• 한국식품영양과학회지
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• 제36권5호
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• pp.534-539
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• 2007

본 연구는 김치로 분리한 우량 종균인 Leu. citreum GJ7의 급성독성을 시험하기 위하여 ICR 마우스에게 1회 Leu. citreum GJ7을 복강 또는 경구투여한 후 사망률, 체중의 변화, 일반 및 임상증상, 육안적 소견 등을 관찰하였다. 복강투여 후 24시간 관찰한 결과, 일부 Leu. citreum GJ7 투여군에서 부분적으로 사망례가 관찰은 되었으나 나머지 시험동물은 계속 생존하여 2,500 mg/kg까지는 평균치사량을 산출할 수 없었다. 또한 5,000 mg/kg을 14일 동안 경구투여하였을 경우에는 사망례가 없었으며, 특이한 임상증상도 관찰되지 않았다. 복강 혹은 경구투여한 후 마우스의 체중변화에 있어서도 대조군과 Leu. citreum GJ7 투여군 사이에 유의성 있는 차이는 보이지 않았으며, 생존동물의 부검결과에서도 내부 장기의 육안적 이상이 관찰되지 않았다. 따라서 Leu. citreum GJ7은 본 실험의 모든 조건에서 $LD_{50}$이 복강투여 시 2,500 mg/kg, 경구투여 시 5,000 mg/kg 이상인 저독성의 안전한 물질로 사료된다.

• BMB Reports
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• 제52권9호
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• pp.548-553
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• 2019

Ets-1 is a prototype of the ETS protein family. Members of the ETS protein family contain a unique ETS domain. Ets-1 is associated with cancer progression and metastasis in many types of cancer. Many studies have shown a link between elevated expression of Ets-1 in cancer biopsies and poor survival. CCR7 is a chemokine that binds to specific ligand CCL21/CCL19. CCR7 expression is associated with tumor metastasis and infiltration into lymph nodes. The objective of this study was to test whether Ets-1 could regulate CCR7 expression and enhance tumor metastasis. Our data showed that CCR7 expression was downregulated in Ets-1-deficient T cells upon T-cell stimulation. Overexpression of Ets-1 increased CCR7 expression in breast cancer cell lines. In contrast, knockdown of Ets-1 reduced CCR7 expression. Ets-1 could directly bind to CCR7 promoter and mediate CCR7 expression in luciferase reporter assays and chromatin immunoprecipitation assays. Transactivation activity of Ets-1 was independent of the Pointed domain of Ets-1. Ets-1 could also enhance $NF-{\kappa}B$ and CBP transactivation of CCR7 promoter. Our results also showed that Ets-1 could modulate cancer cell transmigration by altering CCR7 expression in transwell assay and wound healing assay. Taken together, our data suggest that Ets-1 can enhance CCR7 expression and contribute to tumor cell migration.

• 약학회지
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• 제37권2호
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• pp.136-142
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• 1993

To a suspension of 1-cyclopropyl-6,8-difluoro-1,4-dihydro-7-{3,7-diazabicyclo[3.3.0]oct-1(5)-en-3-yl}-4-oxo-3-quinoline carboxylic acid(C1) in sodium hydroxide solution and water is added dropwise with stirring carbon disulfide. [6R-[6$\alpha$, 7$\beta$(Z)]]-7-[[[2-Amino-4-thiazoly)methoxyimino]-acetyl]amino]-3-[[[[7-( 3-carboxy-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-7-guinolonyl)-3,7-diazabicyclo[3.3.0]oct-1(5)-en-3-yl]thioxomethyl]thio]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-2-carboxylic acid (DACD) was synthesized from 1-cyclopropyl-6,8-difluoro-1,4-dihydro-7-[7-(mercapto) thioxomethyl-[3,7-dia zabicyclo[3.3.0]oct-1(5)-en-3-yl}]-4-oxo-3-quinoline carboxylic acid disodium salt(C2) and cefotaxime. The invitro activity of novel dual-action cephalosporin, DACD, was compared with the in vitro activities of CENO(cefotaxime 3'-norfloxacin dithiocarbamate), cefotaxime, and norfloxacin against a variety of bacterial species. In vitro activity of DACD was superior to that of norfloxacin against Streptococcus pyogenes. Against Gram-positive and Gram-negative bacteria, its activity was almost equal to that of CENO.

