본 연구는 관상가치가 있는 자생 참두메부추와 갯부추를 절화소재로 이용하고자 수행되었다. 실험은 절화가 수확된 직후, gibberellic acid(GA3) 50, 75, 100mg·L-1, silver thiosulfate(STS) 0.1, 0.3, 0.5mM, 8-hydroxyquinoline sulfate(8-HQS) 25, 50, 100mg·L-1, 그리고 시중에 판매되 고 있는 Chrysal 8mL·L-1, Floralife 10mL·L-1의 보존용액 에 처리되었다. 참두메부추의 절화수명 연장에는 Chrysal 보 존용액 처리가 가장 효과적이었으며 다음으로 75mg·L-1 GA3 처리가 효과적이었다. 한편 8-HQS와 STS는 참두메부추의 절화수명을 단축하고 줄기가 갈변하는 등의 부정적인 영향을 끼쳤다. Chrysal과 더불어 Floralife 보존용액 처리는 절화 참두메부추의 상대 생체중변화율을 높이는데 효과가 있었다. 반면 갯부추는 100mg·L-1 GA3 처리에서 절화수명이 유일하 게 7일까지 연장되었다. GA3 보존용액 처리를 제외한 다른 처리에서 갯부추의 절화수명은 증류수인 대조구보다 비슷하 거나 약간 높은 수준이었다. 절화 갯부추의 수분흡수율은 실 험 초반 100mg·L-1 8-HQS 처리에서, 상대 생체중변화율은 Chrysal 보존용액 처리에서 가장 높게 조사되었으나 두 처 리 모두 절화수명이 유의하게 연장되지 않았다. 갯부추는 100mg·L-1 GA3 처리에서 절화수명을 비롯한 절화품질이 가 장 우수하였다.

본 연구는 다양한 보존용액이 절화 수명에 미치는 영향과, 절단된 두메부추(Allium dumebuchum H.J.Choi)의 줄기의 수분흡수율 및 상대 생체중을 평가하여 두메부추를 절화로 개발 하기 위해 수행되었다. 두메부추 절화가 수확된 후, gibberellic acid(GA3) 50, 75, 100mg･L-1, 8-hydroxyquinoline sulfate(8-HQS) 25, 50, 100mg･L-1, silver thiosulfate(STS) 0.1, 0.3, 0.5mM, 그리고 Chrysal 8mL･L-1, Floralife 10mL･L-1의 보존용액에 처리되었다. 실험기간 동안 환경조건으로 온도는 24℃로 유지되었으며 상대 습도 43±2.1%, 평균 광도는 22.81±1.2μmol･m- 2･s-1, 일장은 9/15h이었다. 두메부추의 절화수명은 대조구인 절화에서 9.0일로 조사된 것에 비해 GA3 100mg･L-1 보존용액 처리된 절화에서 14.0일로 가장 높게 측정되었다. 수분흡 수율 또한 GA3 100mg･L-1 처리에서 실험이 종료되는 시점에 0.07mL･g-1･d-1로 조사되어 다른 처리보다 높았다. 상대 생체 중은 시판중인 절화수명 연장제 Floralife와 Chrysal 보존용액 처리가 GA3 처리보다 유의하게 높게 조사되었다. GA3를 절화 보존용액으로 사용한 결과, 두메부추는 다른 처리들에 비해 높은 수분흡수율로 절화수명이 대조구보다 평균 5일이상 연장 되었다. 그러나, 8-HQS와 STS 보존용액 처리는 대조구에 비하여 두메부추 절화수명에 큰 차이가 없었다.

Streptococcus mutans and Streptococcus sobrinus play important roles in dental caries. Coptis chinensis is a natural product with antimicrobial activity against enterobacteria; however, its effects on oral streptococci are still unknown. Therefore, the effects of C. chinensis on the growth and biofilm formation of the representative cariogenic bacteria S. mutans and S. sobrinus were investigated for the possible use of C. chinensis as an anticaries agent. The C. chinensis extract was diluted with sterile distilled water, and 0.1–2.5% of the extract was used in the experiment. The effects of the C. chinensis extract on the growth and glucan formation of S. mutans and S. sobrinus were measured by viable cell counting and spectrophotometry at 650 nm absorbance, respectively. Crystal violet staining was also carried out to confirm the C. chinensis extract’s inhibitory effect on biofilm formation. The C. chinensis extract significantly inhibited the growth of S. mutans and S. sobrinus at concentrations of ≥ 0.3% as compared with the control group. The viable cell count of colonies decreased by 1.7-fold and 1.2-fold at 2.5% and 1.25%, respectively, compared with the control group. The biofilm formation of S. mutans and S. sobrinus was inhibited by > 20-fold at C. chinensis extract concentrations of ≥ 1.25% as compared with the control group. In summary, the C. chinensis extract inhibited the growth and biofilm and glucan formation of S. mutans and S. sobrinus . Therefore, C. chinensis might be a potential candidate for controlling dental caries.

