Isotope-labelled GA metabolites were identified by GC-MS. following HPLC fr
actionation of extracts derived from fruits or shoots, that had been incuba
ted with [H-2]- and [H-3]- GA(1) or [H-2]- and [H-3]- GA(3) GA(1) (1)was co
nverted into GA(8) (10) by developing fruits and vegetative shoots of sweet
cherry (Prunus avium cv. 'Stella'), while GA(3) (4) was converted into GA(
3)-isolactone (17). Other metabolites of each GA were detected but were not
identified unequivocally. These included a metabolite of GA(1) (1) in frui
tlets that was mure polar (by reverse phase HPLC) than GA(x) (10) and a met
abolite of similar polarity to GA(87) (6). was obtained after incubating fr
uitlets with GA (4). However, no evidence was obtained to suggest that GA(8
7) (6) was a metabolite of GA(3) (4) or that GA(85) (2) was a metabolite of
GA(1) (1) in these tissues, under the conditions used. The pattern of meta
bolites obtained from vegetative tissues was similar to that from fruitlets
. However. the results suggested that GA(1) (1) and GA(3) (4) were metaboli
sed at a greater rate in shoots from mature trees than in shoots from seedl
ings, and that GA(1) (I)was metabolised more rapidly than GA(3) (4) in juve
nile and mature shoots. We conclude from these observations that GA(3). (4)
is not a precursor of GA(87) (6) and GA(32) (5), also, that GA(1) (I) is n
ot a precursor of GA(85) (2) and GA(86), (3) in developing fruits or in veg
etative: shoots of sweet cherry. 2001 Elsevier Science Ltd. All rights rese
rved.