Biosynthesis of cyanogenic glucosides in butterflies and moths: Effective incorporation of 2-methylpropanenitrile and 2-methylbutanenitrile into linamarin and lotaustralin by Zygaena and Heliconius species (Lepidoptera)

¹⁴C-labelled 2-methylpropanenitrile and 2-methylbutanenitrile were administered to larvae and imagines of Heliconius melpomone and to larvae of Zygaena trifolii and the incorporation into the cyanogenic glucosides, linamarin and lotaustralin, was measured. Both species incorporated the precursors at all stages tested, at a high level of 15–72%, thereby indicating that the nitriles are probale intermediates in the lepidopteran biosynthesis of linamarin and lotaustralin from valine and isoleucine respectively.     

Origin of Cyanide in Cultures of a Psychrophilic Basidiomycete

An unidentified psychrophilic basidiomycete used valine and isoleucine as precursors to hydrocyanic acid (HCN). As probable intermediates in the pathway from valine and isoleucine two cyanogenic glucosides, linamarin and lotaustralin, were demonstrated in fungus cultures. The fungus contained two beta-glucosidases and an oxynitrilase which, acting together, were capable of releasing cyanide from both linamarin and lotaustralin. The two beta-glucosidases were purified and compared as to pH optimum, Michaelis constant, energy of activation, thermal stability, and substrate specificity. The products of methyl ethyl ketone cyanohydrin and acetone cyanohydrin dissociation by the oxynitrilase were demonstrated to be HCN together with methyl ethyl ketone and acetone, respectively. The oxynitrilase attacked aliphatic hydroxynitriles, but showed no activity on aromatic hydroxynitriles.     

Co-occurrence of Valine/Isoleucine-derived and cyclopentenoid cyanogens in a Passiflora species

The valine/isoleucine-derived cyanogenic glycosides linamarin and lotaustralin have been isolated together with the cyclopentenoid cyanogen passibiflorin from Passiflora lutea. This is only the second report of the production of cyanogenic glycosides from more than one biosynthetic pathway in individuals of a single species.     

The biosynthesis of cyanogenic glucosides in Linum usitatissimum (linen flax) in Vitro

Microsomal preparations from dark-grown Linum usitatissimum (linen flax) seedlings synthesize acetone cyanohydrin, the precursor of the cyanogenic glucoside linamarin, from valine in the presence of NADPH. N-Hydroxyvaline and isobutyraldoxime, which are predicted intermediates in the pathway, are also converted into products. These microsomal preparations also convert isoleucine into 2-butanone cyanohydrin the precursor of lotaustralin. The biosynthetic activity is located exclusively in the developing cotyledons.     

Photosynthetic and Dark Fixation of 14CO2 in Detached Soybean Cotyledons

Detached soybean cotyledons fixed CO₂ both in the light and dark. Carbon dioxide fixed by the light and dark reactions replaced only a small portion of CO₂ lost by respiration up to the 10th day. In the dark most of the ¹⁴C label was found in the acidic fraction, while in the light 65 per cent of the activity was found in the neutral and basic fractions.     

Properties of a microsomal enzyme system from Linum usitatissimum (linen flax) which oxidizes valine to acetone cyanohydrin and isoleucine to 2-methylbutanone cyanohydrin

Microsomal preparations from flax seedlings have recently been shown to convert L-valine to acetone cyanohydrin, the precursor of the cyanogenic glucoside linamarin [A. J. Cutler and E. E. Conn (1981) Arch. Biochem. Biophys. 212, 468-474]. Further details of this four-step biosynthetic sequence and also details of the analogous reactions in lotaustralin biosynthesis have been obtained. The lotaustralin precursor, 2-methylbutyraldoxime, is the best substrate for cyanide production (Vmax = 413 nmol h-1 g fresh wt-1) and inhibits the conversion of valine and isoleucine into products. Similarly, the linamarin precursor isobutyraldoxime is an excellent substrate (Vmax = 400 nmol h-1 g fresh wt-1) and also inhibits oxidation of the amino acids. The substrate specificity of the oxime-metabolizing step is low and a variety of aliphatic oximes are converted to cyanide. On the other hand, the activity of the microsomal extract is highly selective with regard to the amino acid substrate since, of the aliphatic amino acids tested, only valine and isoleucine are metabolized. We were unable to demonstrate product formation from isobutyronitrile (a linamarin precursor) but did observe detectable cyanide formation from 2-methylcyanobutane, the corresponding precursor of lotaustralin. Competition experiments showed that the biosynthesis of linamarin and lotaustralin is not likely to be catalyzed by separate enzyme systems.     