Phagocytosis is a fundamental process in which phagocytes capture and ingest foreign particles including pathogenic bacteria. Several oral pathogens have anti-phagocytic strategies, which allow them to escape from and survive in phagocytes. Impaired bacteria phagocytosis increases inflammation and contributes to inflammatory diseases. The purpose of this study is to investigate the influences of various agents on oral pathogenic phagocytosis. To determine phagocytosis, Streptococcus mutans, Fusobacterium nucleatum, Aggregatibacter actinomycetemcomitans and Porphyromonas gingivalis were stained with 5-(and-6)-carboxyfluorescein diacetate succinimidyl ester (CFSE), and was measured using flowcytometery and confocal microscopy. The influencing factors on phagocytosis were evaluated through the pretreatment of ROS inhibitor (N-acetyl-L-cysteine (NAC)), lysozyme, potassium chloride (KCI) and adenosine triphosphate (ATP) in THP-1 cells. Expression of pro-inflammatory cytokines was determined by enzyme-linked immunosorbent assay (ELISA). The phagocytosis of various bacteria increased in a MOI-dependent manner. Among the tested bacteria, phagocytosis of P. gingivalis showed the highest fluorescent intensity at same infection time. Among the tested inhibitors, the NAC treatment significantly inhibited phagocytosis in all tested bacteria. In addition, NAC treatment indicated a similar pattern under the confocal microscopy. Moreover, NAC treatment significantly increased the bacteriainduced secretion of IL-1β among the tested inhibitors. Taken together, we conclude that the phagocytosis occurs differently depending on each bacterium. Down-regulation by ROS production inhibited phagocytosis and lead increased of oral pathogens-associated inflammation.

The objective of this study was to determine the effects of E. coli on boar sperm quality and reproductive performance in sows after artificial insemination. Three different levels of E. coli were artificially inoculated to semen with following concentrations; Control, 500, 5,000 and 50,000 colony forming unit (cfu)/ml. Semen samples were preserved at 17℃ for 5 days. Sperm motility was significantly decreased (p<0.05) on day 3 in the group inoculated with 5,000cfu/ml compared to control groups. In all treatment groups, sperm motility was gradually decreased as storage time increased, but the decline pattern was more drastic in the groups inoculated with 5,000 and 50,000 cfu/ml groups from day 3 (p<0.05) compared to control group. After 3 day of storage at 17℃, sperm viability in sample inoculated with the highest concentration (50,000 cfu/ml) of bacteria was less (p<0.05) than that of control group. The pH of semen sample pH was maintained 7.2～7.5 in all groups during the experimental period. No differences (p>0.05) were found for both storage time and bacterial concentration. The pregnancy rate and live born piglets tend to decrease by increasing the concentration of E. coli in semen. In particular, the rate of pregnancy was lower in the group inoculated with 50,000 cfu/ml (58.3%) compare to the other groups (81.8, 75.0, 76.5%). These results suggest that the contamination of E. coli in boar semen negatively affects fertilizing ability of boar sperm and the reproductive performance obtained from sows after artificial insemination.

Human embryonic stem (ES) cells retain the capacity for self‐renewal, are pluripotent and differentiate into the three embryonic germ layer cells. The regulatory transcription factors Oct4, Nanog and Sox2 play an important role in maintaining the pluripotency of human ES cells. The aim of this research was to identify unknown genes upregulated in human ES cells along with Oct4, Nanog, and Sox2. This study characterizes an unknown gene, named chromosome 1 open reading frame 31 (C1orf31) mapping to chromosome 1q42.2. The product of C1orf31 is the hypothetical protein LOC388753 having a cytochrome c oxidase subunit VIb (COX6b) motif. In order to compare expression levels of C1orf‐ 31 in human ES cells, human embryoid body cells, vascular angiogenic progenitor cells (VAPCs), cord‐blood endothelial progenitor cells (CB‐EPCs) and somatic cell lines, we performed RT‐PCR analysis. Interestingly, C1orf31 was highly expressed in human ES cells, cancer cell lines and SV40‐immortalized cells. It has a similar expression pattern to the Oct4 gene in human ES cells and cancer cells. Also, the expression level of C1orf31 was shown to be upregulated in the S phase and early G2 phase of synchronized HeLa cells, leading us to purpose that it may be involved in the S/G2 transition process. For these reasons, we assume that C1orf31 may play a role in on differentiation of human ES cells and carcinogenesis.