Publication Date
2015
Document Type
Dissertation/Thesis
First Advisor
Calvo, Ana M.
Degree Name
M.S. (Master of Science)
Legacy Department
Department of Biological Sciences
LCSH
Biology; Microbiology; Genetics; Aspergillus flavus; Microbiology; Genetics--Research
Abstract
The Aspergillus genus includes species which cause beneficial effects, while others are detrimental, among them, the opportunistic plant and animal pathogen Aspergillus flavus. A. flavus is a known producer of mutagenic and carcinogenic mycotoxins denominated Aflatoxins (AF). Aflatoxin contamination on agriculturally important crops such as maize, peanut, sorghum and tree nuts leads to numerous health issues and economic losses worldwide. We have identified a 14-3-3 homologous gene in A. flavus, artA. In this study we show that artA regulates morphological development and secondary metabolism. The artA deletion mutant presented a decrease in vegetative growth and an increase in conidial production. Normal levels of artA are also required for sclerotial development. Over-expression of artA resulted in a decrease in sclerotial production and in a delay in maturation of these resistant structures. Importantly, artA has a role in AF production. Both deletion and over-expression of artA result in an increase of AF, particularly in the absence of this regulator. Furthermore, artA also affects the production of an unknown fungal secondary metabolite.
Recommended Citation
Ibarra, Beatriz A., "Characterization of the putative 14-3-3 protein, artA, in Aspergillus flavus" (2015). Graduate Research Theses & Dissertations. 1756.
https://huskiecommons.lib.niu.edu/allgraduate-thesesdissertations/1756
Extent
58 pages
Language
eng
Publisher
Northern Illinois University
Rights Statement
In Copyright
Rights Statement 2
NIU theses are protected by copyright. They may be viewed from Huskie Commons for any purpose, but reproduction or distribution in any format is prohibited without the written permission of the authors.
Media Type
Text
Comments
Advisors: Ana M. Calvo.||Committee members: Thomas Sims; Shengde Zhou.