Comparative Basipetal Transport of 6-Benzylaminopurine-8-14C, Gibberellin A3-3H, IAA-2-14C, and Sucrose-14C in the Root of Intact Citrus aurantium Seedlings

The transport and distribution of IAA-2-¹⁴C, gibberellin A₃-³H, 6-benzylaminopurine-8-¹⁴C and sucrose-¹⁴C (U) were studied in whole seedlings of Citrus aurantium L. after “replacing” the root tip with the solution of radiochemicals. All four substances were transported basipetally in the root and were distributed to the stem and leaves. The pattern of distribution of the label from 6-benzylaminopurine was similar to that of sucrose, while a considerably larger amount of gibberellin A₃ was transported to basal regions of the root, away from the tip, and into the shoot. Contrary to these three substances, the basipetal transport of IAA in the root was very low, and the majority of the label was retained in the terminal sections of the root. It is suggested that the different efficiencies at which various hormones move in the transpiration stream in the root may be an important factor in the attainment of a certain balance of hormones in the shoot.     

Chlorophyll turnover in etiolated greening barley transferred to darkness: Isotopic (1-14C glutamic acid) evidence of dark chlorophyll synthesis in the absence of chlorophyll accumulation

Synthesis of chlorophyll was initiated in 5- to 6-day-old dark-grown barley (Hordeum vulgare L. cv. Clipper)seedlings by exposing them to light in the presence of 1-¹⁴ C glutamic acid supplied via the roots.The plants were then returned to darkness. At the end of light treatment (_T) and after 7 or 18 h dark treatment chlorophylls a and b were extracted, quantified (μgleaf¹). purified by HPLC to their magnesium-free derivatives (pheophytin a and b) and their molar radioactivities determined. After 2 h exposure to light followed by 6 h illumination in the presence of 1-¹⁴ C glutamic acid, seedlings had accumulated 4-7 nmol chlorophyll leaf¹ and had incorporated between 900-1 350 Bq (g fresh weight)¹ of radioactive label into the chlorophyll pool. When seedlings were transferred to darkness, label continued to be incorporated and after 18 h the radioactivity of the chlorophyll pool had increased by 300-700 Bq (g fresh weight)¹. Net chlorophyll content, however, remained constant during dark treatment. The increase in radioactivity of the chlorophyll pool in darkness represented the difference between a net increase of label incorporated into chlorophyll a and a small loss of label from chlorophyll b. The absence of measurable radioactivity in the phytol moiety of labelled chlorophyll a, extracted at the endof dark treatment, demonstrated thatincorporation of label was into the tetrapyrrole moiely of chlorophyll and not into the phytol chain. Light-independent incorporation of 1-¹⁴ C glutamic acid into chlorophyll of greening barley seedlings transferred to darkness indicates that chlorophyll synthesis continues when light is withheld. We interpret the net gain in radioactivity of chlorophyll in darkness, in the absence of a net gain in chlorophyll content, to chlorophyll turnover i.e. to simultaneous synthesis and breakdown of chlorophyll when etiolated greening barley seedlings are transferred to darkness.     

14C-Studies on Apple Trees. II. Distribution of Photosynthates from Top and Base Leaves from Extension Shoots

The photosynthates from leaves from extension shoots may be used either for new growth of the shoot itself, or for growth in other parts of the tree. An attempt has been made to elucidate this problem by determining the content of ¹⁴C in long shoots to which ¹⁴CO₂ was applied either through fully developed leaves at the base, or through very young leaves at the apex. In the case of ¹⁴C application at the base, 80 per cent or more of the ¹⁴C initially taken up disappears from the shoot, and only a very minor part is translocated upwards in the shoot. When the leaves at the apex are exposed, on the other hand, 80 per cent of the ¹⁴C absorbed is retained in the leaves and shoot components treated as long as there is still considerable terminal growth taking place, although a small percentage is deposited in the lower parts of the shoot. At the same time, a much higher proportion is incorporated into methanol-insoluble components. As terminal growth decreases, a larger proportion of the ¹⁴C activity of the apex leaves also disappears from the shoot. The distribution of activity between the sorbitol, sucrose, glucose and fructose fractions was not significantly different in young and in fully developed leaves. The ¹⁴C labelling in the sugar fraction was highest for sorbitol, then sucrose, but decreases with time compared to glucose and fructose.     

