Literature DB >> 7235692

Heparinase production by Flavobacterium heparinum.

P M Galliher, C L Cooney, R Langer, R J Linhardt.   

Abstract

Heparinase production by Flavobacterium heparinum in complex protein digest medium, with heparin employed as the inducer, has been studied and improved. The maximum productivity of heparinase has been increased 156-fold over that achieved by previously published methods to 375 U/liter per h in the complex medium. Rapid deactivation of heparinase activity, both specific and total, was observed at the onset of the stationary phase. Nutritional studies on growth and heparinase production showed an obligate requirement for L-histidine and no vitamin requirement. L-Methionine partially relieved the L-histidine requirement. A defined medium containing glucose, ammonium sulfate, basal salts, L-methionine, and L-histidine was developed for growth and heparinase production. The growth rate in this medium was 0.21 h-1, which is 40%, higher than that in complex medium. The maximum volumetric productivity of heparinase in the defined medium was increased to 1,475 U/liter per h, providing a 640-fold increase over that achieved by previously published methods. No rapid deactivation was observed. An examination of alternate inducers for heparinase showed that heparin degradation products, hyaluronic acid, heparin monosulfate, N-acetyl-D-glucosamine, and maltose, induce heparinase in complex medium. An Azure A assay was modified and fully developed to measure the heparin concentration during fermentation and the heparinase specific activity of crude extracts of F. heparinum obtained from sonication, thus negating the need for further purification to measure activity."

Entities:  

Mesh:

Substances:

Year:  1981        PMID: 7235692      PMCID: PMC243699          DOI: 10.1128/aem.41.2.360-365.1981

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  7 in total

1.  Bacterial degradation of heparin.

Authors:  A N PAYZA; E D KORN
Journal:  Nature       Date:  1956-01-14       Impact factor: 49.962

2.  Characterization of an intracellular protease isolated from Bacillus thuringiensis sporulating cells and able to modify homologous RNA polymerase.

Authors:  M M Lecadet; M Lescourret; A Klier
Journal:  Eur J Biochem       Date:  1977-10-03

3.  Sequential degradation of heparin in Flavobacterium heparinum. Purification and properties of five enzymes involved in heparin degradation.

Authors:  C P Dietrich; M E Silva; Y M Michelacci
Journal:  J Biol Chem       Date:  1973-09-25       Impact factor: 5.157

4.  Isolation and characterization of oligosaccharides obtained from heparin by the action of heparinase.

Authors:  A Linker; P Hovingh
Journal:  Biochemistry       Date:  1972-02-15       Impact factor: 3.162

5.  Novel heparin degradation products. Isolation and characterization of novel disaccharides and oligosaccharides produced from heparin by bacterial degradation.

Authors:  C P Dietrich
Journal:  Biochem J       Date:  1968-07       Impact factor: 3.857

6.  Presence of heparan sulfate in the glomerular basement membrane.

Authors:  Y S Kanwar; M G Farquhar
Journal:  Proc Natl Acad Sci U S A       Date:  1979-03       Impact factor: 11.205

Review 7.  Heparin: an old drug with a new paradigm.

Authors:  L B Jacques
Journal:  Science       Date:  1979-11-02       Impact factor: 47.728

  7 in total
  21 in total

1.  Specific plate assay for bacterial heparinase.

Authors:  J J Zimmermann; R Langer; C L Cooney
Journal:  Appl Environ Microbiol       Date:  1990-11       Impact factor: 4.792

2.  Isolation and expression in Escherichia coli of hepB and hepC, genes coding for the glycosaminoglycan-degrading enzymes heparinase II and heparinase III, respectively, from Flavobacterium heparinum.

Authors:  H Su; F Blain; R A Musil; J J Zimmermann; K Gu; D C Bennett
Journal:  Appl Environ Microbiol       Date:  1996-08       Impact factor: 4.792

3.  Isolation and expression in Escherichia coli of cslA and cslB, genes coding for the chondroitin sulfate-degrading enzymes chondroitinase AC and chondroitinase B, respectively, from Flavobacterium heparinum.

Authors:  A L Tkalec; D Fink; F Blain; G Zhang-Sun; M Laliberte; D C Bennett; K Gu; J J Zimmermann; H Su
Journal:  Appl Environ Microbiol       Date:  2000-01       Impact factor: 4.792

4.  Ex vivo model of an immobilized-enzyme reactor.

Authors:  H Bernstein; R Langer
Journal:  Proc Natl Acad Sci U S A       Date:  1988-11       Impact factor: 11.205

5.  Large scale preparation and characterization of mucopolysaccharase contamination free heparinase.

Authors:  V C Yang; H Bernstein; C L Cooney; R Langer
Journal:  Appl Biochem Biotechnol       Date:  1987 Sep-Dec       Impact factor: 2.926

Review 6.  Polysaccharide lyases.

Authors:  R J Linhardt; P M Galliher; C L Cooney
Journal:  Appl Biochem Biotechnol       Date:  1986-04       Impact factor: 2.926

7.  NMR methods to monitor the enzymatic depolymerization of heparin.

Authors:  John F K Limtiaco; Szabolcs Beni; Christopher J Jones; Derek J Langeslay; Cynthia K Larive
Journal:  Anal Bioanal Chem       Date:  2010-09-04       Impact factor: 4.142

8.  Bioreactor based on suspended particles of immobilized enzyme.

Authors:  L E Freed; G V Vunjak-Novakovic; P A Drinker; R Langer
Journal:  Ann Biomed Eng       Date:  1993       Impact factor: 3.934

9.  The release of heparinase from the periplasmic space of Flavobacterium heparinum by three-step osmotic shock.

Authors:  J J Zimmermann; K Oddie; R Langer; C L Cooney
Journal:  Appl Biochem Biotechnol       Date:  1991-08       Impact factor: 2.926

10.  Purification, characterization and specificity of chondroitin lyases and glycuronidase from Flavobacterium heparinum.

Authors:  K Gu; R J Linhardt; M Laliberté; K Gu; J Zimmermann
Journal:  Biochem J       Date:  1995-12-01       Impact factor: 3.857

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.