Production of alkaloids and differentiation in a submerged culture ofClaviceps purpurea (Fr.) Tul

The submerged culture of the Claviceps purpurea strain studied was polymorphous. In the process of alkaloid synthesis, cytodifferentiation preceded biochemical differentiation. The onset of the alkaloid phase was characterized by: predominance of chlamydospores in the culture, the presence of vegetative cells with reduced or arrested proliferation, maximum acetylCoA carboxylase activity, the maximum amount of total fatty acids, an over-average cell pool tryptophan level and minimum tryptophan synthetase activity. Intracellular ricinoleic acid was an indicator of differentiation of the culture towards alkaloid formation and also of alkaloid synthesis. The cytodifferentiation period in the initial phases of fermentation, when the cell has several alternative possibilities of development, is regarded as the most sensitive sector of the regulatory mechanisms of alkaloid formation.     

Biosynthesis of ergotamine by Claviceps purpurea (Fr.) Tul

1. Partially purified ceramide trihexoside alpha-galactosidase from human liver was studied by using ceramide trihexoside specifically tritiated in the terminal galactose. 2. The hydrolysis of ceramide trihexoside was absolutely dependent on a mixture of sodium taurocholate and Triton X-100 and was markedly inhibited by human serum albumin and by NaCl. 3. The Lineweaver-Burk plot for ceramide trihexoside hydrolysis was upward curving. Ceramide lactoside inhibited hydrolysis of all concentrations of ceramide trihexoside. Ceramide digalactoside stimulated hydrolysis of low concentrations of ceramide trihexoside, but inhibited hydrolysis of high concentrations of the lipid. 4. alpha-Galactosidase activity assayed with the synthetic substrate 4-methylumbelliferyl alpha-d-galactopyranoside fractionated together with activity assayed with the natural substrate ceramide trihexoside. Both activities had identical heat-inactivation kinetics. 5. Characteristics of the hydrolysis of the synthetic substrate differed considerably from those of the natural substrate, including pH optimum, shape of the Lineweaver-Burk plot, and differential effects of inhibitors and activators. Mutual inhibition of hydrolysis between the synthetic and natural substrates was predominantly non-competitive. 6. These results are discussed in the light of special problems involved in the hydrolysis of lipids in an aqueous milieu.     

Changes of the cytoplasmic ultrastructure during development of sclerotia in Claviceps purpurea (Fr.) Tul.

The development of sclerotia of Claviceps purpurea was investigated by light and electron microscopy. During the first days after infection sterigma and conidiospores are formed. The spores show a moderately developed vacuolar system, they are thick walled and contain about 20% lipid (related to the cell volume) embedded in glycogen. The sterigma are cylindrical unicellular hyphae with electron dense cytoplasm and isolated strongly contrasted lipid droplets. In maturing sclerotia the hyphae become septated with increasingly thick cell walls and a large lipid content. The lipid forms small droplets in young cells, while in the mature sclerotium it occurs in the form of very large drops, occupying the major part of the cell. Simultaneously the composition of the lipid is changed. The mature cells have several nuclei. They are partially connected by osmiophilic substances, forming a network of intercellular spaces.Abbreviations HEPES N-2-hydroxyethylpiperazine-N'-2-ethanesulfonic acid - DMSO Dimethylsulfoxide     

Studies on Claviceps purpurea (Fr.) Tul. parasitic on Phragmites communis Trin

Isolates from C. purpurea sclerotia occurring naturally on Phragmites communis usually sporulated vigorously on the culture medium employed, and their failure to produce alkaloid in vitro was associated with a thin white growth form. Such isolates also failed to produce sclerotia on the host plants tested. A variant having a plectenchymatic morphology in vitro and producing a thick pigmented non-sporulating growth form yielded alkaloid (up to approximately 300μg/ml mainly δ8–9 and δ9–10 lysergic acids and chanoclavine) in surface or submerged culture and developed typical ergot sclerotia (containing 0·2-0·4% alkaloid, mainly ergotoxine and ergotamine) in vivo. Improved alkaloid yield in vitro was obtained from a strain reselected after passing through a parasitic phase. Aetiological aspects of the P. communis ergot are discussed.     

Improved medium for saprophytic production of ergot alkaloids by Claviceps purpurea (Fr.) Tul

Studies were undertaken on the production of ergot alkaloids in saprophytic culture employing two strains of C. purpurea. In an attempt to improve the yield of the alkaloids and to develop a cheaper medium, the commonly used carbohydrate source, mannitol, was replaced with different types of starches and starchy materials as these are comparatively much cheaper than mannitol. Results indicated that, in stationary cultures, certain starches enhanced the yield greatly, while in shaker cultures starches could replace mannitol for equivalent yields.     

