Literature DB >> 822843

Purification and properties of pantothenase from Pseudomonas fluorescens.

R K Airas, E A Hietanen, V T Nurmikko.   

Abstract

Pantothenase (EC 3.5.1.22) from Pseudomonas fluorescens UK-1 was purified to homogeneity as judged by disc-gel electrophoresis and isoelectric focusing. The purification procedure consisted of four steps: DEAE-Sephadex chromatography, (NH4)2SO4 precipitation, hydroxyapatite chromatography and preparative polyacrylamide-gel electrophoresis. Gel filtration on Ultrogel AcA 34 was used to determine the molecular weight, and sodium dodecyl sulphate/polyacrylamide-gel electrophoresis to study the subunit molecular weight. The enzyme appeared to be composed of two subunits with mol.wts. of approx. 50000 each. The total mol.wt. of the enzyme was thus about 100000. The isoelectric point was 4.7 at 10 degrees C.

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Year:  1976        PMID: 822843      PMCID: PMC1163867          DOI: 10.1042/bj1570409

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  9 in total

1.  DISC ELECTROPHORESIS. II. METHOD AND APPLICATION TO HUMAN SERUM PROTEINS.

Authors:  B J DAVIS
Journal:  Ann N Y Acad Sci       Date:  1964-12-28       Impact factor: 5.691

2.  Spectroscopic determination of tryptophan and tyrosine in proteins.

Authors:  H Edelhoch
Journal:  Biochemistry       Date:  1967-07       Impact factor: 3.162

3.  Kinetic studies on pantothenase from Pseudomonas fluorescens. Effects of pH on substrate and inhibitor binding.

Authors:  K Airas
Journal:  Biochem J       Date:  1976-08-01       Impact factor: 3.857

4.  Thermal inactivation and reactivation of an enzyme in vivo. Pantothenate hydrolase of Pseudomonas fluorescens.

Authors:  R K Airas
Journal:  Biochem J       Date:  1972-11       Impact factor: 3.857

5.  Measurement of molecular weights by electrophoresis on SDS-acrylamide gel.

Authors:  K Weber; J R Pringle; M Osborn
Journal:  Methods Enzymol       Date:  1972       Impact factor: 1.600

6.  Sensitive biuret method for determination of protein in an impure system such as whole bacteria.

Authors:  A L Koch; S L Putnam
Journal:  Anal Biochem       Date:  1971-11       Impact factor: 3.365

7.  The bacterial degradation of pantothenic acid. I. Over-all nature of the reaction.

Authors:  C T Goodhue; E E Snell
Journal:  Biochemistry       Date:  1966-02       Impact factor: 3.162

8.  The bacterial degradation of pantothenic acid. II. Pantothenate hydrolase.

Authors:  V Nurmikko; E Salo; H Hakola; K Mäkinen; E E Snell
Journal:  Biochemistry       Date:  1966-02       Impact factor: 3.162

9.  The aerobic pseudomonads: a taxonomic study.

Authors:  R Y Stanier; N J Palleroni; M Doudoroff
Journal:  J Gen Microbiol       Date:  1966-05
  9 in total
  2 in total

1.  Kinetic studies on pantothenase from Pseudomonas fluorescens. Effects of pH on substrate and inhibitor binding.

Authors:  K Airas
Journal:  Biochem J       Date:  1976-08-01       Impact factor: 3.857

2.  Pantothenases from pseudomonads produce either pantoyl lactone or pantoic acid.

Authors:  R K Airas
Journal:  Biochem J       Date:  1988-03-01       Impact factor: 3.857

  2 in total

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