Camalexin (BioDeep_00000397970)

Main id: BioDeep_00000000646

 

PANOMIX_OTCML-2023 Antitumor activity natural product


代谢物信息卡片


3-(1,3-thiazol-2-yl)-1H-indole

化学式: C11H8N2S (200.0408)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C12=C(C=CC=C2)NC=C1C3=NC=CS3
InChI: InChI=1S/C11H8N2S/c1-2-4-10-8(3-1)9(7-13-10)11-12-5-6-14-11/h1-7,13H

描述信息

D000890 - Anti-Infective Agents
IPB_RECORD: 278; CONFIDENCE confident structure
Camalexin is a phytoalexin isolated from Camelina sativa (Cruciferae) with antibacterial, antifungal, antiproliferative and anticancer activities. Camalexin can induce reactive oxygen species (ROS) production[1][2][3].

同义名列表

3 个代谢物同义名

3-(1,3-thiazol-2-yl)-1H-indole; 2-(3-Indolyl)thiazole; Camalexin



数据库引用编号

14 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(0)

PlantCyc(0)

代谢反应

0 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

21 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有：

  • PubMed: 来源于PubMed文献库中的文献信息，我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表，这个列表按照代谢物同时出现的文献数量降序排序，取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘，得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序，取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中，存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称，可以跳转到相关代谢物的信息页面。

亚细胞结构定位 关联基因列表
Cytoplasm 9 CAT, DOCK6, GGPS1, HPGDS, MAPK3, MAPK6, MKS1, PIN4, RPS2
Peripheral membrane protein 1 CYP1B1
Endoplasmic reticulum membrane 2 CYP1B1, FMO1
Nucleus 6 IRX1, MAPK3, MAPK6, MYB, PIN4, RPS2
cytosol 13 BAK1, CAT, DOCK6, GCLM, GGPS1, GSR, HAO2, HPGDS, MAPK3, MAPK6, MKS1, MYB, RPS2
centrosome 1 MKS1
nucleoplasm 7 GGPS1, HPGDS, MAPK3, MAPK6, MYB, PIN4, RPS2
RNA polymerase II transcription regulator complex 1 MYB
cell surface 2 TNFRSF10B, TNR
glutamatergic synapse 2 MAPK3, TNR
Golgi apparatus 1 MAPK3
plasma membrane 3 MAPK3, NPR1, TNFRSF10B
Membrane 8 BAK1, CAT, CYP1B1, MKS1, MYB, NPR1, RPS2, TNFRSF10B
caveola 1 MAPK3
extracellular exosome 3 CAT, GSR, RPS2
endoplasmic reticulum 2 BAK1, FMO1
extracellular space 1 TNR
perinuclear region of cytoplasm 2 DOCK6, GGPS1
Schaffer collateral - CA1 synapse 1 TNR
mitochondrion 5 BAK1, CAT, CYP1B1, GSR, MAPK3
protein-containing complex 2 CAT, MAPK6
intracellular membrane-bounded organelle 3 CAT, CYP1B1, HPGDS
Microsome membrane 1 CYP1B1
extracellular region 2 CAT, TNR
Mitochondrion outer membrane 1 BAK1
Single-pass membrane protein 2 BAK1, FMO1
mitochondrial outer membrane 1 BAK1
mitochondrial matrix 3 CAT, GSR, PIN4
BAK complex 1 BAK1
Bcl-2 family protein complex 1 BAK1
external side of plasma membrane 1 GSR
Secreted, extracellular space, extracellular matrix 1 TNR
Z disc 1 GGPS1
nucleolus 1 PIN4
Early endosome 1 MAPK3
Cytoplasm, perinuclear region 2 DOCK6, GGPS1
Membrane raft 1 TNR
pore complex 1 BAK1
Cell junction, focal adhesion 1 MAPK3
focal adhesion 3 CAT, MAPK3, RPS2
spindle 1 PIN4
Peroxisome 2 CAT, HAO2
Peroxisome matrix 1 CAT
peroxisomal matrix 2 CAT, HAO2
peroxisomal membrane 1 CAT
collagen-containing extracellular matrix 1 TNR
Late endosome 1 MAPK3
receptor complex 1 NPR1
ciliary basal body 1 MKS1
chromatin 1 IRX1
Chromosome 1 PIN4
cytoskeleton 2 MAPK3, MKS1
Cytoplasm, cytoskeleton, cilium basal body 1 MKS1
centriole 1 MKS1
Nucleus, nucleolus 1 RPS2
nuclear envelope 1 MAPK3
Membrane, caveola 1 MAPK3
pseudopodium 1 MAPK3
Cytoplasm, myofibril, sarcomere, Z line 1 GGPS1
ficolin-1-rich granule lumen 1 CAT
secretory granule lumen 1 CAT
endoplasmic reticulum lumen 2 FMO1, MAPK3
nuclear matrix 1 MYB
perineuronal net 1 TNR
MKS complex 1 MKS1
cytosolic ribosome 1 RPS2
ribosome 1 RPS2
catalase complex 1 CAT
cytosolic small ribosomal subunit 1 RPS2
ANPR-A receptor complex 1 NPR1
tenascin complex 1 TNR
glutamate-cysteine ligase complex 1 GCLM
small ribosomal subunit 1 RPS2
septin cytoskeleton 1 MAPK6
preribosome 1 PIN4


