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Auxin inhibitors

Efforts may now have been successful Whereas normal tobacco cells require auxin for division, sequence tagged (TDNA) lines encoding an adenylyl cyclase were obtained which were auxin-independent but cAMP-dependent. From one line (axi 141), a complementary DNA encoding adenylyl cyclase has been isolated with characteristic leucine repeats and similarity to yeast adenylyl cyclase (Ichikawa et al., 1997). The result seems not to be the expression of an alternative division pathway from the normal auxin-driven division since it is blocked by auxin inhibitors and is activated by cAMP and the cyclase activator forskolin. Perhaps a link to G-protein at the membrane will now bring plant growth regulation even closer to that of animals. [Pg.239]

ABA was discovered by three independent lines of research.548 Cams and coworkers found that an auxin inhibitor, abscisin, was involved in the abscission of immature cotton fruits. However, Ohkuma and other... [Pg.53]

Adventitious shoot formation occurred when the roots were cultured onto auxin-free medium as mentioned above. Since the decrease of auxin levels seemed to be important for the adventitious shoot formation, the influences of auxin inhibitors on shoot formation on the cultured root segments were investigated. The auxin polar transport inhibitor, 2,3,... [Pg.680]

Table 12. Influences of auxin inhibitors on shoot formation on the cultured root segments... Table 12. Influences of auxin inhibitors on shoot formation on the cultured root segments...
Plant hormone biosynthesis and metabolism are influenced and modified, too, as already mentioned, by a large number of typical secondary plant constituents of quite different structures (Eef. 5, 6). For instance, it has been shown that some oi-disubstituted acetic acid derivatives are active both as antiauxins and as inhibitors of the biosynthesis of cyclic terpenoids. Thus, some more simple model compounds synthesized by ourselves, for example substituted a-phenoxy-isobutyrio acids, are not only competitive auxin inhibitors but they are also able to inhibit both the gibberellin and sterol biosynthesis. The same is true for some well known plant growth retardants, such as CCO or AMO 1618, which are inhibitors of gibberellin biosynthesis both in plants and in Fus ium moniliforme, but at the same time they are inhibiting and modifying also the biosynthesis of steroids in the respective organisms as well as in animal in vitro systems (Eef. 29) ... [Pg.7]

Auxin inhibitor herbicides include the so-called wild oat herbicides shown in Figure 5.22. Their classification as auxin inhibitors is based on their inhibition of auxin-induced responses in auxin bioassays and their antagonism of auxin herbicides. " This anti-auxin activity of diclofop-methyl is almost certainly secondary in importance to its inhibition of acetyl-CoA carboxylase (see Chapter 3). [Pg.159]

Other auxin-like herbicides (2,48) include the chlorobenzoic acids, eg, dicamba and chloramben, and miscellaneous compounds such as picloram, a substituted picolinic acid, and naptalam (see Table 1). Naptalam is not halogenated and is reported to function as an antiauxin, competitively blocking lAA action (199). TIBA is an antiauxin used in receptor site and other plant growth studies at the molecular level (201). Diclofop-methyl and diclofop are also potent, rapid inhibitors of auxin-stimulated response in monocots (93,94). Diclofop is reported to act as a proton ionophore, dissipating cell membrane potential and perturbing membrane functions. [Pg.46]

In addition to inhibitory chemicals which enter the plant from the external environment, many endogenous inhibitors appear to function as regulators of seed germination and plant growth and development. The interrelationships between endogenous inhibitors and growth promoters such as the auxins, gibberellins, and kinins remain to be elucidated. [Pg.120]

Inhibition of tomato and barley plants growing in soils infested with Centaurea repens (knapweed) was reported by Fletcher and Renney (38). A toxic component was isolated in highest concentration from the foliage of knapweed. The inhibitor was considered to be an indole alkaloid or auxin precursor because of its ultraviolet absorption spectrum and the positive reactions obtained with Salkowski and Ehrlich reagents. The presence of the inhibitor was considered to explain partially the rapid establishment of Centaura spp. in almost pure stands. [Pg.135]

