EFFECTS OF PHENOLIC INHIBITORS ON GROWTH AND METABOLISM OF GLUCOSE-UL-14C IN PAUL'S SCARLET ROSE CELL-SUSPENSION CULTURES

ABSTRACT Paul's Scarlet rose cell-suspension cultures were incubated in varying concentrations of the following phenolic inhibitors; chlorogenic acid, cinnamic acid, p-coumaric acid, ferulic acid, and scopoletin. All test compounds except chlorogenic acid were completely inhibitory at a 10⁻³m concentration, resulting in death of the cells prior to completion of the growth cycle. To assess the cellular effects of two commonly named plant inhibitors, ferulic and cinnamic acids, these compounds were provided to cultures during incubation of cells with glucose-UL-¹⁴C. Incubation of cells with glucose-UL-¹⁴C in the presence of 10⁻⁴m ferulic acid resulted in increased incorporation of ¹⁴C into the soluble lipid fraction along with decreased incorporation of ¹⁴C into protein, organic acids, and soluble amino acids. Treatment of the cells with 10⁻⁵m cinnamic acid during the incubation period resulted in a significant decrease in incorporation of ¹⁴C into protein. These alterations in the flow of carbon into cellular constituents when cells are treated with cinnamic and ferulic acids explain, at least in part, why these compounds inhibit growth, seed germination, and seedling development.     

INFLUENCE OF CERTAIN PLANT GROWTH REGULATORS AND CROWN-GALL RELATED SUBSTANCES ON BUD FORMATION AND GAMETOPHORE DEVELOPMENT OF THE MOSS PYLAISIELLA SELWYNII

Bud formation and gametophore development were studied in the moss Pylaisiella selwynii (Kindb.) Steere and Anderson grown from spores in a liquid medium consisting of inorganic salts. Indoleacetic acid and ethrel increased bud formation within a narrow concentration range. Copious bud formation was obtained with the five cytokinins tested at concentrations varying from 5 X 10⁻⁶ to 5 X 10⁻¹⁴ M. Except for about 10 % of the buds obtained with 6-γ, γ-dimethylallylaminopurine at 5 times 10⁻¹⁴ m, the cytokinin-induced buds failed to develop into normal gametophores. Octopine, lysopine, and octopinic acid, substances obtained from crown-gall tumors, increased bud formation at 10⁻³ m. On lysopine-treated plants these buds developed into typical gametophores. Gemma-like structures were obtained with octopine but no gametophores. l -arginine and l -lysine, the amino acids which respectively occur in octopine and lysopine, failed to induce gametophore formation although buds were obtained with 10⁻³ m lysine. γ-Guanidinobutyric acid induced bud formation at 10⁻³ m, but these buds developed into highly abnormal gametophores. The failure of buds obtained with many of these treatments to develop into gametophores appeared to result from the formation of new cell walls in other than the normal geometrical relationship during initial divisions of the pro-bud. The relevance of the findings to the crown-gall problem is discussed.     

Regulatory effects of exogenous branched-chain amino acids in Nicotiana plumbaginifolia cell suspension cultures

Nicotiana plumbaginifolia suspension cultured cells were grown on medium supplemented with valine, leucine and isoleucine, singly or in combination. The effects of the three branched-chain amino acids on cell growth rate and on the activity of acetohydroxyacid synthase (AHAS), the first enzyme (and the main regulative site) of their biosynthetic pathway, were studied. Results showed that valine and leucine, at concentrations ranging from 10^–4 to 10^–3 M, inhibit growth, and at higher doses (from 10^–2 to 10^–1 M) AHAS activity. Growth, but not AHAS activity, was affected also by isoleucine. The addition of ammonium succinate to the culture medium, in order to counteract a possible general inhibitory effect of these compounds on nitrogen metabolism, relieved only partially their cytotoxicity. Feeding cells with equimolar mixtures of the three amino acids resulted in a minor but reproducible decrease in AHAS level, which was proportional to the dose. A similar result was obtained also on N. plumbaginifolia seedlings, suggesting that in this species a modulation of enzyme level could play a role in controlling the flow of metabolites through the pathway.Abbreviations AHAS acetohydroxyacid synthase - BCAA branched-chain amino acids - FAD flavin adenine dinucleotide - GS glutamine synthetase - TPP thiamine pyrophosphate     

