Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 12 de 12
Filter
Add more filters










Publication year range
1.
Phytochemistry ; 56(6): 577-81, 2001 Mar.
Article in English | MEDLINE | ID: mdl-11281135

ABSTRACT

From the exudate of germinating sunflower (Helianthus annuus L.) seeds was isolated a stereoisomer of diversifolide, 4, 15-dinor-3-hydroxy-1(5)-xanthene-12,8-olide (designated sundiversifolide) as determined by analysis of its IR, APCI-, ESI- and HR-MS and 13C and 1H NMR spectra. This substance inhibited shoot and root growth of cat's-eyes by about 50% at a concentration of 30 ppm. It also showed species-selective activity on the shoot and root growth of tested plants. When cat's-eyes seeds were incubated together with sunflower seeds, the cat's-eyes growth was inhibited. Furthermore, it was detected from an extract of river sand when sunflower seeds were incubated on the sand. These results indicate that sundiversifolide has an allelopathic function in sunflower plants.


Subject(s)
Helianthus/chemistry , Seeds/chemistry , Xanthenes/chemistry , Helianthus/physiology , Plant Roots/drug effects , Plant Roots/growth & development , Plant Shoots/drug effects , Plant Shoots/growth & development , Plants/drug effects , Seeds/physiology , Species Specificity , Stereoisomerism , Xanthenes/isolation & purification , Xanthenes/pharmacology
2.
Phytochemistry ; 54(3): 275-9, 2000 Jun.
Article in English | MEDLINE | ID: mdl-10870181

ABSTRACT

The distribution of natural growth inhibitors, the raphanusanins (isomers of 3-(methylthio)methylene-2-pyrrolidinethione) and their precursors (4-methylthio-3-butenyl glucosinolate (MTBG) and 4-methylthio-3-butenyl isothiocyanate (MTBI), between illuminated and shaded halves of radish hypocotyls during phototropic curvature was analyzed using a physicochemical assay. Phototropic stimulation rapidly decreased MTBG content, and abruptly increased contents of MTBI and raphanusanins in the illuminated halves of radish hypocotyls within 30 min after the onset of unilateral illumination. Content in the shaded halves was similar to that in dark controls. When MTBG, MTBI, and raphanusanins at endogenous levels were applied unilaterally to etiolated hypocotyls, MTBI and raphanusanins caused hypocotyls to bend but MTBG showed no activity. Blue illumination promoted myrosinase (thioglucosidase) activity, which releases MTBI from MTBG, in hypocotyls after 10 min, although enzyme activity in dark controls did not change. These results suggest that phototropic stimulation promotes myrosinase activity in the illuminated side of radish hypocotyls, releasing bioactive MTBI from inactive MTBG and simultaneously producing bioactive raphanusanins.


Subject(s)
Phototropism/physiology , Pyrrolidines/metabolism , Thioglucosides/metabolism , Thiones/metabolism , Vegetables/metabolism , Darkness , Hypocotyl/metabolism , Kinetics , Light , Plant Growth Regulators/metabolism
3.
J Plant Growth Regul ; 18(2): 65-67, 1999 Oct.
Article in English | MEDLINE | ID: mdl-10552134

ABSTRACT

The allelopathy of a serious weed, barnyard grass (Echinochloa crus-galli L.), was investigated. Root exudates of young barnyard grass showed allelopathic effects and plant-selective activity and inhibited root elongation of all plants tested. With respect to shoot growth, the exudates did not show inhibition of barnyard grass only. The allelopathic substance was isolated and identified as p-hydroxymandelic acid by NMR. p-Hydroxymandelic acid strongly inhibited shoot growth and root elongation of all plants tested. The effects of three congeners of p-hydroxymandelic acid were tested on rice shoot growth. In the biological activity exhibited in rice, shoot growth was related to the hydroxyl groups.