• BMB Reports
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• 제40권4호
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• pp.539-546
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• 2007

The lysozymes encoded by bacteriophage T7 and K11 are both bifunctional enzymes sharing an extensive sequence homology (75%). The constructions of chimeric lysozymes were carried out by swapping the N-terminal and C-terminal domains between phage T7 and K11 lysozymes. This technique generated two chimeras, T7K11-lysozyme (N-terminal T7 domain and C-terminal K11 domain) and K11T7-lysozyme (N-terminal K11 domain and C-terminal T7 domain), which are both enzymatically active. The amidase activity of T7K11-lysozyme is comparable with the parental enzymes while K11T7-lysozyme exhibits an activity that is approximately 45% greater than the wild-type lysozymes. Moreover, these chimeric constructs have optimum pH of 7.2-7.4 similar to the parental lysozymes but exhibit greater thermal stabilities. On the other hand, the chimeras inhibit transcription comparable with the parental lysozymes depending on the source of their N-terminals. Taken together, our results indicated that domain swapping technique localizes the N-terminal region as the domain responsible for the transcription inhibition specificity of the wild type T7 and K11 lysozymes. Furthermore, we were able to develop a simple and rapid purification scheme in purifying both the wild-type and chimeric lysozymes.

• Asian-Australasian Journal of Animal Sciences
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• 제3권2호
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• pp.121-123
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• 1990

A CRD experiment with unequal numbers of hens were assigned at random to three treatment groups, 1) separation of chicks from hen at 21 days after hatching 2) separation of chicks from hen at 7 days and 3) hens were allowed to brood the chicks(no separation) up to 10 weeks of age, to determine the productive and reproductive performance of hens and their chicks. The mean cycle length (one hatch to another) was 72.8 days for the 7-day group as compared with 87.7 days and 83.4 days for the 21-day and the no separation groups, respectively (p<.0l). The broody period was 28.5 days for the 7-day group compared with 43.9 and 42.6 days for the 21 days and the no separation groups, respectively (p<.0l). The end of the broody period to the start of lay varied from 8.0 to 8.7 days. The number of eggs laid per clutch were 12.3 for the 21-day group, compared with 11.5 and 10.1 for the 7-day and no separation groups, respectively (p<.05). This is due to the longer (p<.05) clutch length of the 21-day group as compared with the 7-day and no separation groups, respectively. The chicks separated from the hens at 21 and 7 days were heavier (p<.01) than the chicks not separated from the hens. Mortalities were highest (p<.05) for chicks separated at 7 days as compared with chicks separated at 21 days and those not separated. We concluded that separating chicks at 7 days from the hen gave the shortest cycle length and broody period, separating the chicks at 21 days gave the longest clutch length and the maximum number of eggs, separating the chicks at 21 and 7 days resulted in heavier chicks and separating the chicks at 7 days resulted in the highest mortality.

• IMMUNE NETWORK
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• 제24권1호
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• pp.9.1-9.21
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• 2024

The cytokine IL-7 plays critical and nonredundant roles in T cell immunity so that the abundance and availability of IL-7 act as key regulatory mechanisms in T cell immunity. Importantly, IL-7 is not produced by T cells themselves but primarily by non-lymphoid lineage stromal cells and epithelial cells that are limited in their numbers. Thus, T cells depend on cell extrinsic IL-7, and the amount of in vivo IL-7 is considered a major factor in maximizing and maintaining the number of T cells in peripheral tissues. Moreover, IL-7 provides metabolic cues and promotes the survival of both naïve and memory T cells. Thus, IL-7 is also essential for the functional fitness of T cells. In this regard, there has been an extensive effort trying to increase the protein abundance of IL-7 in vivo, with the aim to augment T cell immunity and harness T cell functions in anti-tumor responses. Such approaches started under experimental animal models, but they recently culminated into clinical studies, with striking effects in re-establishing T cell immunity in immunocompromised patients, as well as boosting anti-tumor effects. Depending on the design, glycosylation, and the structure of recombinantly engineered IL-7 proteins and their mimetics, recombinant IL-7 molecules have shown dramatic differences in their stability, efficacy, cellular effects, and overall immune functions. The current review is aimed to summarize the past and present efforts in the field that led to clinical trials, and to highlight the therapeutical significance of IL-7 biology as a master regulator of T cell immunity.

