generated eighteen experimental trials with overall acceptance as the responses. According to the statistical analyses, OOVB demonstrated a ratio containing onion vinegar, water, brown sugar, apple extracts and Omija extracts of 10, 72.3, 4.4, 12.2 and 1.1 (weight ratio), respectively. The OOVB revealed desirable nutrition values (phenolics compounds 19.3 mg/100 g, total flavonoids 3.1 mg/100 g, quercetin 1.9 mg/100). The OOVB displayed antibacterial effects in Gram negative Enterobacter aerogenes, Escherichia coli, Salmonella typhimurium and Gram positive Staphylococcus aureus. The findings revealed that OOVB was 18% in DPPH radical inhibitionand 11% in superoxide dismutase-like activity thus, OOVB has nutritional value and good quality as well as potential biological activities for functional beverages.