THE UTILIZATION OFD-AMINO ACIDS BY YEASTS

1967 ◽  
Vol 13 (7) ◽  
pp. 777-788 ◽  
Author(s):  
T. A. LaRue ◽  
J. F. T. Spencer

Ninety-one strains of yeast from 19 genera were examined for their ability to utilize single L- and D-amino acids as the nitrogen source for growth. Eighty strains from 17 genera were able to grow on at least one D-amino acid. The most readily utilized were alanine, α-amino butyric acid, leucine, and serine. D-Cysteine was used by few species. The utilization of D-amino acids is of little use in classifying or identifying yeasts.

1984 ◽  
Vol 102 (3) ◽  
pp. 667-672 ◽  
Author(s):  
G. Ashbell ◽  
H. H. Theune ◽  
D. Sklan

SummaryChanges in distribution of amino acid nitrogen of chopped wheat plants ensiled at shooting and flowering when wilted, and at the milk and dough stages as fresh material, were determined as affected by addition of 0·8% propionic acid (PrA) or 2·2% urea phosphate-calcium propionate (UP-CaPr). Analyses were carried out after an ensiling period of 90 days and after a further aerobic exposure period (AE) of 7 days.Total amino acid (TAA) contents in the dry matter (D.M.) during the fermentation period and in the AE were stable in untreated material (UM) and treated material. Concentration of essential amino acids decreased during fermentation, this decrease being higher in the UM. The free amino acids were low in the fresh material (18·6% of TAA) but increased in the ensiled material to ca. 71 % of the TAA in the silage. In the AE this level was 63% in UM and 69% in treated material. The ammonia-N contents increased during fermentation in UM and especially in the UP-CaPr treatments, while the opposite occurred in the PrA treatments.The concentrations of and changes in 21 amino acids (AAs) are given. The highest AA concentrations recorded in the fresh material were those of arginine, lysine, glutamic acid, alanine, leucine, proline and glycine. The most marked increments in AAs as a result of fermentation were those of ornithine, γ-amino butyric acid, threonine and methionine. Marked decreases were observed in glutamine, arginine and glutamic acid. PrA increased mainly arginine, asparagine and glutamine, whereas γ-amino butyric acid decreased; UP-CaPr increased arginine, asparagine, lysine and glutamic acid (in silage only) and reduced γ-amino butyric acid and glutamine (in AE only).


1954 ◽  
Vol 45 (1) ◽  
pp. 36-40 ◽  
Author(s):  
Hamish Robertson ◽  
A. John G. Barnett

1. An investigation has been made into the changes that take place in the free amino-acid pattern when kale-water slurries are allowed to ferment under conditions of (a) aeration, (b) anaerobiasis and (c) partial sterilization with sulphur dioxide.2. It has been found that, with aerated mixtures, the loss of free amino-acids is virtually complete within 2 weeks, while there is only a slight loss with the anaerobic mixtures. With mixtures containing sulphur dioxide no loss of amino-acids occur.3. The formation of α-amino butyric acid possibly from threonine has been noted.


1968 ◽  
Vol 10 (2) ◽  
pp. 362-368 ◽  
Author(s):  
Patricia Sarvella ◽  
B. J. Stojanovic

The free and protein amino acid patterns present in the leaves of the species of the genus Gossy pium were determined. The presence or absence of the free amino acids except for glycine and γ-amino butyric acid did not appear to be of value for separation of the species. However, the patterns of the protein amino acids varied between the genomes, and seemed to separate the species. These patterns were separated into groups similar to those found for the DNA-base ratios and the cytotaxonomic grouping of the species.


2021 ◽  
Author(s):  
Jin-Tian Ma ◽  
Li-Sheng Wang ◽  
Zhi Chai ◽  
Xin-Feng Chen ◽  
Bo-Cheng Tang ◽  
...  

Quinazoline skeletons are synthesized by amino acids catabolism/reconstruction combined with dimethyl sulfoxide insertion/cyclization for the first time. The amino acid acts as a carbon and nitrogen source through HI-mediated catabolism...


Nature ◽  
1950 ◽  
Vol 165 (4201) ◽  
pp. 716-717 ◽  
Author(s):  
A. C. HULME ◽  
W. ARTHINGTON

1975 ◽  
Vol 21 (3) ◽  
pp. 414-417 ◽  
Author(s):  
Yasuyuki Doi ◽  
Akikatsu Kataura

Abstract Free amino acids in the tonsils of 20 individuals were measured column chromatographically. Those always found in readily detectable amounts included O-phosphoserine, taurine, O-phosphoethanolamine, aspartic acid, hydroxyproline, threonine, serine, glutamic acid, proline, glycine, alanine, α-amino-n-butyric acid, valine, cystine, methionine, isoleucine, leucine, tyrosine, phenylalanine, ornithine, γ-amino-butyric acid, lysine, histidine, and arginine. Results were compared for three clinical pathological groups and for four age groups. Some abnormal values may result from the pathological conditions.


1965 ◽  
Vol 20 (4) ◽  
pp. 307-312 ◽  
Author(s):  
P. S. Chen ◽  
F. Hanimann

By using the automatic amino acid analyzer (model 120 B, Beckman) the free ninhydrin-positive components in the methanol extracts of Drosophila melanogaster were fractionated. Compared to the conventional paper partition chromatography the great advantage of this technique is the distinct separation of such amino acids like leucine, isoleucine, phenylalanine, valine, methionine, γ-amino-butyric acid as well as the basic components ornithine, lysine, histidine and arginine. Furthermore, the occurrence of phosphoserine, tyrosine phosphate, ethanolamine, phosphoethanolamine and glycerophosphoethanolamine was identified. The metabolic significance of these substances is discussed.


1978 ◽  
Vol 24 (11) ◽  
pp. 1346-1357 ◽  
Author(s):  
Mariette Carels ◽  
David Shepherd

Monascus major ATCC 16362 and Monascus rubiginosus ATCC 16367 were cultivated aerobically on media containing nitrate or ammonium as nitrogen source to which the following modifications were made: (1) pH adjusted to 2.5 before sterilization; (2) addition of yeast extract; (3) addition of amino acids in identical proportions and concentrations to those found in yeast extract; (4) adjustment of pH to 2.5 after addition of amino acids.The addition of amino acids in the form of yeast extract increased mycelium formation and reduced conidiation and pigment production. The addition of an amino acid mixture did not increase mycelium formation to the same extent as yeast extract but increased the number of conidia, while pigment production was reduced, especially when nitrate was the nitrogen source. As the amino acids are taken up after conidial formation has started, it would appear that it is not the amino acids themselves which are directly responsible for the induction of conidiation. The addition of amino acids inhibits nitrate and ammonium uptake suggesting the need for an early intracellular nitrogen limitation to induce conidiation. Lowering the pH inhibits the formation of conidia and increases pigment production; also the effect of amino acid addition is totally annulled.The pH of the medium is all important in regulating the formation of conidia and pigment production. The possible effects of the pH on the uptake of certain medium components is discussed, as well as their possible control of certain metabolic pathways which ultimately determines the availability of intermediates for conidiation and pigment production.


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