1.Anti-Helicobacter pylori Compounds from Maackia amurensis.
Woo Sung PARK ; Ji Yeong BAE ; Hye Jin KIM ; Min Gab KIM ; Woo Kon LEE ; Hyung Lyun KANG ; Seung Chul BAIK ; Kyung Mook LIM ; Mi Kyeong LEE ; Mi Jeong AHN
Natural Product Sciences 2015;21(1):49-53
Eight isoflavonoid compounds were isolated from the EtOAc fraction of Maackia amurensis which had shown the highest anti-Helicobacter pylori activity among the fractions, using medium pressure liquid chromatography and recrystallization. Based on the spectroscopic data including 1H-NMR, 13C-NMR, HMBC and MS data, the chemical structures of the isolates were determined to be (-)-medicarpin (1), afromosin (2), formononetin (3), tectorigenin (4), prunetin (5), wistin (6), tectoridin (7) and ononin (8). Anti-H. pylori activity of each compound was evaluated with broth dilution assay. As a result, (-)-medicarpin (1), tectorigenin (4) and wistin (6) showed anti-H. pylori activity. (-)-Medicarpin (1) exhibited the most potent growth inhibitory activity against H. pylori with the minimal inhibitory concentration (MIC)90 of 25 microM, and tectorigenin (4) with MIC90 of 100 microM ranked the second. This is the first study to show the anti-H. pylori activity of M. amurensis, and it is suggested that the stem bark of M. amurensis or the EtOAc fraction or the isolated compounds can be a new natural source for the treatment of H. pylori infection.
Chromatography, Liquid
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Maackia*
2.Structure kinetic model of Maackia amurensis cells in suspension culture.
Kai LUO ; Xue-Qiang ZHA ; Jian-Ping LUO
Chinese Journal of Biotechnology 2007;23(4):657-661
A structure kinetic model was established for describing the relationship among cell growth, genistein formation and substrate utilization in suspension culture of Maackia amurensis. In this model, sucrose uptake, structure components production, intermediate matter changes, cell respiration loss and secondary metabolite (genistein) production were all predicted. The parameter sensitivity test was indicated that intermediate matter self-catalysis rate constant (k(b1)), structure component synthesis rate constant (k(b2)) and secondary metabolite synthesis rate constant (k(p)) were the most sensitive parameters for this model. If k(b1), k(b2) or k(p) are changed by 10%, the range of the aim function value would be changed by 12.8%, 4.61% and 2.54%, respectively. Adjustment of the other parameters only aroused a change of less than 0.5% in the aim function value. The predicted values were in good agreement with those obtained experimentally.
Cell Culture Techniques
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Cells, Cultured
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Kinetics
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Maackia
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cytology
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Models, Biological
3.Wood Decay Fungi in South Korea: Polypores from Seoul.
Yeongseon JANG ; Seokyoon JANG ; Jaejung LEE ; Hwanhwi LEE ; Hanbyul LEE ; Young Min LEE ; Joo Hyun HONG ; Mihee MIN ; Young Woon LIM ; Changmu KIM ; Jae Jin KIM
Mycobiology 2014;42(2):140-146
In Seoul, a majority of plant communities have undergone significant changes over the last few decades; however, how wood decay fungi have responded and adapted to the changes in vegetation remains unknown. Through an ongoing investigation of Korean indigenous fungi, ca. 300 specimens with poroid basidiocarp were collected in Seoul during 2008~2012. Morphological examination and molecular analysis using the internal transcribed spacer and nuclear large subunit ribosomal DNA region sequences helped identify 38 species belonging to 28 genera, 10 families, and 5 orders in this area. Among them, three polypores, Abundisporus pubertatis, Coriolopsis strumosa, and Perenniporia maackiae were found to be new to South Korea.
