Hostname: page-component-848d4c4894-xm8r8 Total loading time: 0 Render date: 2024-06-20T12:36:42.215Z Has data issue: false hasContentIssue false

Bovine milk N-acetyl-β-D-glucosaminidase and its significance in the detection of abnormal udder secretions

Published online by Cambridge University Press:  01 June 2009

B. J. Kitchen
Affiliation:
Otto Madsen Dairy Research Laboratory, Department of Primary Industries, Hamilton, Brisbane, Australia, 4007
G. Middleton
Affiliation:
Otto Madsen Dairy Research Laboratory, Department of Primary Industries, Hamilton, Brisbane, Australia, 4007
M. Salmon
Affiliation:
Otto Madsen Dairy Research Laboratory, Department of Primary Industries, Hamilton, Brisbane, Australia, 4007

Summary

A new spectrofluorimetric assay procedure for bovine milk N-acetyl-β-D-glucosaminidase (NAGase) is described for use as a routine screening test for the detection of abnormal uddersecretions. This procedure uses 4-methylumbel-liferyl-N-acetyl-β-D-glucosaminide as substrate. On the basis of the greater sample throughput, increased product sensitivity detection of NAGase and the absence of turbidity problems, it is considered to be superior to a previously reported spectrophotometric procedure (Kitchen, 1976). The correlation coefficient between the somatic cell count and the fluorimetric procedure using 243 quarter fore-milk samples was 0·86. Distribution studies on bovine milk and mammary gland homogenates indicated that this enzyme activity was located predominantly in the soluble whey protein fraction and the post-microsomal supernatant. Mammary gland secretory cells contained high levels of NAGase and appeared to be the major source of the enzyme in milk whilst NAGase from other sources (white blood cells, blood serum) contributed only a minor proportion (5–15%) of the total activity in milk. The implications of these findings on the value of the NAGase test as a means of mastitis diagnosis are discussed.

Type
Original Articles
Copyright
Copyright © Proprietors of Journal of Dairy Research 1978

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Brown, R. W., Morse, G. E., Newbould, F. H. S. & Slanetz, L. W. (1969). Microbiological Procedures for the Diagnosis of Bovine Mastitis, pp. 45. Washington, D.C.: National Mastitis Council.Google Scholar
Carlson, G. P. & Kaneko, J. J. (1973). Proceedings of the Society for Experimental Biology and Medicine 142, 853.Google Scholar
Chandler, R. L., Reid, I. M., Harrison, R. & France, B. R. (1974). Journal of Comparative Pathology 84, 517.Google Scholar
Harmon, R. J., Schanbacher, F. L., Ferguson, L. C. & Smith, K. L. (1975). American Journal of Veterinary Research 36, 1001.Google Scholar
Harmon, R. J., Schanbacher, F. L., Ferguson, L. C. & Smith, K. L. (1976). Infection and Immunity 13, 533.Google Scholar
Janzen, J. J. (1968). Journal of Dairy Science 51, 1857.CrossRefGoogle Scholar
Kitchen, B. J. (1974). Biochimica et Biophysica Acta 356, 257.CrossRefGoogle Scholar
Kitchen, B. J. (1976). Journal of Dairy Research 43, 251.CrossRefGoogle Scholar
Kitchen, B. J. & Middleton, G. (1976 a). Australian Veterinary Journal 52, 102.Google Scholar
Kitchen, B. J. & Middleton, G. (1976 b). Journal of Dairy Research 43, 491.CrossRefGoogle Scholar
Linzell, J. L. & Peaker, M. (1971). Physiological Reviews 51, 564.CrossRefGoogle Scholar
Mellors, A. (1968). Canadian Journal of Biochemistry 46, 451.Google Scholar
Patton, S., Hood, L. F. & Patton, J. S. (1969). Journal of Lipid Research 10, 260.CrossRefGoogle Scholar
Plantz, P. E. & Patton, S. (1973). Biochimica et Biophysica Acta 291, 51.CrossRefGoogle Scholar