• Asian Pacific Journal of Cancer Prevention
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• 제13권3호
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• pp.1049-1052
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• 2012

The purpose of this study was to evaluate expression and prognostic value of matrix metalloproteinase-7 (MMP-7) in colorectal cancer (CRC) patients. CRC tissues and corresponding distal normal mucosa tissues of 118 CRC patients were assessed by immunohistochemistry. Correlations between MMP-7 expression, patients' clinic pathological features, and overall survival rate were analyzed. We found that positive expression of MMP-7 in CRC tissues was significantly higher than that in distal normal mucosa (61.0% vs. 39.8%, p =0.001). Poor histological differentiation, advanced clinical stage and lymph node metastasis were significantly correlated with MMP-7 expression in CRC. The overall survival rate was significantly higher in the MMP-7 negative group than the positive group (Log-rank test= 9.957, p= 0.002). MMP-7 appeared as a significant independent prognostic factor through multivariate survival analysis. Collectively, we found MMP-7 expression to be correlated with progression and metastasis of CRC and thus could be used as a predictive marker of prognosis in CRC patients.

• 미생물학회지
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• 제37권1호
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• pp.37-41
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• 2001

Pleurotus ostreatus에서는 10.2 kb와 7.2 kb의 미토콘드리아 선상 플라스미드 DNA가 존재함이 발견되었다. 이 플라스미드 DNA의 양쪽 5'말단에는 단백질이 공유 결합되어있다고 알려져 있다. 최근에 P.ostreatus의 10.2 kb 미토콘드리아 선상 플라스미드 DNA를 다른 곰팡이의 선상 플라스미드 DNA에 존재하는 open reading frame(ORF)와 비교 분석하여 Podospora anserina의 플라스미드 pAL2의 DNA polymerase 및 RNA polymerase 암호부위와 유사성이 있음이 확인되었다. 본 연구에서는 7.2 kb선상 DNA를 HindIII잘라서 얻은 2조각의 절편(4.7 kb, 2.3 kb)을 클로닝하고 염기 서열을 분석하였다. 클로닝된 7 kb 절편에는 3개의 ORF,즉 ORF1(2982 bp, 993 amino acids), ORF2(2703 bp, 900 amino acids), ORF3(771 bp, 256 amino acids)가 존재함을 확인하였다 또한, 이들의 ORF를 분석한 결과, DNA polymerase와 RNA polymerase 암호부위와 유사성 이 있음을 확인하였다.

• 대한화학회지
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• 제21권2호
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• pp.139-148
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• 1977

2-푸르푸랄과 5-알킬-2-푸르푸랄류 가운데 5-메틸-2-푸르푸랄, 5-이소프로필-2-푸르푸랄, 5-삼차부틸-2-푸르푸랄, 5-이소아밀-2-푸르푸랄, 그리고 5-니트로-2-푸르푸랄 등의 옥심 생성반응 속도 정수를 pH 7인 완충용액내 반응온도 15∼$45^{\circ}C$에서 구하였다. 이 반응은 2차반응이며 활성화 에너지는 각각 5.50, 7.22, 7.03, 7.49, 7.78 그리고 4.97 kcal/mole이다. 5-알킬-2-푸르푸랄류에 대하여는 Hammett식이 성립되고 반응온도 15, 25, 35, $45^{\circ}C$에서 반응정수는 각각 2.010, 1.756, 1.541, 1.311 등이 계산되었다.

• Bulletin of the Korean Chemical Society
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• 제33권7호
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• pp.2287-2294
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• 2012

Deep blue fluorescent host materials based on a novel spiro[benzo[c]fluorene-7,9'-fluorene] core structure with side aromatic wings in the 5- and 9-positions, namely, 5,9-di(naphthalen-2-yl)spiro[benzo[c]fluorene-7,9'-fluorene] (DN-SBFF), 5,9-bis(4-t-butylphenyl)spiro[benzo[c]fluorene-7,9'-fluorene] (BP-SBFF), and 5,9-bis(4-fluorophenyl)spiro[benzo[c]fluorene-7,9'-fluorene] (FP-SBFF), were designed and successfully prepared using the Suzuki reaction. The physical properties of these materials and their EL characteristics as blue host materials doped with N,N,N',N'-tetraphenylspiro[benzo[c]fluorene-7,9'-fluorene]-5,9-diamine (TPA-SBFF) were investigated. The device used comprised ITO/N,N'-diphenyl-N,N'-bis[4-(phenyl-m-tolyl-amino)phenyl]-biphenyl-4,4'-diamine (DNTPD)/N,N'-di(1-naphthyl)-N,N'-diphenylbenzidine (NPB)/(FP-SBFF):dopant x%/tris(8-hydroxyquinoline)aluminum ($Alq_3$)/LiF. The device obtained using FP-SBFF doped with TPA-SBFF showed high color purity (0.13, 0.18) and an efficiency of 6.61 cd/A at 7 V.