Literature DB >> 3247288

The effect of compactional pressure on urease activity.

C L Teng1, M J Groves.   

Abstract

Jack bean urease is a proteinaceous enzyme, MW approximately 489 kD, readily soluble in water but losing activity when sheared in solution at stresses as low as 2.5 Pa. There is a need for controlled-release forms of many of the new genetically engineered peptide and polypeptide drugs with high specific activities. The simplest form of controlled release would be a sterile compressed pellet of the active component inserted subdermally. However, "activity" may be lost on compaction. Urease can be regarded as a model protein which may lose activity when sheared during compaction in the dry state. Tablets of urease weighing 100 mg were compressed over a range of pressures from 60 to 1750 MPa. No relative loss of activity would be detected following compaction at pressures up to 474 MPa. Above this limiting pressure there was a 50% loss of relative activity, evidently by a compactional effect on the protein quaternary and tertiary structures. No direct relationship was observed between stress (compactional pressure) and inactivation.

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Year:  1988        PMID: 3247288     DOI: 10.1023/a:1015988718381

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  17 in total

1.  A thermochemical study of the hydrolysis of urea by urease.

Authors:  N D Jespersen
Journal:  J Am Chem Soc       Date:  1975-04-02       Impact factor: 15.419

2.  A rapid and precise method for the determination of urea.

Authors:  J K FAWCETT; J E SCOTT
Journal:  J Clin Pathol       Date:  1960-03       Impact factor: 3.411

3.  Emerging trends in biotechnology: a perspective from the pharmaceutical industry.

Authors:  W Szkrybalo
Journal:  Pharm Res       Date:  1987-10       Impact factor: 4.200

4.  A study of the structural subunits of urease obtained during controlled dissociation.

Authors:  C C Contaxis; F J Reithel
Journal:  Can J Biochem       Date:  1972-05

5.  Enzyme inactivation with shearing.

Authors:  S E Charm; B L Wong
Journal:  Biotechnol Bioeng       Date:  1970-11       Impact factor: 4.530

6.  Inhibition of urease by metal ions.

Authors:  R B Hughes; S A Katz; S E Stubbins
Journal:  Enzymologia       Date:  1969-06-30

7.  [Studies on inactivation of powder enzyme by shearing operation (author's transl)].

Authors:  I Horikoshi; N Takeguchi; M Morii; A Sano
Journal:  Yakugaku Zasshi       Date:  1977-02       Impact factor: 0.302

8.  Electron microscopy of negatively stained jackbean urease at three levels of quaternary structure, and comparison with hydrodynamic studies.

Authors:  W N Fishbein; W F Engler; J L Griffin; W Scurzl; G F Bahr
Journal:  Eur J Biochem       Date:  1977-02-15

9.  [Molecular galenics. 12. Inactivation of pepsin by pressure-mechanical denaturation of proteins].

Authors:  R Hüttenrauch; I Keiner
Journal:  Pharmazie       Date:  1976-08       Impact factor: 1.267

10.  The subunit structure of jack-bean urease.

Authors:  C J Bailey; D Boulter
Journal:  Biochem J       Date:  1969-07       Impact factor: 3.857

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  1 in total

1.  The effect of compactional pressure on a wheat germ lipase preparation.

Authors:  M H Zarrintan; C D Teng; M J Groves
Journal:  Pharm Res       Date:  1990-03       Impact factor: 4.200

  1 in total

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