文献列表

  • Jogindra Naik, Shivi Tyagi, Ruchika Rajput, Pawan Kumar, Boas Pucker, Naveen C Bisht, Prashant Misra, Ralf Stracke, Ashutosh Pandey. Flavonols have opposite effects on the interrelated glucosinolate and camalexin biosynthetic pathways in Arabidopsis thaliana. Journal of experimental botany. 2023 Oct; ?(?):. doi: 10.1093/jxb/erad391. [PMID: 37813680]
  • Zi-Jie Li, Shu-Ya Tang, Hong-Shan Gao, Jin-Yao Ren, Pei-Ling Xu, Wen-Pan Dong, Ying Zheng, Wei Yang, Yi-Yang Yu, Jian-Hua Guo, Yu-Ming Luo, Dong-Dong Niu, Chun-Hao Jiang. Plant growth-promoting rhizobacterium Bacillus cereus AR156 induced systemic resistance against multiple pathogens by priming of camalexin synthesis. Plant, cell & environment. 2023 Sep; ?(?):. doi: 10.1111/pce.14729. [PMID: 37775913]
  • Bibek Aryal, Jian Xia, Zehan Hu, Michael Stumpe, Tashi Tsering, Jie Liu, John Huynh, Yoichiro Fukao, Nina Glöckner, Hsin-Yao Huang, Gloria Sáncho-Andrés, Konrad Pakula, Joerg Ziegler, Karin Gorzolka, Marta Zwiewka, Tomasz Nodzynski, Klaus Harter, Clara Sánchez-Rodríguez, Michał Jasiński, Sabine Rosahl, Markus M Geisler. An LRR receptor kinase controls ABC transporter substrate preferences during plant growth-defense decisions. Current biology : CB. 2023 Apr; ?(?):. doi: 10.1016/j.cub.2023.04.029. [PMID: 37146609]
  • Anamika A Rawat, Michael Hartmann, Anne Harzen, Raphael Lugan, Sara Christina Stolze, Celine Forzani, Laura Abts, Sophie Reißenweber, Naganand Rayapuram, Hirofumi Nakagami, Jürgen Zeier, Heribert Hirt. OXIDATIVE SIGNAL-INDUCIBLE1 induces immunity by coordinating N-hydroxypipecolic acid, salicylic acid, and camalexin synthesis. The New phytologist. 2023 02; 237(4):1285-1301. doi: 10.1111/nph.18592. [PMID: 36319610]
  • Anna Koprivova, Melina Schwier, Vanessa Volz, Stanislav Kopriva. Shoot-root interaction in control of camalexin exudation in Arabidopsis. Journal of experimental botany. 2023 Jan; ?(?):. doi: 10.1093/jxb/erad031. [PMID: 36651631]
  • Ching-Han Chang, Wu-Guei Wang, Pei-Yu Su, Yu-Shuo Chen, Tri-Phuong Nguyen, Jian Xu, Masaru Ohme-Takagi, Tetsuro Mimura, Ping-Fu Hou, Hao-Jen Huang. The involvement of AtMKK1 and AtMKK3 in plant-deleterious microbial volatile compounds-induced defense responses. Plant molecular biology. 2023 Jan; 111(1-2):21-36. doi: 10.1007/s11103-022-01308-2. [PMID: 36109466]
  • Beatriz Val-Torregrosa, Mireia Bundó, Mani Deepika Mallavarapu, Tzyy-Jen Chiou, Victor Flors, Blanca San Segundo. Loss-of-function of NITROGEN LIMITATION ADAPTATION confers disease resistance in Arabidopsis by modulating hormone signaling and camalexin content. Plant science : an international journal of experimental plant biology. 2022 Oct; 323(?):111374. doi: 10.1016/j.plantsci.2022.111374. [PMID: 35839945]
