Casique-Arroyo Gabriela, Bideshi Dennis, Salcedo-Hernández Rubén, Barboza-Corona José Eleazar
Departamento de Ingeniería en Alimentos, Instituto de Ciencias Agrícolas, Universidad de Guanajuato, Apartado postal 311, Irapuato, Guanajuato, 36500, Mexico.
Antonie Van Leeuwenhoek. 2007 Jul;92(1):1-9. doi: 10.1007/s10482-006-9127-1. Epub 2006 Nov 30.
Bacillus thuringiensis subsp. kurstaki HD-73 was transformed with the homologous endochitinase gene chiA74 of B. thuringiensis subsp. kenyae LBIT-82 under the regulation of its own promoter and Shine-Dalgarno sequence. The plasmid, pEHchiA74, which harbors chiA74, was detected by southern blot analysis and showed high segregational stability when the recombinant strain was grown in a medium without antibiotic. The recombinant bacterium transformed with pEHchiA74 showed an improvement in chitinolytic activity three times that of the wild-type strain. Expression of ChiA74 did not have any deleterious effect on the crystal morphology and size, but sporulation and Cry1Ac production in rich medium (nutrient broth with glucose) was reduced by approximately 30%. No significant increase in the toxicity of the transformant bacterium toward Plutella xylostella was detected using the same amount of total protein. However, it is possible that ChiA74 synthesis compensated for the decrease in net Cry1Ac synthesis and toxicity observed with the recombinant strain.
苏云金芽孢杆菌库尔斯塔克亚种HD-73在其自身启动子和Shine-Dalgarno序列的调控下,用苏云金芽孢杆菌肯尼亚亚种LBIT-82的同源内切几丁质酶基因chiA74进行转化。通过Southern印迹分析检测到携带chiA74的质粒pEHchiA74,当重组菌株在不含抗生素的培养基中生长时,该质粒显示出高分离稳定性。用pEHchiA74转化的重组细菌的几丁质分解活性提高到野生型菌株的三倍。ChiA74的表达对晶体形态和大小没有任何有害影响,但在丰富培养基(含葡萄糖的营养肉汤)中的孢子形成和Cry1Ac产量降低了约30%。使用相同量的总蛋白未检测到转化细菌对小菜蛾的毒性有显著增加。然而,ChiA74的合成有可能补偿了重组菌株中观察到的Cry1Ac净合成和毒性的降低。