Effect of Abscisic Acid on the Activities of Photosynthetic Enzymes and 14CO2 Fixation Products in Leaves of Pennisetum typhoides Seedlings

Abscisic acid inhibited the rate of ¹⁴CO₂ fixation in leaves of Pennisetum typhoides (Burm. f.) Stapf & Hubbard seedlings, but increased the activities of phosphoenol-pyruvate-carboxylase and malic enzyme. The leaves of the seedlings grown in the presence of abscisic acid incorporated, in comparison to the control, more radioactivity in the fraction of organic acids, but less radioactivity was recorded in the amino acid fraction. On the other hand, gibberellic acid which also inhibits photosynthetic ¹⁴CO₂ assimilation and decreases the activities of photosynthetic enzymes, favours greater incorporation in alanine, and reduces that in malate. It is deduced that bio-regulants can greatly influence the flow of ¹⁴C into individual photosynthetic products. As in growth, abscisic and gibberellic acids in combination tended to antagonize each other in their effects on enzyme activity as well as in incorporation of ¹⁴CO₂ into photosynthetic products.     

Labelling of lupine nodule metabolites with 14CO2 assimilated from the leaves

On feeding ¹⁴CO₂ to the shoots of lupine (25 mCi per plant) 30 min was the minimal time needed to determine the incorporation of label into bacteroid compounds. The predominant incorporation, exhibited in all root, nodule and bacteroid samples after 30 min exposure, was into sucrose (45–90% of the corresponding fraction radioactivity) of the neutral fraction; into malate (30–40%) of the acid fraction; into aspartic acid and asparagine (60–80% in sum) of the basic fraction. The composition of carbon compounds containing the greatest amount of ¹⁴C in the cytosol of nodules and in bacteroids was similar. Their radioactivity after 30 min exposure was for bacteroids (nCi per g of bacteroid fr. wt): sucrose 5.73, glucose 1.00, malate 0.15, succinate 0.11; for the nodule cytosol (nCi per g of nodule fr. wt): sucrose 200.00, glucose 8.40, malate 9.34, succinate 8.50. Thus it was demonstrated that in lupine, sucrose is the main photoassimilate entering not only into nodules but also into bacteroids. The biosynthesis of aspartic acid and asparagine occurs during nitrogen fixation in bacteroids.     

14C-Studies on Apple Trees. I. The Effect of the Fruit on the Translocation and Distribution of Photosynthates

The presence of fruits affects the translocation and distribution of photosynthates from apple leaves to other organs of the tree. An attempt has been made to study the relationship in greater detail by following the distribution of ¹⁴C introduced in the form of ¹⁴CO₂ on shoots with and without fruits, respectively. Determinations of the ¹⁴C-content were made on different parts of the shoot sampled at varying intervals after the introduction of the tracer. The ^l4C-labelling and the content of sorbitol and sugar in the leaves were determined by means of paper chromatography. A total of nearly 90 per cent of the ¹⁴C taken up by the leaves can be transferred to a fruit close by, the majority during the first 4 to 5 days following the addition of the ¹⁴C. The content of ¹⁴C in the leaves is reduced more rapidly in shoots with fruits than in those without. Young leaves retain more of the added ¹⁴C than do fully developed ones. The greatest changes with time are found in the methanol-soluble ¹⁴C-compounds. Immediately following application, the leaves contain 58 to 80 per cent of the ¹⁴C added in sorbitol, 7 to 9 per cent in sucrose, and 1 to 4 per cent in the form of glucose. Within 5 days after the introduction of ¹⁴C the amount of ¹⁴C-sorbitol is reduced very considerably, while in certain cases the amount of ¹⁴C-glucose increases. The ¹⁴C-sorbitol content was higher in leaves from shoots without fruits than in those from fruit-bearing shoots, and this applied also to the total contents of sorbitol and of glucose.     

