981 research outputs found
Early transcriptional response of terpenoid metabolism to Colletotrichum gloeosporioides in a resistant wild strawberry Fragaria nilgerrensis
No full textMehmood, Nasir, Yuan, Yuan, Ali, Mohammed, Ali, Muhammad, Iftikhar, Junaid, Cheng, Chunzhen, Lyu, Meiling, Wu, Binghua (2021): Early transcriptional response of terpenoid metabolism to Colletotrichum gloeosporioides in a resistant wild strawberry Fragaria nilgerrensis. Phytochemistry (112590) 181: 1-12, DOI: 10.1016/j.phytochem.2020.112590, URL: http://dx.doi.org/10.1016/j.phytochem.2020.11259
Timomenus nevilli Burr 1904
No full textTimomenus nevilli (Burr, 1904) Opisthocosmia nevilli Burr, 1904: 309. Eparchus nevilli Burr, 1907: 121. Timomenus nevilli Burr, 1910: 197. Measurements. Total body: ♂ 10.0‒21.0, ♀ 13.0‒ 18.5; forceps: ♂ 5.5‒10.5, ♀ 5.0‒8.0. Material. 2 ♀♀, Motuo, Tibet, China, elev. 1350m, 1979. IX. 8, collected by Jin Gen-Tao & Wu Jian-Yi; 3 ♀♀, Beibeng, Motuo, Tibet, China, elev. 940m, 1979. X. 17‒24, collected by Jin Gen-Tao & Wu Jian-Yi; 2 ♂♂, 3 ♀♀, Motuo, Tibet, China, elev. 1310‒1470m, 1980. II. 10‒27, collected by Jin Gen-Tao & Wu Jian-Yi. Distribution. China (Fujian, Tibet), India, Bhutan; Nepal, Sikkim.Published as part of Sun, Meiling, Li, Kai & Liu, Xianwei, 2016, Three new species of the subfamily Opisthocosmiinae from China (Dermaptera, Forficulidae), with new synonymies and combinations, pp. 359-371 in Zootaxa 4109 (3) on page 363, DOI: 10.11646/zootaxa.4109.3.6, http://zenodo.org/record/26607
sj-tif-1-onc-10.1177_11795549221092218 – Supplemental material for The Establishment and Experimental Verification of an lncRNA-Derived CD8+ T Cell Infiltration ceRNA Network in Colorectal Cancer
No full textSupplemental material, sj-tif-1-onc-10.1177_11795549221092218 for The Establishment and Experimental Verification of an lncRNA-Derived CD8+ T Cell Infiltration ceRNA Network in Colorectal Cancer by Qi Wu, Zhiyuan Zhang, Meiling Ji, Tao Yan, Yudong Jiang, Yijiao Chen, Jiang Chang, Jicheng Zhang, Dong Tang, Dexiang Zhu and Ye Wei in Clinical Medicine Insights: Oncology</p
sj-jpg-2-onc-10.1177_11795549221092218 – Supplemental material for The Establishment and Experimental Verification of an lncRNA-Derived CD8+ T Cell Infiltration ceRNA Network in Colorectal Cancer
No full textSupplemental material, sj-jpg-2-onc-10.1177_11795549221092218 for The Establishment and Experimental Verification of an lncRNA-Derived CD8+ T Cell Infiltration ceRNA Network in Colorectal Cancer by Qi Wu, Zhiyuan Zhang, Meiling Ji, Tao Yan, Yudong Jiang, Yijiao Chen, Jiang Chang, Jicheng Zhang, Dong Tang, Dexiang Zhu and Ye Wei in Clinical Medicine Insights: Oncology</p
Cordax armatus De Haan 1842
