Retroelements in higher plants.

Representatives of several classes of retroelements have been characterized in a broad range of plant species, where they appear at variable and sometimes very high copy numbers. So far, only a very small number of plant elements have been shown to be active, and this activity seems to be restricted to specific situations of 'genomic shock'. Although it is not yet known whether the presence of retroelements is linked to the high level of variability found in plant genomes, it is now clear that retrotransposons are ancient and ubiquitous components of plant genomes, and could play an important role in plant evolution.     

Cytokinin effect on protein synthesis in vivo in higher plants

The influence of naphthalene-1-acetic acid and kinetin on protein synthesis in vivo was investigated by measuring the incorporation of radioactive amino acids into polypeptides of synthesizing polysomes. The second subculture of sterile pith tissue of Nicotiana tabacum L. cv. Wisconsin 38 grown on a medium containing only a minimum of growth substances was further starved in a small volume of medium lacking auxin and cytokinin for 12 h. An incubation period of 4 h with [¹⁴C]amino acids followed. The last 30 min of those incubations were carried out in the presence of actinomycin D and the last 20 min were performed under different conditions: a) without any growth substances, b) with naphthalene-l-acetic acid, c) with kinetin. By measuring the differences of the specific radioactivities of the polysomes the following results were revealed: 1) Kinetin increases the protein synthesis by an average of 35%-2) Auxin has no effect on protein synthesis.Abbreviations Act. D actinomycin D - NAA naphthalene-1-acetic acid Part of a Diplomarbeit, University of Bonn 1976     

Somatic hybridization in higher plants.

Somatic hybridization in higher plants has come into focus since methods have been established for protoplast fusion and uptake of foreign DNA and organelles by protoplasts. Polyethylene glycol (PEG) was an effective agent for inducing fusion. Treatment of protoplasts with PEG resulted in 5 to 30% heterospecific fusion products. Protoplasts of different species, genera and even families were compatible when fused. A number of protoplast combinations (soybean + corn, soybean + pea, soybean + tobacco, carrot + barley, etc.) provided fusion products which underwent cell division and callus formation. Fusion products initially were heterokaryocytes. In dividing heterokaryocytes, random distribution of mitotic nuclei was observed to be accompanied by multiple wall formation and to result in chimeral callus. Juxtaposition of mitotic nuclei suggested nuclear fusion and hybrid formation. Fusion of heterospecific interphase nuclei was demonstrated in soybean + pea and carrot + barley heterokaryons. Provided parental protoplasts carry suitable markers, the fusion products can be recognized. For the isolation and cloning of hybrid cells, fusion experiments must be supplemented with a selective system. Complementation of two non-allelic genes that prevent or inhibit growth under special culture conditions appears as the principle on which to base the selection of somatic hybrids. As protoplasts of some species have been induced to regenerate entire plants, the development of hybrid plants from protoplast fusion products is feasible and has already been demonstrated for tobacco.     

Chloroplast promoters from higher plants.

This survey compiles 60 chloroplast promoter sequences from higher plants published to date and compares them with these sequences from procaryotic systems. The current evidence demonstrates that structurally defined chloroplast promoters are, in most cases, functionally active in initiating gene expression in chloroplasts.     

Sugar sensing in higher plants.

Sugar repression of photosynthetic genes is likely a central control mechanism mediating energy homeostasis in a wide range of algae and higher plants. It overrides light activation and is coupled to developmental and environmental regulations. How sugar signals are sensed and transduced to the nucleus remains unclear. To elucidate sugar-sensing mechanisms, we monitored the effects of a variety of sugars, glucose analogs, and metabolic intermediates on photosynthetic fusion genes in a sensitive and versatile maize protoplast transient expression system. The results show that sugars that are the substrates of hexokinase (HK) cause repression at a low concentration (1 to 10 mM), indicating a low degree of specificity and the irrelevance of osmotic change. Studies with various glucose analogs suggest that glucose transport across the plasma membrane is necessary but not sufficient to trigger repression, whereas subsequent phosphorylation by HK may be required. The effectiveness of 2-deoxyglucose, a nonmetabolizable glucose analog, and the ineffectiveness of various metabolic intermediates in eliciting repression eliminate the involvement of glycolysis and other metabolic pathways. Replenishing intracellular phosphate and ATP diminished by hexoses does not overcome repression. Because mannoheptulose, a specific HK inhibitor, blocks the severe repression triggered by 2-deoxyglucose and yet the phosphorylated products per se do not act as repression signals, we propose that HK may have dual functions and may act as a key sensor and signal transmitter of sugar repression in higher plants.     