14C-Studies on Apple Trees III. The Influence of Season on Storage and Mobilization of Labelled Compounds

The present paper reports an attempt to elucidate the storage and mobilization processes in 1-year-old apple rootstocks by studying the ¹⁴C content of different parts of the tree following application of ¹⁴CO₂. The translocation of the ¹⁴C taken up from the leaves to other parts proceeds at the highest rate during the first few days after the application of ¹⁴C. The distribution in shoots, trunk and roots after application of ¹⁴C during May, July, August, and in part of September depends in particular upon the intensity of growth in the various parts. From the lime of the application of ¹⁴C until leaf-fall, 40–50 per cent of the ¹⁴C initially absorbed disappears from the tree. After exposure to ¹⁴C during October, and in part of September, a relatively large part of the ¹⁴C applied goes to the root. In this case there is a considerable reduction in the ¹⁴C-conlent from leaf-fall to the following spring after leafing, especially in the root, although relatively speaking reduction is also considerable in the bark of the parts above ground, and it is most pronounced in the methanol (80 %) soluble fraction. The reduction takes place primarily during spring, and comprises, after application during October, for the whole tree 20–25 per cent of the ¹⁴C initially absorbed. Only 13–17 per cent of this amount was recovered in the newly developed shoots and leaves in the following June.     

14C-Studies on Apple Trees. VIII. The Seasonal Variation and Nature of Reserves

The nature, seasonal variation and mobilization of reserves in Malus × domestica have been studied by means of ¹⁴C, carbohydrate analyses and extractions of xylem sap. Following exposure to ¹⁴CO₂ in the autumn, the majority of the ¹⁴C absorbed is found in the root. During the winter and in particular the spring the amounts of ¹⁴C in the top and root are reduced to approximately 40 per cent of the autumn values; in the root the amount of dry matter was also considerably reduced. In the tops, most of the ¹⁴C absorbed was found as methanol (80 %)-soluble ¹⁴C which also showed the greatest seasonal reduction; sorbitol, sucrose or glucose in particular are responsible for the decrease in concentration within this fraction. Maximum values for methanol-insoluble ¹⁴C were found in March. In the root, the highest values for absolute changes were found for methanolinsoluble ¹⁴C. Hydrolysis of this fraction showed considerable activity in glucose. In the root there was also considerable activity in a precipitated fraction of the methanol extract. Eluates of xylem sap from apple branches contained primarily sorbitol, the highest concentration of which was found at the beginning of March. For a tree with a dry matter weight of about 300 g, the utilization of reserves from the tree in the spring was calculated to be at least 13 g of dry matter. However, only a minor part (less than 25 per cent) of the latter appears to serve as building material for new growth.     

14CO2 Fixation and Compartmentation of Carbon Metabolism in a Recombined Chloroplast- 'Cytoplasm' System

The Compartmentation of ¹⁴CO₂ fixation and concomitant metabolism of ^l4C-iabelled products in a recombined system, composed of isolated intact spinach (Spinacia oleracea) chloroplasls and a ‘cytoplasm’ fraction, has been studied. Addition of ‘cytoplasm’ to chloroplasts fixing ¹⁴CO₂ increased the label in hexoae monophosphates outside the chloroplasts at the expense of excreted dihydroxyacetone phosphate. The label in ammo acids was increased both inside and outside the chloroplasts. The results support the view that chloroplasls are not able to make 2-oxoacids for amino acid synthesis directly from fixed CO₂, but have to co-operate with the cytoplasm and other organelles. The results also show that recombined systems can be useful for studies on the compartmen tation of carbon metabolism in pholosynthesizing plant tissues.     

SIMULTANEOUS INCORPORATION OF ORALLY ADMINISTERED [9, 10-3H2]OLEIC AND [1-14C]LINOLEIC ACIDS INTO LIPIDS OF THE ADULT RAT BRAIN

