1.Chemical constituents from stems of Cistanche deserticola cultured in Tarim desert.
Ze-Dong NAN ; Ming-Bo ZHAO ; Yong JIANG ; Peng-Fei TU
China Journal of Chinese Materia Medica 2013;38(16):2665-2670
In order to clarify the chemical constituents of Cistanche deserticola cultured in Tarim desert, a systematically phytochemical investigation was carried out. The chemical constituents were isolated by column chromatography, over silica gel, Sephadex LH-20, MCI gel, ODS and semi-preparative HPLC, and their structures were determined on the basis of MS, NMR spectroscopic data analysis, physicochemical properties and/or comparison with literature data Seventeen compounds were isolated from the 85% ethanol extract of the stems of C. deserticola cultured in Tarim desert. Their structures were identified as salsaside B (1), syringin (2), demethyl syrinyin (3), coniferin (4), (2E,6E)-3,7-dimethyl-8-hydroxyoctadien-1-O-beta-D-glucoside (5), (+)-syringaresinol (6), 2S,3S, 4S-trihydroxypentanoic acid (7), panaxytriol (8), beta-sitosterol-3-O-beta-D-xylopyranoside (9), androsin (10), 3-methyl-but-2-en-1-yl-beta-D-glucopyranoside (11), benzyl-glucopyranoside (12), 4-hydroxybenzyl-beta-D-glucoside (13), nicotinamide (14), p-hydroxybenzoic acid (15), 4-hydroxy-benzeneethanol (16), and galactitol (17). Compounds 3, 6-13 were isolated from this genus for the first time, and compounds 1, 4 and 5 were obtained from this species for the first time.
Cistanche
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chemistry
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growth & development
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Desert Climate
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Drugs, Chinese Herbal
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analysis
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isolation & purification
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Plant Stems
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chemistry
2.Effect of harvest times on yield and quality of Isatidis Folium in Longzhong semi-arid region.
Wenwen TANG ; Xinyang ZHANG ; You HE ; Xiaojun JIN
China Journal of Chinese Materia Medica 2011;36(8):955-958
Different harvest times of Isatidis Folium had a significant effect on the yield and the quality of Isatidis Radix and Isatidis Folium. The harvest could increase the yield of Isatidis Folium, but reduce the yield of Isatidis Radix, the quality of Isatidis Radix and Isatidis Folium. One, two and three harvests of the Isatidis Folium reduced the yield of Isatidis Radix as 18.3%, 58.6%, 67.4% and increased the yield of the Folium as 107.3%, 86.3% and 116.6%. Ethanol-soluble extract of Isatidis Radix was 42.50%, 42.24%, 31.77%, which were 1.19%, 1.79%, 26.13% lower than those of the control, respectively. The water-soluble extract, indirubin, indigo content reduced with increase of the harvest times. Indirubin contents with two or three times harvests were higher than that of the control, but the content of water-soluble extract, ethanol-soluble extract, indigo were lower than those of the control.
Agriculture
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methods
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Desert Climate
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Drugs, Chinese Herbal
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chemistry
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metabolism
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Indigo Carmine
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Indoles
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metabolism
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Isatis
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metabolism
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Plant Leaves
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chemistry
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metabolism
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Plant Roots
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chemistry
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metabolism
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Quality Control
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Time Factors
3.A novel endogenous badnavirus exists in Alhagi sparsifolia.
Yong-Chao LI ; Jian-Guo SHEN ; Guo-Huan ZHAO ; Qin YAO ; Wei-Min LI
Journal of Zhejiang University. Science. B 2018;19(4):274-284
We report the recovery of a 7068-nt viral sequence from the "viral fossils" embedded in the genome of Alhagi sparsifolia, a typical desert plant. Although the full viral genome remains to be completed, the putative genome structure, the deduced amino acids and phylogenetic analysis unambiguously demonstrate that this viral sequence represents a novel species of the genus Badnavirus. The putative virus is tentatively termed Alhagi bacilliform virus (ABV). Southern blotting and inverse polymerase chain reaction (PCR) data indicate that the ABV-related sequence is integrated into the A. sparsifolia genome, and probably does not give rise to functional episomal virus. Molecular evidence that the ABV sequence exists widely in A. sparsifolia is also presented. To our knowledge, this is the first endogenous badnavirus identified from plants in the Gobi desert, and may provide new clues on the evolution, geographical distribution as well as the host range of the badnaviruses.
Badnavirus/genetics*
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Biological Evolution
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Desert Climate
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Fabaceae/virology*
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Genes, Plant
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Genetic Variation
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Genome, Viral
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Geography
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Open Reading Frames
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Phylogeny
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Plant Diseases/virology*
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Plasmids
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Sequence Analysis, RNA
4.Effects of seed priming on drought tolerence in Prunella vulgaris.
Qiaosheng GUO ; Xianxiu ZHANG ; Xuelian SHEN ; Yuhang CHEN
China Journal of Chinese Materia Medica 2009;34(10):1195-1198
OBJECTIVETo explore an effective way to increase drought tolerance of Prunella vulgaris seed.
METHODThe treatment of drought stress to P. vulgaris seeds was made by the different concentrations of PEG solutions. Primed seeds germinated under 25% PEG.
RESULTAs concentrations of PEG increasing, seed germination percentage, germination index and vitality index reduced. Primed with 20%-25% PEG, 300-500 mg x L(-1) GA3 and 1.6%-2.0% KNO3-KH2PO4 could enhance three population seeds germination index and vitality index under drought stress. Treated with NaCl, seeds germination percentage and germination index of two population increased, which came from Nanjing Zijinshan and Anhui Jinzhai, respectively, while those of seeds from Gansu Chengxian reduced.
