de la Fuente-Salcido Norma M, Casados-Vázquez Luz E, García-Pérez Ada P, Barboza-Pérez Uriel E, Bideshi Dennis K, Salcedo-Hernández Rubén, García-Almendarez Blanca E, Barboza-Corona José E
Aniversidad Autónoma de Coahuila, Escuela de Ciencias Biológicas, Torreón, Coahuila, 27104, México.
Posgrado en Biociencias, División de Ciencias de la Vida, Universidad de Guanajuato Campus Irapuato-Salamanca, Irapuato, Guanajuato, 36500, México.
Microbiologyopen. 2016 Oct;5(5):819-829. doi: 10.1002/mbo3.372. Epub 2016 May 12.
Bacillus thuringiensis subsp. tenebrionis DSM-2803 has been studied extensively and spore/crystal mixtures of this strain are used widely in commercial products to control coleopteran pests. The endochitinase chiA Btt gene of B. thuringiensis subsp. tenebrionis DSM-2803 was cloned and expressed in Escherichia coli. The recombinant 6x-histidine tagged protein (rChiA Btt, ~74 kDa), was purified by a HiTrap Ni affinity column. The K of rChiA Btt was 0.847 μmol L and its optimal activity occurred at pH 7 and ~40°C. Most divalent cations reduced endochitinase activity but only Hg abolished activity of the enzyme. We report for the first time the characterization of a chitinase synthesized by B. thuringiensis subsp. tenebrionis DSM-2803, and show that the purified rChiA74 Btt reduced the radial growth and increased the hyphal density of Colletotrichium gloeosporioides, the etiological agent of "anthracnose" in plants.
苏云金芽孢杆菌暗黑亚种DSM-2803已得到广泛研究,该菌株的孢子/晶体混合物被广泛用于商业产品中以防治鞘翅目害虫。苏云金芽孢杆菌暗黑亚种DSM-2803的内切几丁质酶chiA Btt基因被克隆并在大肠杆菌中表达。重组的带有6x-组氨酸标签的蛋白(rChiA Btt,约74 kDa)通过HiTrap Ni亲和柱进行纯化。rChiA Btt的Km为0.847 μmol L,其最佳活性出现在pH 7和约40°C条件下。大多数二价阳离子会降低内切几丁质酶的活性,但只有Hg会使该酶失活。我们首次报道了苏云金芽孢杆菌暗黑亚种DSM-2803合成的几丁质酶的特性,并表明纯化的rChiA74 Btt降低了植物“炭疽病”病原体胶孢炭疽菌的径向生长并增加了其菌丝密度。