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1.
J Exp Bot ; 62(8): 2827-40, 2011 May.
Artigo em Inglês | MEDLINE | ID: mdl-21282330

RESUMO

Cytokinins (CKs) are plant hormones affecting numerous developmental processes. Zeatin and its derivatives are the most important group of isoprenoid CKs. Zeatin occurs as two isomers: while trans-zeatin (transZ) was found to be a bioactive substance, cis-zeatin (cisZ) was reported to have a weak biological impact. Even though cisZ derivatives are abundant in various plant materials their biological role is still unknown. The comprehensive screen of land plants presented here suggests that cisZ-type CKs occur ubiquitously in the plant kingdom but their abundance might correlate with a strategy of life rather than with evolutionary complexity. Changing levels of transZ and cisZ during Arabidopsis ontogenesis show that levels of the two zeatin isomers can differ significantly during the life span of the plant, with cisZ-type CKs prevalent in the developmental stages associated with limited growth. A survey of the bioassays employed illustrates mild activity of cisZ and its derivatives. No cis↔trans isomerization, which would account for the effects of cisZ, was observed in tobacco cells and oat leaves. Differences in uptake between the two isomers resulting in distinct bioactivity have not been detected. In contrast, cisZ and transZ have a different metabolic fate in oat and tobacco. Analysis of a CK-degrading enzyme, cytokinin oxidase/dehydrogenase (CKX), reveals that Arabidopsis possesses two isoforms, AtCKX1 expressed in stages of active growth, and AtCKX7, both of which have the highest affinity for the cisZ isomer. Based on the present results, the conceivable function of cisZ-type CKs as delicate regulators of CK responses in plants under growth-limiting conditions is hypothesized.


Assuntos
Plantas/metabolismo , Zeatina/metabolismo , Arabidopsis/enzimologia , Arabidopsis/crescimento & desenvolvimento , Avena/metabolismo , Biocatálise , Bioensaio , Transporte Biológico , Células Cultivadas , Isomerismo , Oxirredutases/metabolismo , Filogenia , Folhas de Planta/metabolismo , Plantas/enzimologia , Isoformas de Proteínas , Sementes/metabolismo , Transdução de Sinais , Especificidade por Substrato , Fatores de Tempo , Nicotiana/citologia , Nicotiana/enzimologia , Trítio/metabolismo , Zeatina/genética
2.
J Plant Physiol ; 236: 88-95, 2019 May.
Artigo em Inglês | MEDLINE | ID: mdl-30939333

RESUMO

Enhanced ultraviolet radiation (UV) is an important environmental factor that may cause reductions in the growth and productivity of plants. In the present work we studied the response to UV-B radiation in leaves of the model legume Lotus japonicus. After UV-B treatment, induction of phenyalanine-ammonia lyase gene expression and enzyme activity was detected. Among the ten genes encoding for PAL found in the L. japonicus genome, LjPAL1 was both the most expressed and the most induced. All the genes encoding for enzymes of the isoflavonoid pathway were also strongly induced; this was paralleled by a marked accumulation of vestitol and isoliquiritigenin. Moreover, accumulation of several other isoflavonoids was also detected. In vitro measurements of the free radical scavenging capacity of vestitol indicated that this compound can be an appropriate free radical scavenger, suggesting a possible role for this molecule in the response to abiotic stress. On the other hand, an increase of flavonol levels was not observed while the expression of the key enzymes for flavonol biosynthesis flavanone-3-hydroxylase and flavonol synthase was decreased. Taken together, these results indicate that L. japonicus follows a peculiar strategy in its response to UV radiation by accumulating isoflavonoids as an possible alternative to accumulation of flavonols as observed in other plant species.


Assuntos
Isoflavonas/biossíntese , Lotus/efeitos da radiação , Cromatografia Líquida de Alta Pressão , Indução Enzimática/efeitos da radiação , Sequestradores de Radicais Livres/metabolismo , Regulação da Expressão Gênica de Plantas/efeitos da radiação , Lotus/metabolismo , Espectrometria de Massas , Fenilalanina Amônia-Liase/metabolismo , Folhas de Planta/metabolismo , Folhas de Planta/efeitos da radiação , Reação em Cadeia da Polimerase em Tempo Real , Raios Ultravioleta
3.
Physiol Plant ; 134(4): 609-23, 2008 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-18823328

RESUMO

Darkness mediates different senescence-related responses depending on the targeting of dark treatment (whole plants or individual leaves) and on the organs that perceive the signal (leaves or cotyledons). As no data are available on the potential role of darkness to promote senescence when applied to individual cotyledons, we have investigated how darkness affects the progression of senescence in either a single or both individually darkened cotyledons of young 10-day-old Cucurbita pepo (zucchini) seedlings. Strong acceleration of senescence was observed when both cotyledons were darkened as judged by the damage in their anatomical structure, deterioration of chloroplast ultrastructure in parallel with decreased photosynthetic rate and photochemical quantum efficiency of PSII. In addition, the endogenous levels of cytokinins (CKs) and IAA were strongly reduced. In a single individually darkened cotyledon, the structure and function of the photosynthetic apparatus as well as the contents of endogenous CKs and IAA were much less affected by darkness, thus suggesting inhibitory effect of the illuminated cotyledon on the senescence of the darkened one. Apparently, the effect of darkness to accelerate/delay senescence in a single darkened cotyledon depends on the light status of the other cotyledon from the pair. The close positive correlation between CK content and the activity of CK oxidase/dehydrogenase (CKX; EC 1.4.3.18/1.5.99.12) suggested that CKX was essentially involved in the mechanisms of downregulation of endogenous CK levels. Our results indicated that CKX-regulated CK signaling could be a possible regulatory mechanism controlling senescence in individually darkened cotyledons.


Assuntos
Cotilédone/metabolismo , Cucurbita/metabolismo , Citocininas/metabolismo , Escuridão , Oxirredutases/metabolismo , Clorofila/metabolismo , Cloroplastos/ultraestrutura , Cotilédone/citologia , Ácidos Indolacéticos/metabolismo , Microscopia Eletrônica de Transmissão , Fotossíntese , Complexo de Proteína do Fotossistema II/metabolismo
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