Dimethylallylpyrophosphate (BioDeep_00000000703)

   

natural product human metabolite PANOMIX_OTCML-2023 Endogenous


代谢物信息卡片


({hydroxy[(3-methylbut-2-en-1-yl)oxy]phosphoryl}oxy)phosphonic acid

化学式: C5H12O7P2 (246.0058)
中文名称: 二甲基丙烯基二磷酸
谱图信息: 最多检出来源 Homo sapiens(blood) 18.39%

分子结构信息

SMILES: CC(=CCOP(=O)(O)OP(=O)(O)O)C
InChI: InChI=1S/C5H12O7P2/c1-5(2)3-4-11-14(9,10)12-13(6,7)8/h3H,4H2,1-2H3,(H,9,10)(H2,6,7,8)

描述信息

Prenyl diphosphate is a prenol phosphate that is a phosphoantigen comprising the O-pyrophosphate of prenol. It has a role as an epitope, a phosphoantigen, an Escherichia coli metabolite and a mouse metabolite. It is a conjugate acid of a prenyl diphosphate(3-).
Dimethylallylpyrophosphate is a metabolite found in or produced by Escherichia coli (strain K12, MG1655).
Dimethylallyl diphosphate is a natural product found in Centaurium erythraea, Streptomyces albidoflavus, and other organisms with data available.
Dimethylallylpyrophosphate is a metabolite found in or produced by Saccharomyces cerevisiae.
Dimethylallylpyrophosphate, also known as 2-isopentenyl diphosphate or delta-prenyl diphosphoric acid, belongs to the class of organic compounds known as isoprenoid phosphates. These are prenol lipids containing a phosphate group linked to an isoprene (2-methylbuta-1,3-diene) unit. Dimethylallylpyrophosphate is a very hydrophobic molecule, practically insoluble in water, and relatively neutral.
Dimethylallyl pyrophosphate (or -diphosphate) (DMAPP) is an intermediate product of both mevalonic acid (MVA) pathway and DOXP/MEP pathway. It is an isomer of isopentenyl pyrophosphate (IPP) and exists in virtually all life forms.
A prenol phosphate that is a phosphoantigen comprising the O-pyrophosphate of prenol.

同义名列表

64 个代谢物同义名

({hydroxy[(3-methylbut-2-en-1-yl)oxy]phosphoryl}oxy)phosphonic acid; 3-methylbut-2-enyl pyrophosphate (dimethylallyl-diphosphate); 2-Buten-1-ol, 3-methyl-, trihydrogen pyrophosphate (7CI,8CI); Diphosphoric acid, mono(3-methyl-2-butenyl) ester (9CI); 3-Methylbut-2-enyl phosphono hydrogen phosphoric acid; gamma,gamma-Dimethyallyl pyrophosphate ammonium salt; Diphosphoric acid, P-(3-methyl-2-buten-1-yl) ester; 2-Buten-1-ol, 3-methyl-, trihydrogen pyrophosphate; Diphosphoric acid, mono(3-methyl-2-butenyl) ester; 3-methyl-but-2-enyl phosphono hydrogen phosphate; Diphosphoric acid mono(3-methyl-2-butenyl) ester; 3-methyl-2-Buten-1-ol trihydrogen pyrophosphate; 3-methylbut-2-enyl phosphono hydrogen phosphate; 3,3-dimethylallyl pyrophosphate, (14)C-labeled; 3-methylbut-2-en-1-yl trihydrogen diphosphate; 2-Buten-1-ol, 3-methyl-, pyrophosphate (6CI); 3-Methyl-2-butenyl trihydrogen diphosphate; Gamma gamma-dimethylallyl pyrophosphate&; 1,1-Dimethyl-4-phenylpiperazinium iodide; gamma,gamma-Dimethylallyl pyrophosphate; 3,3-Dimethylallyl pyrophosphoric acid; delta2-Isopentenyl diphosphoric acid; 3-methyl-2-Buten-1-ol pyrophosphate; Dimethylallyl pyrophosphoric acid; Δ2-isopentenyl diphosphoric acid; 3-Methyl-2-butenyl pyrophosphate; Dimethylallylpyrophosphoric acid; 3-methylbut-2-enyl pyrophosphate; γ,γ-Dimethylallyl pyrophosphate; 2-Isopentenyl diphosphoric acid; Dimethylallyl diphosphoric acid; 3,3-dimethylallyl pyrophosphate; delta-Prenyl diphosphoric acid; delta2-Isopentenyl diphosphate; delta2-isopentenyl-diphosphate; Monoprenyl diphosphoric acid; Dimethylallyl pyrophosphate; dimethylallyl-pyrophosphate; Dimethylally pyrophosphate; Δ-prenyl diphosphoric acid; dimethylallylpyrophosphate; Prenol pyrophosphoric acid; Δ2-isopentenyl diphosphate; 2-Isopentenyl diphosphate; dimethylallyl-diphosphate; Dimethylallyl diphosphate; delta-Prenyl diphosphate; Prenyl diphosphoric acid; Monoprenyl diphosphate; Δ-prenyl diphosphate; Prenol pyrophosphate; prenyl-diphosphate; Prenyl diphosphate; dimethylallyl-PPi; Dimethylallyl-PP; DMADP cpd; DMAPP; DMPP; 1x07; IPE; 3-methyl-2-butenyl-1-diphosphoric acid, triammonium salt; DMAPP (ammonium salt); Dimethylallyl diphosphate; Dimethylallyl diphosphate



