Abstracts - faqs.org

Abstracts

Biological sciences

Search abstracts:
Abstracts » Biological sciences

One-step purification of nisin A by immunoaffinity chromatography

Article Abstract:

A research was conducted to study the purification of lantibiotic nisin A, a ribosomally synthesized and posttranslationally modified antimicrobial peptide, to homogeneity using a single-step immunoaffinity chromatography method. Anti-nisin A monoclonal antibodies were coupled to a HiTrap N-hydroxysuccinimide-activated column from Pharmacia. A reverse-phase chromatography column was utilized to determine the purity of nisin A obtained from the culture supernatant of L. lactis. Results showed that the purification procedure was efficient, specific and reproducible.

Author: Hernandez, Pablo E., Rodriguez, Juan M., Suarez, Ana M., Azcona, Juan I., Sanz, Bernabe
Publisher: American Society for Microbiology
Publication Name: Applied and Environmental Microbiology
Subject: Biological sciences
ISSN: 0099-2240
Year: 1997
Usage, Chromatography

User Contributions:

Comment about this article or add new information about this topic:

CAPTCHA


Generation of polyclonal antibodies against nisin: immunization strategies and immunoassay development

Article Abstract:

The conjugates of the antimicrobial lanthionine-containing peptide nisin A (nisA) with keyhole limpet hemocyanin (nisA-KLH) induce formation of polyclonal antibodies with high relative affinity and sensitivity in immunized mice. The nisA conjugate with cholera toxin induces antibodies with low affinity and sensitivity. A competitive direct enzyme-linked immunosorbent assay detects five to 100 ng/ml of the antibodies induced by nisA-KLH. The polyclonal antibodies cross-react with nisZ but not with bacteriocins lacking lanthionine.

Author: Hernandez, Pablo E., Azcona-Olivera, Juan I., Rodriguez, Juan M., Suarez, Ana M.
Publisher: American Society for Microbiology
Publication Name: Applied and Environmental Microbiology
Subject: Biological sciences
ISSN: 0099-2240
Year: 1996
Analysis, Anti-infective agents, Enzyme-linked immunosorbent assay, Antibodies

User Contributions:

Comment about this article or add new information about this topic:

CAPTCHA


PCR detection of the lactocin S structural gene in bacteriocin-producing Lactobacilli from meat

Article Abstract:

The basic molecular biology techniques are suitable to study the strains which are capable of producing bacteriocins. The primer for the PCR amplification of the structural genes of bacteriocins should be selected carefully. Hybridization analysis confirmed the amplification of 75-bp fragment of the gene.

Author: Hernandez, Pablo E., Rodriguez, Juan M., Cintas, Luis M., Casaus, Pilar, Suarez, Ana
Publisher: American Society for Microbiology
Publication Name: Applied and Environmental Microbiology
Subject: Biological sciences
ISSN: 0099-2240
Year: 1995
Methods, Lactobacillus, Molecular biology

User Contributions:

Comment about this article or add new information about this topic:

CAPTCHA


Subjects list: Research, Peptides
Similar abstracts:
  • Abstracts: Overgrowth syndromes and the regulation of signaling complexes by proteoglycans. Recurrent 10q22-q23 deletions: A genomic disorder on 10q associated with cognitive and behavioral abnormalities
  • Abstracts: Identification of epichloe endophytes in planta by a microsatellite-based PCR fingerprinting assay with automated analysis
  • Abstracts: Genetic association of apolipoprotein E with age-related macular degeneration. A critical appraisal of the scientific basis of commercial genomic profiles used to assess health risks and personalize health interventions
  • Abstracts: P-element-induced variation in metabolic regulation in Drosophila. Spontaneous mutation rate of modifiers of metabolism in Drosophila
  • Abstracts: Characterization and environmental regulation of outer membrane proteins in Xenorhabdus nematophilus. Purification and characterization of Xenorhabdicin, a phage tail-like bacteriocin, from the lysogenic strain F1 of Xenorhabdus nematophilus
This website is not affiliated with document authors or copyright owners. This page is provided for informational purposes only. Unintentional errors are possible.
Some parts © 2025 Advameg, Inc.