FACTORS AFFECTING THE TOXICITY OF SEVERAL LICHEN ACIDS: EFFECT OF PH AND LICHEN ACID CONCENTRATION

The effect of pH 5–8 and lichen acid concentration gradients (2.7 times 10⁻² - 2.7 times 10⁻⁶ m ) on the toxicity of the following lichen acids: usnic, lecanoric, evernic, vulpinic, stictic, fumarpro-tocetraric, psoromic, and atranorin, on spores of Funaria hygrometrica was tested. Percent germination and sporeling growth were used as indicators of toxicity. None of the lichen acids were significantly toxic, for either percent germination or sporeling growth at concentrations equal to or below 2.7 times 10⁻⁵ m at pH 7.0, but many of the lichen acids which increased in toxicity at values different from pH 7 may have been toxic at lower concentrations if a different pH was used for the assay. Lichen acid toxicity showed a good correlation with pH for the parameter of spore germination, or sporeling growth, or both. Some lichen acids did not inhibit germination but were effective in retarding sporeling growth, or vice versa. This observation is discussed in relation to changing fatty acids and other lipid composition as germination occurs. Two of the three O-methylated lichen acids (evernic and psoromic) were among the most effective in inhibiting growth over all, but at lower pH values these were less effective than non-O-methylated lichen acids. Stictic, which is also an O-methylated lichen acid, was the least effective inhibitor over all the pH values for both parameters, while vulpinic was the most toxic over all the pH values. The order of relative toxicity for the lichen acids is different, depending on the pH and concentration at which they are tested and depending on the parameter measured. Thus, in an ecological sense, it is difficult to evaluate the adaptive significance of a particular compound or group of compounds without knowing what factors influence the toxicity of those compounds and how these factors vary in the organism's habitat.     

EFFECTS OF MAPLE SYRUP URINE DISEASE METABOLITES ON MOUSE l-FIBROBLASTS IN VITRO: A FINE STRUCTURAL AND BIOCHEMICAL STUDY

—The branched-chain amino and ketoacids [i.e. l -leucine, l -isoleucine, l -valine, alpha-ketoisocaproic acid (AKICA), alpha-keto-beta-methylvaleric acid (AKBMVA) and alpha-ketoisovaleric acid (AKIVA)] were administered to mouse strain l fibroblasts in tissue culture in an attempt to study the effects of increased levels of the compounds in an in vitro system. All of these compounds are found to be elevated in the blood of patients with Maple Syrup Urine Disease (MSUD). With AKICA, l -leucine, AKIVA and AKBMVA, there was a decreased growth rate at concentrations of 10 to 30 times the levels found in Maple Syrup Urine Disease. Combined administration of the above six compounds at the maximum blood levels noted in MSUD produced a significantly decreased growth rate. Electron microscopic studies revealed numerous annulate lamellae in cells treated with AKICA and in those treated with a combination of all six MSUD compounds. AKICA-treated cells contained elevated concentrations per cell of free fatty acids, triglycerides, sterols and some classes of phospholipids. Isotope labelling experiments were performed using [U-¹⁴C] AKICA and [³H]isoleucine, which were added to l -cell suspension cultures containing various levels of unlabelled AKICA. Labelled AKICA and isoleucine were both taken up by the cells. The net uptake of isoleucine was inhibited by AKICA in concentrations found in MSUD. Folch-Lees extraction of cells treated with labelled AKICA revealed increased ¹⁴C counts only in the lower lipid phase. The growth inhibition and annulate lamellae observed with AKICA treatment may be due to an arrest of the cells in phase G₁ of the cell growth cycle, possibly due to decreased isoleucine uptake. It is proposed that a similarly-mediated arrest in the proliferation of oligodendroglial cells during the critical period of myelination gliosis might account for the myelination abnormalities reported in MSUD.     

