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Keywords: Arabidopsis
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Articles
Biochem J (2025) 482 (09): 451–466.
Published: 06 May 2025
... under the Creative Commons Attribution License 4.0 (CC BY) . Arabidopsis iron metals plants sensing transport The first-row transition metal iron is the most abundant and used metal in cells [ 1 ]. Iron is widely used as a cofactor, participating in oxidation–reduction reactions...
Includes: Supplementary data
Articles
Biochem J (2025) BCJ20240685.
Published: 17 April 2025
... Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 Plants Arabidopsis Metals Iron Transport Sensing Plants Arabidopsis Metals Iron Transport Sensing Plants Arabidopsis Metals Iron Transport Sensing arabidopsis...
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Biochem J (2023) 480 (5): 307–318.
Published: 09 March 2023
...) in the cyanobacterium Synechocystis sp. PCC 6803. However, the sensitivity to ROS of chloroplast-localized EF-Tu (cpEF-Tu) of plants remains to be elucidated. In the present study, we generated a recombinant cpEF-Tu protein of Arabidopsis thaliana and examined its sensitivity to ROS in vitro . In cpEF-Tu that lacked...
Includes: Supplementary data
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Biochem J (2020) 477 (1): 173–189.
Published: 10 January 2020
...Marco Pedretti; Carolina Conter; Paola Dominici; Alessandra Astegno Arabidopsis centrin 2, also known as calmodulin-like protein 19 (CML19), is a member of the EF-hand superfamily of calcium (Ca 2+ )-binding proteins. In addition to the notion that CML19 interacts with the nucleotide excision...
Includes: Supplementary data
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Biochem J (2019) 476 (7): 1105–1107.
Published: 10 April 2019
..., recent work suggests that the chemical versatility of these proteins contributes to metabolite repair. In this issue of the Biochemical Journal , Niehaus et al. demonstrate that the Nit1 nitrilase from Arabidopsis thaliana functions as a metabolite repair enzyme that removes deaminated glutathione from...
Articles
Biochem J (2014) 463 (1): 145–155.
Published: 08 September 2014
... Arabidopsis and maize TenA_E proteins (At3g16990, GRMZM2G080501) hydrolysed amino-HMP to HMP and, far more actively, hydrolysed the N -formyl derivative of amino-HMP to amino-HMP. Ablating the At3g16990 gene in a line with a null mutation in the HMP biosynthesis gene ThiC prevented its rescue by amino-HMP...
Includes: Supplementary data
Articles
Biochem J (2014) 459 (1): 15–25.
Published: 14 March 2014
...Kirby N. Swatek; Rashaun S. Wilson; Nagib Ahsan; Rebecca L. Tritz; Jay J. Thelen Plant 14-3-3 proteins are phosphorylated at multiple sites in vivo ; however, the protein kinase(s) responsible are unknown. Of the 34 CPK (calcium-dependent protein kinase) paralogues in Arabidopsis thaliana , three...
Includes: Supplementary data
Articles
Biochem J (2014) 457 (1): 127–136.
Published: 10 December 2013
.... In the present study, we examined the biochemical properties, subcellular localization and tissue-specific distribution of Arabidopsis CML43. Our data indicate that CML43 displays characteristics typical of Ca 2+ sensors, including high-affinity Ca 2+ binding, conformational changes upon Ca 2+ binding...
Includes: Supplementary data
Articles
Biochem J (2013) 449 (2): 373–388.
Published: 14 December 2012
... processes. In the present study we characterized a silique-abundant gene AtDOF ( Arabidopsis thaliana DOF ) 4.2 for its functions in Arabidopsis . AtDOF4.2 is localized in the nuclear region and has transcriptional activation activity in both yeast and plant protoplast assays. The T-M-D motif in AtDOF4.2...
Includes: Supplementary data
Articles
Biochem J (2012) 448 (3): 353–363.