Relatively few sites of growth-modifying or growth-inhibitory action have been identified at the cellular and molecular level. Consequently, the exact action of, and relationships between, auxins, gib-berellins, kinins, and growth inhibitors remain to be elucidated. [Pg.138]

A. M. Hirsch, R. V. Bhuvaneswari, J. G. Torrey and T. Bisseling, Early nodulin genes are induced in alfalfa root outgrowths elicited by auxin transport inhibitors. Proc. Natl. Acad. Sci. U.S.A. 86 1244-1248 (1989). [Pg.320]

None of these had pronounced herbicidal activity but rather PGR activity. Compound % for example, has been shown to be an auxin transport inhibitor, a property probably shared by the other members of this class also. A structure activity analysis for this group of compounds has been reported by Katekar ( ) ... [Pg.33]

Phenolic compounds naturally occurring in plants have induced many physiological responses that duplicate those reported for ozone and/or peroxyacetylnitrate (PAN). Chlorogenic acid is a competitive inhibitor of lAA-oxidase (35) and plant growth is adversely affected by increased concentrations of auxins (36). Concentrations of chlorogenic acid are increased in tobacco tissue exposed to ozone ( ) Phenols inhibit ATP synthesis (37), oxidative phosphorylation ( ) and SH enzyme activity (27) they increase respiration (38), reduce CO2 fixation (22), modify both membrane permeability (40) and oxidation rate of reduced NADH... [Pg.102]

Light decreased the auxin response of etiolated peas without affecting the auxin level if light activates or produces an inhibitor which interacts... [Pg.409]

Inhibitors of protein synthesis have been shown to block both the rapid and slow auxin-mediated growth responses. How do you explain these observations ... [Pg.597]

Figure 3. Development of BS and BI cellulase activity in apices of pea seedlings. Intact seedlings were sprayed with the auxin analogue 2,4-D and decapitated seedlings were painted with the natural auxin IAA with or without an inhibitor of DNA synthesis, FUdR. All treatments resulted in massive swelling at the pea apex because of cell expansion cell divisions also occurred, but not in the presence of FUdR (6). Cellulases were extracted as described in Figure 1 and assayed in unpurified form. Figure 3. Development of BS and BI cellulase activity in apices of pea seedlings. Intact seedlings were sprayed with the auxin analogue 2,4-D and decapitated seedlings were painted with the natural auxin IAA with or without an inhibitor of DNA synthesis, FUdR. All treatments resulted in massive swelling at the pea apex because of cell expansion cell divisions also occurred, but not in the presence of FUdR (6). Cellulases were extracted as described in Figure 1 and assayed in unpurified form.
Bailly A, Sovero V, Vincenzetti V, Santelia D, Bartnik D, Koenig BW, Mancuso S, Martinoia E, Geisler. 2008. Modulation of P-glycoproteins by auxin transport inhibitors is mediated by interaction with immunophilins. J Biol Chem 283 21817— 21826. [Pg.531]


See other pages where Auxin inhibitors is mentioned: [Pg.223]    [Pg.329]    [Pg.155]    [Pg.54]    [Pg.159]    [Pg.223]    [Pg.329]    [Pg.155]    [Pg.54]    [Pg.159]    [Pg.46]    [Pg.47]    [Pg.105]    [Pg.139]    [Pg.125]    [Pg.422]    [Pg.336]    [Pg.431]    [Pg.387]    [Pg.408]    [Pg.423]    [Pg.657]    [Pg.1052]    [Pg.594]    [Pg.46]    [Pg.46]    [Pg.345]    [Pg.354]    [Pg.226]    [Pg.231]    [Pg.514]    [Pg.525]    [Pg.189]   
See also in sourсe #XX -- [ Pg.681 ]

See also in sourсe #XX -- [ Pg.681 ]




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Auxin polar, inhibitors

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Auxins inhibitor herbicides

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