Biotransformation of Homofolate from a Growth Inhibitor to a Growth-Promoting Derivative

Chemotherapy ◽  
1983 ◽  
Vol 29 (6) ◽  
pp. 436-441 ◽  
Author(s):  
Nathan Grossowicz ◽  
Samuel Waxman
1974 ◽  
Vol 22 (3) ◽  
pp. 429 ◽  
Author(s):  
V Rajagopal ◽  
IM Rao

Tomato plants were grown at three nitrogen levels: normal supply (control), moderate deficiency (one-eighth the normal supply – 1/8N) and acute deficiency (-N). Plant heights were reduced by 51.4 and 75.7 % respectively at 40 days under the latter two treatments compared with control plants. The biological activity of growth-promoting and growth-inhibiting substances was determined in the shoot apices of the three sets of plants at three stages: 20, 30 and 40 days after sowing. In general, the endogenous auxin was higher in control than in 1/8N and - N plants. The growth inhibitor level was higher in -N plants than in control and 118N plants. Gibberellin activity was less in nitrogen- starved plants than in controls. - N plants exhibited not only loss of gibberellins but an accumulation of inhibitors at the last stage. A negative correlation between growth promotors (auxins and gibberellins) and growth inhibitors was evident. The interaction between auxins, gibberellins and inhibitors is discussed.


1984 ◽  
Vol 246 (3) ◽  
pp. C351-C354 ◽  
Author(s):  
L. J. Mordan ◽  
F. G. Toback

The factors that stimulate kidney growth in K+-deficient animals are unknown. Cultures of renal epithelial cells (BSC-1 line) were used to study this phenomenon because their growth is accelerated in medium containing a reduced K+ concentration. We tested the hypothesis that growth induced by low-K+ medium is mediated by factors produced by the cells; i.e., is subject to autocrine control. Low-K+ (3.2 mM) or control (5.4 mM) medium was conditioned by placing it on confluent cultures of BSC-1 cells for 1 h and was then collected. The K+ concentration of the low-K+ conditioned medium was then adjusted to the control value by addition of KCl. This conditioned medium stimulated growth of fresh cultures of cells to the same extent as did unconditioned low-K+ medium. The appearance of growth-promoting activity was maximal at a K+ concentration of 3.2 mM during conditioning of the medium. Low-K+ conditioned medium, corrected to a K+ concentration of 5.4 mM, required 6 h to commit cells to enhanced proliferation. Growth-stimulating activity in low-K+ conditioned medium was antagonized by a purified growth inhibitor produced by the cells. These observations are consistent with the hypothesis that autocrine products with opposite effects on growth can regulate proliferation of renal epithelial cells.


1971 ◽  
Vol 19 (3) ◽  
pp. 273 ◽  
Author(s):  
N Sreeramulu ◽  
IM Rao

Growth substances in developing seeds of dormant and non-dormant cultivars of groundnut were chromatographically separated, and their content at various RF values estimated by the rice coleoptile bioassay technique. Growth promotors increased from 20 to 30 days in the acidic and neutral fractions of the dormant and non-dormant seeds. From 30 days onwards, growth promotors decreased while inhibitors accumulated, but their relative proportions varied in the two types of seeds. In mature non-dormant seeds, the content of growth promotors in the acidic fraction was higher than that of inhibitors; in dormant seeds it was lower. In the neutral fraction the content of inhibitors was higher than that of promotors in seeds of both types. The balance of growth-promoting and inhibiting substances in relation to seed development and dormancy is discussed, and it is concluded that the acidic inhibitors are responsible for dormancy in groundnut seeds.


1960 ◽  
Vol 38 (6) ◽  
pp. 875-881 ◽  
Author(s):  
F. R. Forsyth ◽  
D. J. Samborski

Optimum growth of etiolated pea stem sections was obtained in a basal solution of 3-indoleacetic acid, cobalt chloride, and sucrose. The final length of pea stem sections was increased when sucrose was added 2, 4, or 6 hours after 3-indoleacetic acid and cobalt were added to the test solution. Benzimidazole at 100 to 200 p.p.m. and kinetin at 1 p.p.m. added to the basal solution inhibited growth of etiolated pea stem sections. Growth.of the pea stem sections was inhibited when they were treated for 4 hours with kinetin plus 3-indoleacetic acid, then transferred to the basal solution for 14 hours. There was no growth inhibition when pea stem sections were treated for 4 hours with kinetin alone, followed by 14 hours on the basal solution. Similar results with kinetin were obtained when barley coleoptiles were used and 2,4-dichlorophenoxyacetic acid was the growth-promoting substance. Ether and hot water extracts of pea stem tissue pretreated with kinetin and 3-indoleacetic acid did not appear to contain a growth inhibitor.


1984 ◽  
Vol 62 (10) ◽  
pp. 2047-2052 ◽  
Author(s):  
S. D. Ray ◽  
M. M. Laloraya

Abscisic acid, a potent growth inhibitor, inhibits hypocotyl growth of Amaranthus caudatus (L.) seedlings. Phenolic compounds when applied with ABA (abscisic acid), antagonize ABA action and restore normal seeding growth. GA (gibberellic acid) promotes hypocotyl growth and on combined application with ABA, the ratio of their concentrations determines the course of the resultant growth. This interaction can be modulated by phenolic compounds. Phenolic compounds in low concentrations when present together with GA and ABA favour GA-induced growth by antagonizing the inhibitory effect of ABA. Inhibitory action of abscisic acid on growth is so far known to be counteracted only by growth-promoting hormones. Antagonistic action of phenolic compounds imparts a dual role to this class of compounds, balancing the effect of growth-promoting and growth-inhibiting hormones.


1990 ◽  
Vol 80 (1) ◽  
pp. 109-113 ◽  
Author(s):  
Ester P. Lorences ◽  
Gordon J. McDougall ◽  
Stephen C. Fry

2019 ◽  
Vol 13 (3) ◽  
pp. 167-173
Author(s):  
Fiona C. Thomas ◽  
Jhodi-Ann Bowie ◽  
Lincoln Hill ◽  
Joelle T. Taknint

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