1.Investigation on continual outbreaks of norovirus caused by the Sydney 2012 G ||.4 strain after a school outbreaks controlled in higher education mega center of Guangzhou.
Yuan JUN ; Wenfeng CAI ; Di BIAO ; Huaping XIE ; Guixiong LIAN ; Xincai XIAO ; Luo LEI ; Yufei LIU ; Zhicong YANG
Chinese Journal of Epidemiology 2014;35(6):755-756
Caliciviridae Infections
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epidemiology
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China
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epidemiology
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Disease Outbreaks
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Female
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Humans
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Male
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Norovirus
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Schools
2.Studies on chemical constituents of aerial parts of Ammopiptanthus mongolicus.
Xiao-Ming TIAN ; Shi-Zhong CHEN ; Peng-Fei TU ; Lian-Di LEI
China Journal of Chinese Materia Medica 2008;33(19):2204-2206
OBJECTIVETo investigate the chemical constituents of the aerial parts of Ammopiptanthus mongolicus.
METHODThe chemical constituents were isolated by various column chromatographic methods. The structures were identified by spectral data.
RESULTTen compounds were isolated and identified as m-hydroxybenzoic acid (1), 1-(4-hydroxyphenyl) ethanone (2), beta-sitosterol (3), (-)-syringaresinol (4), (+)-lariciresinol (5), blumenol A (6), blumenol B (7), beta-daucosterol (8), coniferin (9), syringin (10).
CONCLUSIONThe ten compounds were obtained from the genus Ammopiptanthus for the first time.
Cinnamates ; chemistry ; Cyclohexanones ; chemistry ; Drugs, Chinese Herbal ; chemistry ; Fabaceae ; chemistry ; Glucosides ; chemistry ; Magnetic Resonance Spectroscopy ; Phenylpropionates ; chemistry ; Plant Components, Aerial ; chemistry ; Sitosterols ; chemistry
3.Chemical constituents from the leaves of Ilex pernyi.
Guang-Bo XIE ; Feng NIU ; Xiao-Jing WANG ; Lian-Di LEI ; Peng-Fei TU
Acta Pharmaceutica Sinica 2008;43(1):60-62
A new compound and five known compounds were isolated from the ethanolic extract of the leaves of Ilex pernyi Franch. Their structures were established on the basis of spectral analysis and identified as trans-isoeugenyl-alpha-L-arabinopynosyl (1 --> 6) -beta-D-glucopyranoside (1) , kaempferol-3-O-sambubioside (2), quercetin-3-O-sambubioside (3), isoquercitrin (4), (+) -syringaresinol-O-beta-D-glucopyranoside (5), amarantholidoside IV (6). Among them, compound 1 is a new phenolic glycoside, named as ilexperphenoside A, and compounds 2-6 were isolated from this plant for the first time.
Glucosides
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chemistry
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isolation & purification
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Glycosides
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chemistry
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isolation & purification
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Ilex
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chemistry
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Molecular Structure
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Plant Leaves
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chemistry
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Plants, Medicinal
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chemistry
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Quercetin
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analogs & derivatives
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chemistry
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isolation & purification
4.Character study of content and correlativity of elements in Radix Astragali obtained from different regions.
Lian-Di LEI ; Li OUYANG ; Ya-Qiong LIU ; Ning-Hua HUANG ; Jing-Yu WANG
China Journal of Chinese Materia Medica 2008;33(3):255-258
OBJECTIVETo study the characters of concentration of 42 elements in Radix Astragali and make an attempt at looking for relationship between the element concentration and regions where samplers are obtained.
METHODDetermining the content of elements in 40 Radix Astragali samples from 7 different provinces by ICP-MS, AFS and ASS. Analyzing the correlation of elements in Radix Astragali using statistic software (Spss).
RESULTFirstly, similar lines of element concentration have been acquired in our research. Secondly, it is observed that the content of elements in the samples shows regional diversity. Thirdly, there are 346 correlative element pairs in correlate analysis. And some of them indicate remarkable correlativity.
CONCLUSIONWith the aid of obtained results, it is concluded that element content in Radix Astragali display special distributing line. Remarkable correlation is presented in some element pairs. The quality of Radix Astragali gained from Neimeng, Shanxi and Gansu are better than those from other regions.
Astragalus Plant ; chemistry ; growth & development ; China ; Elements ; Geography
5.Studies on triterpenoid constituents in leaf of Ilex pernyi.
Guang-Bo XIE ; Si-Xiang ZHOU ; Lian-Di LEI ; Peng-Fei TU
China Journal of Chinese Materia Medica 2007;32(18):1890-1892
OBJECTIVETo investigate the chemical constituents of Ilex pernyi.
