Plant growth regulators and the physiological limitations to yield in sugar beet

Improvements in seed germination, the early establishment of leaf cover, storage root development and the control of bolting would all increase the yield of sugar beet in the UK. Plant growth at these stages of development is controlled by genotype and by climatic factors acting through endogenous growth substances and is potentially capable of modification by applied growth regulators. For example, sugar beet responds to changes in daylength and spectral quality of light at the end of the day by increasing lamina and petiole growth, light interception and plant growth rate. Changes in endogenous gibberellins in young leaves of plants growing in different photoperiods and the responses of these leaves to applied gibberellic acid are presented as evidence for the involvement of gibberellins in leaf expansion in sugar beet.     

Effects of terbinafine on growth, squalene, and steryl ester content of a celery cell suspension culture

The allylamine terbinafine inhibited growth of a celery (Apium graveolens) cell suspension culture (I₅₀ = 90 μM) and blocked the action of squalene epoxidase, resulting in an accumulation of squalene and a decrease in the sterol content of the cells. Celery cells were tolerant to squalene accumulation; inhibition of growth of cultures was associated with a fall in the free sterol content below about 1 μg sterol/mg dry wt of cells. At Day 14, untreated celery cells contained about 60% of the total sterol in the esterified form. However, the steryl ester pool was considerably lower in terbinafine-treated cells which may reflect an attempt to maintain the free sterol content above a threshold value. The composition of free sterols of terbinafine-treated cells was different from control cultures, suggesting that terbinafine has a second site of inhibition on the pathway to major sterols in plants.     

Effects of triazole inhibitors of sterol biosynthesis on the free and esterified sterol composition of celery cell suspension cultures

Treatment of celery cell suspension cultures with paclobutrazol and three other triazoles resulted in decreased growth and an accumulation of 14α-methylsterols in both the free sterol and the steryl ester pools, thus indicating that the triazoles were inhibiting the action of the plant obtusifoliol 14α-demethylase system. Obtusifoliol, 14α-methylcampesta-8,24(24¹)-dien-3β-ol and 14α-methylcampest-8-en-3β-ol were the main 14α-methylsterols to increase in the free sterol pool. In the presence of the triazoles the steryl esters became virtually depleted of sitosterol, campesterol, stigmasterol and isofucosterol, which were replaced by 14α-methylsterols with obtusifoliol becoming the dominant esterified sterol. Treatment of the celery culture with a fourth triazole which did not have a noticeable effect on growth and caused negligible accumulation of 14α-methylsterols in the free sterol pool nevertheless produced some enrichment of the steryl esters in obtusifoliol. The results indicate that, following triazole treatment, a rapid esterification of the accumulating 14α-methylsterol intermediates occurs before they start to build up in significant amount in the free sterol pool.