ACTIONS OF l- AND d-HOMOCYSTEATE IN RAT CNS: A CORRELATION BETWEEN LOW-AFFINITY UPTAKE AND THE TIME COURSES OF EXCITATION BY MICROELECTROPHORETICALLY APPLIED L-GLUTAMATE ANALOGUES

Abstract— A correlation has been attempted between the uptake characteristics of l - and d -homocysteate and the time courses of neuronal excitation by these and other amino acids related to l -glutamate. The uptake of l - and d -homocysteate and of l -[³⁵S]homocysteate was studied in individual slices of rat cerebral cortex at 37°C. Tissue: medium ratios attained over l0 min for the unlabelled enantiomers at 2.5 mM were 3.7 for l -homocysteate but only 0.8 for the d -isomer. The uptake of l -[³⁵S]homocysteate over the concentration range 0.09 μm -2 mm can be attributed mainly to a low-affinity transport process with K_m approx 3 mm and V_max 1.7 μmol/g/min, but a high-affinity process of low V_max may make a minor contribution at the lower concentrations within this range. In terms of dependence on energy metabolism and [Na⁺], and on inhibition by p-chloromercuriphenylsulphonate, ouabain and structural analogues of the amino acid, the main uptake system for L-[³⁵S]homocysteate appears to be similar to that mediating low-affinity uptake of l -glutamate and other acidic amino acids. d -Homocysteate was but a weak inhibitor of this uptake system compared with other structural analogues. The time courses of excitation by 6 amino acids were determined by microelectrophoretic application to rat spinal neurones. d -Homocysteate induced responses with recovery times considerably longer than those of the other amino acids; this correlates with the absence of rapid uptake systems demonstrated for this amino acid in cortical tissue. d -Glutamate and l -homocysteate, which are only accumulated by low-affinity transport mechanisms, induced responses with recovery periods similar to those of l -glutamate, l -aspartate and d -aspartate, which are accumulated by both high- and low-affinity uptake systems. Although contributions of other factors to the observed time courses, such as rates of association and dissociation of the amino acid-receptor complexes, cannot be excluded, the present results are consistent with the hypothesis that low-affinity uptake systems of high V_max play an important role in the rapid termination of the effects of amino acid excitants.     

THE INFLUENCE OF PHOTOPERIOD AND EXOGENOUS NITROGEN-CONTAINING COMPOUNDS ON THE REPRODUCTIVE CYCLES OF THE LIVERWORT CEPHALOZIA MEDIA

The effects of photoperiod and a number of metabolites (inorganic nitrogenous compounds, amino acids, and growth substances) on reproductive differentiation in the leafy liverwort Cephalozia media Lindb. were studied under axenic conditions. The increase or decrease in the number of branches bearing localized reproductive structures was used to determine the influence of the experimental variables on the regulation of both asexual and sexual phases of reproductivity (production of gemmae and gametangia). Within the context of photoperiodic control, the magnitude of the normal reproductive response was significantly stimulated or inhibited by low concentrations of certain amino acids or kinetin. Certain metabolites (10^-6M concentrations of arginine, cysteine, tryptophan plus kinetin) were able to overcome photoperiodic control of the reproductive response. Generally, organic compounds which stimulated asexual reproductivity under short photoperiod inhibited sexual reproductivity under long photoperiod. Exogenous inorganic nitrogen did not significantly affect the asexual or sexual reproductive response.     

SYNTHETIC AMINO ACIDS AND THE NATURE OF l-DOPA TRANSPORT AT THE BLOOD-BRAIN BARRIER

—The blood-brain barrier transport of amino acids has been measured using the carotid injection technique in the rat. The synthetic amino acids, 2-aminobicyclo(2,2,1)heptane-2-carboxylic acid (BCH) and α-(methylamino)isobutyric acid (MeAIB), were model substrates in the Ehrlich cell for the leucine (L) and alanine (A) neutral amino acid transport mechanisms, respectively. The uptake (±)b-[carboxyl-¹⁴C]BCH at the same rate for the five brain regions tested suggested a similarity between regions for the L transport mechanism. At injectant concentrations of 0·1 mm (similar to naturally occurring aromatic neutral amino acids), BCH was mainly taken up by a saturable mediated transport mechanism (K₁, 0·16 mm and V_max, 0·03/μmol/g per min). At higher concentrations, uptake by a nonsaturable or diffusional mechanism could be demonstrated. When BCH was added as a second amino acid to l -[3-¹⁴C]DOPA, the saturable component of l -DOPA transport was significantly inhibited. MeAIB had no measurable effect on the rate of l -DOPA transport. These results suggested that the mediated transport mechanism for l -DOPA at the cerebral capillaries is similar to the l -neutral amino acid transport system.     