—The incorporation of an orally administered mixture of [9,10-³H₂joleic acid and [1-¹⁴C]linoleic acid into the brain and spinal cord lipids was maximal after 24 h compared with 4 h for extraneural tissue. In the latter, both acids were utilized equally well for triglyceride biosynthesis, but linoleate entered phosphatidylcholine more rapidly than oleate. Oleic acid was preferentially incorporated into newly synthesized cholesterol esters although 4 h after dosing most cholesterol esters present in serum were formed preferentially from linoleate presumably by the action of lecithin-cholesterol acyl transferase. In neural tissue, a considerable amount of [1-¹⁴C]linoleate was metabolized to higher polyunsaturated fatty acids, whereas in the case of oleate, 90 per cent of the tritium activity remained in monoenic acids at all time periods studied. Both acids were initially incorporated most rapidly into the lecithin fraction of brain and spinal cord, but after 7 days diacyl phosphatidylethanolamine had the highest specific activity. These data are consistent with the view that the uptake of labelled fatty acids by the brain takes place principally as free acids but that some uptake of esterified forms, probably largely as phosphatidylcholine, also occurs. The low linoleate content of the brain and probably also of cerebrospinal fluid cannot be explained on the basis of a selective restriction on the uptake of this lipid from plasma.     

Cyclopentenylglycine,a precursor of deidaclin in Turnera ulmifolia

When [2-¹⁴C]cyclopentenylglycine was synthesized and fed to seedlings of Turnera ulmifolia, the label was incorporated into the nitrile group of the cyanogenic glycoside deidaclin. The amino acid cyclopentenylglycine was also found to occur naturally in Turnera ulmifolia. These findings indicate that cyclopentenyl cyanogenic glycosides are synthesized from the corresponding amino acids by the same pathway utilized in the biosynthesis of other cyanogenic glycosides.     

14C-studies on Apple Trees. IX. Seasonal Changes in the Formation of Fruit Constituents and their Subsequent Conversions

The formation and subsequent conversions of ¹⁴C-labelled compounds were followed in fruits of Malus domestica cvs. Golden Delicious and Cox's Orange Pippin after labelling proximate leaves with ¹⁴CO₂ at different times during the growing season. A few hours after labelling of the leaves, the larger share of fruit ¹⁴C was detected in sorbitol. This share descreased rapidly except in the late autumn. When labelling about 1 July (c. 1 month after bloom), 40–60% of the fruit ¹⁴C was permanently fixed in the methanol and water insoluble fraction. 25% or more was primarily found in organic acids, but this declined during the season to a few per cent. When labelling at the end of July, the dominating feature was the establishment of a peak of temporarily insoluble ¹⁴C, returning back to the soluble form through October and November. This was particularly pronounced in‘Cox's Organe Pippin'. Labelling with ¹⁴C at the end of August and at the end of September yielded increasing amounts of ¹⁴C in sugars. The labelling of fructose predominated, but as the autumn progressed the amount of label in sucrose increased. This was due to a conversion from ¹⁴C-compounds of older origin as well as to a larger share of the imported assimilates turning into sucrose at this time of the year. During prolonged storage of harvested fruits at 3°C, ¹⁴C in fructose increased at the expense of ¹⁴C in sucrose.     

Changes in protein fractions and leucine-[14C] incorporation during Sorghum grain development

Incorporation of leucine and changes in different protein fractions have been studied during Sorghum grain development. Most of the label from the injected leucine-[¹⁴C] was found in glutelin and residue fraction towards later stages of maturity. The label in albumin, globulin and prolamin decreased with a concomitant increase in label in glutelin and residue proteins. The concentration of lysine, aspartic acid and glycine decreased while that of leucine, proline, alanine, tyrosine, phenylalanine, and cystine increased during grain development. Increase in serine, methionine, valine and isoleucine was only marginal. The proportion of glutamic acid was high at all stages of grain development. Glutelin fraction resolved into two peaks on gel chromatography, only one of which with higher MW was labelled, while in albumin both the peaks were found to be labelled. Tannin content also increased during grain development.     

Translocation of 14C-labelled assimilates in cabbage during club root development

The effects of infection of root systems by Plasmodiophora brassicae on the translocation of ¹⁴C-labelled assimilates from the first and third leaves of cabbage seedlings were investigated. During the early phases of Plasmodium development, there were small differences in the distribution patterns of ¹⁴C-labelled assimilate between healthy and infected seedlings. At the end of growth of plasmodia and during resting spore formation, both first and third leaves exported more assimilates than corresponding leaves of healthy seedlings. When the infected roots were dissected into various regions after exposure of the fed leaves to ¹⁴CO₂, more assimilate accumulated in the club root region than in any other part.