A bacterial assay for rapid screening of IAA catabolic enzymes

. 2019 ; 15 () : 126. [epub] 20191104

Status PubMed-not-MEDLINE Jazyk angličtina Země Velká Británie, Anglie Médium electronic-ecollection

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid31700527

BACKGROUND: Plants rely on concentration gradients of the native auxin, indole-3-acetic acid (IAA), to modulate plant growth and development. Both metabolic and transport processes participate in the dynamic regulation of IAA homeostasis. Free IAA levels can be reduced by inactivation mechanisms, such as conjugation and degradation. IAA can be conjugated via ester linkage to glucose, or via amide linkage to amino acids, and degraded via oxidation. Members of the UDP glucosyl transferase (UGT) family catalyze the conversion of IAA to indole-3-acetyl-1-glucosyl ester (IAGlc); by contrast, IAA is irreversibly converted to indole-3-acetyl-l-aspartic acid (IAAsp) and indole-3-acetyl glutamic acid (IAGlu) by Group II of the GRETCHEN HAGEN3 (GH3) family of acyl amido synthetases. Dioxygenase for auxin oxidation (DAO) irreversibly oxidizes IAA to oxindole-3-acetic acid (oxIAA) and, in turn, oxIAA can be further glucosylated to oxindole-3-acetyl-1-glucosyl ester (oxIAGlc) by UGTs. These metabolic pathways have been identified based on mutant analyses, in vitro activity measurements, and in planta feeding assays. In vitro assays for studying protein activity are based on producing Arabidopsis enzymes in a recombinant form in bacteria or yeast followed by recombinant protein purification. However, the need to extract and purify the recombinant proteins represents a major obstacle when performing in vitro assays. RESULTS: In this work we report a rapid, reproducible and cheap method to screen the enzymatic activity of recombinant proteins that are known to inactivate IAA. The enzymatic reactions are carried out directly in bacteria that produce the recombinant protein. The enzymatic products can be measured by direct injection of a small supernatant fraction from the bacterial culture on ultrahigh-performance liquid chromatography coupled to electrospray ionization tandem spectrometry (UHPLC-ESI-MS/MS). Experimental procedures were optimized for testing the activity of different classes of IAA-modifying enzymes without the need to purify recombinant protein. CONCLUSIONS: This new method represents an alternative to existing in vitro assays. It can be applied to the analysis of IAA metabolites that are produced upon supplementation of substrate to engineered bacterial cultures and can be used for a rapid screening of orthologous candidate genes from non-model species.

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Vanneste S, Friml J. Auxin: a trigger for change in plant development. Cell. 2009;136(6):1005–1016. doi: 10.1016/j.cell.2009.03.001. PubMed DOI

Friml J, Vieten A, Sauer M, Weijers D, Schwarz H, Hamann T, et al. Efflux dependent auxin gradients establish the apical-basal axis of Arabidopsis. Nature. 2003;426(6963):147–153. doi: 10.1038/nature02085. PubMed DOI

Benková E, Ivanchenko MG, Friml J, Shishkova S, Dubrovsky JG. A morphogenetic trigger: is there an emerging concept in plant developmental biology? Trends Plant Sci. 2009;14(4):189–193. doi: 10.1016/j.tplants.2009.01.006. PubMed DOI

Petersson SV, Johansson AI, Kowalczyk M, Makoveychuk A, Wang JY, Moritz T, et al. An auxin gradient and maximum in the Arabidopsis root apex shown by high-resolution cell-specific analysis of IAA distribution and synthesis. Plant Cell. 2009;21(6):1659–1668. doi: 10.1105/tpc.109.066480. PubMed DOI PMC

Ljung K. Auxin metabolism and homeostasis during plant development. Development. 2013;140(5):943–950. doi: 10.1242/dev.086363. PubMed DOI

Zhao Y. Essential roles of local auxin biosynthesis in plant development and in adaptation to environmental changes. Annu Rev Plant Biol. 2018;69(1):417–435. doi: 10.1146/annurev-arplant-042817-040226. PubMed DOI