Emergence and phytopathological properties of a new strain of Claviceps purpurea (Fr.) Tul. on rye

The emergence of a new stable strain of Claviceps purpurea is described. The strain formed the sphacelial stage very weakly on rye, and was unlikely therefore to be able to initiate an epidemic under field conditions, but the sclerotia contained chanoclavine as the major alkaloid in contrast to the ergotamine component of the parent strain. Isolates of C. purpurea derived from ryegrass ergots were also shown to parasitize rye.     

The cellular role of nitrogen in the biosynthesis of alkaloids by submerged culture of Claviceps purpurea (Fr.) Tul.

Asparagine was a superior nitrogen source for clavine-alkaloid production in Claviceps purpurea. Its transport into the cell excedded the cell's biosynthetic need for this amino acid. Asparagine entered the cell without degradation. This disturbed the relative pool sizes of various amino acids resulting in a change in the genetically determined ratio at which amino acids were utilized for protein synthesis. Overproduction of alkaloids (4500 mug.ml-1) may be associated with increased availability of tryptophan because of the enhanced assimilation of asparagine-derived ammonia via glutamine synthetase (EC 6.3.1.2). However, ammonium salts in the fermentation broth led to a depression of the alkaloid yield. Partial replacement of the ammonium salt by aspartic acid elevated alkaloid production.     

Isolation of the Ergot Strain Claviceps purpurea(Fr.) Tul. VKM-F-3662D Producing the Lactamic Alkaloid Ergocornam

A new ergot strain, VKM-F-3662D, producing lactamic alkaloid ergocornam with concomitant alkaloids valinamide and ergometrine, was isolated during selective work with sclerotium MS-462, which was obtained from ergocryptine ergot strain VKM-F-2642D. The structure of these alkaloids was determined by ¹H and ¹³C NMR.     

Morphological differentiation of cells in submerged cultures of Claviceps purpurea (Fr.) Tul., producing alkaloids]

Differentiation of the cells of the submerged culture of Claviceps purpurea (Fr.) Tul. was studied by electron microscopy. Two types of oviform cell were found: (1) the conidia which had one nucleus and vacuolized cytoplasm and were not involved in the production of alkaloids; (2) the chlamydospores with two nuclei, homogeneous cytoplasm, and high content in lipids. The chlamydospores, like the cells of sclerotia, were found to produce alkoloids.     

Isolation of the ergot (Claviceps purpurea (Fr.) Tul., strain VKM-F-366D), producing the lactamic alkaloid ergocornam

A new ergot strain VKM-F-3662D producing lactamic alkaloid ergocornam with concomitant alkaloids valinamide and ergometrine was isolated during selective works with sclerotium MS-462, which was obtained from ergocryptine ergot strain VKM-F-2642D. The structure of these alkaloids was determined by 1H and 13C NMR.     

Effect of immobilization on the stability ofClaviceps purpurea protoplasts

Summary Protoplasts released with high efficiency from vegetative and productive hyphae ofClaviceps purpurea were immobilized in 2% Ca-alginate. The yield of active immobilized protoplasts depended upon the age of the mycelium from which protoplasts were derived and was found to be 25–43% in comparison with native hyphae. During incubation in a modified production medium immobilized protoplasts were stable for at least 10–12 days. No external growth of regenerated hyphae from spherical beads of alginate gel with entrapped protoplasts was observed for 13–15 days of the batchwise incubation.     

Influence of auxins on growth ofClaviceps purpurea (Fries) tulasne in saprophytic cultures

A 10⁻³ m β-indolebutyric and 2,4-dichlorophenoxyacetic acid concentration stimulated the fresh weight increase and dry matter production in the mycelium of staticClaviceps purpurea cultures to 170–180% of the control value. Higher concentrations severely inhibited growth. α-Naphthylacetic acid was less active. β-Indoleacetic acid differed markedly from the other auxins, as it stimulated the fresh weight increase, but at the same time inhibited dry matter production. In submerse cultivation, the differences between the test auxins disappeared; none of them stimulated growth and only inhibition of growth, by concentrations of over 10⁻⁵–10⁻⁴ m, was observed. The used strain did not produce alkaloids in saprophytic cultures, even in the presence of auxins.     

An Electron-Microscope Study of Host Penetration and Early Stages of Haustorium Formation of Peronospora parasitica (Fr.) Tul. on Cabbage Cotyledons

Penetration of the epidermis of cabbage cotyledons and haustoriumdevelopment by Peronospora parasitica within 12 hours of sporegermination was studied by means of the electron microscope.The ultrastructure of appressoria, penetrating hyphae, developinghaustorium and host cells associated with the invading parasiteare described. The mechanism of penetration and the terminologyconcerned with the ultrastructure of host-parasite interfacesare discussed.