数据库引用编号

32 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(8)

BioCyc(2)

PlantCyc(0)

代谢反应

894 个相关的代谢反应过程信息。

Reactome(76)

BioCyc(7)

WikiPathways(5)

Plant Reactome(738)

INOH(2)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(66)

PharmGKB(0)

24 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 10 FDPS, FNTA, GGPS1, IDI2, IPP, MAPKAPK3, MAPT, MVD, MVK, NFE2L2
Peripheral membrane protein 2 CYP1B1, MAPT
Endoplasmic reticulum membrane 5 ACAT1, CYP1B1, FDFT1, HMGCR, HSP90B1
Nucleus 4 HSP90B1, MAPKAPK3, MAPT, NFE2L2
cytosol 12 FDPS, FNTA, GGPS1, HSP90B1, IDI2, MAPKAPK3, MAPT, MVD, MVK, NFE2L2, PDSS2, XYLB
dendrite 1 MAPT
centrosome 1 NFE2L2
nucleoplasm 4 FDPS, GGPS1, MAPKAPK3, NFE2L2
RNA polymerase II transcription regulator complex 1 NFE2L2
Cell membrane 2 MAPT, SLC38A3
Cytoplasmic side 1 MAPT
Cell projection, axon 1 MAPT
Multi-pass membrane protein 4 ACAT1, FDFT1, HMGCR, SLC38A3
cell surface 1 EPCAM
Golgi apparatus 1 NFE2L2
growth cone 1 MAPT
neuronal cell body 1 MAPT
smooth endoplasmic reticulum 1 HSP90B1
Cytoplasm, cytosol 2 MAPT, NFE2L2
plasma membrane 5 EPCAM, FNTA, MAPT, NFE2L2, SLC38A3
Membrane 7 ACAT1, CYP1B1, FDFT1, FDPS, HMGCR, HSP90B1, SLC38A3
apical plasma membrane 2 EPCAM, SLC38A3
axon 1 MAPT
basolateral plasma membrane 2 EPCAM, SLC38A3
extracellular exosome 3 ACAT1, EPCAM, HSP90B1
endoplasmic reticulum 4 ACAT1, FDFT1, HMGCR, HSP90B1
perinuclear region of cytoplasm 2 GGPS1, HSP90B1
Cell junction, tight junction 1 EPCAM
bicellular tight junction 1 EPCAM
mitochondrion 5 ACAT1, CYP1B1, MAPT, PDSS1, PDSS2
protein-containing complex 1 HSP90B1
intracellular membrane-bounded organelle 3 CYP1B1, IDI2, MVK
Microsome membrane 1 CYP1B1
Single-pass type I membrane protein 1 EPCAM
Secreted 1 MAPT
extracellular region 2 HSP90B1, MAPT
mitochondrial matrix 4 ACAT1, FDPS, PDSS1, PDSS2
actin cytoskeleton 1 IPP
dendritic spine 1 MAPT
Z disc 1 GGPS1
microtubule cytoskeleton 1 MAPT
axon cytoplasm 1 MAPT
midbody 1 HSP90B1
Cytoplasm, perinuclear region 1 GGPS1
Membrane raft 1 MAPT
Cytoplasm, cytoskeleton 1 MAPT
focal adhesion 1 HSP90B1
microtubule 1 MAPT
axolemma 1 MAPT
Peroxisome 3 FDPS, IDI2, MVK
peroxisomal membrane 1 HMGCR
collagen-containing extracellular matrix 1 HSP90B1
lateral plasma membrane 1 EPCAM
nuclear speck 1 MAPT
neuron projection 1 MAPT
chromatin 1 NFE2L2
mediator complex 1 NFE2L2
microtubule associated complex 1 FNTA
cytoplasmic ribonucleoprotein granule 1 MAPT
Basolateral cell membrane 1 SLC38A3
Cell projection, dendrite 1 MAPT
Melanosome 1 HSP90B1
cell body 1 MAPT
sperm plasma membrane 1 HSP90B1
Peroxisome membrane 1 HMGCR
Cytoplasm, myofibril, sarcomere, Z line 1 GGPS1
endoplasmic reticulum lumen 1 HSP90B1
Sarcoplasmic reticulum lumen 1 HSP90B1
Lateral cell membrane 1 EPCAM
protein-DNA complex 1 NFE2L2
somatodendritic compartment 1 MAPT
nuclear periphery 1 MAPT
transferase complex 2 PDSS1, PDSS2
glial cell projection 1 MAPT
endocytic vesicle lumen 1 HSP90B1
neurofibrillary tangle 1 MAPT
endoplasmic reticulum chaperone complex 1 HSP90B1
main axon 1 MAPT
tubulin complex 1 MAPT
CAAX-protein geranylgeranyltransferase complex 1 FNTA
protein farnesyltransferase complex 1 FNTA
heterotetrameric polyprenyl diphosphate synthase complex 2 PDSS1, PDSS2


