Kinetin-8-(14)C degraded rapidly upon drying on living or inert surfaces. However, when care was exercised to avoid taking solutions to dryness during fractionation of plant extracts containing (14)C-kinetin and before partitioning by thin layer chromatography, little degradation occurred. A procedure for 24-hour ethyl acetate partitioning, using a continuous liquid-liquid extractor, which perm...

Kinetin-induced expansion of lettuce (Lactuca sativa) cotyledons and inhibition of root are accompanied by parallel changes in protein nitrogen. However, during its inhibition of the longitudinal growth and water uptake of hypocotyl and pea (Pisum sativum) epicotyl sections kinetin markedly stimulates protein synthesis. Kinetin seems to separate auxin induced effects on protein synthesis and wa...

In hypocotyl segments of mung bean (Phaseolus mungo L.) seedlings, exogenously supplied indoleacetic acid was rapidly conjugated mainly into indoleacetylaspartic acid, which was inactive in inducing ethylene production. Kinetin is known to stimulate indoleacetic acid-induced ethylene production. The mechanism of kinetin action on indoleacetic acid-induced ethylene production by hypocotyl segmen...

Two field experiments in 1993 and 1994 as well as a laboratory germination experiment were conducted on the Egyptian cotton cultivar Giza 75 (Gossypium barbadense) to determine the effect of six concentrations of kinetin (6-furfurylaminopurine) ranging from 0 to 10.0 mg l(-1) and three different methods of application: (A) seeds were soaked for 24 h before germination (laboratory experiment) or...

The interaction between kinetin and naphthaleneacetic acid in the regulation of senescence of excised tissue of mature broccoli leaves has been used to examine the extent of synchrony between changes in chlorophyll, RNA, and protein. Kinetin increased the net uptake of 14C-labeled orotic acid and leucine. Naphthaleneacetic acid decreased the effect of kinetin on net uptake after long treatment,...

Permeability changes of Allium cepa cells were studied by a plasmometric method. Onion epidermis was floated in phosphate buffer solution with kinetin (2.5 milligrams/liter), or buffer without kinetin as a control, for 10 hours. The treated and control tissues were then transferred to one of the following four permeants: thiourea, urea, maloamide, dimethylurea.Kinetin treatment increased the pe...

Effect of growth hormones i.e., gibberellic acid (GA3), indole-3-acetic acid (IAA) and Kinetin was studied on the root of Cicer arietinum L. after forty-five and sixty days of treatments and compared with control. The application of GA3 alone and in combination with IAA or Kinetin or both caused extension growth and insignificant increase in the number of rootlets accompanied with decrease in t...

We tested the ability of N(6)-furfuryladenine (kinetin) to protect against oxidative and glycoxidative protein damage generated in vitro by sugars and by an iron/ascorbate system. At 50 microM, kinetin was more efficient (82% inhibition) than adenine (49% inhibition) to inhibit the bovine serum albumin (BSA)-pentosidine formation in slow and fast glycation/glycoxidation models. Kinetin also inh...

This research was undertaken for optimizing simple and reproducible protocol on indirect regeneration in tomato using kinetin. The effect of kinetin for efficient callus production was studied and its results were interpreted. Hypocotyls and cotyledons were used as explants and effect on callus derived regeneration was greatly influenced by addition of kinetin in media. The individually positio...

Excised pith tissue from Nicotiana glauca or the tumor-prone hybrid N. glauca x N. langsdorffii has no growth requirement for exogenous cytokinins. Addition of kinetin to cultures of these lines results in growth inhibition at a kinetin concentration 1000-fold lower than the optimal level for kinetin-requiring lines. Cytological comparison of the kinetin-inhibited 2N hybrid and glauca tissues w...