• 한국생물공학회:학술대회논문집
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• 한국생물공학회 2005년도 생물공학의 동향(XVII)
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• pp.997-997
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• 2005

• 한국잠사학회:학술대회논문집
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• 한국잠사학회 2004년도 제47회 춘계 학술연구 발표회
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• pp.54-54
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• 2004

• 대한약학회:학술대회논문집
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• 대한약학회 2001년도 Proceedings of International Convention of the Pharmaceutical Society of Korea
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• pp.279.2-279.2
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• 2001

• 한국약용작물학회지
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• 제10권4호
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• pp.294-297
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• 2002

A gene coding for the GST of cotton (Gh-5) was cloned into Escherichia coli and experssed. The enzyme remained within the cytoplasm of E. coli. An 696 bp open reading frame was in the 988 base pair fragment of the recombinant plasmid pET-30b(+). The deduced protein sequence consists of 232 amino acids and has a molecular mass of 30235.58 Da. The cloned enzyme conjugated reduced glutathione and 1-chloro-2,4-dinitrobenzene (CDNB). Plant GST cDNA was expressed in microbe and produced polypeptide had function as an enzyme.

• 한국식품영양과학회지
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• 제40권8호
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• pp.1092-1098
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• 2011

본 연구에서는 당뇨병의 치료에 중요한 저해요인으로 제기되고 있는 당뇨합병증을 예방하고자 녹황색 채소 등을 통해 식사 시 한국인들이 쉽게 섭취할 수 있는 ${\beta}$-carotene의 혈관계 합병증 예방효과를 분석하고자 하였다. 간 미토콘드리아에서의 catalase 활성은 ${\beta}$-carotene을 급여한 비당뇨군에서 유의적으로 높은 활성을 나타내었으나 당뇨군에서는 ${\beta}$-carotene 급여에 의한 영향을 나타내지 않았다. 간 사이토졸 내의 superoxide dismutase 활성은 ${\beta}$-carotene을 급여하지 않은 당뇨군에서 그 활성이 가장 저하되었으나 ${\beta}$-carotene 공급에 의해 유의적으로 증가되었다. 간 사이토졸 내의 glutathione-S-transferase 활성은 ${\beta}$-carotene의 급여에 의한 차이가 없었다. 간 마이크로솜에서의 glucose-6-phosphatase 활성은 대조군에 비하여 ${\beta}$-carotene을 급여하지 않은 당뇨군에서 유의적으로 높게 나타났으나 ${\beta}$-carotene을 급여한 당뇨군에서는 활성이 유의적으로 저하되었다. 간조직의 환원형 glutathione 함량은 당뇨군에서 유의적으로 감소되었으며, 당뇨군에서 ${\beta}$-carotene의 급여로 증가하였다. 이상의 결과에서 볼 때 ${\beta}$-carotene의 섭취는 당뇨 유도에 의한 산화스트레스가 증가된 생리적 상태에서 glutathione의 소모를 감소시키고, 항산화 효소계 중 특히 superoxide dismutase 활성을 유도하여 과산화 라디칼을 환원시킴으로써 활성산소에 의해 유발되는 산화적 손상의 일차적 방어에 관여한 것으로 여겨진다. 따라서 인체시험 등을 통한 후속연구와 연계하여 ${\beta}$-carotene 수준을 적절하게 보충 섭취한다면 당뇨로 인한 항산화계 활성의 변화를 조절함으로써 산화스트레스에 대한 보호효과를 나타내어 당뇨병 합병증의 예방에 기여할 수 있을 것으로 여겨진다.

• Fisheries and Aquatic Sciences
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• 제4권2호
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• pp.88-92
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• 2001

To examine effects of cadmium on the respiratory burst of kidney phagocytes and antioxidant defense in liver, juvenile red seabream Pagrus major were fed a cadmium-incorporated diet $(1g\;CdC1_2/kg\;diet)$. The respiratory burst activity measured by chemiluminescence (CL) was significantly reduced by oral intake of cadmium. Lipid peroxidation in liver expressed as thiobarbituric acid reactive substances (TBARS) was significantly higher in the fish fed a cadmium-incorporated diet than that of the fish fed a control diet both on Day 3 and Day 9. Liver Glutathione S-transferase (GST) activitiy was significantly increased both on Day 3 and Day 9 by feeding a cadmium-incorporated diet, when compared with the controls. From the present results, it can be concluded that oral intake of cadmium in red seabream is associated with marked reduction of respiratory burst capacity of kidney phagocytes which can elevate susceptibility of fish against infecting pathogens. Cadmium administration also elicits significant increment of lipid peroxidation in liver, and fish try to detoxify cadmium by increasing GST activity.