Published: 21 November 2012
.... NTL6 is a plant-specific NAC [NAM/ATAF1/2/CUC2] transcription factor that is expressed as a dormant plasma membrane-associated form in Arabidopsis . Proteolytic processing of NTL6 is triggered by abiotic stresses and ABA (abscisic acid). In the present study, we show that NTL6 is linked directly...
Includes: Supplementary data
Articles
Biochem J (2012) 446 (2): e5–e7.
Published: 14 August 2012
...Brian E. Ellis Plants contain hundreds of protein kinases that are believed to provide cellular signal transduction services, but the identities of the proteins they are targeting are largely unknown. Using an Arabidopsis MAPK (mitogen-activated protein kinase) (MPK6) as a model, Sörensson et al...
Articles
Biochem J (2012) 446 (2): 271–278.
Published: 14 August 2012
... specificity towards substrates. In the present study, we used a random positional peptide library to search for consensus phosphorylation sequences for Arabidopsis MAPKs MPK3 and MPK6. These experiments indicated a preference towards the sequence L/P-P/X- S -P-R/K for both kinases. After bioinformatic...
Includes: Supplementary data
Articles
Biochem J (2012) 445 (3): 393–401.
Published: 13 July 2012
... to histones during the plant DNA damage response is currently poorly understood. Several different acetylated H3 and H4 N-terminal peptides following X-ray treatment were identified using MS analysis of purified histones, revealing previously unseen patterns of histone acetylation in Arabidopsis . Immunoblot...
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Biochem J (2012) 442 (3): 551–561.
Published: 24 February 2012
...) transporter, designated BCD1 (BUSH-AND-CHLOROTIC-DWARF 1), contributes to iron homoeostasis during stress responses and senescence in Arabidopsis . The BCD1 gene is induced by excessive iron, but repressed by iron deficiency. It is also induced by cellular and tissue damage occurring under osmotic stress...
Includes: Supplementary data
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Biochem J (2011) 439 (2): 207–214.
Published: 28 September 2011
... from Arabidopsis thaliana leaves. Several novel super- and mega-complexes including PS (photosystem) I, PSII and LHCs (light-harvesting complexes) in various combinations are reported. 1 These authors contributed equally to this work. 2 To whom correspondence should be addressed (email...
Includes: Supplementary data
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Biochem J (2011) 437 (3): 505–513.
Published: 13 July 2011
...Elizabeth Allen; Annick Moing; Jonathan A. D. Wattis; Tony Larson; Mickaël Maucourt; Ian A. Graham; Dominique Rolin; Mark A. Hooks ACN1 (acetate non-utilizing 1) is a short-chain acyl-CoA synthetase which recycles free acetate to acetyl-CoA in peroxisomes of Arabidopsis . Pulse-chase [2- 13 C...
Includes: Supplementary data
Articles
Biochem J (2010) 427 (3): 359–367.
Published: 14 April 2010
... of cold-inducible PR (pathogenesis-related) genes in Arabidopsis . In the present study, we show that proteolytic processing of NTL6 is regulated by cold-induced remodelling of membrane fluidity. NTL6 processing was stimulated rapidly by cold. The protein stability of NTL6 was also enhanced by cold...
Articles
Biochem J (2010) 425 (2): 389–399.
Published: 23 December 2009
...), a tocochromanol with a structure similar to γ-tocopherol and γ-tocotrienol, but with a C-40 prenyl side chain. PC-8 formation was abolished in the Arabidopsis thaliana tocopherol cyclase mutant vte1 , but accumulated in VTE1-overexpressing plants, in agreement with a role of tocopherol cyclase (VTE1) in PC-8...
Includes: Supplementary data
Articles
Biochem J (2009) 424 (2): 169–177.