5.
J Plant Growth Regul ; 17(4): 215-219, 1998 Dec.
Article in English | MEDLINE | ID: mdl-9892744

ABSTRACT

The effect of disaccharide lepidimoide on light-induced chlorophyll accumulation was studied in cotyledons of sunflower (Helianthus annuus L.) seedlings and detached cucumber (Cucumis sativus L.) cotyledons. From studies on the structure-activity relationships of lepidimoide, its analogs, and sucrose with respect to light-induced chlorophyll accumulation in the cotyledons of sunflower seedlings, both lepidimoide and the free carboxylic acid of lepidimoide (lepidimoic acid) showed the highest promoting activity, whereas the hydrogenated lepidimoide, which lacks a double bond in the C4, 5 position in uronic acid, showed lower activity than lepidimoide; however, sucrose exhibited very weak activity. These results suggest that lepidimoide acts as a new type of plant growth regulator, not simply as a carbon source providing energy. Lepidimoide promoted not only light-induced chlorophyll accumulation in sunflower cotyledons but also light-induced 5-aminolevulinic acid content, which is considered to be a rate-limiting step in chlorophyll biosynthesis. Lepidimoide with cytokinin stimulated the accumulation of chlorophyll and 5-aminolevulinic acid additively. In detached cucumber cotyledons, lepidimoide also promoted light-induced chlorophyll accumulation. These results indicate that lepidimoide, in cooperation with cytokinin, causes light-induced chlorophyll accumulation in the cotyledons of several dicot plant species by affecting the level of 5-aminolevulinic acid. Key Words. 5-Aminolevulinic acid accumulation-Chlorophyll accumulation-Cucumis sativus-Cytokinin-Helianthus annuus-Lepidimoic acid-Lepidimoide-Structure-activity relationship

6.
DNA Seq ; 8(4): 235-9, 1998 Mar.
Article in English | MEDLINE | ID: mdl-10520452

ABSTRACT

We isolated and determined a nucleotide sequence of a cDNA clone encoding a protein homologous to maize major auxin-binding protein (ABP1) from a cDNA library of oat coleoptiles. The deduced amino acid sequence of this clone contained an N-linked glycosylation signal and an ER-retention signal. Furthermore, two domains that were important to interact with auxins, were conserved in this clone at amino acid level.


Subject(s)
Avena/genetics , DNA, Complementary/genetics , Plant Proteins , Receptors, Cell Surface/genetics , Amino Acid Sequence , Base Sequence , DNA, Plant/genetics , Indoleacetic Acids/metabolism , Molecular Sequence Data , Receptors, Cell Surface/chemistry , Receptors, Cell Surface/metabolism , Sequence Alignment , Sequence Analysis, DNA
7.
DNA Seq ; 9(5-6): 329-33, 1998.
Article in English | MEDLINE | ID: mdl-10524760

ABSTRACT

A gene homologue to the auxin-inducible SAUR (Small Auxin Up RNAs) of soybean was isolated from a cDNA and a genomic library of radish. The cDNA clone was about 470 bp in length and contained a DST (Down STream) element that was involved in mRNA instability in the 3'-untranslated region. The genomic clone contained two short sequences that related to auxin-responsible core sequences (AGTCTC and TATCCCAC) in its promoter region. The radish SAUR transcript was accumulated by auxin and cycloheximide treatments in the same way as that in other plant species. However, the NDE and DUE elements that were reported in all of the other SAUR gene promoters were not conserved in this radish SAUR gene. The results suggest that the promoter activity of the SAUR gene will be regulated by only two short sequences.


Subject(s)
Plant Proteins/chemistry , Plant Proteins/genetics , Vegetables/genetics , Amino Acid Sequence , Base Sequence , Blotting, Northern , Blotting, Southern , Gene Expression Regulation, Plant , Indoleacetic Acids/metabolism , Molecular Sequence Data , Plant Roots/chemistry , Promoter Regions, Genetic , Sequence Analysis, DNA , Vegetables/chemistry
8.
J Antibiot (Tokyo) ; 49(5): 414-7, 1996 May.
Article in English | MEDLINE | ID: mdl-8682716

ABSTRACT

New protein farnesyltransferase inhibitors, andrastins A-C, have been discovered in the cultured broth of Penicillium sp. FO-3929. Andrastins extracted from broth supernatant were purified by silica gel chromatography, ODS chromatography and HPLC. The IC50 of andrastins A, B, and C against protein farnesyltransferase were 24.9, 47.1, and 13.3 microM, respectively.


