Isolation and Expression of Enolase Gene in Fusarium oxysporum f. sp. lycopersici

被引:8
作者
Lizbeth Macias-Sanchez, Karla [1 ]
Garcia-Soto, Jesus [2 ]
Roncero, M. Isabel G. [3 ]
Hernandez-Monjaraz, Wendy [1 ]
Caudillo-Perez, Cesar [1 ]
Guadalupe Martinez-Cadena, Ma. [2 ]
机构
[1] Inst Politecn Nacl UPIIG IPN, Unidad Profes Interdisciplinaria Ingn Campus Guan, Guanajuato 36275, Mexico
[2] Univ Guanajuato, Dept Biol, Div Ciencias Nat & Exactas, Guanajuato 36000, Gto, Mexico
[3] Univ Cordoba, Dept Genet, E-14071 Cordoba, Spain
关键词
Enolase; Glucose; Fusarium; Expression; Copy number; ASPERGILLUS-ORYZAE; FILAMENTOUS FUNGUS; GLYCOLYTIC GENES; SACCHAROMYCES-CEREVISIAE; MOLECULAR-CLONING; CELL-WALL; PROTEIN; IDENTIFICATION; ACTIVATION; DELETION;
D O I
10.1007/s12010-014-1338-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Fusarium oxysporum f. sp. lycopersici is a fungus responsible for the tomato disease known as fusariosis. Enolase, which is the enzyme that catalyzes the reaction of 2-phosphoglycerate to phosphoenolpyruvate, is present during glycolysis. Enolase genes have been isolated from bacteria and fungi, among other organisms. In this research, a large portion of the enolase, eno, gene sequence was isolated from F. oxysporum and compared with those of other microorganisms, revealing a similarity of 51-69 %. We analyzed the copy number of the eno gene and determined that only a single copy is present in F. oxysporum, as in several fungi, such as Candida albicans and Aspergillus oryzae. We also detected the expression of the eno gene by reverse transcription-polymerase chain reaction during in vitro growth under two growth conditions where glucose was used as the carbon source, and we observed the same eno gene expression levels under both growth conditions.
引用
收藏
页码:902 / 908
页数:7
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