Distribution of radiomanganese in the rumen of sheep

1981 ◽  
Vol 59 (1) ◽  
pp. 76-83 ◽  
Author(s):  
M. Ivan

Twelve sheep, each prepared with a rumen fistula, were divided into three groups of four and fed three dietary levels of manganese (22, 300, and 3000 μg/g dry matter) for 11 weeks. The sheep were then dosed with radioactive manganese and samples of rumen contents were taken via the rumen fistula at 1, 7, and 13 h after dosing. The sheep were immediately killed after the last sampling and total rumen contents were mixed and sampled. Rumen fluid was separated from all samples and fractionated by centrifugation into protozoa plus plant particles, bacteria, and cell-free fraction. The bacterial cells were disrupted and fractionated into cell walls and cytoplasm. The cytoplasmic protein was precipitated with trichloroacetic acid.Although the concentration of radiomanganese in rumen fluid decreased with time after dosing from 14.4–17.8 to 6.1–9.3% of dose/L the protozoal and bacterial uptakes of radiomanganese were not significantly different and ranged from 26.5 to 40.6% and 18.9 to 31.7% of total in the rumen fluid, respectively. There was also no effect of dietary concentration of manganese on the uptake and distribution of radiomanganese in the rumen fluid fractions. However, on the average more radiomanganese was found in the bacterial cell walls (48.1–75.3% of total in bacteria) and less in the cytoplasm (51.9–24.7% of total in bacteria) with increasing dietary manganese. Very little radioactivity was found in the trichloroacetic acid precipitated cytoplasm (1.79–0.78% of total in cytoplasm). Concentrations of manganese in the bacteria and bacterial cell walls were higher than, and closely related with, those in the diet. Specific activities of radiomanganese decreased in all fractions with increasing dietary manganese. Approximately 15–17% of the total radiomanganese in the rumen contents at 13 h after dosing was found in the protozoal fraction and 10–15% was found in the bacterial fraction; only approximately 21% of the radiomanganese remained in cell-free fraction of the rumen fluid in each dietary treatment.

2018 ◽  
Vol 2018 ◽  
pp. 1-9 ◽  
Author(s):  
Wenxue Chen ◽  
Lan Zou ◽  
Weijun Chen ◽  
Yueying Hu ◽  
Haiming Chen

The chemical composition and antimicrobial mechanism of action of black pepper chloroform extract (BPCE) were investigated, as well as the potential antibacterial activities of BPCE against Escherichia coli and Staphylococcus aureus. The results showed that 1H-Cycloprop[e]azulen-7-ol, decahydro-1,1,7-trimethyl-4-methylene-, [1ar-(1aα,4aα,7β,7a,β,7bα.)]- (8.39%) and 2-methylene-4,8,8-trimethyl-4-vinyl-bicyclo[5.2.0]nonane (6.92%) were identified as the two primary components of BPCE. The release of intracellular transaminases from bacteria after being incubated with BPCE revealed that the bacterial cell walls and membranes were degraded and that protein synthesis was inhibited to some extent. The inhibition of bacterial Na+/K+-ATPase activity upon the addition of BPCE also indicated an enhanced permeability of bacterial cell membranes. Moreover, an analysis of hexokinase and pyruvate kinase activities showed that BPCE affected the metabolic rate of glycolysis and disrupted the normal metabolism of bacteria. This phenomenon was supported by an observed accumulation of lactic acid (LA) in the treated bacterial cells. Overall, our results indicated that BPCE damaged bacterial cell walls and membranes, which was followed by a disruption of bacterial cell respiration.


1968 ◽  
Vol 243 (11) ◽  
pp. 3169-3179 ◽  
Author(s):  
D J Tipper ◽  
J L Strominger

1981 ◽  
Vol 256 (17) ◽  
pp. 9229-9234
Author(s):  
E Benedetti ◽  
B Di Blasio ◽  
V Pavone ◽  
C Pedone ◽  
C Toniolo ◽  
...  

1970 ◽  
Vol 245 (14) ◽  
pp. 3675-3682
Author(s):  
Roland Plapp ◽  
Jack L. Strominger

1966 ◽  
Vol 116 ◽  
pp. 487-515 ◽  
Author(s):  
John S. Anderson ◽  
Pauline M. Meadow ◽  
Mary A. Haskin ◽  
Jack L. Strominger

1991 ◽  
Vol 260 (1) ◽  
pp. R126-R133 ◽  
Author(s):  
L. Johannsen ◽  
J. Wecke ◽  
F. Obal ◽  
J. M. Krueger

Muramyl peptides have a variety of biological effects in mammals, including enhancement of the immune response, sleep, and body temperature. Although mammals lack biosynthetic pathways for muramyl peptides, they are found in mammals and are well known as components of bacterial cell walls. This suggests that phagocytic mammalian cells digest bacterial cell walls and produce biologically active muramyl peptides. Staphylococcal cell walls were radioactively labeled during growth of the bacteria. During the digestion of these radiolabeled bacteria, murine bone marrow macrophages produced low-molecular-weight substances that coeluted chromatographically with the radioactive cell wall marker. Further separation of these substances using reversed-phase high-performance liquid chromatography resulted in the isolation of substances with high specific biological activity. Intracerebroventricular injection of rabbits with these substances induced an increase in slow-wave sleep and body temperature and a suppression of rapid-eye-movement sleep. The characteristics of the biological responses and the chromatographic behavior of the active components are consistent with those of muramyl peptides. The ability of macrophages to tailor muramyl peptides from peptidoglycan may provide an amplification step for the immune response. Muramyl peptides released by macrophages may also act as mediators for various facets of the acute phase response elicited by bacterial infections such as fever and sleep.


1965 ◽  
Vol 11 (1) ◽  
pp. 109-118 ◽  
Author(s):  
D. C. Gillespie ◽  
F. D. Cook

Soil organisms belonging to the myxobacter group and predatory on molds, yeasts, nematodes, and streptomycetes as well as on a wide range of bacteria elaborate at least two extracellular enzymes: a protease and a lysin. The protease hydrolyzes casein and haemoglobin and is inactive against bacterial cell walls while the lysin hydrolyzes bacterial cell walls but is inactive on proteins. These enzymes have been separated on hydroxylapatite columns and some of their properties are described. The predatory action of many of the isolates may be explained by the secretion and subsequent action of these two enzymes.


1982 ◽  
Vol 38 (3) ◽  
pp. 817-824 ◽  
Author(s):  
T Ogawa ◽  
S Kotani ◽  
K Fukuda ◽  
Y Tsukamoto ◽  
M Mori ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document