Ludwig-Müller J. Auxin conjugates: their role for plant development and in the evolution of land plants. J Exp Bot. 2011;62(6):1757–1773. doi: 10.1093/jxb/erq412. PubMed DOI

Zhang J, Peer WA. Auxin homeostasis: the DAO of catabolism. J Exp Bot. 2017;68(12):3145–3154. doi: 10.1093/jxb/erx221. PubMed DOI

Staswick PE, Serban B, Rowe M, Tiryaki I, Maldonado MT, et al. Characterization of an Arabidopsis enzyme family that conjugates amino acids to indole-3-acetic acid. Plant Cell. 2005;17:617–627. doi: 10.1105/tpc.104.026690. PubMed DOI PMC

Westfall CS, Herrmann J, Chen Q, Wang S, Jez JM. Modulating plant hormones by enzyme action. Plant Signal Behav. 2011;5(12):1607–1612. doi: 10.4161/psb.5.12.13941. PubMed DOI PMC

Ruiz Rosquete M, Barbez E, Kleine-Vehn J. Cellular auxin homeostasis: gatekeeping is housekeeping. Mol Plant. 2012;5(4):772–786. doi: 10.1093/mp/ssr109. PubMed DOI

Östin A, Kowalyczk M, Bhalerao RP, Sandberg G. Metabolism of indole-3-acetic acid in Arabidopsis. Plant Physiol. 1998;118(1):285–296. doi: 10.1104/pp.118.1.285. PubMed DOI PMC

Campanella JJ, Smith SM, Leibu D, Wexler S, Ludwig-Müller J. The auxin conjugate hydrolase family of Medicago truncatula and their expression during the interaction with two symbionts. J Plant Growth Regul. 2008;27:26–38. doi: 10.1007/s00344-007-9027-2. DOI

Jackson RG, Lim EK, Li Y, Kowalczyk M, Sandberg G, Hoggett J, et al. Identification and biochemical characterization of an Arabidopsis indole-3-acetic acid glucosyltransferase. J Biol Chem. 2001;276:4350–4356. doi: 10.1074/jbc.M006185200. PubMed DOI

Jin SH, Ma XM, Han P, Wang B, Sun YG, Zhang GZ, et al. UGT74D1 is a novel auxin glycosyltransferase from Arabidopsis thaliana. PLoS ONE. 2013;8(4):1–11. PubMed PMC

Tanaka K, Hayashi KI, Natsume M, Kamiya Y, Sakakibara H, Kawaide H, et al. UGT74D1 catalyzes the glucosylation of 2-oxindole-3-acetic acid in the auxin metabolic pathway in arabidopsis. Plant Cell Physiol. 2014;55(1):218–228. doi: 10.1093/pcp/pct173. PubMed DOI PMC

Kowalyczk M, Sandberg G. Quantitative analysis of indole-3-acetic acid metabolites in Arabidopsis. Plant Physiol. 2001;127:1845–1853. doi: 10.1104/pp.010525. PubMed DOI PMC

Novák O, Hényková E, Sairanen I, Kowalczyk M, Pospíšil T, et al. Tissue-specific profiling of the Arabidopsis thaliana auxin metabolome. Plant J. 2012;72:523–536. doi: 10.1111/j.1365-313X.2012.05085.x. PubMed DOI

Porco S, Pěnčík A, Rashed A, Voß U, Casanova-Sáez R, Bishopp A, et al. Dioxygenase-encoding AtDAO1 gene controls IAA oxidation and homeostasis in Arabidopsis. Proc Natl Acad Sci. 2016;113(39):11016–11021. doi: 10.1073/pnas.1604375113. PubMed DOI PMC

Zhang J, Lin JE, Harris C, Campos Mastrotti Pereira F, Wu F, Blakeslee JJ, et al. DAO1 catalyzes temporal and tissue-specific oxidative inactivation of auxin in Arabidopsis thaliana. Proc Natl Acad Sci. 2016;113(39):11010–11015. doi: 10.1073/pnas.1604769113. PubMed DOI PMC