文献列表

  • Xuan Song, Chang Liu, Khalid H Dhiloo, Chao-Qun Yi, Tian-Tao Zhang, Yong-Jun Zhang. Functional characterization of a geranylgeranyl diphosphate synthase in the leaf beetle Monolepta hieroglyphica. Archives of insect biochemistry and physiology. 2024 Feb; 115(2):e22088. doi: 10.1002/arch.22088. [PMID: 38349673]
  • Guo Wei, Yudie Chen, Jianwen Wang, Liguo Feng. Molecular cloning and characterization of farnesyl diphosphate synthase from Rosa rugosa Thunb associated with salinity stress. PeerJ. 2024; 12(?):e16929. doi: 10.7717/peerj.16929. [PMID: 38435988]
  • Abira Sahu, Mohammad Golam Mostofa, Sarathi M Weraduwage, Thomas D Sharkey. Hydroxymethylbutenyl diphosphate accumulation reveals MEP pathway regulation for high CO2-induced suppression of isoprene emission. Proceedings of the National Academy of Sciences of the United States of America. 2023 10; 120(41):e2309536120. doi: 10.1073/pnas.2309536120. [PMID: 37782800]
  • Natalie Fiutek, Matthew B Couger, Stacy Pirro, Scott W Roy, José R de la Torre, Edward F Connor. Genomic Assessment of the Contribution of the Wolbachia Endosymbiont of Eurosta solidaginis to Gall Induction. International journal of molecular sciences. 2023 Jun; 24(11):. doi: 10.3390/ijms24119613. [PMID: 37298563]
  • Jiahao Liang, De Wang, Xin Li, Weiwen Huang, Chun Xie, Minghui Fu, Hongmei Zhang, Qiong Meng. In Silico Genome-Wide Mining and Analysis of Terpene Synthase Gene Family in Hevea Brasiliensis. Biochemical genetics. 2023 Jun; 61(3):1185-1209. doi: 10.1007/s10528-022-10311-7. [PMID: 36534333]
  • Toni Krause, Piera Wiesinger, Diego González-Cabanelas, Nathalie Lackus, Tobias G Köllner, Thomas Klüpfel, Jonathan Williams, Johann Rohwer, Jonathan Gershenzon, Axel Schmidt. HDR, the last enzyme in the MEP pathway, differently regulates isoprenoid biosynthesis in two woody plants. Plant physiology. 2023 Feb; ?(?):. doi: 10.1093/plphys/kiad110. [PMID: 36848194]
  • Hirosuke Oku, Ishmael Mutanda, Masashi Inafuku. Molecular characteristics of isoprene synthase and its control effects on isoprene emissions from tropical trees. Journal of plant research. 2023 Jan; 136(1):63-82. doi: 10.1007/s10265-022-01418-4. [PMID: 36367585]
  • Xueni Di, David Ortega-Alarcon, Ramu Kakumanu, Javier Iglesias-Fernandez, Lucia Diaz, Edward E K Baidoo, Adrian Velazquez-Campoy, Manuel Rodríguez-Concepción, Jordi Perez-Gil. MEP pathway products allosterically promote monomerization of deoxy-D-xylulose-5-phosphate synthase to feedback-regulate their supply. Plant communications. 2022 Dec; ?(?):100512. doi: 10.1016/j.xplc.2022.100512. [PMID: 36575800]
  • Ülo Niinemets, Bahtijor Rasulov, Eero Talts. CO2 -responsiveness of leaf isoprene emission: Why do species differ?. Plant, cell & environment. 2021 09; 44(9):3049-3063. doi: 10.1111/pce.14131. [PMID: 34155641]