Published: 11 November 2009
... formation from UDP-Glc was 0.24. Phylogenetic analysis revealed that PsUGE1 forms a group with Arabidopsis UDP-Glc 4-epimerases, AtUGE1 and AtUGE3, apart from a group including AtUGE2, AtUGE4 and AtUGE5. Similar to rPsUGE1, recombinant AtUGE1 and AtUGE3 expressed in E. coli showed high UDP-Xyl 4-epimerase...
Includes: Supplementary data
Articles
Biochem J (2009) 420 (1): 57–65.
Published: 28 April 2009
... important functions for PEPC and PPCK (PEPC kinase) in plant acclimation to nutritional P i deprivation. However, little is known about the genetic origin or phosphorylation status of native PEPCs from −P i (P i -deficient) plants. The transfer of Arabidopsis suspension cells or seedlings to −P i growth...
Includes: Supplementary data
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Biochem J (2009) 418 (1): 145–154.
Published: 28 January 2009
... detoxification mechanism for metals. Cation transport into the vacuole can be mediated by CAX (cation exchanger) transporters. The Arabidopsis thaliana AtCAX2 transporter was shown previously to transport Ca 2+ , Cd 2+ and Mn 2+ . To assess the conservation of the functional and regulatory characteristics...
Includes: Supplementary data
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Biochem J (2008) 415 (3): e1–e3.
Published: 15 October 2008
... come from the study of animal cells, and this is where we start the discussion. Arabidopsis clathrin coated vesicle endocytosis phosphoinositide © The Authors Journal compilation © 2008 Biochemical Society 2008 11 9 2008 18 9 2008 1 email [email protected]...
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Biochem J (2008) 409 (1): 27–41.
Published: 11 December 2007
... to further our understanding of network regulation. 1 To whom correspondence should be addressed (email [email protected] ). 14 8 2007 11 9 2007 14 9 2007 © The Authors Journal compilation © 2008 Biochemical Society 2008 Arabidopsis metabolic control...
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Biochem J (2007) 406 (3): 399–406.
Published: 29 August 2007
...Mark A. Hooks; James E. Turner; Elaine C. Murphy; Katherine A. Johnston; Sally Burr; Szymon Jarosławski The Arabidopsis acn (acetate non-utilizing) mutants were isolated by fluoroacetate-resistant germination and seedling establishment. We report the characterization of the acn2 mutant...
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Biochem J (2007) 405 (1): 191–198.
Published: 13 June 2007
.... The mechanisms involved in P i sensing and signal transduction are not completely understood. In the present study we report that a previously uncharacterized transcription factor, BHLH32, acts as a negative regulator of a range of P i starvation-induced processes in Arabidopsis . In bhlh32 mutant plants in P i...
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Biochem J (2006) 394 (1): 95–103.
Published: 27 January 2006
...-phosphorylation of Ins(1,3,4,5,6) P 5 (inositol 1,3,4,5,6-pentakisphosphate). A human orthologue, HsIPK1 , is able to substitute for yeast ScIPK1 , restoring Ins P 6 production in a Saccharomyces cerevisiae mutant strain lacking the ScIPK1 open reading frame ( ScIpk1 Δ). We have identified an Arabidopsis genomic...
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Biochem J (2004) 379 (3): 601–607.
Published: 01 May 2004
... A–Sepharose. Internal sequence analysis of a 55 kDa protein identified in the extract following 2700-fold purification revealed strong similarity to the primary sequence of GLPQ, a bacterial GPX-PDE. To confirm the identity of plant GPX-PDE, an Arabidopsis thaliana cDNA similar to that encoding the bacterial...
Articles
Biochem J (2001) 355 (3): 671–679.
Published: 24 April 2001
... purified from etiolated mung-bean ( Phaseolus aureus ) shoots, native XETs purified from lentil ( Lens culinaris ) and nasturtium ( Tropaeolum majus ) seeds, and three insect-cell-produced thale-cress ( Arabidopsis thaliana ) XETs (EXGT, TCH4 and MERI-5)]. All such product profiles showed a good fit...