METHODThe chemical constituents were isolated by various column chromatographic methods. The structures were identified by spectral data.
RESULTEight triterpenoid compounds were isolated and identified as ursolic acid (1), lupeol (2), alpha-amyrin (3), uvaol (4), 3beta-hydroxyurs-11-ene-13beta-olide (5), pomolic acid (6), lup-20 (29)-ene-3beta, 24-diol (7), 3beta, 23-dihydroxy-urs-12-en-28-oic acid (8).
CONCLUSIONThe eight compounds were obtained from this plant for the first time.
Ilex ; chemistry ; Oleanolic Acid ; analogs & derivatives ; chemistry ; isolation & purification ; Plant Leaves ; chemistry ; Plants, Medicinal ; chemistry ; Triterpenes ; chemistry ; isolation & purification
6.Molecular epidemiological characteristics of Streptococcus pyogenes strains involved in an outbreak of scarlet fever in China, 2011.
Yuan Hai YOU ; Yan Yan SONG ; Xiao Mei YAN ; Hai Bin WANG ; Meng Han ZHANG ; Xiao Xia TAO ; Lei Lei LI ; Yu Xin ZHANG ; Xi Hong JIANG ; Bing Hua ZHANG ; Hao ZHOU ; Di XIAO ; Lian Mei JIN ; Zi Jian FENG ; Feng Ji LUO ; Jian Zhong ZHANG
Biomedical and Environmental Sciences 2013;26(11):877-885
OBJECTIVETo investigate molecular characterization of streptococcus pyogenes isolates involved in an outbreak of scarlet fever in China in 2011.
METHODSSeventy-four Streptococcal pyogenes involved in an outbreak of scarlet fever were isolated from pediatric patients in the areas with high incidence in China from May to August of 2011. Emm genotyping, pulsed-field gel electrophoresis (PFGE), superantigen (SAg) genes and antimicrobial susceptibility profiling were analyzed for these isolates.
RESULTSA total of 4 different emm types were identified. Emm12 was the most prevalent type which contained four predominating PFGE patterns corresponding to four different virulence and superantigen profiles. Emm12 (79.7%) and emm1 (14.9%) accounted for approximately 94% of all the isolates. The speA gene was all negative in emm12 isolates and positive in emm1 isolates. All strains were resistant to erythromycin, and 89.4% of them were resistant to erythromycin, tracycline, and clindamycin simultaneously.
CONCLUSIONSeveral highly diversified clones with a high macrolide resistance rate comprise a predominant proportion of circulating strains, though no new emm type was found in this outbreak. The data provide a baseline for further surveillance of scarlet fever, which may contribute to the explanation of the outbreak and development of a GAS vaccine in China.
Anti-Bacterial Agents ; administration & dosage ; therapeutic use ; Child ; China ; epidemiology ; Disease Outbreaks ; Drug Resistance, Bacterial ; Electrophoresis, Gel, Pulsed-Field ; Humans ; Incidence ; Molecular Epidemiology ; Scarlet Fever ; drug therapy ; epidemiology ; microbiology ; Streptococcus pyogenes ; drug effects ; genetics ; isolation & purification ; pathogenicity ; Virulence
7.Study of heterologous efficient synthesis of cucurbitadienol.
Shou-Lian LI ; Dong WANG ; Yi LIU ; Ting-Ting LIN ; Jin-Lei TANG ; Er-Bing HUA ; Xue-Li ZHANG ; Zhu-Bo DAI ; Lu-Qi HUANG
China Journal of Chinese Materia Medica 2017;42(17):3326-3331
Cucurbitadienol has anti-inflammation, anti-cancer activities, and acts as a precursor of traditional Chinese medicine active ingredients mogroside and cucurbitacine. For construction of a Sacchromyces cerevisiae cell factory for production of cucurbitadienol, we firstly cloned a cucurbitadienol synthase (CBS) gene from Siraitia grosvenorii. Then, through heterologous expression of CBS in the triterpenoid chassis strain WD-2091, the engineered strain could produced 27.44 mg•L ⁻¹ cucurbitadienol, which was determined by GC-MS. Further regulation of CBS expression led to cucurbitadienol's titer increasing by 202.07% and reaching 82.89 mg•L ⁻¹ in the shake flask fermentation and 1 724.10 mg•L ⁻¹ in the high cell density fermentation. Our research promotes the cucurbitane-type tetracyclic triterpenoids synthesis pathway analysis progress and provides the basis for further obtaining cell factories for production of cucurbitadienol tetracyclic triterpenoids.