  • Toni Krause, Michael Reichelt, Jonathan Gershenzon, Axel Schmidt. Analysis of the isoprenoid pathway intermediates, dimethylallyl diphosphate and isopentenyl diphosphate, from crude plant extracts by liquid chromatography tandem mass spectrometry. Phytochemical analysis : PCA. 2020 Nov; 31(6):770-777. doi: 10.1002/pca.2941. [PMID: 32337807]
  • Xin Jin, Can Baysal, Lihong Gao, Vicente Medina, Margit Drapal, Xiuzhen Ni, Yanmin Sheng, Lianxuan Shi, Teresa Capell, Paul D Fraser, Paul Christou, Changfu Zhu. The subcellular localization of two isopentenyl diphosphate isomerases in rice suggests a role for the endoplasmic reticulum in isoprenoid biosynthesis. Plant cell reports. 2020 Jan; 39(1):119-133. doi: 10.1007/s00299-019-02479-x. [PMID: 31679061]
  • Sarada D Tetali. Terpenes and isoprenoids: a wealth of compounds for global use. Planta. 2019 Jan; 249(1):1-8. doi: 10.1007/s00425-018-3056-x. [PMID: 30467631]
  • Xi Zhang, Tianyang Guo, Tong Xiang, Yiyang Dong, Jichuan Zhang, Liqun Zhang. Quantitation of isoprenoids for natural rubber biosynthesis in natural rubber latex by liquid chromatography with tandem mass spectrometry. Journal of chromatography. A. 2018 Jul; 1558(?):115-119. doi: 10.1016/j.chroma.2018.05.006. [PMID: 29773339]
  • Bahtijor Rasulov, Eero Talts, Irina Bichele, Ülo Niinemets. Evidence That Isoprene Emission Is Not Limited by Cytosolic Metabolites. Exogenous Malate Does Not Invert the Reverse Sensitivity of Isoprene Emission to High [CO2]. Plant physiology. 2018 02; 176(2):1573-1586. doi: 10.1104/pp.17.01463. [PMID: 29233849]
  • Chun-Li Liu, Jing-Yi Cai, Hao-Ran Bi, Tian-Wei Tan. A novel DMAPP-responding genetic circuit sensor for high-throughput screening and evolving isoprene synthase. Applied microbiology and biotechnology. 2018 Feb; 102(3):1381-1391. doi: 10.1007/s00253-017-8676-8. [PMID: 29243081]
  • Hiroyuki Kajiura, Nobuaki Suzuki, Yuji Tokumoto, Takuya Yoshizawa, Shinya Takeno, Kazuhito Fujiyama, Yoshinobu Kaneko, Hiroyoshi Matsumura, Yoshihisa Nakazawa. Two Eucommia farnesyl diphosphate synthases exhibit distinct enzymatic properties leading to end product preferences. Biochimie. 2017 Aug; 139(?):95-106. doi: 10.1016/j.biochi.2017.05.001. [PMID: 28478108]
  • Bok-Kyu Shin, Mihyang Kim, Jaehong Han. Exceptionally high percentage of IPP synthesis by Ginkgo biloba IspH is mainly due to Phe residue in the active site. Phytochemistry. 2017 Apr; 136(?):9-14. doi: 10.1016/j.phytochem.2017.01.012. [PMID: 28139297]
  • Julie E Chaves, Paloma Rueda Romero, Henning Kirst, Anastasios Melis. Role of isopentenyl-diphosphate isomerase in heterologous cyanobacterial (Synechocystis) isoprene production. Photosynthesis research. 2016 Dec; 130(1-3):517-527. doi: 10.1007/s11120-016-0293-3. [PMID: 27412351]