Clinorotation effect on thermodynamic efficiency of energy transformation in chloroplasts of higher plants

The aim of the work was to estimate the effect of clinorotation on thermodynamic coupling and efficiency of the process of photosynthetic energy transformation in chloroplasts using nonequilibrium thermodynamics approach. These parameters were calculated from experimentally determined net photosynthetic oxygen evolution at static head [(Je)sh], uncoupled rate of the oxygen evolution (Jo)unc and net rate of ATP production. It was found that in chloroplasts isolated from control and clinorotated pea plants coefficient of thermodynamic coupling of photophosphorylation (q) was 0.94 and 0.91 respectively. Optimal thermodynamic efficiency (eta opt) of the systems were calculated as 0.64 and 0.6 for control and clinorotation plants. Thus the data of the work show that thermodynamic efficiency of light energy transformation in higher plants is under influence of imitated weightlessness conditions.     

The effect of some oligo-amines and -guanidines on membrane permeability in higher plants

The effect of a series of oligo-amines and -guanidines on the membranes of higher plants has been tested by measuring the efflux of betacyanin from beet root discs, and the loss of total ions from beet root and swede discs, beet and spinach leaf discs and apple cells in suspension culture. All of the naturally occurring di- and polyamines tested showed relatively little toxicity. Betacyanin efflux from beet root discs was reduced by diamines [NH₂(CH₂)_xNH₂] up to x = 10 or less. Ion efflux was minimal at x = 7. Within the triamine series [NH₂(CH₂)_xNH(CH₂)₃NH₂] for x = 8 or less, betacyanin efflux was reduced or unaffected, although total ion loss was increased by the triamines when x = 4 or more and especially by the longer chain amines (to x = 10). Similar behaviour was found in the tetra-amine series [NH₂(CH₂)₃NH(CH₂)_xNH(CH₂)₃NH₂] with betacyanin efflux reduced for x = 2–4 (spermine). Although spermine potentiated the toxicity effects of Guazatine {[NH₂C(NH)NH(CH₂)₈]₂NH} and Dodine [NH₂C(NH)NH(CH₂)₁₁,Me] in beet root discs, spermine and calcium ions reduced the ion efflux caused by these toxic guanidines and also by Synthalin B [NH₂C(NH)NH(CH₂)₁₂NHC(NH)NH₂] in swede discs, spinach leaves and apple cells. No significant reversal of ion loss was detected with putrescine, cadaverine or spermidine in swede discs. In the homologous series of monoguanidines [NH₂C(NH)NH(CH₂)_x?1Me] for x up to 18, greatest toxicity was shown for x = 10 and 11 in both betacyanin loss and total ion efflux in beet root discs. Greatest ion efflux from the apple cell suspension was found with x = 11 and 12. In the homologous series of diguanidines [NH₂C(NH)NH(CH₂),NHC(NH)NH₂] for x = 2–12 greatest toxicity was shown for x = 12 (the longest chain tested) in beet root and in the efflux of ions from apple cell suspension. Technical Guazatine was considerably more phytotoxic than pure Guazatine in all systems tested. p-Chloromercuribenzoate (p-CMB) potentiates the loss of betacyanin and total ions caused by Guazatine, Synthalin B, and Dodine in beet root discs. This effect of p-CMB is reversed by subsequent incubation in cysteine or mercaptoethanol, prior to treatment with the guanidines.     

Antimutagenicity of secondary metabolites from higher plants.

Higher plants contain both mutagens and antimutagens and are susceptible to mutagenesis but screening programs for detection of antimutagenesis rarely employ higher plant systems. Short-term bacterial and mammalian tissue culture systems are the norm. Using modified screening tests for detecting antimutagenic agents, higher plants have been shown to contain a variety of structurally novel antimutagenic agents. Systematic bioassay-directed methodology resulted in the isolation in pure form and biological and chemical characterization of the responsible individual active components from various plants. The methodology in use is illustrated by the isolation of cinnamic acid, cinnamyl cinnamate and cinnamyl ricinoleate as the active constituents of the classic medicinal plant product, Styrax asiatica. The methods which may be used to reveal structure-activity relationships and to explore putative molecular modes of action are illustrated with excerpts from the same study.     

The thioredoxin h system of higher plants.

In plants, thioredoxins h are encoded by a multigenic family of genes (eight in Arabidopsis thaliana, at least five in Populus sp.). The multiplicity of these isoforms raises the question of their specificity. This review focuses on thioredoxins h in two plant models: Arabidopsis and poplar. Thioredoxins h can be divided into three different subgroups according to the analysis of their primary structure. This paper describes the biochemical properties of each subgroup. Recent data in the field indicate that subgroup members differ by their subcellular localization as well as their reduction pathways suggesting specific functions for each subgroup. The development of proteomic tools has also increased considerably the number of potential thioredoxin targets, showing the importance of thioredoxins h in plants.