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Table 1 Primers used for PCR construction and amplification of chiA74 ∆s p and chiA74 ∆s p-gfp

From: Bacillus thuringiensis subsp. kurstaki HD1 as a factory to synthesize alkali-labile ChiA74∆sp chitinase inclusions, Cry crystals and spores for applied use

Primer

Sequencea

chiA74-13

F: 5′-TCCCCGCGG ATG TCACCAAAGCAAAGTCAAAAAATTGTTGGGTAC-3′

chiA74-12

R: 5′-TCCCCGCGG TTCTCCTTTCAAAATAAAAGATATATTTAAAGGC-3′

gfp-1

F: 5′- ATGGCTAGCAAAGGAGAAGAACTTT-3′

gfp-3

R: 5′- GGTCAGATCT TTATTTGTAGAGCTCATCCAT -3′

chiA74-C

F: 5′- GGTCAGATCT ACGTAATATCCATTAATTACTTCACTA -3′

chiA74-B

R: 5′- GTTTTCGCTAATGACGGCATTTAAAAG -3′

cyt-STAB-1

F: 5′-CGGAATTCTATTTTCGATTTC-3′

chiA74-3

R: 5-AACTGCAG CGAAAGCCTTTCCCTAACAGGTGACTATC-3′

ery-1

F: 5-AAAACTGCAG CTTAAGAGTGTGTTGATAGTGC-3′

ery-2

R: 5-ATAAGAATGCGGCCGC CCCCGTAGGCGCTAGGGACC-3

  1. aArtificial start ATG codon (bold type) used to initiate the chitinase translation, and the restriction endonuclease cleavage sites SacII, BglII, PstI and NotI (italics) are shown.