  • Bahtijor Rasulov, Eero Talts, Ülo Niinemets. Spectacular Oscillations in Plant Isoprene Emission under Transient Conditions Explain the Enigmatic CO2 Response. Plant physiology. 2016 12; 172(4):2275-2285. doi: 10.1104/pp.16.01002. [PMID: 27770061]
  • Tianhong Yang, Lingling Fang, Agnes M Rimando, Victor Sobolev, Keithanne Mockaitis, Fabricio Medina-Bolivar. A Stilbenoid-Specific Prenyltransferase Utilizes Dimethylallyl Pyrophosphate from the Plastidic Terpenoid Pathway. Plant physiology. 2016 08; 171(4):2483-98. doi: 10.1104/pp.16.00610. [PMID: 27356974]
  • Lemeng Dong, Esmer Jongedijk, Harro Bouwmeester, Alexander Van Der Krol. Monoterpene biosynthesis potential of plant subcellular compartments. The New phytologist. 2016 Jan; 209(2):679-90. doi: 10.1111/nph.13629. [PMID: 26356766]
  • Aparajita Banerjee, Alyssa L Preiser, Thomas D Sharkey. Engineering of Recombinant Poplar Deoxy-D-Xylulose-5-Phosphate Synthase (PtDXS) by Site-Directed Mutagenesis Improves Its Activity. PloS one. 2016; 11(8):e0161534. doi: 10.1371/journal.pone.0161534. [PMID: 27548482]
  • Ülo Niinemets, Zhihong Sun, Eero Talts. Controls of the quantum yield and saturation light of isoprene emission in different-aged aspen leaves. Plant, cell & environment. 2015 Dec; 38(12):2707-20. doi: 10.1111/pce.12582. [PMID: 26037962]
  • Laura K Henry, Michael Gutensohn, Suzanne T Thomas, Joseph P Noel, Natalia Dudareva. Orthologs of the archaeal isopentenyl phosphate kinase regulate terpenoid production in plants. Proceedings of the National Academy of Sciences of the United States of America. 2015 Aug; 112(32):10050-5. doi: 10.1073/pnas.1504798112. [PMID: 26216978]
  • Bahtijor Rasulov, Irina Bichele, Katja Hüve, Vivian Vislap, Ülo Niinemets. Acclimation of isoprene emission and photosynthesis to growth temperature in hybrid aspen: resolving structural and physiological controls. Plant, cell & environment. 2015 Apr; 38(4):751-66. doi: 10.1111/pce.12435. [PMID: 25158785]
  • Cinzia Formighieri, Anastasios Melis. Carbon partitioning to the terpenoid biosynthetic pathway enables heterologous β-phellandrene production in Escherichia coli cultures. Archives of microbiology. 2014 Dec; 196(12):853-61. doi: 10.1007/s00203-014-1024-9. [PMID: 25116411]
  • Sergiy G Krasutsky, Marek Urbansky, Chad E Davis, Christian Lherbet, Robert M Coates, C Dale Poulter. Synthesis of methylerythritol phosphate analogues and their evaluation as alternate substrates for IspDF and IspE from Agrobacterium tumefaciens. The Journal of organic chemistry. 2014 Oct; 79(19):9170-8. doi: 10.1021/jo501529k. [PMID: 25184438]