  • Dimitri Bréard, Thibault Barrit, Daniel Sochard, Sophie Aligon, Elisabeth Planchet, Béatrice Teulat, Josiane Le Corff, Claire Campion, David Guilet. Development of a quantification method for routine analysis of glucosinolates and camalexin in brassicaceous small-sized samples by simultaneous extraction prior to liquid chromatography determination. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 2022 Aug; 1205(?):123348. doi: 10.1016/j.jchromb.2022.123348. [PMID: 35777257]
  • Kevin L Cox. Stronger together: Ethylene, jasmonic acid, and MAPK signaling pathways synergistically induce camalexin synthesis for plant disease resistance. The Plant cell. 2022 07; 34(8):2829-2830. doi: 10.1093/plcell/koac155. [PMID: 35652267]
  • Ngoc Huu Nguyen, Patricia Trotel-Aziz, Sandra Villaume, Fanja Rabenoelina, Christophe Clément, Fabienne Baillieul, Aziz Aziz. Priming of camalexin accumulation in induced systemic resistance by beneficial bacteria against Botrytis cinerea and Pseudomonas syringae pv. tomato DC3000. Journal of experimental botany. 2022 06; 73(11):3743-3757. doi: 10.1093/jxb/erac070. [PMID: 35191984]
  • Ngoc Huu Nguyen, Patricia Trotel-Aziz, Christophe Clément, Philippe Jeandet, Fabienne Baillieul, Aziz Aziz. Camalexin accumulation as a component of plant immunity during interactions with pathogens and beneficial microbes. Planta. 2022 May; 255(6):116. doi: 10.1007/s00425-022-03907-1. [PMID: 35511374]
  • Ancai Liao, Lin Li, Tienan Wang, Aidang Lu, Ziwen Wang, Qingmin Wang. Discovery of Phytoalexin Camalexin and Its Derivatives as Novel Antiviral and Antiphytopathogenic-Fungus Agents. Journal of agricultural and food chemistry. 2022 Mar; 70(8):2554-2563. doi: 10.1021/acs.jafc.1c07805. [PMID: 35179026]
  • Yihao Li, Kun Liu, Ganlu Tong, Chao Xi, Jin Liu, Heping Zhao, Yingdian Wang, Dongtao Ren, Shengcheng Han. MPK3/MPK6-mediated phosphorylation of ERF72 positively regulates resistance to Botrytis cinerea through directly and indirectly activating the transcription of camalexin biosynthesis enzymes. Journal of experimental botany. 2022 01; 73(1):413-428. doi: 10.1093/jxb/erab415. [PMID: 34499162]
  • D S Makhazen, G N Veremeichik, Y N Shkryl, G K Tchernoded, V P Grigorchuk, V P Bulgakov. Inhibition of the JAZ1 gene causes activation of camalexin biosynthesis in Arabidopsis callus cultures. Journal of biotechnology. 2021 Dec; 342(?):102-113. doi: 10.1016/j.jbiotec.2021.10.012. [PMID: 34736953]
  • Kangmei Zhao, Deze Kong, Benjamin Jin, Christina D Smolke, Seung Yon Rhee. A novel bivalent chromatin associates with rapid induction of camalexin biosynthesis genes in response to a pathogen signal in Arabidopsis. eLife. 2021 09; 10(?):. doi: 10.7554/elife.69508. [PMID: 34523419]
