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Adsorption of soluble proteins to rumen bacteria and the role of adsorption in proteolysis

Published online by Cambridge University Press:  24 July 2007

R. J. Wallace
Affiliation:
Rowett Research InstituteBucksburn, Aberdeen AB2 9SB
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Abstract

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1. Following the addition of I4C-labelled casein to mixed rumen bacteria at 39°, some radioactivity was adsorbed to the bacteria before the casein was hydrolysed. At O°, the rate of hydrolysis was greatly diminished but adsorption still occurred, and this enabled a study of the adsorption mechanism to be made.

2. The adsorption of 14C-labelled casein to rumen bacteria was a saturable process. The maximum binding capacity was about 10 μ I4C-labelled casein/mg bacterial protein.

3. The ability of bacteria to adsorb 14C-labelled casein was abolished when they had been boiled for 5 min. Boiling caused the release of material from the bacteria which rendered some undigested protein soluble in 50 g trichloroacetic acid/l.

4. Adsorbed 14C-labelled casein could be partly displaced by the addition of Triton XI00 or an excess of unlabelled casein, or by boiling, or by removal of capsular material by blending. Adsorbed 14C-labelled haemoglobin could similarly be displaced by an excess of cold casein.

5. When an excess of casein was added to bacteria to which glucose-6-phosphate dehydrogenase (EC I. I.I.49) and glucosephosphate isomerase (EC 5.3. I.9) had been adsorbed, little active enzyme was displaced.

6. The susceptibility of different 14C-labelled proteins to hydrolysis corresponded to their relative adsorption affinities.

7. The pattern of sensitivity to inhibitors of the adsorption mechanism was the same as that for the inhibition of the bacterial hydrolysis of 14C-labelled casein, and the synthetic substrates leucine p-nitroanilide and benzoyl arginine p-nitroanilide.

8. It was concluded that the adsorption site and the catalytic site for proteolysis by rumen bacteria are probably identical and so not likely to be subject to independent manipulation.

Type
Papers on General Nutrition
Copyright
Copyright © The Nutrition Society 1985

References

Blackburn, T. H. (1968). Journal of General Microbiology 53, 3751.CrossRefGoogle Scholar
Blackburn, T. H. & Hobson, P. N. (1960). Journal of General Microbiology 22, 272281.CrossRefGoogle Scholar
Brock, F. M., Forsberg, C. W. & Buchanan-Smith, J. G. (1982). Applied and Environmental Microbiology 44, 561569.CrossRefGoogle Scholar
Hazlewood, G. P. & Edwards, R. (1981). Journal of General Microbiology 125, 1115.Google Scholar
Herbert, D., Phipps, P. J. & Strange, R. E. (1971). Methods in Microbiology 5B, 209344.CrossRefGoogle Scholar
Kopecny, J. & Wallace, R. J. (1982). Applied and Environmental Microbiology 43, 10261033.CrossRefGoogle Scholar
Mangan, J. L. (1972). British Journal of Nutrition 27, 261283.CrossRefGoogle Scholar
Nugent, J. H. A., Jones, W. T., Jordan, D. J. & Mangan, J. L. (1983). British Journal of Nutrition 50, 357368.CrossRefGoogle Scholar
Nugent, J. H. A. & Mangan, J. L. (1981). British Journal of Nutrition 46, 3959.CrossRefGoogle Scholar
Wallace, R. J. (1983). British Journal of Nutrition 50, 345355.CrossRefGoogle Scholar
Wallace, R. J. & Kopecny, J. (1983). Applied and Environmental Microbiology 45, 212217.CrossRefGoogle Scholar
Wright, D. E. (1967). Applied Microbiology 15, 547550.CrossRefGoogle Scholar