Synthesis of auxin

The inhibition of the synthesis of auxin by D-galactose was also shown to be a contributory factor in the retardation of growth ofA vena coleoptiles.538-539 On the other hand, D-galactose-induced evolution of ethylene is known to retard the growth of mung-bean seedlings.540... 

Dahm, H., Sitek, J. M., and Strzelczyk, E. (1977). Synthesis of auxins by bacterial isolated from the roots of pine seedlings inoculated with rusty forest soil. Pol. I. Soil Sci. 10, 131-137. 

The T-DNA (transferred DNA) region of the Ti plasmid carries the genes which are transferred to, integrated, and expressed in recipient plant cells. T-DNA from pTi contains genes which promote the synthesis of auxins, C3rtokinins... 

The induction of PAL activity by the two growth factors can be separated in time so that they may act at different sites within the cell to bring about the response (40). Auxin added at the time of subculture of the tissue changes the pattern of protein synthesis of the cells by changing the transcription pattern of the mRNA after two hours (43). Kinetin does not have this effect (44). 

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... 

Further studies are required to fully elucidate the role of flavonoids in auxin regulation in vivo to determine, for example, whether changes in the synthesis or deposition of specific flavonoids within the cell act to change the rate or direction of auxin transport. There is the question of how such different organs or developmental outcomes as nodules, lateral roots,... 

Two aliphatic acids possess, for grasses, many of the growth-distortion and toxicity effects associated with the synthetic auxins on dicotyledonous plants. Trichloroacetic acid and 2,2-dichloropropionic acid (dalapon), as the sodium salts, have been called grass "hormones or auxins, although Wilkinson184 could find no growth stimulation at low concentrations, and described dalapon as an antiauxin from its interference with indole-3-acetic acid effects. The herbicidal properties of trichloroacetate do not depend on its protein-denaturing ability, and those of 2,2-dichloropropionic acid involve, at least indirectly, the synthesis of pantothenic acid. 

These observations are consistent with the conclusion that auxin treatment leads to the synthesis of BS cellulase, which then accumulates in smooth ER vesicles. There is direct evidence that the synthesis occurs in rough ER vesicles (11). Cellulase activity was shown (25) to increase in RNA-rich pea microsomes, provided these were isolated from auxin-treated tissue, when the preparations were incubated with ingredients necessary for carrying out protein synthesis in vitro. Messenger RNA (mRNA) from these microsomes has been translated in a different ribo-somal system and shown to synthesize BS cellulase protein (II). Thus, it is legitimate to use the term "induction to apply to the ability of auxin to evoke the appearance of mRNA for BS cellulase. 

Fig. 1. Ethylene biosynthesis. The numbered enzymes are (1) methionine adenosyltransferase, (2) ACC (l-aminocyclopropane-l-carboxylic acid) synthase, (3) ethylene forming enzyme (EFE), (4) 5 -methylthio-adenosine nucleosidase, (5) 5 -methylthioribose kinase. Regulation of the synthesis of ACC synthase and EFE are important steps in the control of ethylene production. ACC synthase requires pyridoxal phosphate and is inhibited by aminoethoxy vinyl glycine EFE requires 02 and is inhibited under anaerobic conditions. Synthesis of both ACC synthase and EFE is stimulated during ripening, senescence, abscission, following mechanical wounding, and treatment with auxins.

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