Cytokinin production gibberellin

There also have been clear indications that interactions of ethylene with auxins, cytokinins, gibberellins and ABA are involved in both ethylene production and action. Generally the effects of ethylene tend to antagonize those of auxins, cytokinins and gibberellins, and tend to reinforce those of ABA, depending, however, on tissue systems involved. Reinforcement of ethylene by ABA and vice versa occurs more frequently in senescence. 

Brassinosteroids are reported to stimulate overall plant growth and development, especially under stress conditions, to enhance auxin-induced growth as well as auxin-induced ethylene production (5, 6). Brassinosteroids interact with most of the phytohormones, such as cytokinins and gibberellins, and in particular with auxin. 

Table 1. Physiological response and current commercial uses of gibberellin an cytokinin products registered in the USA and Europe...

Sitton D, Itai C, Kende H (1972) Decreased cytokinin production in the roots as a factor in shoot senescence. Planta 73 296-300 Skene KGM (1967) Gibberellin-like substances in root exudate of Vitis vinifera. Planta 74 250-265... 

Such questions have been raised for the catabolic products of auxins, abscisic acid, conjugates of auxins, and gibberellin, and for the hormonal role of cytokinins and auxins in tRNA molecules, but are not reviewed in this article (17). A satisfactory answer to this question requires elucidation of the cellular mechanisms (discussed in this paper) that are believed to be primarily under hormonal regulation. 

At the preclimacteric stage of development, just prior to the rise in ethylene production the concentrations of auxins, gibberellins, and cytokinins are assumed to be very low. 

Auxins (67), gibberellins (68), cytokinins (69), and abscisic acid (67) can enhance the production of ethylene if added in concentrations that are generally considered stronger than tissue levels. Paradoxically, ethylene was one of the first chemicals identified as a potent defoliant (70), and now it has been shown to be a natural product of plant tissues that seems to regulate abscission (68, 71) as well as an influence on a host of other physiological reactions (7). 

Chloro-3-methyl-4-nitro-lH-pyrazole (Release) has no auxin-, gib-berellin-, or cytokinin-like activity, yet it is an ejffective abscission agent. At the present, there is no evidence to indicate that Release retards auxin, gibberellin, or cytokinin activity. It does stimulate and enhance the tissue production of ethylene (105). Release is fairly stable, and there is no indication that it is degraded by the tissue to ethylene per se (106). 

Two compounds common in plant metabolism are believed to be precursors of isoprenoid cytokinins in plants adenosine-5 -monophosphate (AMP) and A -isopentenylpyrophos-phate (iPP). As a final product of the mevalonate pathway, the latter substance serves also as a precursor for a wide spectrum of metabolites including some other plant hormones, as abscisic acid, gibberellins and brassinosteroids. The hypothetical scheme of reactions resulting in the formation of iPA, Z and DHZ is given in Fig. 2. The enzyme of entry into isoprenoid cytokinin formation is A -isopentenylpyrophosphate 5 -AMP-A -iso-pentenyltransferase (EC 2.5.1.8, trivially named cytokinin synthetase ). This enzyme activity was first detected in a cell-free preparation from the slime mould Dictyostelium discoideum [7,8]. Later the enzyme from higher plants (cytokinin-independent tobacco callus [9,10] and immature Zea mays kernels [11]) was described and the data were recently summarised in [12], The enzyme is very specific as far as the substrate is concerned [13,14] only the nucleotide AMP can be converted and only iPP (with a double bond in A position) may function as a side chain donor. 

Poly(c -l,4-isoprene) belongs to the family of polyisoprenoids, which are the most structurally diverse and abundant natural products known, with more than 23,000 primary and secondary metabolites. This huge family comprises, for example, sterols which display not only structural functions (control of biological membrane fluidity) but also hormonal functions (steroid hormones). Key phyto-hormones, such as abscisic acid, gibberellins and cytokinins, are isoprenoids too. Moreover, isoprenoids are used in protein prenylation, which is a key step in the activation and the localization of metabolic enzymes in many organisms. The first common step of all isoprenoid biosynthesis pathways is the formation of isopentenyl diphosphate (IPP). ... 

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