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Volume 7, Issue 2 (Suppl)

J Ecosyst Ecography, an open access journal

ISSN:2157-7625

September 18-20, 2017

September 18-20, 2017 Toronto, Canada

Joint Conference

International Conference on

International Conference on

Environmental Microbiology and Microbial Ecology

&

Ecology and Ecosystems

Catherine Cesa-Luna et al., J Ecosyst Ecography 2017, 7:2 (Suppl)

DOI: 10.4172/2157-7625-C1-030

Antagonism of

Pseudomonas

sp. EMM-1 and its potential as biocontrol agent

Catherine Cesa-Luna, Joel de la Cruz-Enríquez, Ana Laura Hernández-Tenorio, Fernando Xicale-Nava, Yolanda Elizabeth Morales-García, Rocío Pérez-y-Terrón,

Antonino Báez-Rogelio, Jesús Muñoz-Rojas

and

Verónica Quintero-Hernández

Benemérita Universidad Autonoma de Puebla, Mexico

B

acteria may exhibit antagonistic interactions to compete for space and nutrients in their habitat. This competition has been

mainly evaluated by double-layer agar and simultaneous inhibition assays. The best known antagonistic bacteria are

Enterococcus

,

Lactococcus

,

Streptomyces

,

Bacillus

,

Pseudomonas

,

Klebsiella

,

Escherichia

and

Burkholderia

due to their potential to produce

inhibitory substances such as broad-spectrum antibiotics, organic acids, siderophores, antifungal and bacteriocins. Our study model,

Pseudomonas

sp. EMM-1, is a Gram-negative bacterium isolated from contaminated soil highly competitive due to the production

of one or more inhibitory substances. It has been demonstrated its antimicrobial activity against diverse beneficial and pathogenic

microorganisms including the genera

Bradyrhizobium

,

Azotobacter

,

Staphylococcus

,

Streptococcus

,

Klebsiella

and

Burkholderia

; as

well as the

phytopathogenic

fungi

Pantoea

and

Fusarium

. In this work the ability of Pseudomonas sp. EMM-1 to inhibit diverse fungi

isolated from soil and plants with fungal diseases, such as

Aspergillum

and

Fusarium

was verified by the double-layer agar assay,

leading us to assume its potential as biocontrol agent.

Biography

Catherine Cesa-Luna has completed her bachelor’s degree in Clinical Chemistry in 2012 from Universidad Veracruzana, México and obtained her master’s degree

in Microbiologic Sciences (Medical Microbiology) in 2016 at the Benemerita Universidad Autónoma de Puebla, Mexico; where she is currently pursuing her Ph.D

in microbiology. She is evaluating the antimicrobial activity of synthetic IsCT-like peptides derived from scorpion venoms on bacteria of clinical interest and also

working on the purification and identification of compounds related to the activity of the inhibitory substance produced by

Pseudomonas

sp. EMM-1.

kathy_cl_3@hotmail.com