  • A Banerjee, T D Sharkey. Methylerythritol 4-phosphate (MEP) pathway metabolic regulation. Natural product reports. 2014 Aug; 31(8):1043-55. doi: 10.1039/c3np70124g. [PMID: 24921065]
  • Andrea Ghirardo, Louwrance Peter Wright, Zhen Bi, Maaria Rosenkranz, Pablo Pulido, Manuel Rodríguez-Concepción, Ülo Niinemets, Nicolas Brüggemann, Jonathan Gershenzon, Jörg-Peter Schnitzler. Metabolic flux analysis of plastidic isoprenoid biosynthesis in poplar leaves emitting and nonemitting isoprene. Plant physiology. 2014 May; 165(1):37-51. doi: 10.1104/pp.114.236018. [PMID: 24590857]
  • Bahtijor Rasulov, Irina Bichele, Agu Laisk, Ülo Niinemets. Competition between isoprene emission and pigment synthesis during leaf development in aspen. Plant, cell & environment. 2014 Mar; 37(3):724-41. doi: 10.1111/pce.12190. [PMID: 24033429]
  • Changfang Zhou, Ziru Li, Amy E Wiberley-Bradford, Sean E Weise, Thomas D Sharkey. Isopentenyl diphosphate and dimethylallyl diphosphate/isopentenyl diphosphate ratio measured with recombinant isopentenyl diphosphate isomerase and isoprene synthase. Analytical biochemistry. 2013 Sep; 440(2):130-6. doi: 10.1016/j.ab.2013.05.028. [PMID: 23747531]
  • Aparajita Banerjee, Yan Wu, Rahul Banerjee, Yue Li, Honggao Yan, Thomas D Sharkey. Feedback inhibition of deoxy-D-xylulose-5-phosphate synthase regulates the methylerythritol 4-phosphate pathway. The Journal of biological chemistry. 2013 Jun; 288(23):16926-16936. doi: 10.1074/jbc.m113.464636. [PMID: 23612965]
  • Sean E Weise, Ziru Li, Allison E Sutter, Alex Corrion, Aparajita Banerjee, Thomas D Sharkey. Measuring dimethylallyl diphosphate available for isoprene synthesis. Analytical biochemistry. 2013 Apr; 435(1):27-34. doi: 10.1016/j.ab.2012.11.031. [PMID: 23262281]
  • Juan A Faraldos, Veronica Gonzalez, Amang Li, Fanglei Yu, Mustafa Köksal, David W Christianson, Rudolf K Allemann. Probing the mechanism of 1,4-conjugate elimination reactions catalyzed by terpene synthases. Journal of the American Chemical Society. 2012 Dec; 134(51):20844-8. doi: 10.1021/ja311022s. [PMID: 23214943]
  • Nobuaki Suzuki, Hirotaka Uefuji, Takashi Nishikawa, Yukio Mukai, Atsushi Yamashita, Masahira Hattori, Naotake Ogasawara, Takeshi Bamba, Ei-ichiro Fukusaki, Akio Kobayashi, Yoshiyuki Ogata, Nozomu Sakurai, Hideyuki Suzuki, Daisuke Shibata, Yoshihisa Nakazawa. Construction and analysis of EST libraries of the trans-polyisoprene producing plant, Eucommia ulmoides Oliver. Planta. 2012 Nov; 236(5):1405-17. doi: 10.1007/s00425-012-1679-x. [PMID: 22729820]
  • Xiao-Min Lu, Xiao-Jiao Hu, Yuan-Zeng Zhao, Wei-Bin Song, Mei Zhang, Zong-Liang Chen, Wei Chen, Yong-Bin Dong, Zhen-Hua Wang, Jin-Sheng Lai. Map-based cloning of zb7 encoding an IPP and DMAPP synthase in the MEP pathway of maize. Molecular plant. 2012 Sep; 5(5):1100-12. doi: 10.1093/mp/sss038. [PMID: 22498772]