NUTRITIONAL REQUIREMENTS OF THE CHYTRID KARLINGIA ASTEROCYSTA,AN OBLIGATE CHITINOPHILE

The nonfilamentous chytrid, Karlingia asterocysta, has been isolated in pure culture on chitin media and the nutritional requirements of a single-spore clone investigated. The fungus displayed an absolute requirement for chitin or preformed N-acetyl-d -glucosamine. This requirement could only be relieved partially by glucose in the presence of limiting acetyl glucosamine concentrations. Under similar conditions other carbohydrates were not utilized. Sulfate was used as a sulfur source and either nitrate or ammonium ion served as nitrogen sources, though growth was better with amino acids. The organism had a very low phosphate optimum (5 × 10^–5 m ) and was inhibited by concentrations at or above 1 × 10^–3 m . The optimal pH range extended from 6.0 to 7.5 and growth decreased rapidly at higher or lower pH values. Thiamine was required at a very low concentration; only 2 μg thiamine-HCl/liter were required for optimal growth. In a rich, agitated medium K. asterocysta completed a single growth cycle (i.e., plant generation) in 70 hr at 25 C.     

EFFECT OF UNDERNUTRITION ON AMINO ACID COMPARTMENTATION IN THE DEVELOPING RAT BRAIN

—Rat pups undernourished through 21 days of age show abnormal patterns of cerebral amino acid metabolism. The pattern of incorporation of radioactivity from l -[U-¹⁴C]leucine into amino acids derived from tricarboxylic acid cycle intermediates was altered, with significantly more ¹⁴C being incorporated into glutamate and aspartate in the underfed rats than in controls. Glutamate compartmentation, manifested in the ratio of specific radioactivities of glutamine to glutamate, developed more slowly in the. diet-restricted group. These results are similar to those seen in neonatally-thyroidectomized rats and suggest decreased growth of neuronal processes. This impairment of amino acid metabolism returns to normal after a 7-week period of adequate nutrition.     

Amino acid requirements for growth of the rabbit blastocyst in vitro

Ten amino acids, namely, arginine, histidine, lysine, tryptophane, methionine, phenylalanine, leucine, valine, threonine and serine were indispensable for growth of rabbit blastocysts in vitro; others were nonessential. Of all the essential amino acids, arginine and lysine were required in relatively high concentrations, 10^?2 M and 10^?3 M, respectively, for optimum growth. Complete omission of the non-essential amino acids from the medium markedly reduced blastocyst growth. Interaction between serine and glycine demonstrated a partial sparing action on serine by glycine, similar to that observed between methionine and cysteine. The amino acid composition of a culture medium capable of providing continuous and consistent growth of rabbit blastocysts in vitro is described.     

Properties of RNA fractions from nuclei of brain cells which stimulate incorporation of amino acids by brain ribosomes

Abstract— The properties of RNA fractions from nuclei of brain cells which were capable of stimulating amino acid incorporation into proteins of an homologous ribosomal system were investigated. RNA was routinely prepared from crude nuclear preparations of rat brain by a method which involved treatment with sodium dodecyl sulphate and phenol at 65°. The capacity of this preparation to stimulate incorporation of radioactivity from a mixture of 15 l -[¹⁴C]amino acids was greatly enhanced by preliminary incubation of the ribosomal system from brain for 5–20 min. The response was markedly dependent upon the concentrations of ribosomes and of the pH 5 fraction. The optimal level of Mg²⁺ for basal incorporation of amino acids into protein was 8 mm ; however, incorporation in the presence of nuclear RNA was greater at higher concentrations of Mg²⁺. The response to nuclear RNA was also enhanced as the K⁺ concentration was increased from 25 to 100 mm . The stimulatory effect of nuclear RNA on incorporation of l -[¹²C]eucine was either unaltered or depressed by addition of a mixture of 19 l -[¹²C]amino acids each at concentrations, of 10^?8, 10^?2, or 10^?1 mm . Under appropriate conditions of incubation, basal rates of incorporation and rates of incorporation stimulated by nuclear RNA were linear for 30 min. The response was proportional to the concentration of nuclear RNA between 34 and 136 μg. RNA prepared from ribosomes of rat brain essentially failed to stimulate incorporation of amino acids over this range of concentrations. Fractionation of nuclear RNA by centrifugation in sucrose density gradients revealed that 75 per cent of the stimulatory activity was in the fraction which sedimented below 12 S and contained about 25 per cent of the total RNA. Most of the remaining activity was in the 18 S region. Less than 5 per cent of the RNA in the lightest fraction (< 12 S) exhibited amino acid-acceptor activity, The stimulatory action of nuclear RNA on incorporation of amino acids was readily destroyed by mild treatment with pancreatic ribonuclease, whereas amino acid-acceptor activity was relatively resistant to this treatment. The results suggest that the brain may contain low molecular weight RNA with properties of messenger RNA.     

