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Keywords: Arabidopsis thaliana
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Biochem J (2022) 479 (18): 1967–1984.
Published: 23 September 2022
... natural chaperones remained elusive. We have now tested cationic peptide fragments of several Arabidopsis thaliana arabinogalactan-proteins (AGPs) as candidates. Fragments of AGP17, 18, 19 and 31 were effective, typically at ∼25 µg/ml (9–19 µM), promoting the boron bridging of 16–20 µM monomeric RG-II...
Includes: Supplementary data
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Biochem J (2020) 477 (24): 4785–4796.
Published: 24 December 2020
... at 20 μM and HOZ concentration varied from 0 to 40 μM. The near-UV and visible range 300–800 nm were scanned. arabidopsis thaliana crystallography protein structure tetrapyrroles Heme is an essential pigment for plants and participates in various key biological processes [ 1...
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Biochem J (2020) 477 (19): 3885–3896.
Published: 12 October 2020
... to confirm that Lys-acetylation at low stoichiometries can be a regulatory mechanism controlling Rubisco maximal activity. The results highlight the need for further use of stoichiometry measurements when determining the biological significance of reversible PTMs like acetylation. Arabidopsis thaliana...
Includes: Supplementary data
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Biochem J (2020) 477 (19): 3743–3767.
Published: 12 October 2020
... Arabidopsis thaliana (henceforth Arabidopsis ). In both ZE and SE, certain events must occur including the establishment of the body axis (polarity), and of the primary and apical meristems. As such, we briefly discuss key factors involved in the initiation of tissue systems during ZE, and speculate...
Includes: Supplementary data
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Biochem J (2020) 477 (16): 3019–3032.
Published: 26 August 2020
... in Arabidopsis thaliana by determining the abundance of different proteins during enrichment of ribosomes from cell cultures using peptide mass spectrometry. The turnover rates of 26 40S subunit r-proteins and 29 60S subunit r-proteins were also determined, showing that half of the ribosome population...
Includes: Supplementary data
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Biochem J (2019) 476 (20): 2939–2952.
Published: 18 October 2019
..., our knowledge on the structural, kinetic and regulatory properties of the enzymes from C 3 species is still limited. In this work, we report the recombinant production and biochemical characterization of two PEPCKs identified in Arabidopsis thaliana : Ath PEPCK1 and Ath PEPCK2. We found that both...
Includes: Supplementary data
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Biochem J (2019) 476 (12): 1781–1790.
Published: 26 June 2019
... Arabidopsis thaliana as described previously [ 26 ] and used as a template for RT-PCR. The gene fragment encoding the predicted mature protein region of G6PDH1 (At5g35790; Phe 51 –Ala 576 ) was amplified with the following oligonucleotide primers: 5′-CATG CCATGG CGTTCTTCGCCGAGAAACATTC-3′ (NcoI) and 5′-CCG...
Includes: Supplementary data
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In Collection
Seeds
Biochem J (2019) 476 (6): 965–974.
Published: 22 March 2019
..., cauliflower, broccoli and Brussel sprouts, belong to the same species, Brassica oleracea L., the nearest crop relative to the model plant Arabidopsis thaliana L. According to the Food and Agriculture Organization (FAO), 3.8 million hectares of cabbage, cauliflower and broccoli were harvested in 2016...
Includes: Supplementary data
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In Collection
Seeds
Biochem J (2019) 476 (5): 843–857.
Published: 12 March 2019
... protein profiling of proteases to evaluate the quality of artificially and naturally aged seeds of Arabidopsis thaliana . Using this approach, we have identified two protease activities with opposite behaviours in aged seeds of Arabidopsis that correlate with the quality status of the seeds. We show...
Includes: Supplementary data
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Biochem J (2019) 476 (5): 783–794.
Published: 06 March 2019
... in Arabidopsis thaliana , in complex with the ALA-interacting subunit 5 (ALIS5). The ATP hydrolytic activity of the ALA2–ALIS5 complex was stimulated in a highly specific manner by phosphatidylserine. Small changes in the stereochemistry or the functional groups of the phosphatidylserine head group affected...
Includes: Supplementary data
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Biochem J (2019) 476 (1): 151–164.
Published: 15 January 2019
... the enzyme activity of Arabidopsis thaliana LACS9 (AtLACS9) by introducing random mutations into its cDNA using error-prone PCR. Two AtLACS9 variants containing multiple amino acid residue substitutions were identified with enhanced enzyme activity. To explore the effect of each amino acid residue...
Includes: Supplementary data
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Biochem J (2018) 475 (1): 61–74.
Published: 02 January 2018
... by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) . Arabidopsis thaliana AUX/IAA proteins protein modification SUMO SUMO chains In vitro sumoylation of substrate NAF ( Figure 1 ) results in the addition...
