Extracts of Alternaria alternata spores and mycelia were prepared. Crossed immunoelectrophoresis showed the presence of at least 40 antigens in these extracts. Analysis of seven commercial extracts by CIEP and isoelectric focusing showed many fewer components and a high degree of variability. Eight of the antigens in the spore extract demonstrable by CIEP were not present in mycelia extracts. This spore-specific fraction was isolated by solid phase immunoadsorption and shown to be potent antigenically and allergenically. The extracts of mycelia, spore and spore-specific fraction demonstrated strong reactivity with 92 Alternaria sensitive patients by both RAST and skin test. About half of the patients were significantly more reactive to spore and/or spore-specific than the mycelia. Many of the spore antigens are either common to or cross-reactive between spore and mycelia but there are a minimum of eight spore-specific antigens, at least one of which is a strong allergen.

Download full-text PDF

Source

Publication Analysis

Top Keywords

spore-specific fraction
8
mycelia spore
8
extracts
5
mycelia
5
spore
5
isolation spore
4
spore specific
4
specific allergens
4
allergens alternaria
4
alternaria extracts
4

Similar Publications

Like many bacteria, possesses two DNA translocases that affect chromosome segregation at different steps. Prior to septum closure, nonsegregated DNA is moved into opposite cell halves by SftA, while septum-entrapped DNA is rescued by SpoIIIE. We have used single-molecule fluorescence microscopy and tracking (SMT) experiments to describe the dynamics of the two different DNA translocases, the cell division protein FtsA and the glycolytic enzyme phosphofructokinase (PfkA), in real time.

View Article and Find Full Text PDF

Germination of dormant Bacillus subtilis spores with specific nutrient germinants is dependent on a number of inner membrane (IM) proteins, including (i) the GerA, GerB, and GerK germinant receptors (GRs) that respond to nutrient germinants; (ii) the GerD protein, essential for optimal GR function; and (iii) SpoVA proteins, essential for the release of the spore-specific molecule dipicolinic acid (DPA) during spore germination. Levels of GR A and C subunit proteins, GerD, and SpoVAD in wild-type spores were determined by Western blot analysis of spore fractions or total disrupted spores by comparison with known amounts of purified proteins. Surprisingly, after disruption of decoated B.

View Article and Find Full Text PDF

The survival of Bacillus pumilus SAFR-032 spores to standard industrial clean room sterilization practices necessitates the development of rapid molecular diagnostic tool(s) for detection and enumeration of viable bacterial spores in industrial clean room environments. This is of importance to maintaining the sterility of clean room processing products. This paper describes the effect of propidium monoazide (PMA) on fluorescence in situ hybridization (FISH) for detecting and enumerating B.

View Article and Find Full Text PDF

Gel-free proteomic identification of the Bacillus subtilis insoluble spore coat protein fraction.

Proteomics

December 2011

Swammerdam Institute for Life Sciences, Department of Mass Spectrometry of Biomacromolecules, University of Amsterdam, The Netherlands.

Species from the genus Bacillus have the ability to form endospores, dormant cellular forms that are able to survive heat and acid preservation techniques commonly used in the food industry. Resistance characteristics of spores towards various environmental stresses are in part attributed to their coat proteins. Previously, 70 proteins have been assigned to the spore coat of Bacillus subtilis using SDS-PAGE, 2-DE gel approaches, protein localization studies and genome-wide transcriptome studies.

View Article and Find Full Text PDF

Localization of the GerD spore germination protein in the Bacillus subtilis spore.

Microbiology (Reading)

April 2009

Department of Molecular Biology and Biotechnology, University of Sheffield, Firth Court, Western Bank, Sheffield S10 2TN, UK.

The GerD protein of Bacillus subtilis is required for efficient spore germination in l-alanine, and for germination in the alternative germinant combination of amino acids plus sugars. Only germination via nutrient receptors is affected in the mutant. The GerD protein is predicted to be a lipoprotein that is produced in the forespore compartment of the sporulating cell.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!