3.Purification and properties of isoflavone-glucosidase.
Ming-Jie XIE ; Ming SONG ; Cui-Xia ZOU ; Chun-Hua XU ; Ming-Chun LU ; Feng-Xie JIN
Chinese Journal of Biotechnology 2006;22(4):635-638
A high activity isoflavone-glucosidase, which hydrolysis glycosides, was obtainde using liquid fermentation from Absidia sp. R strain. The isoflavone-glucosidase was purified 11 folds with yielding rate of 10.9% after ammonium sulfate precipitation and DEAE-Cellocuse (DE-52) ion exchange chromatography. SDS-PAGE results showed that the molecular weight is 53kD. And the optimum temperature, the optimum pH, Km and pI of the enzyme are 50 deegrees C, 5.0, 1.3 x 10(-2) mol/L and 3.2, respectively. The isoflavone-glucosidase is also rather stable under 60 degrees C and in pH range from 5.0 to 7.0. The enzyme can be activated by Co2+ and Ca2+, and be inhibited by Ag+ and Cu2+.
Absidia
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enzymology
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Glucosidases
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isolation & purification
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metabolism
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Hydrogen-Ion Concentration
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Isoflavones
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metabolism
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Temperature
4.The correlation and clinic value of p53,p16,PCNA protein expressions in patients with esophageal carcinoma
Zhong-Ming WANG ; Xiu-Cui LI ; Gui-Rong LIU ; Yong-Mei SUN ; Chun-Luan YUAN ;
Cancer Research and Clinic 2006;0(10):-
Objective To study the expression of p53,p16,PCNA protein in esophageal carcinoma and its relationship to sexual distinction,the location of disease,the biological level,the depth of invasion and lymph node metastasis.Methods 118 patients with esophageal carcinoma were included in the study,all of them were treated for the first time.p53,p16 and PCNA protein in the 118 cases of esophageal carcinoma were detected by immunohistochemical assay(SP technique). Results The positive expression of p53, p16, PCNA protein in 118 patients was 80 %(92/118),42%(50/118)and 97%(115/118),respectively.The positive expression of p53,PCNA protein were irrelated to the sexual distinction,the location of disease,the biological level,the depth of invasion and the lymph node metastasis.The loss of p16 was significantly related to the depth of invasion and the lymph node metastasis(P
5.Expression and significance of RECK, metalloproteinase-9 and vascular endothelial growth factor-C in colorectal cancer.
Hong ZHANG ; Jin-chun CONG ; Ming-ming CUI ; Yong FENG ; Chun-sheng CHEN
Chinese Journal of Gastrointestinal Surgery 2010;13(9):695-698
OBJECTIVETo investigate the expression of reversion-inducing cysteine-rich protein with Kazal motifs (RECK), matrix metalloproteinase-9 (MMP-9), and vascular endothelial growth factor-C (VEGF-C) in colorectal cancer.
METHODSS-P immunohistochemistry was used to detect the expression of RECK, MMP-9 and VEGF-C in colorectal cancer specimen. Colorectal mucosal tissue at least 10 cm away from the tumor was used as control.
RESULTSThe positive expression of RECK in colorectal cancer was significantly lower than that in the controls(53.3% vs. 100%, P<0.05). Both MMP-9 and VEGF-C were over expressed compared with the controls(86.7% vs. 23.3% and 71.7% vs. 13.3% respectively, P<0.01). The expression of RECK was negatively correlated with that of MMP-9 and VEGF-C, and the expression of MMP-9 was positively correlated with that of VEGF-C. There were significant associations between the expression of these proteins and lymph node metastasis, distant metastasis, and TNM staging (all P<0.05).
CONCLUSIONSRECK expression is low in colorectal cancer, while MMP-9 and VEGF-C expressions are high. Combined testing of these 3 markers is important in the evaluation of tumor metastasis and invasion, and is helpful in the prediction of the prognosis.