No full textCordax armatus (De Haan, 1842) (Figs. 13‒16) Forficula armatus De Haan, 1842: 243. Opisthocosmia armata Bormans, 1888: 444. Cordax armatus Burr, 1910: 185. Measurements. Total body: ♂ 13.0‒18.0, ♀ 14.0‒18.0; forceps: ♂ 5.5, ♀ 5.0‒6.0. Material. 1 ♂, Da’an, Fujian, 1959. VI. 25, collected by Jin Gen-Tao & Lin Yang-Ming; 1 ♂, Beibeng, Motuo, Tibet, China, elev. 1050m, 1979. VII. 24, collected by Jin Gen-Tao & Wu Jian-Yi; 2 ♂♂, 4 ♀♀, Beibeng, Motuo, Tibet, China, 1979. VIII. 5 ‒XI. 6, collected by Jin Gen-Tao & Wu Jian-Yi; 1 ♀, Didong, Motuo, Tibet, China, elev. 920m, 1980. VII. 5, collected by Jin Gen-Tao & Wu Jian-Yi; 2 ♂♂, 3 ♀♀, Jinxiu, Guangxi, China, 1981. IX. 17 ‒X. 21, collected by Jin Gen-Tao; 1 ♂, Old Mountain, Jinxiu, Guangxi, China, elev. 1100m, 1981. X. 13, collected by Jin Gen-Tao; 1 ♀, Hekou, Yunnan, China, elev. 130m, 1982. VI. 5, collected by Jin Gen-Tao & Wu Jian-Yi; 1 ♀, Huangniushi, Jiulian Mountain, Jiangxi, elev. 500m, 1986. IX. 10, collected by Jin Gen-Tao & Lin Yang-Ming; 1 ♂, Sancha River, Jinghong, Yunnan, China, 1995. XI. 11‒12, collected by Xu Wen-Hong; 2 ♀♀, Sancha River, Xishuangbanna, Yunnan, China, elev. 750m, 2009. VI. 9‒10, collected by Liu Xian-Wei et al.; 1 ♂, 2 ♀♀, Nonggang, Longzhou, Guangxi, China, elev. 200m, 2013. VII. 10‒13, collected by Zhang Hai-Guang et al.; 2 ♂♂, Dongsai, Maolan, Libo, Guizhou, China, elev. 600‒700m, 2014. VIII. 9‒10, collected by Sun Mei-Ling; 2 ♀♀, Weng’ang, Maolan, Libo, Guizhou, China, elev. 500‒800m, 2014. VIII. 9‒11, collected by Sun Mei-Ling. Distribution. China (Fujian, Jiangxi, Hainan, Guangxi, Yunnan, Tibet, Guizhou), Burma, Borneo, Celebes, Sumatra.Published as part of Sun, Meiling, Li, Kai & Liu, Xianwei, 2016, Three new species of the subfamily Opisthocosmiinae from China (Dermaptera, Forficulidae), with new synonymies and combinations, pp. 359-371 in Zootaxa 4109 (3) on page 365, DOI: 10.11646/zootaxa.4109.3.6, http://zenodo.org/record/26607
Timomenus lugens Bormans 1894
No full text<i>Timomenus lugens</i> (Bormans, 1894) <p> <i>Opisthocosmia lugens</i> Bormans, 1894: 308. <i>Eparchus lugens</i> Burr, 1907: 121.</p> <p> <i>Timomenus lugens</i> Burr, 1910: 93.</p> <p> <b>Measurements.</b> Total body: ♂ 13.0‒22.0, ♀ 10.0‒21.0; forceps: ♂ 4.0‒10.0, ♀ 3.5‒9.5.</p> <p> <b>Material.</b> 1♂, Menghai, Yunnan, China, 1973. XI.27, collected by Hu Jin-Lin; 1♂, Beibeng, Motuo, Tibet, China, 1979. VIII.12, collected by Jin Gen-Tao & Wu Jian-Yi; 1♀, Didong, Motuo, Tibet, China, elev. 1120m, 1979. XI.21, collected by Jin Gen-Tao & Wu Jian-Yi; 1♂, 5♀♀, Motuo, Tibet, China, elev. 980‒1520m, 1980. II.10‒V.29, collected by Jin Gen-Tao & Wu Jian-Yi; 1♀, Jinping, Yunnan, China, elev. 1350m, 1982. VI.13, collected by Jin Gen-Tao & Wu Jian-Yi; 1♀, Mengla, Yunnan, China, 1991. IX.3, collected by Liu Zu-Yao <i>et al.</i>; 1♀, Mangshi, Yunnan, China, 1991. IX.22, collected by Liu Zu-Yao <i>et al.</i>; 4♂♂, 3♀♀, Jinuo, Yunnan, China, 1995. VIII.5–9, collected by Liu Xian-Wei <i>et al.</i>; 1♂, 2♀♀, Mawei, Pingbian, Yunnan, China, elev. 900‒950m, 2009. V.22‒23, collected by Liu Xian-Wei <i>et al.</i>; 1♂, Sancha River, Xishuangbanna, Yunnan, China, elev. 750m, 2009. VI.9‒10, collected by Liu Xian-Wei <i>et al..</i></p> <p> <b>Distribution.</b> China (Hubei, Zhejiang, Jiangxi, Guangxi, Sichuan, Yunnan, Tibet), Myanmar, India, Bhutan, Thailand, Malaysia.</p>Published as part of <i>Sun, Meiling, Li, Kai & Liu, Xianwei, 2016, Three new species of the subfamily Opisthocosmiinae from China (Dermaptera, Forficulidae), with new synonymies and combinations, pp. 359-371 in Zootaxa 4109 (3)</i> on page 363, DOI: 10.11646/zootaxa.4109.3.6, <a href="http://zenodo.org/record/266075">http://zenodo.org/record/266075</a>