  • Ayumi Kosaka, Marta Pastorczyk, Mariola Piślewska-Bednarek, Takumi Nishiuchi, Erika Ono, Haruka Suemoto, Atsushi Ishikawa, Henning Frerigmann, Masanori Kaido, Kazuyuki Mise, Paweł Bednarek, Yoshitaka Takano. Tryptophan-derived metabolites and BAK1 separately contribute to Arabidopsis postinvasive immunity against Alternaria brassicicola. Scientific reports. 2021 01; 11(1):1488. doi: 10.1038/s41598-020-79562-x. [PMID: 33452278]
  • Chang Ge, Wensheng Zhao, Lanchun Nie, Shance Niu, Siyu Fang, Yaqian Duan, Jiateng Zhao, Kedong Guo, Qian Zhang. Transcriptome profiling reveals the occurrence mechanism of bisexual flowers in melon (Cucumis melo L.). Plant science : an international journal of experimental plant biology. 2020 Dec; 301(?):110694. doi: 10.1016/j.plantsci.2020.110694. [PMID: 33218617]
  • Liuyi Yang, Yan Zhang, Rongxia Guan, Sen Li, Xuwen Xu, Shuqun Zhang, Juan Xu. Co-regulation of indole glucosinolates and camalexin biosynthesis by CPK5/CPK6 and MPK3/MPK6 signaling pathways. Journal of integrative plant biology. 2020 Nov; 62(11):1780-1796. doi: 10.1111/jipb.12973. [PMID: 32449805]
  • Jinggeng Zhou, Xiaoyang Wang, Yunxia He, Tian Sang, Pengcheng Wang, Shaojun Dai, Shuqun Zhang, Xiangzong Meng. Differential Phosphorylation of the Transcription Factor WRKY33 by the Protein Kinases CPK5/CPK6 and MPK3/MPK6 Cooperatively Regulates Camalexin Biosynthesis in Arabidopsis. The Plant cell. 2020 08; 32(8):2621-2638. doi: 10.1105/tpc.19.00971. [PMID: 32439826]
  • Baoda Han, Yunhe Jiang, Guoxin Cui, Jianing Mi, M Rob G Roelfsema, Grégory Mouille, Julien Sechet, Salim Al-Babili, Manuel Aranda, Heribert Hirt. CATION-CHLORIDE CO-TRANSPORTER 1 (CCC1) Mediates Plant Resistance against Pseudomonas syringae. Plant physiology. 2020 02; 182(2):1052-1065. doi: 10.1104/pp.19.01279. [PMID: 31806735]
  • Karen J Kloth, Ilka N Abreu, Nicolas Delhomme, Ivan Petřík, Cloé Villard, Cecilia Ström, Fariba Amini, Ondřej Novák, Thomas Moritz, Benedicte R Albrectsen. PECTIN ACETYLESTERASE9 Affects the Transcriptome and Metabolome and Delays Aphid Feeding. Plant physiology. 2019 12; 181(4):1704-1720. doi: 10.1104/pp.19.00635. [PMID: 31551361]
  • Céline Caseys. A Plant Metabolon Efficiently Mass-Produces Phytochemical Defenses. The Plant cell. 2019 11; 31(11):2554-2555. doi: 10.1105/tpc.19.00699. [PMID: 31511314]
  • Stefanie Mucha, Stephanie Heinzlmeir, Verena Kriechbaumer, Benjamin Strickland, Charlotte Kirchhelle, Manisha Choudhary, Natalie Kowalski, Ruth Eichmann, Ralph Hückelhoven, Erwin Grill, Bernhard Kuster, Erich Glawischnig. The Formation of a Camalexin Biosynthetic Metabolon. The Plant cell. 2019 11; 31(11):2697-2710. doi: 10.1105/tpc.19.00403. [PMID: 31511315]