CONCLUSIONTreated with PEG, GA3, KNO3-KH2 PO4 under proper concentration, seed vigor, seed resistance under drought stress would increase.
Desert Climate ; Droughts ; Germination ; drug effects ; Kinetin ; pharmacology ; Osmotic Pressure ; drug effects ; Plant Growth Regulators ; pharmacology ; Plant Proteins ; Prunella ; drug effects ; physiology ; Seeds ; drug effects ; physiology ; Sodium ; pharmacology ; Sodium Chloride ; pharmacology ; Temperature
5.Frequency of group A rotavirus with mixed G and P genotypes in bovines: predominance of G3 genotype and its emergence in combination with G8/G10 types.
Yashpal S MALIK ; Kuldeep SHARMA ; Nirupama VAID ; Somendu CHAKRAVARTI ; K M CHANDRASHEKAR ; Sanjay S BASERA ; Rashmi SINGH ; MINAKSHI ; Gaya PRASAD ; Baldev R GULATI ; Kiren N BHILEGAONKAR ; Awadh B PANDEY
Journal of Veterinary Science 2012;13(3):271-278
The present study describes the genotypic distribution of rotaviruses (RVs) in an Indian bovine population with unexpectedly higher proportions of G3 alone or in combination of G8/G10. PCR-genotyping confirmed that 39.4% (13/33) of the prevalent RVs were the G3 type while 60.6% (20/33) were dual G3G10 or G3G8 types. P typing revealed that 93.9% (31/33) of the samples were P[11] while 6.1% (2/33) possessed a dual P[1]P[11] type. Sequence analysis of the VP7 gene from G3 strains viz. B-46, 0970, and BR-133 showed that these strains had sequence identities of 90.5% to 100% with other bovine G3 strains. The highest identity (98.9% to 100%) was observed with RUBV3 bovine G3 strains from eastern India. The G3 strains (B-46, 0970, and BR-133) showed 97.5% to 98.8% sequence homologies with the Indian equine RV strain Erv-80. Phylogenetic analysis demonstrated that G3 strains clustered with bovine RUBV3 and J-63, and equine Erv-80 G3. Overall, these results confirmed that the incidence of infection by RVs with the G3 genotype and mixed genotypes in the bovine population was higher than previously predicted. This finding reinforces the importance of constantly monitoring circulating viral strains with the G3 genotype in future surveillance studies.
Animals
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Cattle
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Cattle Diseases/epidemiology/*virology
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Desert Climate
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Feces/virology
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Genotype
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India/epidemiology
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Molecular Sequence Data
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Phylogeny
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RNA, Viral/genetics
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Reverse Transcriptase Polymerase Chain Reaction/veterinary
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Rotavirus/classification/*genetics/isolation & purification
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Rotavirus Infections/epidemiology/*veterinary/virology
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Sequence Analysis, Protein/veterinary
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Sequence Analysis, RNA/veterinary
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Sequence Homology
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Tropical Climate
6.Separation and identification of endophytic fungi from desert plant Cynanchum komarovii.
Hai-Jing DUAN ; Ting HAN ; Xiu-Li WU ; Na LI ; Jing CHEN ; Lu-Ping QIN
China Journal of Chinese Materia Medica 2013;38(3):325-330
OBJECTIVEThe research aimed to investigate the entophytic fungal community of Cynanchum Komarrovii, including the biodiversity in different organs and the correlations with ecological environment. Endophytic fungi with patent bioactivity were also rapidly screened.
METHODPDA medium was used to isolate and purify the endophytic fungi from C. komarovii living in Shaanxi and Ningxia district, respectively. The strains were identified based on the morphological characteristics of the fungi and similarity of 5.8S gene and internal transcribed spacer (ITS) sequence. Pyriculaia oryzae model was applied to preliminarily screen the active fungi.
RESULTNinety-four strains of endophytic fungi were isolated and identified to 9 species, 13 genera, 9 families and 6 orders, among them, 47 strains were from the plants living in Ningxia. And then, 5 of them were isolated from roots, 14 from branches, and 28 from leaves. They were identified belonging to 8 species, 9 genera, 5 families and 4 orders. Additionally, 47 strains were from the plants living in Shaanxi. 16 were isolated from the roots, 18 from branches, 13 from leaves. They were identified belonging to 5 species, 8 genera, 6 families and 4 orders. By preliminary screening, 18 strains of endophytes completely inhibited the germination of conidium, which showed a potential bioactivity for these fungi. Both N4 and S17 strains had stronger growth inhibition effect.
CONCLUSIONEndophytic fungi from desert plant C. komarovii have the feature of diversity. Different geographical environment and type of organizations lead to the significant difference on the quantity and the species composition. Most of fungi in Ningxia C. komarovii distribute in leaves. However, most of those in Shaanxi C. komarovii distribute in stems and leaves. It also indicated that endophytes from C. komarovii had a strong antifungal activity.
Antifungal Agents ; pharmacology ; Biodiversity ; China ; Culture Media, Conditioned ; pharmacology ; Cynanchum ; microbiology ; DNA, Ribosomal Spacer ; genetics ; Desert Climate ; Endophytes ; classification ; genetics ; isolation & purification ; Fungi ; classification ; genetics ; isolation & purification ; Genetic Variation ; Magnaporthe ; drug effects ; growth & development ; Microbial Sensitivity Tests ; Phylogeny ; Plant Leaves ; microbiology ; Plant Roots ; microbiology ; Plant Stems ; microbiology ; RNA, Ribosomal, 5.8S ; genetics ; Species Specificity