ENVIRONMENTAL AND HORMONAL CONTROL OF TURION GERMINATION IN MYRIOPHYLLUM VERTICILLATUM

Germination, or outgrowth, of Myriophyllum verticillatum turions involves a series of visible changes starting with reflexing of leaves followed by extension and curving of the axis, and then by root formation. Before abscission, turions grow out in response to long days (16 hr) but not short days (8 hr). After abscission, turions show maximal dormancy which can be fully broken by a cold treatment (4 C). Turions are heterogeneous in degree of dormancy and ability to respond to less complete dormancy-breaking treatments, e.g., long days at 20 C. Cytokinins (10^-6 m) break dormancy of non-cold-treated turions, whereas gibberellic acid (GA₃) is ineffective except at high concentrations (10^-3 m). Continuous treatment with cytokinins causes abnormal development after germination. GA₃, on the other hand, induces apparently normal development even at high concentration. Indoleacetic acid (IAA) induces outgrowth only at high concentrations (10^-3 - 10^-4 m), but these concentrations also produce abnormal development. Abscisic acid (ABA, 10^-5 m) retards outgrowth of cold-treated turions and can completely suppress it in non-cold-treated turions. The activity of ABA-like substances in turions remains about the same before and during germination, whereas other (unidentified) acidic inhibitors decrease markedly. The cytokinin activity changes in a complex pattern.     

PROPERTIES OF TYROSINE HYDROXYLASE IN PERIPHERAL NERVES

Approximately 80 per cent of tyrosine hydroxylase activity in bovine mandibular nerve and rabbit sciatic nerve was soluble, and the rest of the activity was particle-bound. The soluble enzyme in bovine mandibular nerve was isolated by ammonium sulphate fractionation (25–35 per cent saturation). The enzyme had a pH optimum at 5·9 in Tris-acetate buffer, and at 6·5 in Tris-HCl or phosphate buffer. The enzyme required a tetrahydropteridine cofactor. K_m values toward various tetrahydropteridines such as l -erythro-tetrahydrobiopterin (a probable natural cofactor), 2-amino-4-hydroxy-6-methyltetrahydropteridine, and 2-amino-4-hydroxy-6,7-dimethyltetrahydropteridine were 2 × 10⁻⁵m , 5 × 10⁻⁵m and 4 × 10⁻⁴m , respectively. The K_m value for tyrosine at 1 × 10⁻³m -2-amino-4-hydroxy-6-methyltetrahydropteridine as a cofactor was 5 × 10⁻⁵m . The enzyme activity was markedly stimulated with Fe²⁺ or catalase, but Fe²⁺ gave higher activity. The activity was inhibited with α, α′-dipyridyl, l -α-methyl-p-tyrosine, and various catecholamines. Among catecholamines, dopamine was the most potent inhibitor. l -5-Hydroxytryptophan was an inhibitor as potent as dopamine. Neither d -5-hydroxytryptophan nor 5-hydroxytryptamine inhibited the enzyme. The inhibition by l -5-hydroxytryptophan was partially competitive with tetrahydrobiopterin at concentrations higher than 9 × 10⁻⁵m , and partially uncompetitive at concentrations lower than 9 × 10⁻⁵m . The addition of heparin or lysolecithin did not affect enzyme activity with tetrahydrobiopterin as cofactor.     

