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Arabidopsis separate antifungal protein from Italian or AtDabb1

机译：拟南芥从意大利或AtDabb1分离抗真菌蛋白

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摘要

More particularly, the present invention relates to a call rekto AtDabb1 antifungal protein isolated from Arabidopsis Italian or coconut tree Kiwoom death ( Collectotrichum coccodes ), gallium pusa oxy Forum ( Fusarium oxysporum ), gallium pusa solani ( Fusarium solani ), tricot der Do Har Jia num ( Trichoderma harzianum ), tricot der corruption to Do ( Trichoderma viride ), Candida albicans ( Candida albicans ) and tree course isophorone Bay gelri ( Trichosporon beigellii ) to inhibit cell growth of plant pathogenic fungi , such relates to the antifungal protein isolated from Arabidopsis AtDabb1 Thalia me.

机译：更具体地，本发明涉及从拟南芥属意大利人或椰子树Kiwoom死亡（ Collectotrichum coccodes ），氧化镓镓论坛（尖孢镰刀菌）中分离出的rekto AtDabb1抗真菌蛋白。，茄子茄（镰刀菌（Fusarium solani ）），特里科（Tricot der Do Har Jia num）（木霉harzianum ），特里科（Tricotder der to do）腐烂（ Trichoderma viride ），白色念珠菌（白色念珠菌）和树过程异佛尔酮湾gel喱（ Trichosporon米歇尔氏菌）抑制植物病原真菌的细胞生长，与从拟南芥AtDabb1分离的抗真菌蛋白有关塔利亚我。 展开▼

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公开/公告号KR101063234B1

专利类型

公开/公告日2011-09-07

原文格式PDF

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申请/专利号KR20080032442

发明设计人 정지현;장호희;박진호;이상열;김선영;이중로;강재숙;김외연;이영미;
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申请日2008-04-08

分类号C12N15/29;C12N15/10;C12N15/09;

国家 KR

入库时间 2022-08-21 17:49:49

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机译：从形式改变的转基因植物和拟南芥（Arabidopsis thaliana）的启动子和蛋白质中分离出最终的1,4-β-葡聚糖酶基因

1. Construction of a chloroplast protein interaction network and functional mining of photosynthetic proteins in Arabidopsis thaliana [J] . Qing-Bo Yu, Yong-Lan Cui, Kang Chong, 细胞研究（英文版） . 2008,第010期

2. Construction of a chloroplast protein interaction network and functional mining of photosynthetic proteins in Arabidopsis thaliana [J] . Qing-Bo Yu, Guang Li, Guan Wang, 细胞研究：英文版 . 2008,第010期

3. Genome-wide Analysis of Ovate Family Proteins in Arabidopsis [J] . Huang Jian-ping, Li Hong-ling, Chang Ying 东北农业大学学报（英文版） . 2012,第003期

4. The Arabidopsis PRCl-like ring-finger proteins are necessary for repression of embryonic traits during vegetative growth [J] . Donghong Chen, Anne Molitor, Chunlin Liu, 细胞研究：英文版 . 2010,第012期

5. Functional characterization of pathogen-responsive protein AtDabb1 with an antifungal activity from Arabidopsis thaliana. [J] . Lee JR, Lee SS, Park SC Biochimica et biophysica acta: BBA: International journal of biochemistry, biophysics and molecular biololgy. Proteins and Proteomics . 2008,第12期

6. Determining Degradation and Synthesis Rates of Arabidopsis Proteins Using the Kinetics of Progressive ~(15)N Labeling of Two-dimensional Gel-separated Protein Spots [J] . Lei Li, Clark J. Nelson, Cory Solheim, Molecular & cellular proteomics: MCP . 2012,第6期

7. Molecular mechanism of Arabidopsis thaliana profilins as antifungal proteins [J] . Seong-Cheol Park, Il Ryong Kim, Jin-Young Kim, Biochimica et Biophysica Acta. General Subjects . 2018,第12期