Peer WA, Cheng Y, Angus M. Evidence of oxidative attenuation of auxin signalling. J Exp Bot. 2013;64:2629–2639. doi: 10.1093/jxb/ert152. PubMed DOI

Pěnčík A, Simonovik B, Petersson SV, Henyková E, Simon S, Greenham K, et al. Regulation of auxin homeostasis and gradients in arabidopsis roots through the formation of the indole-3-acetic acid catabolite 2-oxindole-3-acetic acid. Plant Cell. 2013;25(10):3858–3870. doi: 10.1105/tpc.113.114421. PubMed DOI PMC

Stepanova AN, Alonso JM. Auxin catabolism unplugged: role of IAA oxidation in auxin homeostasis. Proc Natl Acad Sci. 2016;113(39):10742–10744. doi: 10.1073/pnas.1613506113. PubMed DOI PMC

Jackson RG, Kowalczyk M, Li Y, Higgins G, Ross J, Sandberg G, et al. Over-expression of an Arabidopsis gene encoding a glucosyltransferase of indole-3-acetic acid: phenotypic characterisation of transgenic lines. Plant J. 2002;32(4):573–583. doi: 10.1046/j.1365-313X.2002.01445.x. PubMed DOI

Böttcher C, Keyzers RA, Boss PK, Davies C. Sequestration of auxin by the indole-3-acetic acid-amido synthetase GH3-1 in grape berry (Vitis vinifera L.) and the proposed role of auxin conjugation during ripening. J Exp Bot. 2010;61(13):3615–3625. doi: 10.1093/jxb/erq174. PubMed DOI

Ludwig-Müller J, Jülke S, Bierfreund NM, Decker EL, Reski R. Moss (Physcomitrella patens) GH3 proteins act in auxin homeostasis. New Phytol. 2009;181(2):323–338. doi: 10.1111/j.1469-8137.2008.02677.x. PubMed DOI

Chen Q, Zhang B, Hicks LM, Wang S, Jez JM. A liquid chromatography-tandem mass spectrometry-based assay for indole-3-acetic acid-amido synthetase. Anal Biochem. 2009;390(2):149–154. doi: 10.1016/j.ab.2009.04.027. PubMed DOI

Chen Q, Westfall CS, Hicks LM, Wang S, Jez JM. Kinetic basis for the conjugation of auxin by a GH3 family. J Biol Chem. 2010;285(39):29780–29786. doi: 10.1074/jbc.M110.146431. PubMed DOI PMC

Zhang S-W, Li C-H, Cao J, Zhang Y-C, Zhang S-Q, Xia Y-F, et al. Altered architecture and enhanced drought tolerance in rice via the down-regulation of indole-3-acetic acid by TLD1/OsGH3.13 activation. Plant Physiol. 2009;151(4):1889–1901. doi: 10.1104/pp.109.146803. PubMed DOI PMC

Drábková LZ, Dobrev PI, Motyka V. Phytohormone profiling across the bryophytes. PLoS ONE. 2015;10(5):1–19. PubMed PMC

Žižková E, Kubeš M, Dobrev PI, Přibyl P, Šimura J, Zahajská L, et al. Control of cytokinin and auxin homeostasis in cyanobacteria and algae. Ann Bot. 2017;119(1):151–166. doi: 10.1093/aob/mcw194. PubMed DOI PMC

Pěnčík A, Casanova-Sàez R, Pilařovà V, Žukauskaitė A, Pinto R, et al. Ultra-rapid auxin metabolite profiling for high-throughput mutant screening in Arabidopsis. J Exp B. 2018;69(10):2569–2579. doi: 10.1093/jxb/ery084. PubMed DOI PMC

Zhao Z, Zhang Y, Liu X, Zhang X, Liu S, et al. A role for a dioxygenase in auxin metabolism and reproductive development in rice. Dev Cell. 2013;27:113–122. doi: 10.1016/j.devcel.2013.09.005. PubMed DOI

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