  • Yunxia He, Juan Xu, Xiaoyang Wang, Xiaomeng He, Yangxiayu Wang, Jinggeng Zhou, Shuqun Zhang, Xiangzong Meng. The Arabidopsis Pleiotropic Drug Resistance Transporters PEN3 and PDR12 Mediate Camalexin Secretion for Resistance to Botrytis cinerea. The Plant cell. 2019 09; 31(9):2206-2222. doi: 10.1105/tpc.19.00239. [PMID: 31239392]
  • Philip Carella. Resistance on Tap: PDR Transporters Direct Antimicrobial Metabolites Toward Invading Pathogens. The Plant cell. 2019 09; 31(9):1943-1944. doi: 10.1105/tpc.19.00470. [PMID: 31266849]
  • Brenden Barco, Yoseph Kim, Nicole K Clay. Expansion of a core regulon by transposable elements promotes Arabidopsis chemical diversity and pathogen defense. Nature communications. 2019 08; 10(1):3444. doi: 10.1038/s41467-019-11406-3. [PMID: 31371717]
  • Anna Koprivova, Stefan Schuck, Richard P Jacoby, Irene Klinkhammer, Bastian Welter, Lisa Leson, Anna Martyn, Julia Nauen, Niklas Grabenhorst, Jan F Mandelkow, Alga Zuccaro, Jürgen Zeier, Stanislav Kopriva. Root-specific camalexin biosynthesis controls the plant growth-promoting effects of multiple bacterial strains. Proceedings of the National Academy of Sciences of the United States of America. 2019 07; 116(31):15735-15744. doi: 10.1073/pnas.1818604116. [PMID: 31311863]
  • J Pastor-Fernández, V Pastor, D Mateu, J Gamir, P Sánchez-Bel, V Flors. Accumulating evidences of callose priming by indole- 3- carboxylic acid in response to Plectospharella cucumerina. Plant signaling & behavior. 2019; 14(7):1608107. doi: 10.1080/15592324.2019.1608107. [PMID: 31010375]
  • M Soledade C Pedras, Abbas Abdoli. Methoxycamalexins and related compounds: Syntheses, antifungal activity and inhibition of brassinin oxidase. Bioorganic & medicinal chemistry. 2018 08; 26(15):4461-4469. doi: 10.1016/j.bmc.2018.07.030. [PMID: 30078606]
  • Will Buswell, Roland E Schwarzenbacher, Estrella Luna, Matthew Sellwood, Beining Chen, Victor Flors, Pierre Pétriacq, Jurriaan Ton. Chemical priming of immunity without costs to plant growth. The New phytologist. 2018 05; 218(3):1205-1216. doi: 10.1111/nph.15062. [PMID: 29465773]
  • Yang Yang, Gang Wang, Wenjun Wu, Shunnan Yao, Xiaoyan Han, Donghua He, Jingsong He, Gaofeng Zheng, Yi Zhao, Zhen Cai, Rui Yu. Camalexin Induces Apoptosis via the ROS-ER Stress-Mitochondrial Apoptosis Pathway in AML Cells. Oxidative medicine and cellular longevity. 2018; 2018(?):7426950. doi: 10.1155/2018/7426950. [PMID: 30538806]
  • Wei Zhang, Jason A Corwin, Daniel Copeland, Julie Feusier, Robert Eshbaugh, Fang Chen, Susana Atwell, Daniel J Kliebenstein. Plastic Transcriptomes Stabilize Immunity to Pathogen Diversity: The Jasmonic Acid and Salicylic Acid Networks within the Arabidopsis/Botrytis Pathosystem. The Plant cell. 2017 Nov; 29(11):2727-2752. doi: 10.1105/tpc.17.00348. [PMID: 29042403]
