UTILIZATION OF ADDED SUBSTRATES BY UREDOSPORES OF WHEAT STEM RUST

1956 ◽  
Vol 2 (6) ◽  
pp. 559-563 ◽  
Author(s):  
P. Shu ◽  
A. C. Neish ◽  
G. A. Ledingham
Keyword(s):  
Carbon Dioxide ◽  
Amino Acids ◽  
Fatty Acids ◽  
Glutamic Acid ◽  
Metabolic Activity ◽  
Stem Rust ◽  
Volatile Fatty Acids ◽  
The Other ◽  
Wheat Stem Rust ◽  
Better Than

Uredospores of wheat stem rust utilized a number of externally-supplied, labelled carbohydrates, amino acids, and volatile fatty acids. The carbon of these substrates appeared in the spore materials and in the carbon dioxide. This metabolic activity, though very weak, is definite. D-Mannose, D-mannitol, D-glucose, sucrose, and D-fructose were utilized better than the other carbohydrates. Glutamic acid gave the highest yield of carbon dioxide while the basic amino acids, L-arginine and L-lysine, were more efficiently incorporated into the spore material.

THE METABOLISM OF PROPIONATE BY WHEAT STEM RUST UREDOSPORES

1963 ◽  
Vol 41 (3) ◽  
pp. 737-743 ◽  
Author(s):  
H. Reisener ◽  
A. J. Finlayson ◽  
W. B. McConnell ◽  
G. A. Ledingham
Keyword(s):  
Carbon Dioxide ◽  
Amino Acids ◽  
Glutamic Acid ◽  
Stem Rust ◽  
Water Extract ◽  
Hot Water ◽  
Insoluble Residue ◽  
Soluble Carbohydrates ◽  
Wheat Stem Rust ◽  
Carbon 14

When uredospores of wheat stem rust were shaken for 3 hours with phosphate buffer (pH 6.2) containing propionate-1-C14, -2-C14, or -3-C14, about 55% of the carbon-14 was removed from the solution. With propionate-1-C14, most of the carbon-14 taken up was released as carbon dioxide-C14, whereas about 20% and 31% of propionate carbon 2 and carbon 3, respectively, was incorporated into the spores. The specific activity of a fraction consisting of the free amino acids of a hot-alcohol and hot-water extract of the spores increased markedly with increase in the position number of propionate in which the carbon-14 was located. A similar relation was observed for other fractions such as soluble carbohydrates, ether-soluble material, organic acids, and insoluble residue from spores. The most active amino acids isolated were glutamic acid, γ-aminobutyric acid, and alanine. Partial degradations showed that with propionate-2-C14 the carboxyl groups of glutamic acid were especially radioactive, whereas with propionate-3-C14 the internal carbons were most radioactive.It is concluded that propionate metabolism in the rust spores involved conversion of carbon 1 to carbon dioxide, and utilization of carbons 2 and 3 as acetate with carbon 2 behaving as the carboxyl carbon.

THE METABOLISM OF PROPIONATE BY WHEAT STEM RUST UREDOSPORES

1963 ◽  
Vol 41 (1) ◽  
pp. 737-743 ◽  
Author(s):  
H. Reisener ◽  
A. J. Finlayson ◽  
W. B. McConnell ◽  
G. A. Ledingham
Keyword(s):  
Carbon Dioxide ◽  
Amino Acids ◽  
Glutamic Acid ◽  
Stem Rust ◽  
Water Extract ◽  
Hot Water ◽  
Insoluble Residue ◽  
Soluble Carbohydrates ◽  
Wheat Stem Rust ◽  
Carbon 14

When uredospores of wheat stem rust were shaken for 3 hours with phosphate buffer (pH 6.2) containing propionate-1-C14, -2-C14, or -3-C14, about 55% of the carbon-14 was removed from the solution. With propionate-1-C14, most of the carbon-14 taken up was released as carbon dioxide-C14, whereas about 20% and 31% of propionate carbon 2 and carbon 3, respectively, was incorporated into the spores. The specific activity of a fraction consisting of the free amino acids of a hot-alcohol and hot-water extract of the spores increased markedly with increase in the position number of propionate in which the carbon-14 was located. A similar relation was observed for other fractions such as soluble carbohydrates, ether-soluble material, organic acids, and insoluble residue from spores. The most active amino acids isolated were glutamic acid, γ-aminobutyric acid, and alanine. Partial degradations showed that with propionate-2-C14 the carboxyl groups of glutamic acid were especially radioactive, whereas with propionate-3-C14 the internal carbons were most radioactive.It is concluded that propionate metabolism in the rust spores involved conversion of carbon 1 to carbon dioxide, and utilization of carbons 2 and 3 as acetate with carbon 2 behaving as the carboxyl carbon.

