scholarly journals A defined medium for the production of lysergic acid alkaloids by Claviceps paspali

1970 ◽  
Vol 12 (4) ◽  
pp. 641-644 ◽  
Author(s):  
A. Mizrahi ◽  
G. Miller
Keyword(s):  
Defined Medium ◽  
Lysergic Acid ◽  
Claviceps Paspali

Production of lysergic acid derivatives with immobilized Claviceps paspali mycelium

1989 ◽  
Vol 32 (1) ◽  
pp. 5-10 ◽  
Author(s):  
Damjana Rozman ◽  
Elizabeta Pertot ◽  
Radovan Komel ◽  
Miro Prošek
Keyword(s):  
Lysergic Acid ◽  
Claviceps Paspali

Production of Lysergic Acid Derivatives by a Strain of Claviceps paspali Stevens and Hall in Submerged Culture

Nature ◽  
1960 ◽  
Vol 187 (4733) ◽  
pp. 238-239 ◽  
Author(s):  
F. ARCAMONE ◽  
C. BONINO ◽  
E. B. CHAIN ◽  
A. FERRETTI ◽  
P. PENNELLA ◽  
...  
Keyword(s):  
Submerged Culture ◽  
Lysergic Acid ◽  
Claviceps Paspali

Radioimmunoassay of Lysergic Acid Derivatives from Claviceps paspali Fermentation Cultures

Planta Medica ◽  
1982 ◽  
Vol 45 (07) ◽  
pp. 161-161
Author(s):  
T. Lehtola ◽  
A. Huhtikangas ◽  
J. Lundell ◽  
T. Vallanen
Keyword(s):  
Lysergic Acid ◽  
Claviceps Paspali

Production of a new lysergic acid derivative in submerged culture by a strain of Claviceps paspali Stevens & Hall

1961 ◽  
Vol 155 (958) ◽  
pp. 26-54 ◽  
Keyword(s):  
Acid Derivative ◽  
Submerged Culture ◽  
Acid Amide ◽  
Transformation Products ◽  
Culture Conditions ◽  
Lysergic Acid ◽  
Morphological Properties ◽  
Isolation And Purification ◽  
High Yields ◽  
Claviceps Paspali

1. The production of a new lysergic acid derivative, identified as D-lysergic acid α -hydroxyethylamide, in submerged culture and in yields up to 1 mg/ml. and above, by a strain of Claviceps paspali Stevens & Hall is reported; this substance can be converted in high yields into D-lysergic acid amide. 2. The morphological properties of this strain under different culture conditions are examined and it is shown that it grows in a form resembling natural sclerotia. 3. The biochemical culture conditions for the production of the new lysergic acid derivative in shake flasks and in stirred fermenters, the course of the fermentation, the methods for the isolation and purification of the substance and its transformation products and some of its chemical and physical properties are described.

scholarly journals Über die Herkunft der Seitenkette im d-Lysergsäure-methylcarbinolamid

1968 ◽  
Vol 23 (2) ◽  
pp. 177-180 ◽  
Author(s):  
D. Gröger ◽  
D. Erge ◽  
H. G. Floss
Keyword(s):  
Aspartic Acid ◽  
Related Compound ◽  
High Efficiency ◽  
Lysergic Acid ◽  
Incorporation Rate ◽  
Side Chain ◽  
Short Term ◽  
Claviceps Paspali

Using a strain of Claviceps paspali Mar 488 it has been shown that alanine-2-C14 is incorporated with high efficiency in the carbinol amide moiety of D-Lysergic acid-α-hydroxyethylamide=II. After feeding of ᴅʟ-alanine-15N, DL-aspartic acid-15N and ʟ-glutamine-CO-15NH2 the highest specific incorporation rate was observed with DL-alanine-15N. Short term experiments with ᴅ,ʟ-alanine-15N revealed, that the greater part of the 15N-excess is localized in the N-atom of the side-chain of II. The carbinolamide moiety of the isolated alkaloid arises probably from alanine or a closely related compound.

