Literature DB >> 5847799

Immunochemical studies on alpha-amylase. 3. Immunochemical relationships among amylases from various microorganisms.

S Sirisinha, P Z Allen.   

Abstract

Sirishinha, Stitaya (University of Rochester School of Medicine and Dentistry, Rochester, N.Y.), and Peter Z. Allen. Immunochemical studies on alpha-amylase. III. Immunochemical relationships among amylases from various microorganisms. J. Bacteriol. 90:1120-1128. 1965.-Immunochemical relationships among amylases obtained from a selected group of microorganisms were examined, and a cross-reaction was detected between the alpha-amylases of Bacillus stearothermophilus and B. subtilis. Immunodiffusion and quantitative precipitin studies, as well as cross-neutralization tests, indicate that B. stearothermophilus alpha-amylase reacts with a portion of antibody present in antisera to crystalline B. subtilis alpha-amylase. Amylases from these two species thus have some aspects of structure in common. Limited data obtained by immunodiffusion suggest that groupings which confer cross-reactivity to the B. stearothermophilus enzyme are lost after exposure to mercaptoethanol in the presence of ethylenediamine-tetraacetate, followed by treatment with iodoacetamide. With the antisera employed and within the concentration range examined, no immunochemical cross-reaction was observed among amylases from Aspergillus oryzae, B. subtilis, B. polymyxa, B. macerans, Pseudomonas saccharophila, and Euglena sanguinis. Immunoelectrophoresis of partially purified B. stearothermophilus alpha-amylase by use of antiserum to the crude enzyme, together with localization of amylase activity in immunoelectrophoretic plates, suggests that B. stearothermophilus alpha-amylase is antigenic in the rabbit.

Entities:  

Mesh:

Substances:

Year:  1965        PMID: 5847799      PMCID: PMC315782          DOI: 10.1128/jb.90.4.1120-1128.1965

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  15 in total

1.  Penicillinase-antipenicillinase.

Authors:  M R POLLOCK
Journal:  Ann N Y Acad Sci       Date:  1963-05-08       Impact factor: 5.691

2.  A method for the determination of amylase in intestinal content.

Authors:  A DAHLQVIST
Journal:  Scand J Clin Lab Invest       Date:  1962       Impact factor: 1.713

3.  Thermostable alpha-amylase of Bacillus stearothermophilus. III. Amino acid composition.

Authors:  L L CAMPBELL; G B MANNING
Journal:  J Biol Chem       Date:  1961-11       Impact factor: 5.157

4.  Thermostable alpha-amylase of Bacillus stearothermophilus. IV. Amino-terminal and carboxyl-terminal amino acid analysis.

Authors:  L L CAMPBELL; P D CLEVELAND
Journal:  J Biol Chem       Date:  1961-11       Impact factor: 5.157

5.  [Changes in the morphological structure of Prowazek's bodies in trachoma patients treated with dibiomycin].

Authors:  N D ZATSEPINA
Journal:  Vestn Oftalmol       Date:  1961 Jul-Aug

6.  Differences in mammalian amylases demonstrated by enzyme inhibition with specific antisera.

Authors:  R L McGEACHIN; J M REYNOLDS
Journal:  J Biol Chem       Date:  1959-06       Impact factor: 5.157

7.  Relationships among amylases determined by rabbit antisera to human salivary amylase.

Authors:  R L MCGEACHIN; J M REYNOLDS; J I HUDDLESTON
Journal:  Arch Biochem Biophys       Date:  1961-05       Impact factor: 4.013

8.  The chromatography of normal serum proteins.

Authors:  M P TOMBS; K B COOKE; D BURSTON; N F MACLAGAN
Journal:  Biochem J       Date:  1961-08       Impact factor: 3.857

9.  A comparison of the properties of penicillinase produced by Bacillus subtilis and Bacillus cereus with and without addition of penicillin.

Authors:  E E MANSON; M R POLLOCK; E J TRIDGELL
Journal:  J Gen Microbiol       Date:  1954-12

10.  [Biosynthesis induced by enzymes; enzymatic adaptation].

Authors:  J MONOD; M COHN
Journal:  Adv Enzymol Relat Subj Biochem       Date:  1952
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.