• Journal of Microbiology and Biotechnology
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• 제19권4호
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• pp.387-390
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• 2009

Microbial UDP-glycosyltransferases can convert many small lipophilic compounds into glycons using uridine-diphosphate-activated sugars. The glycosylation of flavonoids affects solubility, stability, and bioavailability. The gene encoding the UDP-glycosyltransferase from Bacillus cereus, BcGT-3, was cloned by PCR and sequenced. BcGT-3 was expressed in Escherichia coli BL21(DE3) with a glutathione S-transferase tag and purified using a glutathione S-transferase affinity column. BcGT-3 was tested for activity on several substrates including genistein, kaempferol, luteolin, naringenin, and quercetin. Flavonols were the best substrates for BcGT-3. The enzyme dominantly glycosylated the 3-hydroxyl group, but the 7-hydroxyl group was glycosylated when the 3-hydroxyl group was not available. The kaempferol reaction products were identified as kaempferol-3-O-glucoside and kaempferol-3,7-O-diglucoside. Kaempferol was the most effective substrate tested. Based on HPLC, LC/MS, and NMR analyses of the reaction products, we conclude that BcGT-3 can be used for the synthesis of kaempferol 3,7-O-diglucose.

• Asian Pacific Journal of Cancer Prevention
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• 제13권9호
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• pp.4417-4421
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• 2012

Objective: The results from studies on associations of the glutathione S-transferase T1 (GSTT1) gene polymorphism and hepatocellular carcinoma (HCC) risk in Chinese populations are still conflicting. This meta-analysis was performed to evaluate the relationship in detail. Methods: Eligible reports were recruited into this meta-analysis from the databases of PubMed, Embase, Cochrane Library and CBM-disc (China Biological Medicine Database). Results were expressed with odds ratios (OR) for dichotomous data, and 95% confidence intervals (CI) were also calculated. Results: Eighteen investigations were identified for the analysis of association between polymorphic deletion of GSTT1 and HCC, consisting of 2,693 patients with HCC and 4,696 controls. Null genotype of GSTT1 was associated with HCC susceptibility in Chinese (OR=1.53, 95%CI: 1.28-1.82; P<0.00001). Conclusion: The GSTT1 null genotype is associated with HCC susceptibility in Chinese.

• Asian Pacific Journal of Cancer Prevention
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• 제14권6호
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• pp.3861-3864
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• 2013

Glutathione S-transferase (GST) enzyme levels are associated with risk of many cancers, including hematologic tumours. We here aimed to investigate the relationships between GSTM1, GSTT1 and GSTP1 polymorphisms and the risk of AML. Genotyping of GSTs was based upon duplex polymerase-chain-reactions with the confronting-two-pair primer (PCR-CTPP) method in 163 cases and 204 controls. Individuals carrying null GSTT1 genotype had a 1.64 fold risk of acute leukemia relative to a non-null genotype (P<0.05). A heavy risk was observed in those carrying combination of null genotypes of GSTM1 and GSTT1 and GSTP1 Val allele genotypes when compared with those carrying wild genotypes, with an OR (95% CI) of 3.39 (1.26-9.26) (P<0.05). These findings indicate that genetic variants of GST and especially the GSTT1 gene have a critical function in the development of AML. Our study offers important insights into the molecular etiology of AML.

• Asian Pacific Journal of Cancer Prevention
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• 제17권10호
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• pp.4719-4722
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• 2016

Background: Glutathione S-transferase M1 (GSTM1) is involved in the detoxification of carcinogenic agents. DNA copy number variants of GSTM1 may be associated with cancer progression and may result in reduced survival time of various cancers. Determination of DNA copy number variants was here used to assess the association between GSTM1 copy number variant and pathological status and survival time of colorectal-cancer patients treated with 5-fluorouracil-based chemotherapy. Methods: One hundred thirteen Thai colorectal-cancer patients were investigated for GSTM1 copy number variant by real-time PCR. Relationships between gene copy number variants and clinico-pathological parameters were determined. Result: Associations were evident between GSTM1 copy number and stage of tumor (P = 0.026) and metastasis at diagnosis (P = 0.049), with odds ratio values of 0.2 and 0.3 respectively. Conclusions: GSTM1 copy number variant was here not related with reduced overall survival for the colorectal-cancer patients receiving 5-FU-based chemotherapy.