Flowers of sour cherry (Prunus cer ants L.) were grown in vitro on liquid M
S-media containing IAA at 5.0 muM and BA at 0.8 muM (controls). The liquid
medium was supplemented with catechin at 68 muM. The flowers were fixed on
paper bridges with the petioles sticked into the liquid medium. Upon treatm
ent with catechin large amounts of callus cells proliferated from the flowe
rs. The fresh weight was 18 fold that of controls. Young fruit tissue of so
ur cherry (P. cerasus) was cultivated on the same media as used for flowers
. With added catechin the fresh weight of the fruit tissues was only 2.2 fo
ld compared with controls. The catechin treatment showed formative cell div
isions, in that already existing parenchyma cells themselves divided about
2-6 times. The number of subdividing cells per unit area was 4.3 times that
of controls. In contrast, the controls showed significantly more leaching
of flavanols into intercellular spaces as compared with the catechin treatm
ents. Additionally, fungus-infected young cherry fruits were sampled in the
orchard. Around the fungal lesions large parenchyma cells were found to su
bdivide themselves several times transversely, similar to the fashion shown
in the catechin-treated fruit pieces. Isoelectrofocusing of cherry-peroxid
ases revealed inhibition of both basic and acidic isoperoxidases by catechi
n. In the stressed wound area, leaching flavanols might act as inhibitors o
f the extremely active IAA peroxidases. Additionally, the rapid oxidation o
f the catechins as verified in our experiments is stimulative for cell deat
h at the fungal infection site.