Open AccessCloning, Sequencing, and Expression of the Chitinase Gene chiA74 from Bacillus thuringiensis
Author(s) -
José E. BarbozaCorona,
Elizabeth NietoMazzocco,
R. Velázquez-Robledo,
Rubén SalcedoHernández,
Mayela Bautista,
Beatriz Jiménez,
Jorge E. Ibarra
Publication year - 2003
Publication title -
applied and environmental microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.552
H-Index - 324
eISSN - 1070-6291
pISSN - 0099-2240
DOI - 10.1128/aem.69.2.1023-1029.2003
Subject(s) - chitinase , bacillus thuringiensis , biology , bacillus cereus , escherichia coli , gene , signal peptide , peptide sequence , microbiology and biotechnology , amino acid , bacillaceae , biochemistry , bacillus subtilis , genetics , bacteria
The endochitinase gene chiA74 from Bacillus thuringiensis serovar kenyae strain LBIT-82 was cloned in Escherichia coli DH5 alpha F'. A sequence of 676 amino acids was deduced when the gene was completely sequenced. A molecular mass of 74 kDa was estimated for the preprotein, which includes a putative 4-kDa signal sequence located at the N terminus. The deduced amino acid sequence showed high degree of identity with other chitinases such as ChiB from Bacillus cereus (98%) and ChiA71 from Bacillus thuringiensis serovar pakistani (70%). Additionally, ChiA74 showed a modular structure comprised of three domains: a catalytic domain, a fibronectin-like domain, and a chitin-binding domain. All three domains showed conserved sequences when compared to other bacterial chitinase sequences. A ca. 70-kDa mature protein expressed by the cloned gene was detected in zymograms, comigrating with a chitinase produced by the LBIT-82 wild-type strain. ChiA74 is active within a wide pH range (4 to 9), although a bimodal activity was shown at pH 4.79 and 6.34. The optimal temperature was estimated at 57.2 degrees C when tested at pH 6. The potential use of ChiA74 as a synergistic agent, along with the B. thuringiensis insecticidal Cry proteins, is discussed.