  • Eliana Gonzales-Vigil, David E Hufnagel, Jeongwoon Kim, Robert L Last, Cornelius S Barry. Evolution of TPS20-related terpene synthases influences chemical diversity in the glandular trichomes of the wild tomato relative Solanum habrochaites. The Plant journal : for cell and molecular biology. 2012 Sep; 71(6):921-35. doi: 10.1111/j.1365-313x.2012.05040.x. [PMID: 22563774]
  • Shuiqin Wu, Zuodong Jiang, Chase Kempinski, S Eric Nybo, Satrio Husodo, Robert Williams, Joe Chappell. Engineering triterpene metabolism in tobacco. Planta. 2012 Sep; 236(3):867-77. doi: 10.1007/s00425-012-1680-4. [PMID: 22729821]
  • Maryam Darabi, Ali Izadi-Darbandi, Ali Masoudi-Nejad, Mohammad Reza Naghavi, Ghorbanali Nemat-Zadeh. Bioinformatics study of the 3-hydroxy-3-methylglotaryl-coenzyme A reductase (HMGR) gene in Gramineae. Molecular biology reports. 2012 Sep; 39(9):8925-35. doi: 10.1007/s11033-012-1761-2. [PMID: 22722993]
  • Michael Behr, Václav Motyka, Fabian Weihmann, Jiří Malbeck, Holger B Deising, Stefan G R Wirsel. Remodeling of cytokinin metabolism at infection sites of Colletotrichum graminicola on maize leaves. Molecular plant-microbe interactions : MPMI. 2012 Aug; 25(8):1073-82. doi: 10.1094/mpmi-01-12-0012-r. [PMID: 22746825]
  • Zhong-Bao Yang, Dejene Eticha, Alfonso Albacete, Idupulapati Madhusudana Rao, Thomas Roitsch, Walter Johannes Horst. Physiological and molecular analysis of the interaction between aluminium toxicity and drought stress in common bean (Phaseolus vulgaris). Journal of experimental botany. 2012 May; 63(8):3109-25. doi: 10.1093/jxb/ers038. [PMID: 22371077]
  • Danilo Aros, Veronica Gonzalez, Rudolf K Allemann, Carsten T Müller, Carlo Rosati, Hilary J Rogers. Volatile emissions of scented Alstroemeria genotypes are dominated by terpenes, and a myrcene synthase gene is highly expressed in scented Alstroemeria flowers. Journal of experimental botany. 2012 Apr; 63(7):2739-52. doi: 10.1093/jxb/err456. [PMID: 22268153]
  • Yimian Ma, Lichai Yuan, Bin Wu, Xian'en Li, Shilin Chen, Shanfa Lu. Genome-wide identification and characterization of novel genes involved in terpenoid biosynthesis in Salvia miltiorrhiza. Journal of experimental botany. 2012 Apr; 63(7):2809-23. doi: 10.1093/jxb/err466. [PMID: 22291132]
  • Motoyoshi Noike, Chengwei Liu, Yusuke Ono, Yoshimitsu Hamano, Tomonobu Toyomasu, Takeshi Sassa, Nobuo Kato, Tohru Dairi. An enzyme catalyzing O-prenylation of the glucose moiety of fusicoccin A, a diterpene glucoside produced by the fungus Phomopsis amygdali. Chembiochem : a European journal of chemical biology. 2012 Mar; 13(4):566-73. doi: 10.1002/cbic.201100725. [PMID: 22287087]
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