Basidiomycota
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Classification
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DNA, Ribosomal
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Fruiting Bodies, Fungal
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Fungi*
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Humans
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Korea
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Maackia
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Phylogeny
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Plants
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Seoul
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Wood*
4.Changes of the Sialoglycoconjugates in the Maxillary Sinus Mucosa of theRabbits after Inoculation of Influenza a Virus.
Jin Hak CHO ; Yin Gyo JUNG ; Chin Saeng CHO ; Kyung You PARK ; Hyun Joon LIM
Korean Journal of Otolaryngology - Head and Neck Surgery 1997;40(4):600-606
The present study was carried out in order to observe the changes in the expression of the sialoglycoconjugates of the rabbit sinus mucosa after inoculation of influenza A virus utilizing a biotin labeled lectins for light microscopy with four different lectins; Maackia amurensis(MAA), Wheat germ agglutinin(WGA), Sambucus nigra(SNA), and Peanut(PNA). A comparison of the affinity of these lectins demonstrated the different distribution of sialoglycoconjugates in the ciliary layer and goblet cells. The normal sinus mucosa stained with four types of lectins showed that the sialoglycoconjugates were mainly distributed in the ciliary layer and goblet cells. Moreover, the main sugar residues of the sialoglycoconjugates were figured out to be consisted of Neu5Ac(alpha2,3)Gal, GlcNAc and Neu5Ac. Influenza A virus infection decreased the staining intensity of the mucosa with MAA, but not with WGA. The staining intensity of PNA, however, was highly increased in the viral infected mucosa. These results suggest that Neu5Ac(alpha2,3)Gal sugar residues may be required as protecting factor or modulator for Influenza A virus infectivity.
Biotin
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Goblet Cells
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Influenza A virus*
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Influenza, Human*
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Lectins
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Maackia
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Maxillary Sinus*
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Microscopy
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Mucous Membrane*
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Sambucus
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Triticum
5.Optimization for isoflavone production in Maackia amurensis suspension cells based on neural networks and accelerating genetic algorithm.
Jian-Ping LUO ; Kai LUO ; Xiao-Yan CHEN ; Shao-Tong JIANG
Chinese Journal of Biotechnology 2004;20(5):759-763
The medium for isoflavone production in Maackia amurensis suspension cells has been optiwised through the artificial neural networks (ANNs) and the real coding based accelerating genetic algorithm (RAGA). Among the ingredients of the medium, nitrogen sources and plant growth regulators were found to be the main factors affecting the production of isoflavone genistein. (NH4)2SO4, KNO3, 2,4-D and 6-BA, 100 approximately 800 mg/L, 1500 approximately 3000 mg/L, 0 approximately 3 mg/L and 0 approximately 1 mg/L respectively, significantly increased genistein yield, in the ranges of effective concentrations. The random ten combinations of these four components generated by RAGA as input data and the genistein yields of ten combinations as output data were used for ANNs-RAGA (the artificial neural networks associated with the accelerating genetic algorithm) modeling. The resultant model showed a high fit between the experimental data and calculating values by ANNs-RAGA. Based on the prediction of the model, the optimum combination of four factors for genistein production was determined on 149.68 mg/L for (NH4)2SO4, 2936.10 mg/L KNO3, 0.01 mg/L 2,4-D and 0.19 mg/L 6-BA. When cells were cultured in the optimized medium, their capability of genistein production was remarkably enhanced to 14.13 mg/L, which was about 19 times higher than that in the original medium. The relative discrepancy between the experimental value and the predictive value of genistein yield from the optimized medium was 7.38%.
Algorithms
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Cells, Cultured
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Culture Media
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Genistein
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metabolism
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Maackia
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metabolism
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Models, Biological
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Neural Networks (Computer)
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Suspensions
6.Expression of Sialic Acids according to the Differentiation of Cultured Human Nasal Epithelial Cells.