THE METABOLISM OF VALERATE-3-C14 AND -5-C14 BY WHEAT STEM RUST UREDOSPORES

1964 ◽  
Vol 42 (3) ◽  
pp. 327-332 ◽  
Author(s):  
H. Reisener ◽  
A. J. Finlayson ◽  
W. B. McConnell
Keyword(s):  
Carbon Dioxide ◽  
Amino Acids ◽  
Glutamic Acid ◽  
Stem Rust ◽  
Phosphate Buffer ◽  
Free Amino Acids ◽  
Free Amino ◽  
Methyl Groups ◽  
Wheat Stem Rust ◽  
Carbon 14

Uredospores of wheat stem rust took up about 90% of the carbon-14 present either as valerate-3-C14 or as valerate-5-C14 in M/30 phosphate buffer pH 6.2 in 3 hours. The initial valerate concentration was 0.017 mM and spores were supplied at the rate of 250 mg/30 ml of buffer. Carbon 3 of the valerate was largely respired as carbon dioxide but carbon 5 was extensively incorporated into spore components. Free amino acids contained about 40% of the radioactivity in the spores labelled with valerate-5-C14 and glutamic acid was highly labelled. Carbon 1 contained 8.1% and carbon 5, 3.8% of the carbon-14 in this glutamic acid and thus internal carbons contained 88%. The results with valerate-3-C14 and with valerate-5-C14 compare well with those of experiments done earlier with propionate-1-C14 and propionate-3-C14 respectively. It is concluded that propionate is formed from carbons 3, 4, and 5 of valerate, and thus that carbon 3 is converted to carbon dioxide, and carbons 4 and 5 to the carboxyl and methyl groups respectively of acetate.

EFFECT OF SHORT-CHAIN FATTY ACIDS ON RESPIRATION OF WHEAT STEM RUST UREDOSPORES

1961 ◽  
Vol 7 (6) ◽  
pp. 865-868 ◽  
Author(s):  
H. J. Reisener ◽  
W. B. McConnell ◽  
G. A. Ledingham
Keyword(s):  
Carbon Dioxide ◽  
Fatty Acids ◽  
Stem Rust ◽  
Short Chain Fatty Acids ◽  
Short Chain ◽  
Puccinia Graminis ◽  
Wheat Stem Rust ◽  
Carbon 14 ◽  
Carboxyl Carbon ◽  
Chain Fatty Acids

Fatty acids added to a suspension of wheat stem rust uredospores (Puccinia graminis var. tritici, race 15B) stimulate respiration. When compared on the basis of equal molar concentration, the utilization of oxygen by spores from wheat grown in the field or in the greenhouse is stimulated by short-chain fatty acids as follows: acetate < propionate < butyrate < valerate. The order for butyrate and valerate is reversed with spores from plants grown under artificial light. Radiotracer experiments indicate that the amount of respired carbon dioxide derived from the carboxyl carbon of the fatty acid added increases markedly with increase in chain length. The addition of exogenous acetate stimulated conversion of spore carbon to carbon dioxide, whereas valerate replaces, in part, spore material as a source of respiratory carbon. Valerate-1-C14 is almost 4 times as effective as acetate-1-C14 for labelling spore material, but the ratio of carbon-14 respired to that incorporated is 2.6 for valerate-1-C14 as compared with 1.5 for acetate-1-C14.

THE UTILIZATION OF AMMONIUM CHLORIDE-15N BY UREDOSPORES OF WHEAT STEM RUST

1966 ◽  
Vol 44 (11) ◽  
pp. 1511-1518 ◽  
Author(s):  
W. B. McConnell ◽  
E. W. Underhill
Keyword(s):  
Amino Acids ◽  
Amino Acid ◽  
Glutamic Acid ◽  
Ammonium Chloride ◽  
Stem Rust ◽  
Organic Nitrogen ◽  
Ammonia Nitrogen ◽  
Ammonium Nitrogen ◽  
Wheat Stem Rust ◽  
Carbon 14