Adult ; Aged ; Colorectal Neoplasms ; genetics ; metabolism ; pathology ; Female ; GPI-Linked Proteins ; metabolism ; Humans ; Male ; Matrix Metalloproteinase 9 ; metabolism ; Middle Aged ; Prognosis ; Vascular Endothelial Growth Factor C ; metabolism
6.Establishment and identification of universal antibody against all subtypes of the influenza A viral hemagglutinins
Changgui LI ; Juan LI ; Chun STELLA ; Ming SHAO ; Shuzhen LIU ; Xiaoyu CUI ; Xuguang LI ; Hanhua FANG ; Junzhi WANG
Chinese Journal of Microbiology and Immunology 2009;29(2):126-129
Objective To establish the universal antibody against all subtypes of the influenza A viral hemagglutinins(HA). Methods All HA sequences from influenza viruses in common domains were analyzed to search for the most conservative re,on of the HA gene. The peptides conjugated to carrier proteins were used to immunize rabbits in order to obtain high titer antibody. Results The most conservative region among all influenza viruses HA genes were 14 amino acids located at the N-terminal of HA2. The antibody titer reached to 1 : 80 000 after 4 injections of the coupled peptides. The achieved antibody was demonstrated by Western blot to bind HA proteins of influenza virus subtypes H1-H13 specifically. Conclusion The universal antibody has been successfully established by immunizing the rabbits with most conservative peptides of HA protein coupled to carrier protein.
7.Detection of TERC gene amplification by fluorescence in-situ hybridization in cervical intraepithelial lesions.
Yan-long YUAN ; Chun-nian HE ; Ming-tang XU ; Cui-qing XU ; Yu-ning SUN ; Huan-fen ZHAO ; Chen CHEN
Chinese Journal of Pathology 2011;40(3):182-186
OBJECTIVETo explore the feasibility and practical value of fluorescence in situ hybridization (FISH) detection of TERC gene amplification in cervical intraepithelial lesions (CIN) and squamous cell carcinoma (SCC).
METHODSTissue microarray was constructed to cover 150 cases of various cervical conditions, including 24 cases of normal cervical mucosa, 78 cases of CINs (CINI, 25 cases; CINII, 21 cases and CINIII, 32 cases) and 48 cases of SCC. FISH was used to detect TERC gene amplification.
RESULTSTERC gene amplification was detected in 8% (2/25) CINI, 47.6% (10/21) CINII, 71.9% (23/32) CINIII and 87.5% (42/48) SCC. There were significant differences among these groups (P < 0.05). The amplification rates of TERC gene in SCC, CINIII and CINII were significantly higher than those of normal cervical epithelium and CINI (P < 0.05). Significant differences were also observed among CINI and CINII, CINIII and SCC (P < 0.05), and between CINII and SCC (P < 0.05). There were no significant differences between normal cervical epithelium and CINI, CINII and CIN III, and between CINIII and SCC (P > 0.05). FISH detection of amplification of TERC gene in CINI and CINII-III demonstrated the following statistics: sensitivity of 62.3%, specificity of 92.0%, accuracy of 71.8%, positive and negative predictive values of 94.3% and 53.5%, respectively.
CONCLUSIONSFISH detection is a reliable method in detecting TERC gene amplification using paraffin tissue sections. When histological evaluation becomes difficult, TERC amplification detectable by FISH may offer a diagnostic distinction of CINI from CINII. Moreover, TERC amplification may be used as a biomarker in predicting CIN progression to invasive cancer.
Adenoma ; diagnosis ; genetics ; Adult ; Aged ; Biomarkers, Tumor ; analysis ; Carcinoma, Squamous Cell ; diagnosis ; genetics ; Cervical Intraepithelial Neoplasia ; diagnosis ; genetics ; Disease Progression ; Female ; Gene Amplification ; Humans ; In Situ Hybridization, Fluorescence ; Middle Aged ; RNA ; genetics ; Sensitivity and Specificity ; Telomerase ; genetics ; Uterine Cervical Neoplasms ; diagnosis ; genetics ; Young Adult
8.Research on output and quality of Panax notoginseng and annual change characteristics of N, P and K nutrients of planting soil under stereo-cultivation.
