On the Mechanism of Action of Growth Regulators
Author(s) -
Robert Muir,
Corwin Hansch
Publication year - 1953
Publication title -
plant physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.554
H-Index - 312
eISSN - 1532-2548
pISSN - 0032-0889
DOI - 10.1104/pp.28.2.218
Subject(s) - phenylacetic acid , coleoptile , benzoic acid , elongation , chemistry , avena , stereochemistry , ring (chemistry) , side chain , substrate (aquarium) , biochemistry , biology , botany , organic chemistry , ecology , materials science , metallurgy , ultimate tensile strength , polymer
Investigations of the effects of various analogues of indoleacetic acid, phenoxyacetic acid, phenylacetic acid and benzoic acid on the elongation of sections of Avena coleoptiles (7, 8, 16, 17) have led to the conclusion that plant growth-regulators react by a nucleophilic substitution at a position on the ring ortho to the carboxyl group or the side chain carrying this group and with the carboxyl group itself. The evidence at hand indicates tna? a cysteinyl unit of a protein is the most likely substrate for the two-point ortho reaction as illustrated below with 2,4-dichlorophenoxyacetic acid.
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