scholarly journals Ammonia production by rumen microorganisms and the enumeration and isolation of bacteria capable of growth on peptides and amino acids from the sheep rumen

1997 ◽  
Vol 37 (Suppl. 1) ◽  
pp. 63-64
Author(s):  
S. Eschenlauer ◽  
CJ Newbold ◽  
N. McKain ◽  
ND Walker ◽  
RJ Wallace
Author(s):  
R.J. Wallace

Protein is broken down by rumen microorganisms via peptides and amino acids to produce ammonia at rates which frequently exceed microbial requirements for N. Much of the ammonia-N formed in this way is eventually excreted as urea. If any of the steps in the degradation sequence could be inhibited, excessive ammonia production would be reduced. More protein, peptides or amino acids would escape fermentation in the rumen, thereby improving the protein nutrition of the host animal.The breakdown of peptides to amino acids is a central part of the degradation sequence. The main enzymic mechanism by which peptides are hydrolysed in the rumen is a bacterial dipeptidyl aminopeptidase, which cleaves dipeptides from the N-terminus of the peptide chain (Wallace & McKain, 1990). Little carboxypeptidase activity appears to be present. The present experiments were undertaken to find out to what extent blocking the N-terminus of peptides enables them to survive degradation in rumen fluid, and to determine which peptides can be protected in this way.


1998 ◽  
Vol 1998 ◽  
pp. 175-175
Author(s):  
C. Atasoglu ◽  
N.D. Walker ◽  
C.J. Newbold ◽  
R.J. Wallace

Ammonia plays an important role in providing N for protein synthesis by rumen microorganisms. Studies using [15N]ammonia or [15N]urea indicate that the proportion of microbial nitrogen derived from ammonia is highly variable, ranging from 18 to 100% (Nolan, 1975; Salter et al., 1979). Peptides and amino acids are also incorporated by rumen microorganisms. They generally stimulate growth (Argyle & Baldwin, 1989), but little is known about the factors which govern the relative proportions of microbial amino acids which are derived from pre-formed amino acids and from ammonia. The present study was undertaken to determine how the concentration of peptides affects ammonia incorporation and the de novo synthesis of individual amino acids by mixed rumen microorganisms.


1998 ◽  
Vol 1998 ◽  
pp. 175-175
Author(s):  
C. Atasoglu ◽  
N.D. Walker ◽  
C.J. Newbold ◽  
R.J. Wallace

Ammonia plays an important role in providing N for protein synthesis by rumen microorganisms. Studies using [15N]ammonia or [15N]urea indicate that the proportion of microbial nitrogen derived from ammonia is highly variable, ranging from 18 to 100% (Nolan, 1975; Salter et al., 1979). Peptides and amino acids are also incorporated by rumen microorganisms. They generally stimulate growth (Argyle & Baldwin, 1989), but little is known about the factors which govern the relative proportions of microbial amino acids which are derived from pre-formed amino acids and from ammonia. The present study was undertaken to determine how the concentration of peptides affects ammonia incorporation and the de novo synthesis of individual amino acids by mixed rumen microorganisms.


1999 ◽  
Vol 1999 ◽  
pp. 212-212 ◽  
Author(s):  
C. Atasoglu ◽  
C.J. Newbold ◽  
R.J. Wallace

Ammonia is thought to be the main source of nitrogen for protein synthesis by the rumen microorganisms, but peptides and amino acids derived from protein degradation are also incorporated into microbial protein. Recent experiments carried out by Atasogluet al.(1998) demonstrated that preformed amino acids decrease the uptake of ammonia into microbial protein and microbial amino acids in a concentration-dependent manner. However, little is known about how rumen ammonia concentrations affect ammonia uptake into microbial protein. The present study was undertaken to determine the influence of rumen ammonia concentrations on ammonia incorporation andde novosynthesis of individual amino acids by the mixed rumen microorganismsin vitro.


1955 ◽  
Vol 33 (1) ◽  
pp. 1-9
Author(s):  
Donn J. Kushner ◽  
Enid Pascoe

The adaptive formation of formic hydrogenlyase in E. coli and of the enzymes oxidizing benzoate, malonate, and L-tyrosine in P. fluorescens is inhibited by benzimidazole. In one strain of E. coli tryptophan and alanine in combination completely reverse the benzimidazole inhibition. In another strain tryptophan partly reverses the inhibition but alanine is without effect. These amino acids are without effect on the benzimidazole inhibition of adaptation in P. fluorescens. Adenine and guanine have no action on the benzimidazole inhibition in both bacterial species.Tryptophan disappears anaerobically in the presence of E. coli. Ammonia production accompanies tryptophan disappearance. This disappearance, which probably involves a destruction of the tryptophan molecule, is inhibited by benzimidazole.


1970 ◽  
Vol 50 (2) ◽  
pp. 397-400 ◽  
Author(s):  
E. A. Ibrahim ◽  
J. R. Ingalls ◽  
D. B. Bragg

not available


1974 ◽  
Vol 20 (2) ◽  
pp. 183-185 ◽  
Author(s):  
B. Emmanuel ◽  
L. P. Milligan ◽  
B. V. Turner

Rumen contents were incubated in vitro with acetate-1-14C. Significant amounts of 14C were incorporated into rumen microbial proteins, nucleic acids, and lipids. Serine, glutamic acid, methionine, and cystine were highly labeled, whereas less, or insignificant radioactivity was found in other amino acids. Acetate was incorporated into a wide range of microbial fatty acids. The quantitative significance of acetate metabolism is discussed.


1991 ◽  
Vol 71 (4) ◽  
pp. 1111-1124 ◽  
Author(s):  
J. Brun-Bellut ◽  
J. M. Kelly ◽  
G. W. Mathison ◽  
R. J. Christopherson

Nitrogen flow and exchanges in the digestive tract were measured in three goats during a dry stage and a subsequent hormonally induced lactation stage. Two diets, formulated with and without urea to contain either a high or low level of crude protein and rumen-degradable protein (RDP), were tested in a crossover experimental design within each stage. The amount of urea nitrogen (N) recycled to the ruminoreticulum was higher (P < 0.05) during lactation (3.5 g d−1) than in the dry stage (0.9 g d−1), as was plasma urea concentration. However, the mean amount of urea recycled was lower (P < 0.05) when the high-RDP diet was fed (1.4 g N d−1) than when the low-RDP diet was fed (3.0 g N d−1), even though the plasma urea concentration tended to be higher in goats fed the high-RDP diet. Of the estimated ruminally available N, 90–110% was incorporated into microbial cells. The proportion of bacterial N derived from rumen ammonia (0.77–0.89) was not influenced by protein source or lactation. Of the amino acids flowing into the duodenum, 69–75% were apparently absorbed in the small intestine, whereas total digestive tract apparent digestibility ranged from 81 to 83%. No more than 60% of the fecal N was derived from undigested bacteria from the rumen. It was concluded that the amount of urea which is recycled to the rumen is under metabolic control and that there is efficient use of ruminally available N by rumen microorganisms. Key words: Goats, lactation, rumen-degradable protein, 15N, urea recycling, amino acids


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