Chun-mei HUANG ; Xiu-ming CUI ; Lei LAN ; Wei-dong CHEN ; Cheng-xiao WANG ; Xiao-yan YANG ; Da-hui LU ; Ye YANG
China Journal of Chinese Materia Medica 2015;40(15):2930-2936
The output and agronomic characters of 3-year-old Panax notoginseng cultured under stereo structure (upper, middle and down layers) were investigated, and the annual change of N, P and K of its planting soil were also studied. Results showed that, compared with field cultured Panax notoginseng, growth vigour and output of stereo-cultivation were significantly lower. But the total production of the 3 layers was 1.6 times of field. The growth vigor and production of P. notoginseng was in the order of upper layer > middle layer > down layer. The content of ginsenoside in rhizome, root tuber and hair root of P. notoginseng was in the order of upper layer > field > middle layer > down layer. Organic matter content and pH of stereo-cultivation soil decreased with the prolonging of planting time, which with the same trend of yield. Organic matter content of stereo-cultivation soil was significantly higher than field, but the pH was significantly lower. Contents of total and available N, P and K in stereo-cultivation soil and field decreased with the prolonging of planting time. The content of N and P were in the order of upper layer > middle layer > yield > down layer, the content of K was in the order of upper layer > middle layer > down layer > yield. Compared with field, the proportion of N and P in the organ of underground (rhizome, root tuber and hair root) of upper layer were increased, while decreased in middle and down layers. Proportion of K in underground decreased significantly of the 3 layers. In conclusion, the agronomic characters and production of stereo-cultivation were significantly lower than that of yield. But the total production of the 3 layers were significantly higher than field of unit area. And the aim of improving land utilization efficiency was achieved. Nutritions in the soil of stereo-cultivation were enough to support the development of P. notoginseng, which was not the cause of weak growth and low production. The absorbing ability of P. notoginseng to N, P and K nutrients was decreased by stereo-cultivation mode. So, improve the growth vigour of P. notoginseng from the perspective of adjusting the stereo-cultivation mode so as to improve the nutrient absorption capacity is the future direction.
Food
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Hydrogen-Ion Concentration
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Nitrogen
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analysis
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Panax notoginseng
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growth & development
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Phosphorus
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analysis
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Potassium
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analysis
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Soil
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chemistry
9.Effect of 2,4-D isooctylester on sperms in tail of epididymis and HSP70 expression of testis tissue in rats.
Guo-Yuan CHEN ; Jian-An CHENG ; Cui-Rong LU ; Wei-Dong LIU ; Ming-Kun HE ; Hua-Wen LI ; Jin-Bo YANG ; Tang-Chun WU
Chinese Journal of Industrial Hygiene and Occupational Diseases 2004;22(4):281-282
2,4-Dichlorophenoxyacetic Acid
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analogs & derivatives
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toxicity
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Animals
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Epididymis
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growth & development
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metabolism
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Female
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HSP70 Heat-Shock Proteins
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biosynthesis
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genetics
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Herbicides
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toxicity
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Male
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Rats
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Rats, Wistar
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Spermatozoa
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drug effects
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growth & development
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metabolism
10.Pharmacokinetic interaction between scutellarin and valsartan in rats.
Ming-Yu CUI ; Chong-Chong TIAN ; Ai-Xia JU ; Chun-Ting ZHANG ; Qiu-Hong LI
Acta Pharmaceutica Sinica 2013;48(4):541-546
Scutellarin is the main effective constituent of breviscapine, a flavonoid mixture isolated from the dried whole plant of Erigeron breviscapus (Vant.) Hand-Mazz, and valsartan is used as an antihypertensive drug. These two drugs have already been clinically used together to treat diabetic nephropathy (DN) in China, and the combined medications showed some enhanced protection against DN. The aim of this study is to investigate the potential pharmacokinetic interaction between scutellarin and valsartan in rats. Breviscapine injection (20 mg x kg(-1), i.v.) and valsartan (15 mg x kg-, i.g.), either alone or together were given to 18 male Sprague-Dawley rats. Concentrations of scutellarin and valsartan were quantified by HPLC, and pharmacokinetic parameters were calculated by non-compartmental methods. We found that the pharmacokinetic parameters of scutellarin altered significantly after co-administration of oral valsartan. The plasma clearance (CL(p)) and the bile clearance (CL(b)) of scutellarin were reduced significantly in the presence of valsartan. After oral administration of valsartan with or without intravenous scutellarin, however, the pharmacokinetic parameters of valsartan were comparable. In conclusion, our data suggests that the concurrent use of valsartan reduces the biliary excretion of scutellarin, and this may be due to the inhibitory effect of valsartan on the biliary excretion of scutellarin mediated by Mrp2 (Multidrug resistance-associated protein 2).
Administration, Intravenous
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Administration, Oral
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Animals
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Antihypertensive Agents
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administration & dosage
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blood
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pharmacokinetics
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Apigenin
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administration & dosage
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blood
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isolation & purification
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pharmacokinetics
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Bile
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metabolism
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Chromatography, High Pressure Liquid
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Drug Interactions
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Erigeron
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chemistry
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Glucuronates
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administration & dosage
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blood
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isolation & purification
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pharmacokinetics
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Male
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Metabolic Clearance Rate
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Multidrug Resistance-Associated Proteins
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metabolism
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Plants, Medicinal
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chemistry
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Random Allocation
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Rats
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Rats, Sprague-Dawley
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Valsartan
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administration & dosage
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blood
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pharmacokinetics