SIGNIFICANCE OF N15 EXCESS IN NITROGENOUS COMPOUNDS OF BIOLOGICAL ORIGIN

1963 ◽  
Vol 41 (1) ◽  
pp. 1089-1097 ◽  
Author(s):  
O. H. Gaebler ◽  
Harold C. Choitz ◽  
Trieste G. Vitti ◽  
Robert Vukmirovich

The purpose of this study was to determine whether the small increase in abundance of N15 normally found in nitrogenous compounds of biological origin is primarily due to mass discrimination in nitrogen metabolism, or to reproducible analytical errors.This problem was approached by repeatedly determining N15 in the same series of nine amino acids, either purchased in chromatographically pure form or isolated from proteins of rat liver, dog serum, and six plant sources. Proteins and amino acids included in the study were selected on the premise that concentration or redistribution of N15 might occur in such processes in urea formation, nitrogen transfer, or nitrogen fixation. Data for N15 excess in a series of alkaloids were also secured.Standard deviations obtained in series of analyses were too small, and values for N15 excess in the same amino acids isolated from different sources too variable, to permit interpreting the observed N15 excess as a reproducible error. Distribution of N15 in amino acids of the animal proteins studied resembled that observed when N15-labelled amino acids or ammonium compounds are given. Differences between results for amino acids of animal and plant origin also supported the idea that the small excess of N15 normally found is metabolically as well as statistically significant. Results for N15 in amide nitrogen likewise supported this view. The smallest excess of N15 occurred in amino acids from proteins of legumes, which fix nitrogen. In synthetic amino acids, the concentration of N15 was more often below than above normal abundance.


1963 ◽  
Vol 41 (5) ◽  
pp. 1089-1097 ◽  
Author(s):  
O. H. Gaebler ◽  
Harold C. Choitz ◽  
Trieste G. Vitti ◽  
Robert Vukmirovich

The purpose of this study was to determine whether the small increase in abundance of N15 normally found in nitrogenous compounds of biological origin is primarily due to mass discrimination in nitrogen metabolism, or to reproducible analytical errors.This problem was approached by repeatedly determining N15 in the same series of nine amino acids, either purchased in chromatographically pure form or isolated from proteins of rat liver, dog serum, and six plant sources. Proteins and amino acids included in the study were selected on the premise that concentration or redistribution of N15 might occur in such processes in urea formation, nitrogen transfer, or nitrogen fixation. Data for N15 excess in a series of alkaloids were also secured.Standard deviations obtained in series of analyses were too small, and values for N15 excess in the same amino acids isolated from different sources too variable, to permit interpreting the observed N15 excess as a reproducible error. Distribution of N15 in amino acids of the animal proteins studied resembled that observed when N15-labelled amino acids or ammonium compounds are given. Differences between results for amino acids of animal and plant origin also supported the idea that the small excess of N15 normally found is metabolically as well as statistically significant. Results for N15 in amide nitrogen likewise supported this view. The smallest excess of N15 occurred in amino acids from proteins of legumes, which fix nitrogen. In synthetic amino acids, the concentration of N15 was more often below than above normal abundance.



1967 ◽  
Vol 13 (11) ◽  
pp. 1509-1519 ◽  
Author(s):  
V. P. Agnihotri ◽  
O. Vaartaja

The utilization of N compounds by P. ultimum Trow (strain I and II), P. rostratum Butler, and P. irregulare Buisman was examined in a chemically denned medium under controlled conditions in surface culture. All species were able to metabolize nitrate, ammonium, and organic nitrogen, and the amount of growth varied with the nitrogen source. In general, yeast extract, peptone, glycine, serine, histidine, cysteine, asparagine, aspartic acid, and glutamic acid supported favorable growth, whereas γ-aminobutyric acid, threonine, and alanine supported poor growth of these fungi. The addition of succinic acid at 0.02 M concentration to ammonium compounds further increased growth of four isolates.Preferential utilization of amino acids from a given mixture was recorded using paper chromatographic techniques. All four isolates gave more vegetative growth on mixtures of amino acids than when they were supplied singly.