Kyung Sik SUH ; Kyung Su KIM ; Jin Woo CHOI ; Joo Heon YOON ; Jeung Gweon LEE
Korean Journal of Otolaryngology - Head and Neck Surgery 1997;40(5):663-669
BACKGROUND: Sialic acid residues are known to play a key role in the normal function of the glycoconjugates. Recently, with the development of specific sialic acid binding lectins such as Maackia seed agglutinin(MAA) and Sambucus nigra agglutinin(SNA), it has made easier to localize the sialic acid residues by the histochemical staining methods. OBJECTIVES: We were to observe the expression of sialic acids according to the differentiation of cultured human nasal epithelial cells by the immunohistochemistry method using Wheat germ agglutinin(WGA), MAA, and SNA. MATERIALS AND METHODS: Human nasal epithelial cell culture was done as floating method for the induction of differentiation. The cultured cells were fixed with 2.5% glutaraldehyde and the epon 812 was used as embedding material. The immunohistochemistry was done as Lim's method. RESULTS: The WGA and MAA positive reactions were noted from the floating zero day through the fourteenth day. The reactions were positive to the squamous-like cells and differentiating cells(ciliated and secretory epithelial cells). The WGA binding patterns were homogeneous but MAA binding patterns were inhomogeneous. The SNA positive reaction was noted only in the fourteenth day and the reaction was inhomogeneous. These results meant that N-acetyl glucosamine and N-acetyl neuraminic acid(alpha 2,3) galactose were expressed from the floating zero day and N-acetyl neuraminic acid(alpha 2,6) galactose was expressed from the floating fourteenth day. CONCLUSION: N-acetyl neuraminic acid(alpha 2,3) galactose may be more important to the primary defence of human nasal epithelial cell. Due to the inhomogeneity of the reaction, the further study using Lowicryl K4M will be needed.
Cells, Cultured
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Epithelial Cells*
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Galactose
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Glucosamine
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Glutaral
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Glycoconjugates
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Humans*
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Immunohistochemistry
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Lectins
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Maackia
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N-Acetylneuraminic Acid*
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Sambucus nigra
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Sialic Acids*
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Triticum
7.Isoflavone glycosides from the bark of Maackia amurensis.
Xiong LI ; Jian-fang LI ; Dong WANG ; Wei-ning WANG ; Zheng CUI
Acta Pharmaceutica Sinica 2009;44(1):63-68
To study the chemical constituents of the Maackia amurensis, the constituents were isolated by various chromatographies and the structures were elucidated on the basis of chemical and spectroscopic data (ESI-MS, 1D and 2D NMR). Thirteen isoflavone glycosides were isolated from the n-BuOH-soluble fraction of the 70% ethanol extract and identified as 7-hydroxy-4',6-dimethoxyisoflavone-7-O-beta-D-glucopyranosyl-(1-->6)-beta-D-glucopyranoside (1), dalsympathetin (2), ononin (3), glycitin (4), genestin (5), saikoisoflavonoside A (6), afrormosin-7-O-beta-D-glucopyranoside (7), gehuain (8), kushenol O (9), 7-hydroxy-4',6-dimethoxyisoflavone-7-O-beta-D-apiofuranosyl-(1-->6)-beta-D-glucopyranoside (10), tectoridin (11), biochanin A 7-O-beta-D-gentiobioside (12) and 7-hydroxy-4'-methoxyisoflavone-7-O-beta-D-apiofuranosy l-(1-->6)-beta-D-glucopyranoside (13). Compound 1 is a new isoflavone glycoside, named as maackiaisoflavonoside, compounds 2, 8, 9, 10, 12 and 13 were isolated from this genus for the first time.
Disaccharides
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chemistry
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isolation & purification
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Isoflavones
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chemistry
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isolation & purification
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Maackia
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chemistry
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Molecular Structure
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Plant Bark
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chemistry
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Plants, Medicinal
;
chemistry
8.Callus formation and its isoflavonoid accumulation in Maackia amurensis.