Fig. 4 in Early transcriptional response of terpenoid metabolism to Colletotrichum gloeosporioides in a resistant wild strawberry Fragaria nilgerrensis
No full textFig. 4. Schematic illustration of general terpenoid biosynthesis pathways showing identified unigenes from F. nilgerrensis leaf transcriptome data. The interconvertible precursors IPP and DMAPP, two phosphorylated C5 unites, are produced by the MVA and MEP pathways which are exchangeable from both compartmentations. The chloroplast is a major site for synthesis of hemiterpene (C5), monoterpenoids (C10), diterpenoids (C20) carotenoids (C40) and chlorophyll, while the cytosol and other organelle are responsible for synthesis of monoterpenoids (C10), sesquiterpene (C15) and triterpene (C30). But that is not strictly conclusive. Arrow with lines indicate reactions catalyzed by enzymes and the encoding genes, with unigenes identified in this experiment boxed. The color highlights are for better visualization. Abbreviations: AACT, acetoacetyl-CoA thiolase; CMK, 4-diphosphocytidyl-2-C-methyl-D-erythritol kinase; DXR, 1-deoxy-D-xylulose 5-phosphate reductase; DXS, 1-deoxy-D-xylulose 5-phosphate synthase; HDR, (E)-4-hydroxy-3-methyl-but-2-enyl diphosphate reductase; HDS, (E)-4-hydroxy-3- methyl-but-2-enyl diphosphate synthase; HMGR, 3-hydroxy-3-methylglutaryl-CoA reductase; HMGS, 3-hydroxy-3-methylglutaryl-CoA synthase; IDI, isopentenyl diphosphate isomerase; MCT, MEP cytidyltransferase; MDC, mevalonate-5-diphosphate decarboxylase; MDS, 2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase; MVK, mevalonate kinase. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)Published as part of Mehmood, Nasir, Yuan, Yuan, Ali, Mohammed, Ali, Muhammad, Iftikhar, Junaid, Cheng, Chunzhen, Lyu, Meiling & Wu, Binghua, 2021, Early transcriptional response of terpenoid metabolism to Colletotrichum gloeosporioides in a resistant wild strawberry Fragaria nilgerrensis, pp. 1-12 in Phytochemistry (112590) 181 on page 7, DOI: 10.1016/j.phytochem.2020.112590, http://zenodo.org/record/829067
Fragaria nilgerrensis leaves
No full text4.2. Isolation of phytochemical and volatile compounds from F. nilgerrensis leaves At different hours (0, 3, 6, 12, 18, 24, 48 and 72 h) after infected with C. gloeosporioides, leaves were removed and collected from the plants, frozen immediately in liquid nitrogen and then stored at 80 ◦ C for future use. Each cryopreserved sample was homogenized in liquid nitrogen by using pestle and mortar. One gram of the powdered samples was mixed with 2 ml saturated NaCl in a 20 