Results 131 to 140 of about 921 (151)

Role of Plant Growth Promoting Rhizobacteria in Agricultural Sustainability-A Review. [PDF]

open access: yesMolecules, 2016
Vejan P   +4 more
europepmc   +1 more source

Molecular and Morphological Changes Induced by Leonardite-based Biostimulant in Beta vulgaris L. [PDF]

open access: yesPlants (Basel), 2019
Barone V   +11 more
europepmc   +1 more source

Improved production and flowering programs for high value poinsettia in the tropics [PDF]

open access: yes
Abdullah, Thohirah Lee   +4 more
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Rapid spectrofluorimetric method for traces of gibberelin

Analytica Chimica Acta, 1997
A new method for determination of gibberelin has been developed, based on the formation of a fluorescent compound with perchloric acid at 100 °C for 6 min. The maximum excitation and emission wavelengths of the fluorescent compound are 416 nm and 457 nm, respectively. Gibberelin in the range 10–800 ng ml−1 can be determined; the 3σ detection limit is 5
Zhiliang Jiang, Xuhong Liu, Aihui Liang
openaire   +1 more source

Gradietn C18 high-performance liquid chromatography of gibberelins

Journal of Chromatography A, 1991
Retention times of 66 gibberellins (GA) in gradient C18 high-performance liquid chromatograhy (HPLC) are reported. These include the retention times of 21 new GAs added to our previously reported 24 GAs. Retention of the other 21 GAs are the ranges estimated from previously reported C8 HPLC.
Jiann-Tsyh Lin   +3 more
openaire   +1 more source

3-hydroxylation of gibberelin A,12-aldehyde in Gibberella fujikuroi strain rec-193A

Phytochemistry, 1973
Abstract When grown on PDL medium for 11 days the strain REC-193A of Gibberella fujikuroi produces the usual range of gibberellins and ent-kaurenoid metabolites. After 3–5 days under the same conditions of culture, this slow growing strain produces virtually none of these metabolites.
John R. Bearder   +2 more
openaire   +1 more source

ChemInform Abstract: PHOTOCHEMICAL REACTIONS. XXVI. MOLECULAR AND CRYSTAL STRUCTURE OF A CYCLOBUTANE ANNELATED GIBBERELIN DERIVATIVE

Chemischer Informationsdienst, 1976
AbstractDie Titelverbindung (II) wird durch Trifluoressigsäure‐katalysierte Wagner‐Meerwein‐Umlagerung des Pseudogibberellin A, ‐ Derivats (I) dargestellt.
L. KUTSCHABSKY   +3 more
openaire   +1 more source

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