1968 ◽  
Vol 14 (11) ◽  
pp. 1253-1258 ◽  
Author(s):  
V. P. Agnihotri

The effects of different nitrogen sources on growth and sclerotial production by Aspergillus niger were determined on a synthetic agar medium. The organism used inorganic, organic, and ammonium nitrogen for growth and sclerotial production. Among the ammonium compounds tested, the chloride, phosphate, sulfate, and carbonate were used poorly, but the nitrate was well utilized. Addition of organic acids to ammonium compounds increased sclerotial production. Raising the concentration of sodium nitrate to a certain level (0.15%) increased the number of sclerotial initials and the number and weight of those which matured. Sodium nitrite curtailed mycelial growth and prevented production of sclerotia. Utilization of nitrite was accelerated by adjusting the pH on the alkaline side from 7.5 to 9.0. Urea supported poor sclerotial production; thiourea inhibited it. Of the amino acids, histidine yielded the most and arginine the least number of sclerotia. In lysine medium, the white cottony sclerotial initials remained fluffy even after 20 days. Sclerotial production decreased significantly when proline, glutamic acid, or leucine were omitted from the basal medium containing 10 amino acids. In general, no correlation existed between the number of sclerotia formed and the dry weight they attained on different nitrogen sources. With certain nitrogen sources sclerotial initials failed to mature.



2020 ◽  
Vol 21 (8) ◽  
pp. 785-798 ◽  
Author(s):  
Abedin Abdallah ◽  
Evera Elemba ◽  
Qingzhen Zhong ◽  
Zewei Sun

The gastrointestinal tract (GIT) of humans and animals is host to a complex community of different microorganisms whose activities significantly influence host nutrition and health through enhanced metabolic capabilities, protection against pathogens, and regulation of the gastrointestinal development and immune system. New molecular technologies and concepts have revealed distinct interactions between the gut microbiota and dietary amino acids (AAs) especially in relation to AA metabolism and utilization in resident bacteria in the digestive tract, and these interactions may play significant roles in host nutrition and health as well as the efficiency of dietary AA supplementation. After the protein is digested and AAs and peptides are absorbed in the small intestine, significant levels of endogenous and exogenous nitrogenous compounds enter the large intestine through the ileocaecal junction. Once they move in the colonic lumen, these compounds are not markedly absorbed by the large intestinal mucosa, but undergo intense proteolysis by colonic microbiota leading to the release of peptides and AAs and result in the production of numerous bacterial metabolites such as ammonia, amines, short-chain fatty acids (SCFAs), branched-chain fatty acids (BCFAs), hydrogen sulfide, organic acids, and phenols. These metabolites influence various signaling pathways in epithelial cells, regulate the mucosal immune system in the host, and modulate gene expression of bacteria which results in the synthesis of enzymes associated with AA metabolism. This review aims to summarize the current literature relating to how the interactions between dietary amino acids and gut microbiota may promote host nutrition and health.



Author(s):  
E. D. S. Corner ◽  
B. S. Newell

A study has been made of the nitrogenous compounds excreted by Calanus helgolandicus (Claus) collected at Plymouth.Most of the excreted nitrogen is in the form of ammonia which accounts for 60–100% (average 74.3%) of the total, and some of the remainder may be lost as urea. There is no evidence for the excretion of measurable amounts of amino acids.Whether the animals are starved or fed they are primarily ammonotelic, and the quantity of ammonia produced at 10° C (3.33 μg/g. dry body wt/day) is not significantly changed when the animals are used at an abnormally high experimental density. This latter condition does, however, lead to the production of large quantities of additional nitrogenous substances that give a positive reaction with ninhydrin.IntroductionThe amounts of nitrogen excreted by zooplankton have been measured by several workers. Harris (1959) used the method of Riley (1953) to estimate the copious quantities of ammonia produced by animals (mainly Acartia tonsa and A. clausi) collected from Long Island Sound; Beers (1964), in laboratory experiments with the chaetognath Sagitta hispida, estimated the excreted ammonia by the procedure of Kruse & Mellon (1952); and Corner, Cowey & Marshall (1965) determined the ammonia excreted by Calanus helgolandicus and C. finmarchicus, using a ninhydrin technique described by Moore & Stein (1954). The methods employed by Harris and by Beers are specific for ammonia: that used by Corner et al. estimates nitrogenous substances (e.g. amino acids) in addition to ammonia, but certain tests were made which seemed to exclude the possibility that these substances contributed significantly to the nitrogen excreted by the animals.



1990 ◽  
Vol 29 (1-2) ◽  
pp. 51-53 ◽  
Author(s):  
A. Dyremark ◽  
M. Ericsson


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