  • Shouan Liu, Jörg Ziegler, Jürgen Zeier, Rainer P Birkenbihl, Imre E Somssich. Botrytis cinerea B05.10 promotes disease development in Arabidopsis by suppressing WRKY33-mediated host immunity. Plant, cell & environment. 2017 Oct; 40(10):2189-2206. doi: 10.1111/pce.13022. [PMID: 28708934]
  • Mrunmay K Giri, Nidhi Singh, Zeeshan Z Banday, Vijayata Singh, Hathi Ram, Deepjyoti Singh, Sudip Chattopadhyay, Ashis K Nandi. GBF1 differentially regulates CAT2 and PAD4 transcription to promote pathogen defense in Arabidopsis thaliana. The Plant journal : for cell and molecular biology. 2017 Sep; 91(5):802-815. doi: 10.1111/tpj.13608. [PMID: 28622438]
  • C Cheval, M Perez, L J Leba, B Ranty, A Perochon, M Reichelt, A Mithöfer, E Robe, C Mazars, J P Galaud, D Aldon. PRR2, a pseudo-response regulator, promotes salicylic acid and camalexin accumulation during plant immunity. Scientific reports. 2017 08; 7(1):6979. doi: 10.1038/s41598-017-07535-8. [PMID: 28765536]
  • Deepa Khare, Hyunju Choi, Sung Un Huh, Barbara Bassin, Jeongsik Kim, Enrico Martinoia, Kee Hoon Sohn, Kyung-Hee Paek, Youngsook Lee. Arabidopsis ABCG34 contributes to defense against necrotrophic pathogens by mediating the secretion of camalexin. Proceedings of the National Academy of Sciences of the United States of America. 2017 07; 114(28):E5712-E5720. doi: 10.1073/pnas.1702259114. [PMID: 28652324]
  • Baptiste Genot, Julien Lang, Souha Berriri, Marie Garmier, Françoise Gilard, Stéphanie Pateyron, Katrien Haustraete, Dominique Van Der Straeten, Heribert Hirt, Jean Colcombet. Constitutively Active Arabidopsis MAP Kinase 3 Triggers Defense Responses Involving Salicylic Acid and SUMM2 Resistance Protein. Plant physiology. 2017 06; 174(2):1238-1249. doi: 10.1104/pp.17.00378. [PMID: 28400495]
  • David C Prince, Ghanasyam Rallapalli, Deyang Xu, Henk-Jan Schoonbeek, Volkan Çevik, Shuta Asai, Eric Kemen, Neftaly Cruz-Mireles, Ariane Kemen, Khaoula Belhaj, Sebastian Schornack, Sophien Kamoun, Eric B Holub, Barbara A Halkier, Jonathan D G Jones. Albugo-imposed changes to tryptophan-derived antimicrobial metabolite biosynthesis may contribute to suppression of non-host resistance to Phytophthora infestans in Arabidopsis thaliana. BMC biology. 2017 03; 15(1):20. doi: 10.1186/s12915-017-0360-z. [PMID: 28320402]
  • Nurmi Pangesti, Michael Reichelt, Judith E van de Mortel, Eleni Kapsomenou, Jonathan Gershenzon, Joop J A van Loon, Marcel Dicke, Ana Pineda. Jasmonic Acid and Ethylene Signaling Pathways Regulate Glucosinolate Levels in Plants During Rhizobacteria-Induced Systemic Resistance Against a Leaf-Chewing Herbivore. Journal of chemical ecology. 2016 Dec; 42(12):1212-1225. doi: 10.1007/s10886-016-0787-7. [PMID: 27848154]