Includes: Supplementary data
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Biochem J (2017) 474 (21): 3675–3687.
Published: 23 October 2017
... in SDS gel-loading buffer, analyzed on SDS–PAGE gels and blotted with anti-GST antibody. Arabidopsis thaliana eukaryotic gene expression myb transcription factor phosphate surface plasmon resonance P1BS probes containing 1× P1BS motif and 2× P1BS motifs were taken from the promoter...
Includes: Supplementary data
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Biochem J (2017) 474 (11): 1789–1801.
Published: 10 May 2017
...John W. Riggs; Judy Callis The Arabidopsis thaliana fructokinase-like proteins FLN1 and FLN2 are required for the differentiation of plastids into photosynthetically competent chloroplasts. However, their specific roles are unknown. FLN1 and FLN2 localize in a multisubunit prokaryotic-type...
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Biochem J (2017) 474 (8): 1347–1360.
Published: 04 April 2017
..., Arabidopsis thaliana genome sequencing has revealed that as many as five Trx subtypes encoded by a total of 10 nuclear genes are targeted to chloroplasts. Because each Trx isoform seems to have a distinct target selectivity, the electron distribution from FTR to multiple Trxs is thought to be the critical...
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Biochem J (2016) 473 (11): 1605–1615.
Published: 27 May 2016
... Arabidopsis thaliana Cdc50 ectodomain disulfide bond flippase N-glycosylation The P-type ATPase superfamily comprises a large number of primary transmembrane-spanning transporters that share the common characteristic of forming a phosphorylated intermediate during their catalytic cycle [ 1 ]. P...
Includes: Supplementary data
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Biochem J (2016) 473 (5): 593–603.
Published: 24 February 2016
... synthesis of ceramides acting to promote programmed cell death [ 13 – 15 ]. Arabidopsis thaliana ceramide enzyme kinetics plant biochemistry sphingolipid Ceramides are organizing components of sphingolipids in the eukaryotic cell. Three ceramide synthase isoforms are found...
Includes: Supplementary data
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Biochem J (2016) 473 (2): 157–166.
Published: 05 January 2016
... to require an active ThMPase for growth. In vitro assays confirmed that these candidates all preferred ThMP to any of 45 other phosphate ester substrates tested. An Arabidopsis thaliana ThMPase homologue (At4g29530) of unknown function whose expression pattern and compartmentation fit with a role in ThDP...
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Biochem J (2015) 467 (1): 91–102.
Published: 20 March 2015
.... This GQS is located within the 5′-UTR of the ATAXIA TELANGIECTASIA-MUTATED AND RAD3-RELATED ( ATR ) mRNA of Arabidopsis thaliana (mouse-ear cress). We show that this GQS is highly stable and is thermodynamically favoured over a competing hairpin structure in the 5′-UTR at physiological K + and Mg 2...
Includes: Supplementary data
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Biochem J (2015) 466 (2): 283–290.
Published: 20 February 2015
... ). 23 10 2014 1 12 2014 12 12 2014 12 12 2014 © The Authors Journal compilation © 2015 Biochemical Society 2015 We show that Arabidopsis thaliana has at least three catalytically active trehalose 6-phosphate synthase isoforms, not one as previously thought, implying...
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Biochem J (2015) 466 (1): 137–145.
Published: 06 February 2015
... in Arabidopsis thaliana and Escherichia coli helps maintain flavin levels. COG3236 proteins thus illustrate two emerging principles in chemical biology: directed overflow metabolism, in which excess flux is diverted out of a pathway, and the pre-emption of damage from reactive metabolites. Subsequent steps...
Includes: Supplementary data
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Biochem J (2014) 459 (2): 289–299.
Published: 28 March 2014
... the Arabidopsis thaliana cpi gene were screened for inactive CPI mutant enzymes on the basis of their ability to genetically complement a Saccharomyces cerevisiae erg7 (defective in oxidosqualene cyclase) ergosterol auxotroph grown in the presence of exogenous cycloeucalenol, and led to the identification of four...
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Biochem J (2012) 448 (2): 243–251.
Published: 07 November 2012
... (email [email protected] or [email protected] ). 15 6 2012 28 8 2012 4 9 2012 4 9 2012 © The Authors Journal compilation © 2012 Biochemical Society 2012 Arabidopsis thaliana glutathione nitrosoglutathione (GSNO) redox...
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Biochem J (2012) 447 (2): 291–299.
Published: 26 September 2012
... All experiments were performed with Arabidopsis thaliana ecotype Columbia (Col0) WT (wild-type) or CPK-overexpressing transgenic lines. For seedling assays, seeds were sterilized and grown in 0.5×Murashige and Skoog liquid medium (Sigma) containing 0.5% sucrose for 9 days at 21°C with a 16 h...