THE EFFECT OF l-DOPA AND AN INHIBITOR OF PERIPHERAL DECARBOXYLATION ON GLUCOSE METABOLISM IN BRAIN1

Abstract– The effect of the administration of l -DOPA plus an inhibitor of peripheral l -aromatic amino acid decarboxylase (aromatic-l -amino-acid carboxy-lyase; EC 4.1.1.28) on the metabolism of glucose in brain was studied by administering [U-^I4C]glucose (20μCi) to three groups of rats: (1) rats that had been injected with l -DOPA (200mg/kg) 28min earlier; (2) rats that had been similarly injected with l -DOPA and also with N-(d,l -seryl)-N′-(2,3,4-trihydroxybenzyl)hydrazine (50 mg/kg), an inhibitor of l -aromatic amino acid decarboxylase, 30min before the l -DOPA; and (3) appropriate controls. The flux of ¹⁴C from glucose in plasma to those amino acids that are in equilibrium with the tricarboxylic acid cycle intermediates was reduced by treatment with l -DOPA and reduced further by treatment with l -DOPA and the decarboxylase inhibitor. Concentrations of glucose in brain and in plasma were increased after treatment with l -DOPA; these increases were attenuated if the inhibitor was given before the l -DOPA. After treatment with l -DOPA, there were decreases in the concentration of aspartate, tryptophan, and tyrosine in brain. After the administration of l -DOPA and the decarboxylase inhibitor, the concentrations in brain of alanine, glutamate, tyrosine, and phenylalanine were greater, and the concentrations of aspartate, leucine, lysine, histidine, arginine, and tryptophan were less than in control rats.     

THE FREE AMINO ACIDS OF HUMAN SPINAL FLUID DETERMINED BY ION EXCHANGE CHROMATOGRAPHY

(1) The free amino acids in human CSF from eighteen subjects have been determined. The analyses were performed on 0-75 ml of CSF by an ion exchange chromatographic method which is capable of detection to the 10^?10 mole level. (2) The amino acids always found in readily detectable amounts were: taurine, threonine, serine, glutamine, glutamic acid, citrulline, glycine, alanine, α-NH₂-n- butyric acid, valine, methionine, isoleucine, leucine, tyrosine, phenylalanine, ethanolamine, ornithine, lysine, histidine and arginine. Urea was present. Aspartic acid and cystine, though always present, occurred in small or trace amounts. Proline was found in four cases and tryptophan in thirteen cases. In addition, twelve unknown peaks were nearly always evident in every chromatogram. (3) Filtrates 10 times more concentrated than those used regularly were prepared from pooled CSF and analysed. These analyses clearly confirmed the presence of those amino acids which were normally in very low concentration and they also served to distinguish the twelve unknown compounds from confusion with baseline artifacts. (4) The distribution of free amino acids in CSF was different from their distribution in blood plasma. (5) Despite a variety of neurological conditions and a wide age span few marked deviations were found in any of the amino acid concentrations.     

DCMU INDUCED INHIBITION OF GROWTH,PHOTOSYNTHESIS AND MOTILITY IN EUDORINA ELEGANS CULTURES

Studies with Eudorina elegans L. were done to provide additional information on the effect of phenyl urea herbicides on phytoplankton. Colonies were grown in various concentrations of DCMU, 3(3,4-dichlorophenyl)-1,1-dimethylurea. DCMU at 10^-5 m induced an algicidic response. DCMU at 10^-7 M and 10^-9 M caused a significant reduction in the growth of colonies. Photosynthesis was significantly inhibited at all concentrations of DCMU. A rapidly growing population of algae treated with 10^-7 m and 10^-9 m DCMU showed a reduced motile/non-motile balance of colonies.     

Seasonal changes in the free amino acids of oat and barley phloem sap in relation to plant growth stage and growth of Rhopalosiphum padi

The concentrations and composition of free amino acids in phloem sap from two cultivars of oats and barley, both susceptible to the aphid Rhopalosiphum padi, were determined by means of high performance liquid chromatography. Sap was collected from excised aphid stylets at three developmental stages (seedlings, tillering plants and plants undergoing stem elongation) from plants given or not given fertiliser and grown outdoors. In connection, the growth of individual R. padi nymphs was estimated at the same phenological stages on plants grown in the greenhouse. The content of free amino acids was consistently higher in seedlings than in plants at the early tillering stage. Only in seedlings did the addition of fertiliser increase amino acid levels. Barley phloem sap contained more free amino acids than that of oats when fertiliser was added and at later developmental stages. Phloem sap of oats and barley showed similar patterns in their composition of free amino acids at the seedling stage, but as the plants grew older the patterns became increasingly different. Plants given fertiliser had higher amounts of dicarboxylic amino acids (glutamic and aspartic acid) than unfertilised plants. The concentrations of γ-amino butyric acid, glycine, histidine, and methionine were very low in all treatments. The relative growth rates of R. padi nymphs were low when amino acid content was low and vice versa. The results are discussed in relation to host plant suitability and plant resistance mechanisms.     

