Azido Auxins
Author(s) -
Alan M. Jones,
L. Lee Melhado,
TsingFen Ho,
Nelson J. Leonard
Publication year - 1984
Publication title -
plant physiology
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 3.554
H-Index - 312
eISSN - 1532-2548
pISSN - 0032-0889
DOI - 10.1104/pp.74.2.295
Subject(s) - auxin , chemistry , botany , biology , biochemistry , gene
The binding constants of three auxin analogs, 4-, 5-, and 6-azidoindole-3-acetic acid (4-, 5-, and 6-N(3)IAA), and of the photoproducts of 5-N(3)IAA to the naphthalene-1-acetic acid (NAA) binding sites of Zea mays L. WF9 x BR38 were determined to evaluate the potential of these analogs as photoaffinity labeling agents. We have found that 4- and 5-N(3)IAA bind to these sites with affinities similar to that of IAA, while 6-N(3)IAA and the photoproducts of 5-N(3)IAA bind less tightly. This binding is fully reversible in the dark. Binding of 5-N(3)IAA becomes covalent and irreversible upon UV irradiation, as evidenced by a 30% loss in NAA binding at sites pretreated with 5-N(3)IAA and UV irradiation, then washed extensively. IAA or NAA, included with this 5-N(3)IAA pretreatment, can protect the sites from blockage, whereas benzoic acid and tryptophan are unable to protect the site, indicating that 5-N(3)IAA specifically labels the auxin sites.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom