Literature DB >> 16348536

Ultrasound treatment for harvesting an aminopeptidase from lactic Acid bacteria and quantitation of the enzyme by enzyme-linked immunosorbent assays.

C Y Boquien1, F Nakache, A Paraf.   

Abstract

Ultrasound treatment of Lactococcus lactis subsp. cremoris AM2 was optimized to release a maximum amount of intracellular aminopeptidase without modifying the antigenicity of the enzyme. The cells were sonicated three times for 30 s at 23 W. Antibodies produced against the aminopeptidase purified from L. lactis subsp. cremoris AM2 enabled us to use immunoblotting to detect the enzyme in the lysates of all of the lactococci tested but not in the lysates of Leuconostoc strains, lactobacilli, and Streptococcus salivarus subsp. thermophilus. A sandwich enzyme-linked immunosorbent assay (ELISA) was developed to quantify the purified aminopeptidase; the detection limit was 4 ng/ml. The aminopeptidase in the supernatant obtained after the ultrasound treatment of strain AM2 cells was detected with the ELISA starting with a total protein concentration of 200 ng/ml. The proportion of equivalent purified aminopeptidase in the supernatant of L. lactis subsp. cremoris AM2 was about 2% of the total protein. Similarly, the aminopeptidase was quantified in different lactococci; the percentages varied between 0.16 and 2%, depending on the strain. The aminopeptidase content in a mixture of several lactic bacteria was also determined with the sandwich ELISA.

Entities:  

Year:  1991        PMID: 16348536      PMCID: PMC183552          DOI: 10.1128/aem.57.8.2211-2216.1991

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


  18 in total

1.  Monoclonal Antibodies to the Cell-Wall-Associated Proteinase of Lactococcus lactis subsp. cremoris Wg2.

Authors:  H Laan; E J Smid; L de Leij; E Schwander; W N Konings
Journal:  Appl Environ Microbiol       Date:  1988-09       Impact factor: 4.792

2.  Purification and Characterization of an Aminopeptidase from Lactococcus lactis subsp. cremoris AM2.

Authors:  E Neviani; C Y Boquien; V Monnet; L P Thanh; J C Gripon
Journal:  Appl Environ Microbiol       Date:  1989-09       Impact factor: 4.792

3.  Purification and Characterization of a Tripeptidase from Lactococcus lactis subsp. cremoris Wg2.

Authors:  B W Bosman; P S Tan; W N Konings
Journal:  Appl Environ Microbiol       Date:  1990-06       Impact factor: 4.792

4.  Purification and Partial Characterization of a Prolyl-Dipeptidyl Aminopeptidase from Lactobacillus helveticus CNRZ 32.

Authors:  N M Khalid; E H Marth
Journal:  Appl Environ Microbiol       Date:  1990-02       Impact factor: 4.792

5.  The Proteolytic Systems of Streptococcus cremoris: an Immunological Analysis.

Authors:  J Hugenholtz; F Exterkate; W N Konings
Journal:  Appl Environ Microbiol       Date:  1984-12       Impact factor: 4.792

6.  Computer-assisted determination of protein concentrations from dye-binding and bicinchoninic acid protein assays performed in microtiter plates.

Authors:  R D Lane; D Federman; J L Flora; B L Beck
Journal:  J Immunol Methods       Date:  1986-09-27       Impact factor: 2.303

7.  Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.

Authors:  H Towbin; T Staehelin; J Gordon
Journal:  Proc Natl Acad Sci U S A       Date:  1979-09       Impact factor: 11.205

8.  Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Authors:  U K Laemmli
Journal:  Nature       Date:  1970-08-15       Impact factor: 49.962

9.  Peptide uptake is essential for growth of Lactococcus lactis on the milk protein casein.

Authors:  E J Smid; R Plapp; W N Konings
Journal:  J Bacteriol       Date:  1989-11       Impact factor: 3.490

10.  Plasmid complements of Streptococcus lactis NCDO 712 and other lactic streptococci after protoplast-induced curing.

Authors:  M J Gasson
Journal:  J Bacteriol       Date:  1983-04       Impact factor: 3.490

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