Characteristics of the active transport of peptides and amino acids by germinating barley embryos

Use of two different assays involving either radioactively labelled substrates or a fluorescent-labelling procedure, gave good agreement for the rates of transport of peptides and amino acids into the scutellum of germinating grains of barley (Hordeum vulgare cv. Maris Otter, Winter). However, evidence was obtained for the enzymic decarboxylation of transpored substrate, which can cause underestimates of transport rates when using radioactively labelled substrates. The peptide Gly-Phe, was shown to be rapidly hydrolysed after uptake, and autoradiography of transported Gly-[U-¹⁴C]Phe indicated a rapid distribution of tracer, i.e. [U-¹⁴C] phenylalanine into the epithelium and sub-epithelial layers of the scutellum. The developmental patterns of transport activity indicate that peptide transport is more important nutritionally during the early stages of germination (1–3 d) whereas amino acids become relatively more important later (4–6 d). A range of amino acids is shown to be actively transported and several compete for uptake. At physiological concentrations, e.g. 2mM, transport of peptides and amino acids is inhibited about 80% by protonophore uncouplers, but at higher concentrations (10–100 mM) passive uptake predominates.Abbreviations Gly glycine - Leu leucine - Phe phenylalanine - Pro proline     

Accumulation of free amino acids and humic substances in a freshwater modular system and their ecological significance

1. Methods for measuring concentrations of total and individual free amino acids (TFAA, FAA), other amino compounds and humic substances (HS) in media containing the following three treatments and the control are described: (i) the non-axenic aquatic macrophyte Ceratophyllum demersum alone; (ii) the pulmonate snail, Biomphalaria glabrata alone; (iii) the snail, plant and the epiphytic bacteria and algae together as a four-component modular system; (iv) control without organisms. 2. TFAA accumulated to give asymptotic values of 2.5 μm , 10 μm and 15 μm in treatments (i), (ii) and (iii), respectively, by the end of the 30-day incubation period. The mass-specific accumulation rate in the treatment with the snail alone [89.4 nmol g^–1 (wet weight minus shell) day^–1] was approximately ten times that with the plant alone [8.4 nmol g^–1 (wet mass) day^–1]. No FAA or HS could be detected at any time in (iv). 3. On the second day of incubation the concentrations of TFAA and of some individual amino acids were significantly higher in the treatment containing the snail and plant together than the sum of the concentrations in the treatments with the plant and snail alone, presumably due to an increase in the snails’ metabolic rate and ‘sloppy feeding’. 4. The differences in the relative abundance of amino compounds accumulating in media conditioned by snails alone (e.g. much larger proportions of ammonia, ethanolamine and phosphoserine than in plant-conditioned media) and plants alone (e.g. larger proportions of asparagine and glutamine than in snail-conditioned media) suggest that snails and plants may derive mutual benefits by exchanging amino compounds. 5. The accumulation patterns of the more recalcitrant HS differ from those of the amino acids in two respects. First, the HS concentrations continued to increase throughout the 30-day incubation period in all three treatments. Second, most of the HS in the module originates from the plant as both the concentrations and mass-specific accumulation rates were significantly higher in the treatment with the plant alone [2.6 mg l^–1, 9.09 μg g^–1 (wet mass) day^–1, respectively] than in the treatment with the snail alone [0.75 mg l^–1 and 7.7 μg g^–1 (wet mass) day^–1, respectively]. 6. The possible reasons for the differences in the accumulation patterns of FAA and HS in the three treatments are discussed. Evidence is also given in support of the testable hypothesis that the four components of the module derive several mutual benefits, including those arising from the release of dissolved organic matter, such as FAA and HS, by living organisms.