When uredospores of wheat stem rust, Puccinia graminis van tritici (race 15B), were incubated with a 3 mM solution of ammonium chloride-15N, a significant amount of nitrogen 15 was converted into organic nitrogen. Most of this organic nitrogen 15 was found in the ethanol and water extracts, with lesser amounts in the buffer and in extracted spores.Amino acids extracted from the spores all contained excess nitrogen 15. Nitrogen 15 from the inorganic source was diluted by factors of 1.7 and 2.7 in free aspartic and glutamic acids respectively; these amino acids were the most heavily labeled with the isotope. Proline was the most weakly labeled amino acid, the nitrogen 15 being diluted by a factor of 102. Good incorporation of nitrogen 15 into glutamic acid compared to simultaneous poor incorporation into the biochemically related amino acid, proline, parallels previous observations made during carbon 14 experiments with rust uredospores.Fourteen "bound" amino acids were isolated after acid hydrolysis of extracted spores. All contained nitrogen 15, the dilution of the added ammonia nitrogen ranging from 96 for glutamic acid to 7660 for proline.The results are taken as evidence that uredospores of wheat stem rust can incorporate ammonium nitrogen into free amino acids and into proteins.

THE COMPONENT FATTY ACIDS OF OILS FOUND IN SPORES OF PLANT RUSTS AND OTHER FUNGI. PART II

1962 ◽  
Vol 8 (3) ◽  
pp. 379-387 ◽  
Author(s):  
A. P. Tulloch ◽  
G. A. Ledingham
Keyword(s):  
Fatty Acids ◽  
Liquid Chromatography ◽  
Stem Rust ◽  
The Other ◽  
Gas Liquid Chromatography ◽  
Wheat Stem Rust ◽  
Alternate Hosts ◽  
Fat Composition

The oils extracted from the spores of 17 species of rusts have been analyzed by gas–liquid chromatography. The spore oils of six species of Puccinia, three species of Cronartium, one species each of Frommea, Hemileia, Phragmidium, and Uromyces contained cis-9, 10-epoxyoctadecanoic acid but it was absent from two species of Gymnosporangium, one species of Puccinia, and one of Uromyces. The Puccinia species include eight races of wheat stem rust which had very similar fat compositions. The different spore forms of wheat and oat stem rust from both the alternate hosts were also quite similar in fat composition. The oils of the spores from the alternate hosts for one of the Gymnosporangium species were similar but for the other species there were marked differences.

EFFECTS OF HYPOGLYCIN A ON THE METABOLISM OF AMINO ACIDS BY LIVER SLICES

1964 ◽  
Vol 42 (1) ◽  
pp. 139-142 ◽  
Author(s):  
S. J. Patrick ◽  
L. C. Stewart
Keyword(s):  
Amino Acids ◽  
Fatty Acids ◽  
Fatty Acid ◽  
Glutamic Acid ◽  
Rat Liver ◽  
Inhibitory Effects ◽  
Liver Slices

The effects of hypoglycin A on the metabolism of L-leucine-C14, L-alanine-C14, and L-glutamic-acid-C14 by rat liver slices have been investigated. Hypoglycin exerted markedly inhibitory effects on the conversion of leucine-C14 to fatty acid, cholesterol, and CO2. Conversion of alanine-C14 and glutamic acid-C14 to fatty acids was also inhibited by hypoglycin. No effects of hypoglycin on the conversion of C14-amino acids into protein or glycogen were demonstrated.

METABOLISM OF AROMATIC COMPOUNDS IN HEALTHY AND RUST-INFECTED PRIMARY LEAVES OF WHEAT: II. STUDIES WITH L-PHENYLALANINE-U-14C, L-TYROSINE-U-14C, AND FERULATE-U-14C

1967 ◽  
Vol 45 (11) ◽  
pp. 2137-2153 ◽  
Author(s):  
A. Fuchs ◽  
R. Rohringer ◽  
D. J. Samborski
Keyword(s):  
Amino Acids ◽  
Stem Rust ◽  
Aromatic Compounds ◽  
The Other ◽  
Major Portion ◽  
Insoluble Residue ◽  
Resistant Reaction ◽  
Wheat Leaves