Jian-ping LUO ; Li-fu WU ; Shao-tong JIANG
China Journal of Chinese Materia Medica 2003;28(12):1138-1141
OBJECTIVETo obtain Maackia amurensis callus and investigate some factors influencing total isoflavonoid production in callus.
METHODDifferent media were used for callus induction from cotyledonary and hypocotyl explants. Total isoflavonoid content was determined by UV spectrophotometer.
RESULTMedium types and hormone combinations influenced both callus formation and their developmental states. MS medium supplemented with NAA/BA or containing 2,4-D was suitable for callus induction from cotyledonary explants. Among the basal media tested, MS, N6 and B5 were suitable for cotyledonary callus formation and SH for hypocotyl callus formation. The formed callus could synthesize isoflavones. Media containing NAA were suitable for isoflavonoid production in cotyledonary callus and media containing 2,4-D/BA were suitable for hypocotyl callus, but 2,4-D/KT at high concentration inhibited the isoflavonoid accumulation in hypocotyl and coytledonary calli. According to the developmentally morphological characters, the formed callus could be classified into four types. II-type callus with yellow in color and friability in texture showed the highest accumulation of isoflavones.
CONCLUSIONThe influences of medium type and hormone combinations on Maackia amurensis callus formation are reflected in both developmentally morphological characters and isoflavonoid accumulation of calli. Yellow, friable callus induced from cotyledonary and hypocotyl explants in MS or N6 medium supplemented with 2,4-D and BA exhibit the optimum growth and isoflavonoid production.
Cotyledon ; growth & development ; metabolism ; Culture Media ; Hypocotyl ; growth & development ; metabolism ; Isoflavones ; analysis ; biosynthesis ; Maackia ; growth & development ; metabolism ; Plant Growth Regulators ; pharmacology ; Plants, Medicinal ; growth & development ; metabolism ; Spectrophotometry, Ultraviolet
9.Tissue distribution of sialic acid-linked influenza virus receptors in beagle dogs.
Zhang Yong NING ; Xin Tao WU ; Yan Fen CHENG ; Wen Bao QI ; Yu Fu AN ; Heng WANG ; Gui Hong ZHANG ; Shou Jun LI
Journal of Veterinary Science 2012;13(3):219-222
Reports of influenza A virus infections in dogs has received considerable attention from veterinarians, virologists, and epidemiologists. Interaction between influenza viral hemagglutinin and cell oligosaccharides containing sialic acid residues results in infection. Sialic acids have an alpha-2,3-linkage to the penultimate galactose in the avian influenza virus receptor and an alpha-2,6-linkage in the human receptor. To date, there are no detailed data on the tissue distribution or histological features of either type of sialic acid-linked influenza virus receptors in beagle dogs, which are common laboratory animals and pets. We conducted the current study to visualize the in situ tissue distribution of both sialic acid-linked influenza virus receptors in various organs of beagle dogs using Maackia amurensis lectin II and Sambucus nigra agglutinin. Both alpha-2,3- and alpha-2,6-sialic acid-linked receptors were detected in the endothelial cells of the respiratory tract and other organs. Endothelial cells of most gastrointestinal organs were negative for alpha-2,3-sialic acid-linked receptors in the dogs. Our results suggested that these canine organs may be affected by influenza virus infection. The findings from our study will also help evaluate the occurrence and development of influenza virus infections in dogs.
Animals
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Dog Diseases/metabolism
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Dogs/metabolism/*virology
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Female
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Influenza A Virus, H5N1 Subtype/*metabolism
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Maackia/chemistry
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Male
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N-Acetylneuraminic Acid/metabolism
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Organ Specificity
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Orthomyxoviridae Infections/metabolism/transmission/veterinary
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Plant Lectins/metabolism
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Receptors, Cell Surface/analysis/chemistry/metabolism
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Receptors, Virus/analysis/chemistry/*metabolism
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Sambucus nigra/chemistry