Includes: Supplementary data
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Biochem J (2012) 444 (2): 227–237.
Published: 11 May 2012
... by methylation, oxidation and ferrochelation reactions. In Arabidopsis thaliana , the ferrochelation step is catalysed by sirohydrochlorin ferrochelatase (SirB), which, unlike its counterparts in bacteria, contains an [Fe–S] cluster. We determined the cluster to be a [4Fe–4S] type, which quickly oxidizes...
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Biochem J (2011) 435 (3): 629–639.
Published: 13 April 2011
... of signalling between the N- and C-terminal domains of DELLA proteins is unresolved. In the present study, we used in vivo and in vitro approaches to characterize di- and tri-partite interactions of the DELLA protein RGL1 (REPRESSOR OF GA1-3-LIKE 1) of Arabidopsis thaliana with the gibberellin receptor GID1A...
Includes: Supplementary data
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Biochem J (2011) 435 (1): 167–174.
Published: 15 March 2011
... unrestricted non-commercial use, distribution and reproduction in any medium, provided the original work is properly cited. Arabidopsis thaliana complex formation degenerated protease domain DEG7 serine protease taxonomic distribution Deg/HtrA (for deg radation of periplasmic proteins/ h...
Includes: Supplementary data
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Biochem J (2010) 430 (2): 295–303.
Published: 13 August 2010
...Marcos A. Tronconi; Mariel C. Gerrard Wheeler; Verónica G. Maurino; María F. Drincovich; Carlos S. Andreo The Arabidopsis thaliana genome contains two genes encoding NAD-MEs [NAD-dependent malic enzymes; NAD-ME1 (TAIR accession number At4G13560) and NAD-ME2 (TAIR accession number At4G00570...
Includes: Supplementary data
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Biochem J (2010) 425 (2): 425–434.
Published: 23 December 2009
... essential for proper photomorphogenesis. Arabidopsis thaliana contains one major biochemically characterized HO (HY1) and three additional putative HOs (HO2, HO3 and HO4). All four proteins are encoded in the nucleus but contain chloroplast translocation sequences at their N-termini. The transit peptides...
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Biochem J (2010) 425 (1): 207–218.
Published: 14 December 2009
... is properly cited. [4Fe-4S]-cluster-containing P-loop NTPase (FSC-NTPase) Arabidopsis thaliana chloroplast high chlorophyll fluorescence 101 (HCF101) iron-sulfur cluster assembly scaffold protein Fe/S clusters (iron-sulfur clusters) are ancient cofactors of proteins required for various...
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Biochem J (2009) 419 (1): 221–230.
Published: 13 March 2009
...Ctirad Hofr; Pavla Šultesová; Michal Zimmermann; Iva Mozgová; Petra Procházková Schrumpfová; Michaela Wimmerová; Jiří Fajkus Proteins that bind telomeric DNA modulate the structure of chromosome ends and control telomere function and maintenance. It has been shown that AtTRB ( Arabidopsis thaliana...
Includes: Supplementary data
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Biochem J (2009) 417 (1): 257–269.
Published: 12 December 2008
... of one of these subunits in Arabidopsis thaliana , ClpR1. Loss of ClpR1 caused a slow-growth phenotype, with chlorotic leaves during early development that later partially recovered upon maturity. Analysis of the Clp proteolytic core in the clpR1 mutant ( clpR1-1 ) revealed approx. 10% of the wild-type...
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Biochem J (2008) 415 (3): 387–399.
Published: 15 October 2008
... [email protected] ). 26 6 2008 5 8 2008 22 8 2008 22 8 2008 © The Authors Journal compilation © 2008 Biochemical Society 2008 All experiments were performed with Arabidopsis thaliana ecotype Columbia 0 (col-0). Plants were grown on soil under exposure to 140 μmol...
Includes: Supplementary data
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Biochem J (2008) 415 (2): 247–255.
Published: 25 September 2008
... in the nucleus. 1 These authors contributed equally to the present study. Arabidopsis thaliana dephosphorylation phosphatase phytochrome p hytochrome- a ssociated p rotein p hosphatase type 2C (PAPP2C) phytochrome-interacting factor 3 (PIF3) Plant light signal transduction...
Includes: Supplementary data
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Biochem J (2008) 412 (2): 275–285.
Published: 14 May 2008
... an important role in the antioxidant system of plants. In the present study we addressed the significance of chloroplast APXs in stress tolerance and signalling in Arabidopsis thaliana . To this end, T-DNA (transfer DNA) insertion mutants tapx , sapx and tapx sapx , lacking the tAPX (thylakoid-bound APX), sAPX...
Includes: Supplementary data