Subject(s)
Alkyl and Aryl Transferases , Androstadienes/isolation & purification , Transferases/antagonists & inhibitors , Androstadienes/chemistry , Androstadienes/pharmacology , Crystallography, X-Ray , Farnesyltranstransferase , Fermentation , Magnetic Resonance Spectroscopy , Microbial Sensitivity Tests , Molecular Structure , Penicillium
9.
Phytochemistry ; 41(3): 671-3, 1996 Feb.
Article in English | MEDLINE | ID: mdl-8835453

ABSTRACT

The structure-activity relationship of lepidimoide and its analogues was investigated by means of the Amaranthus caudatus L. hypocotyl elongation test. In addition, the activities of alpha-D-galacturonic acid and L-(+)-rhamnose, which are component sugars of lepidimoide, were also studied. The carboxylic acid free type of lepidimoide showed growth-promoting activity as high as the original lepidimoide (sodium type). The acetylated compound showed considerably higher activity than lepidimoide, whereas the methylated lepidimoide did not show any activity. The hydroxylated lepidimoide without a double bond in the C-4,5 position showed lower activity. The sugar alcohol type of lepidimoide [2-O-(alpha-D-glucopyranosyl)-L-rhamnose] showed the highest activity in all the compounds studied. alpha-D-Galacturonic acid, L-(+)-rhamnose and their mixtures, which are component sugars of lepidimoide, exhibited only slight or no activity, respectively. D-Glucose and the mixture of D-glucose and L-(+)-rhamnose were also slightly active or inactive. These data suggest that the active sites in the chemical structure of the lepidimoide are the uronic acid derivative bearing an alpha,beta-unsaturated carboxylate bonded to rhamnose via an alpha-glucoside linkage and a double bond in the C-4,5 position in the uronic acid.


Subject(s)
Disaccharides/chemistry , Disaccharides/pharmacology , Plants/chemistry , Carbohydrate Sequence , Molecular Sequence Data , Structure-Activity Relationship
10.
J Chem Ecol ; 20(2): 309-14, 1994 Feb.
Article in English | MEDLINE | ID: mdl-24242056

ABSTRACT

The allelopathic potential of oat (Avena sativa L.) extracts was investigated under laboratory conditions. The ethyl ether-, acetone-, and water-soluble fractions obtained from the extract of oat shoots inhibited the germination and growth of roots and hypocotyls of lettuce (Lactuca sativa L.). The inhibitory activity of the water-soluble fraction was maximum, followed by that of ethyl ether-soluble and acetone-soluble fraction. An active principle of the water-soluble fraction was isolated and its structure was determined by spectral data asL-tryptophan.L-Tryptophan inhibited the growth of hypocotyls and roots of lettuce seedlings at concentrations greater than 0.03 and 0.1 mM, respectively. These results suggested thatL-tryptophan may be an allelochemical which affects the growth or germination of different plant species.

11.
Plant Physiol ; 100(2): 1059-61, 1992 Oct.
Article in English | MEDLINE | ID: mdl-16653018

ABSTRACT

A new allelopathic substance that promoted the shoot growth of different plant species but inhibited the root growth was isolated as an amorphous powder from mucilage of germinated cress (Lepidium sativum L.) seeds. This substance was identified as sodium 2-O-rhamnopyranosyl-4-deoxy-threo-hex-4-enopyranosiduronate (designated lepidimoide) from the mass and the nuclear magnetic resonance and infrared spectra coupled with some chemical evidence. Lepidimoide promoted the hypocotyl growth of etiolated Amaranthus caudatus L. at concentrations higher than 3 mum and inhibited the root growth at concentrations higher than 100 mum. The growth-promoting activity in hypocotyls was 20 or 30 times as much as that of gibberellic acid.

SELECTION OF CITATIONS
SEARCH DETAIL
...