Metabolic changes in a conidia-induced Claviceps paspali strain during submerged fermentation

1987 ◽  
Vol 33 (7) ◽  
pp. 602-606 ◽  
Author(s):  
V. Gaberc-Porekar ◽  
H. Sočič ◽  
E. Pertot ◽  
S. Miličić
Keyword(s):  
Nutrient Uptake ◽  
Mutant Strain ◽  
Submerged Fermentation ◽  
Parent Strain ◽  
Lysergic Acid ◽  
Mutagenic Treatment ◽  
Γ Irradiation ◽  
Metabolic Pattern ◽  
Metabolic Activities ◽  
Claviceps Paspali

Chemical changes in the mycelium of the conidial Claviceps paspali mutant strain, isolated after γ irradiation, were followed during the course of submerged fermentation and compared with the mycelial parent strain; both strains are capable of producing simple lysergic acid derivatives. The syntheses of lipids, carbohydrates, phosphates, nucleic acids, proteins, and alkaloids, as well as nutrient uptake, were determined. It was found that conidiation induced by mutagenic treatment was accompanied by a set of changes in the metabolic pattern. In the conidial mutant, the primary and secondary metabolic activities were repressed and the protein to nonprotein compound ratio of the cells was changed in favour of protein compounds.

Formation of a Lysergic Acid Derivative during the Parasitic Development of a Strain of Claviceps paspali Stevens and Hall

Nature ◽  
1964 ◽  
Vol 202 (4929) ◽  
pp. 312-313 ◽  
Author(s):  
P. BIANCHI ◽  
E. B. CHAIN ◽  
P. G. MANTLE ◽  
A. TONOLO
Keyword(s):  
Acid Derivative ◽  
Lysergic Acid ◽  
Claviceps Paspali

Primary culture of rat ependymal cells in serum-free defined medium

1986 ◽  
Vol 390 (2) ◽  
pp. 199-209 ◽  
Author(s):  
M WEIBEL ◽  
B PETTMANN ◽  
J ARTAULT ◽  
M SENSENBRENNER ◽  
G LABOURDETTE
Keyword(s):  
Primary Culture ◽  
Defined Medium ◽  
Ependymal Cells ◽  
Serum Free

scholarly journals Transcriptional Profiling of Porcine Blastocysts Produced In Vitro in a Chemically Defined Culture Medium

Animals ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 1414
Author(s):  
Josep M. Cambra ◽  
Emilio A. Martinez ◽  
Heriberto Rodriguez-Martinez ◽  
Maria A. Gil ◽  
Cristina Cuello
Keyword(s):  
Culture Medium ◽  
Embryo Quality ◽  
Transcriptional Profiling ◽  
Defined Medium ◽  
Platelet Factor ◽  
Defined Media ◽  
Defined Culture ◽  
The Impact

The development of chemically defined media is a growing trend in in vitro embryo production (IVP). Recently, traditional undefined culture medium with bovine serum albumin (BSA) has been successfully replaced by a chemically defined medium using substances with embryotrophic properties such as platelet factor 4 (PF4). Although the use of this medium sustains IVP, the impact of defined media on the embryonic transcriptome has not been fully elucidated. This study analyzed the transcriptome of porcine IVP blastocysts, cultured in defined (PF4 group) and undefined media (BSA group) by microarrays. In vivo-derived blastocysts (IVV group) were used as a standard of maximum embryo quality. The results showed no differentially expressed genes (DEG) between the PF4 and BSA groups. However, a total of 2780 and 2577 DEGs were detected when comparing the PF4 or the BSA group with the IVV group, respectively. Most of these genes were common in both in vitro groups (2132) and present in some enriched pathways, such as cell cycle, lysosome and/or metabolic pathways. These results show that IVP conditions strongly affect embryo transcriptome and that the defined culture medium with PF4 is a guaranteed replacement for traditional culture with BSA.

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