ml-head-space vial, in which an internal standard (10 μl of 8.08 mg /L 2,6-dimethyl-4-heptanone (cat. Nr. W353701 from Sigma–Aldrich, Shanghai, China) was added. Before subjecting the mixtures for SPME extraction, each vial was heated at 60 ◦ C for 10 min. Subsequently, the headspace of the sample vial was exposed to a 65 μm divinylbenzene/carboxen/polydimethylsilioxan fiber (Supelco, Bellefonte, PA, USA) for 20 min at 60 ◦ C to complete the extraction. Relative abundance of the compounds was quantified by peak area determination and normalized to the mass of the internal standard. We pooled samples from three plants for one biological replication and the experiment was performed twice which gave similar results. Data are shown as mean without significant test in the Results section.Published as part of Mehmood, Nasir, Yuan, Yuan, Ali, Mohammed, Ali, Muhammad, Iftikhar, Junaid, Cheng, Chunzhen, Lyu, Meiling & Wu, Binghua, 2021, Early transcriptional response of terpenoid metabolism to Colletotrichum gloeosporioides in a resistant wild strawberry Fragaria nilgerrensis, pp. 1-12 in Phytochemistry (112590) (112590) 181 on page 7, DOI: 10.1016/j.phytochem.2020.112590, http://zenodo.org/record/829067
Fig. 7 in Early transcriptional response of terpenoid metabolism to Colletotrichum gloeosporioides in a resistant wild strawberry Fragaria nilgerrensis
No full textFig. 7. Phylogenetic relationship of the five FnTPS candidates with other known terpene synthases and a sequence alignment showing the conserved protein motifs. (A) A maximum-likelihood tree of the TPS proteins depicting the TPS-a, TPS-b, TPS-d, TPS-e/f, and TPS-g clades, with bootstrap values greater than 50% shown for the branching. The scale bar corresponds to 6% amino acid substitution. The five F. nilgerrensis proteins are in red. Selected proteins with available three-dimensional structural data are shown in bold using their PDB code followed by the abbreviated species name. The known enzymatic products are in light blue followed with the UniProt Accession numbers of the proteins. (B) Alignment of the five candidates FnTPSs with α-farnesene synthase from apple (Malus domestica) and α-bergamotene synthase from Lavender (Lavandula Angustifolia). The DxDD motif of typical class II terpene synthases in FnTPS6 is boxed and the highly conserved class I DDxxD as well as the lesser conserved RRx8W and NSE/DTE motifs are indicated. The color regime of amino acids is set in Bioedit version 7.2.6. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)Published as part of Mehmood, Nasir, Yuan, Yuan, Ali, Mohammed, Ali, Muhammad, Iftikhar, Junaid, Cheng, Chunzhen, Lyu, Meiling & Wu, Binghua, 2021, Early transcriptional response of terpenoid metabolism to Colletotrichum gloeosporioides in a resistant wild strawberry Fragaria nilgerrensis, pp. 1-12 in Phytochemistry (112590) 181 on page 10, DOI: 10.1016/j.phytochem.2020.112590, http://zenodo.org/record/829067
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