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  • Bo Wang, Xinghua Qin, Juan Wu, Hongying Deng, Yuan Li, Hailian Yang, Zhongzhou Chen, Guoqin Liu, Dongtao Ren. Analysis of crystal structure of Arabidopsis MPK6 and generation of its mutants with higher activity. Scientific reports. 2016 05; 6(?):25646. doi: 10.1038/srep25646. [PMID: 27160427]
  • Elia Stahl, Patricia Bellwon, Stefan Huber, Klaus Schlaeppi, Friederike Bernsdorff, Armelle Vallat-Michel, Felix Mauch, Jürgen Zeier. Regulatory and Functional Aspects of Indolic Metabolism in Plant Systemic Acquired Resistance. Molecular plant. 2016 05; 9(5):662-681. doi: 10.1016/j.molp.2016.01.005. [PMID: 26802249]
  • Alexandra Chapman, Christian Lindermayr, Erich Glawischnig. Expression of antimicrobial peptides under control of a camalexin-biosynthetic promoter confers enhanced resistance against Pseudomonas syringae. Phytochemistry. 2016 Feb; 122(?):76-80. doi: 10.1016/j.phytochem.2016.01.001. [PMID: 26795461]
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  • Huijuan Mo, Xingfen Wang, Yan Zhang, Guiyin Zhang, Jinfa Zhang, Zhiying Ma. Cotton polyamine oxidase is required for spermine and camalexin signalling in the defence response to Verticillium dahliae. The Plant journal : for cell and molecular biology. 2015 Sep; 83(6):962-75. doi: 10.1111/tpj.12941. [PMID: 26221980]
  • Teresa M Müller, Christoph Böttcher, Robert Morbitzer, Cornelia C Götz, Johannes Lehmann, Thomas Lahaye, Erich Glawischnig. TRANSCRIPTION ACTIVATOR-LIKE EFFECTOR NUCLEASE-Mediated Generation and Metabolic Analysis of Camalexin-Deficient cyp71a12 cyp71a13 Double Knockout Lines. Plant physiology. 2015 Jul; 168(3):849-58. doi: 10.1104/pp.15.00481. [PMID: 25953104]
  • Stefanie Mucha, Dirk Walther, Teresa M Müller, Dirk K Hincha, Erich Glawischnig. Substantial reprogramming of the Eutrema salsugineum (Thellungiella salsuginea) transcriptome in response to UV and silver nitrate challenge. BMC plant biology. 2015 Jun; 15(?):137. doi: 10.1186/s12870-015-0506-5. [PMID: 26063239]
  • Yanting Zhao, Jiansheng Wang, Yuanyuan Liu, Huiying Miao, Congxi Cai, Zhiyong Shao, Rongfang Guo, Bo Sun, Chengguo Jia, Liping Zhang, Tamara Gigolashvili, Qiaomei Wang. Classic myrosinase-dependent degradation of indole glucosinolate attenuates fumonisin B1-induced programmed cell death in Arabidopsis. The Plant journal : for cell and molecular biology. 2015 Mar; 81(6):920-33. doi: 10.1111/tpj.12778. [PMID: 25645692]
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  • Miriam D Cargnel, Patricia V Demkura, Carlos L Ballaré. Linking phytochrome to plant immunity: low red : far-red ratios increase Arabidopsis susceptibility to Botrytis cinerea by reducing the biosynthesis of indolic glucosinolates and camalexin. The New phytologist. 2014 Oct; 204(2):342-54. doi: 10.1111/nph.13032. [PMID: 25236170]
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