8. Molecular Docking Approach Study of Binding Performance of Antifungal Proteins [C] . Satya Narayan Sahu, Maheswata Moharana, Rojalin Sahu, International Conference on Advances in Basic Sciences . 2019

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10. Determining Degradation and Synthesis Rates of Arabidopsis Proteins Using the Kinetics of Progressive 15N Labeling of Two-dimensional Gel-separated Protein Spots [O] . Lei Li, Clark J. Nelson, Cory Solheim, 2012

11. The pyrenoidal linker protein EPYC1 phase separates with hybrid Arabidopsis–Chlamydomonas Rubisco through interactions with the algal Rubisco small subunit [O] . Nicky Atkinson, Christos N Velanis, Tobias Wunder, 2019

1. BACKGROUND： Vibrio vulnifi cus inside the body could activate the NF-!B signaling pathwayand initiate the inflammatory cascade. The lung is one of the earliest organs affected by sepsisassociated with acute lung injury. High mobility group protein B1 （HMGB1） is an important late-actingpro-infl ammatory cytokine involving in the pathophysiology of sepsis. It is also involved in the injuryprocess in the lung, liver and intestine. There has been no report on the involvement of HMGB1 inVibrio vulnifi cus sepsis-induced lung injury.METHODS： Sixty rats were randomly divided into a normal control group （group A, n=10） anda Vibrio vulnificus sepsis group （group B, n=50）. Sepsis was induced in the rats by subcutaneousinjection of Vibrio vulnificus （concentration 6×108 cfu/mL, volume 0.1 mL/100g）） into the left lowerlimbs. The rats in group B were sacrifi ced separately 1, 6, 12, 24, and 48 hours after the infection.Their lungs were stored as specimens, lung water content was measured, and lung pathology wasobserved under a light microscope. The expressions of the HMGB1 gene and protein in the lungswere detected by RT-PCR and Western blot. Data were analyzed with one-way analysis of variance（ANOVA） and the LSD method for pair-wise comparison between the two groups. P〈0.05 wasconsidered statistically signifi cant.RESULTS： Compared to group A （0.652±0.177）, HMGB1 mRNA expression in the lungs ofgroup B was signifi cantly higher at 0 hour （1.161±0.358, P=0.013）, 24 hours （1.679±0.235, P=0.000）,and 48 hours （1.258±0.274, P=0.004）（P〈0.05）, and peaked at 24 hours. Compared to group A（0.594±0.190）, HMGB1 protein expression at 6 hours （1.408±0.567, P=0.026） after infection wassignificantly increased （P〈0. 05）, and peaked at 24 hours （2.415±1.064, P=0.000） after infection.Compared to group A （0.699±0.054）, lung water content was significantly increased at 6 hours（0.759±0.030, P=0.001）,12 hours （0.767±0.023, P=0.000）, 24 hours （0.771±0.043, P=0.000） and 48hours （0.789±0.137, P=0.000） after infection （P〈0.05）. Compared to group A, pathological changesat 12 hours in group B indicate marked pulmonary vascular congestion, interstitial edema andinfl ammatory infi ltration. Alveolar cavity collapse and boundaries of the alveolar septum could not beclearly identifi ed.CONCLUSION： Vibrio vulnifi cus sepsis can lead to injury in rat lungs, and increased HMGB1expression in lung tissue may be one of the mechanisms for injury from Vibrio vulnifi cus sepsis. [J] . Qiao-meng Qiu ,Zhong-wang Li ,Lu-ming Tang . 世界急诊医学杂志(英文) . 2011,第4期

2. 黑豆中分离的一个24KDa具有抗真菌活性的胰蛋白酶抑制蛋白 [C] . Biao Shao ,邵彪 ,Shaoyun Wang . 华东六省一市生物化学与分子生物学会2008年学术交流会 . 2008

3. 产抗真菌蛋白菌株筛选与抗真菌蛋白分离纯化 [A] . 陈洪元 . 2011