Wheat leaves infected with stem rust, especially those of susceptible plants, contained more phenylalanine and tyrosine than healthy leaves. The utilization of phenylalanine was increased in both the susceptible and resistant reaction, but the utilization of tyrosine was increased only in the susceptible reaction. No evidence of interconversion of these amino acids was obtained.In n-butanol extracts, which contained glycosides, many constituents were labelled after feeding of L-phenylalanine-U-14C. Most of the n-butanol extractives from resistant-reacting leaves contained more label than those from susceptible-reacting leaves or from healthy leaves. However, one of the n-butanol extractives from susceptible-reacting leaves was 5–10 times as active as that isolated from the other tissues.With L-phenylalanine-U-14C and ferulate-U-14C as precursors, more activity was recovered in insoluble than in soluble esters (of ferulate and p-coumarate). With L-tyrosine-U-14C as precursor, the reverse was observed. After infection, the proportion of label in insoluble esters increased more in resistant leaves than it did in susceptible leaves, regardless of the precursor used.A major portion of the activity from these precursors was recovered in the insoluble residue that contained protein and other polymers. In the experiment with L-phenylalanine-U-14C, this residue was fractionated into protein and non-hydrolyzable material. Susceptible-reacting leaves contained equal amounts of activity in these fractions, while resistant-reacting leaves incorporated 2.5 times as much activity into the non-hydrolyzable material as into protein.

scholarly journals Utilization in vivo of glucose and volatile fatty acids by sheep brain for the synthesis of acidic amino acids

1966 ◽  
Vol 101 (3) ◽  
pp. 591-597 ◽  
Author(s):  
R M O'Neal ◽  
R E Koeppe ◽  
E I Williams
Keyword(s):  
Amino Acids ◽  
Fatty Acids ◽  
Glutamic Acid ◽  
Aspartic Acid ◽  
Free Amino Acids ◽  
Free Amino ◽  
Specific Activity ◽  
Tricarboxylic Acid Cycle ◽  
Sheep Brain ◽  
The Brain

1. Free glutamic acid, aspartic acid, glutamic acid from glutamine and, in some instances, the glutamic acid from glutathione and the aspartic acid from N-acetyl-aspartic acid were isolated from the brains of sheep and assayed for radioactivity after intravenous injection of [2-(14)C]glucose, [1-(14)C]acetate, [1-(14)C]butyrate or [2-(14)C]propionate. These brain components were also isolated and analysed from rats that had been given [2-(14)C]propionate. The results indicate that, as in rat brain, glucose is by far the best precursor of the free amino acids of sheep brain. 2. Degradation of the glutamate of brain yielded labelling patterns consistent with the proposal that the major route of pyruvate metabolism in brain is via acetyl-CoA, and that the short-chain fatty acids enter the brain without prior metabolism by other tissue and are metabolized in brain via the tricarboxylic acid cycle. 3. When labelled glucose was used as a precursor, glutamate always had a higher specific activity than glutamine; when labelled fatty acids were used, the reverse was true. These findings add support and complexity to the concept of the metabolic; compartmentation' of the free amino acids of brain. 4. The results from experiments with labelled propionate strongly suggest that brain metabolizes propionate via succinate and that this metabolic route may be a limited but important source of dicarboxylic acids in the brain.

Utilisation of the end products of ruminant digestion

1957 ◽  
Vol 1957 ◽  
pp. 3-15 ◽  
Author(s):  
D. G. Armstrong ◽  
K. L. Blaxter ◽  
N. McC. Graham
Keyword(s):  
Amino Acids ◽  
Fatty Acids ◽  
Quantitative Data ◽  
Volatile Fatty Acids ◽  
Energy Requirement ◽  
The Body ◽  
Energy Requirements ◽  
Dietary Carbohydrate ◽  
Body Tissues ◽  
End Products

The work of the late Sir Joseph Barcroft and his collaborators (see Elsden & Phillipson, 1948) left little doubt that, in ruminants, the end products of the bacterial dissimilation of dietary carbohydrate included large amounts of the steam-volatile fatty acids—acetic, propionic and butyric acids. More recently, el Shazly (1952a, b) has shown that the steam-volatile fatty acids also arise together with ammonia during the bacterial breakdown of amino-acids in the rumen. Studies by Pfander & Phillipson (1953) and Schambye (1955) further indicate that the acids are absorbed from the digestive tract in amounts that suggest they make a major contribution to the energy requirement of the animal. Quantitative data relative to the amounts absorbed, however, are difficult to obtain. Carroll & Hungate (1954) have calculated that in cattle some 6,000-12,000 Cal. of energy are available from the acids produced by fermentation in the rumen. With sheep, Phillipson & Cuthbertson (1956) have calculated from the results of Schambye (1951a, b; 1955) that at least 600-1,200 Cal. of energy in the form of steam-volatile fatty acids could be absorbed every 24 hrs. Since the fasting heat production of the steer is about 6,500 Cal./24 hrs. and that of the sheep about 1,100 Cal./24 hrs. it is clear that if the fatty acids can be utilised efficiently by the body tissues, they could make a major contribution to the energy requirements, at least those for maintenance.

Sign in / Sign up

Export Citation Format

Share Document