Cloning and expression of chitinase A, B, and C (chiA, chiB, chiC) genes from Serratia marcescens originating from Helicoverpa armigera and determining their activities

Three genes encoding chitinase A (chiA), B (chiB), and C (chiC) were amplified from a bacterium that was isolated from a naturally dead Helicoverpa armigera larva and identified as Serratia marcescens based on 16S rRNA gene sequence analysis (KF823633 accession number). The open reading frames (ORFs) were identified as 1692, 1500, and 1443 base pairs for chiA, chiB, and chiC genes, respectively. These sequences were submitted to the GenBank with accession numbers KF823630 (chiA), KF823631 (chiB), and KF823632 (chiC). Comparison of the deduced amino acid sequences with those of other bacterial chitinases revealed that the 3 chitinases contain the catalytic domain. Furthermore, all 3 chitinases showed 99% similarity to the S. marcescens WW4 strain at the amino acid level. The chitinases were overexpressed in Escherichia coli. Expressed proteins were purified and their activities were tested using colloidal chitin as substrate. Reasonable pH and temperature ranges were also determined as 7-11 and 33-37 °C, respectively. Insecticidal activities of these proteins were tested on the larvae of Malacosoma neustria and H. armigera. Test results showed that 1000 U/mL ChiA, ChiB, and ChiC have 47%, 50%, and 66% insecticidal activities on M. neustria, and 80%, 45%, and 50% insecticidal activities on H. armigera larvae within 10 days, respectively.

Cloning and expression of chitinase A, B, and C (chiA, chiB, chiC) genes from Serratia marcescens originating from Helicoverpa armigera and determining their activities

Three genes encoding chitinase A (chiA), B (chiB), and C (chiC) were amplified from a bacterium that was isolated from a naturally dead Helicoverpa armigera larva and identified as Serratia marcescens based on 16S rRNA gene sequence analysis (KF823633 accession number). The open reading frames (ORFs) were identified as 1692, 1500, and 1443 base pairs for chiA, chiB, and chiC genes, respectively. These sequences were submitted to the GenBank with accession numbers KF823630 (chiA), KF823631 (chiB), and KF823632 (chiC). Comparison of the deduced amino acid sequences with those of other bacterial chitinases revealed that the 3 chitinases contain the catalytic domain. Furthermore, all 3 chitinases showed 99% similarity to the S. marcescens WW4 strain at the amino acid level. The chitinases were overexpressed in Escherichia coli. Expressed proteins were purified and their activities were tested using colloidal chitin as substrate. Reasonable pH and temperature ranges were also determined as 7-11 and 33-37 °C, respectively. Insecticidal activities of these proteins were tested on the larvae of Malacosoma neustria and H. armigera. Test results showed that 1000 U/mL ChiA, ChiB, and ChiC have 47%, 50%, and 66% insecticidal activities on M. neustria, and 80%, 45%, and 50% insecticidal activities on H. armigera larvae within 10 days, respectively.
Turkish Journal of Biology-Cover
  • ISSN: 1300-0152
  • Yayın Aralığı: 6
  • Yayıncı: TÜBİTAK
Sayıdaki Diğer Makaleler

Cloning and expression of chitinase A, B, and C (chiA, chiB, chiC) genes from Serratia marcescens originating from Helicoverpa armigera and determining their activities

Mehtap DANIŞMAZOĞLU, İsmail DEMİR, Kazım SEZEN, Hacer MURATOĞLU, Remziye NALÇACIOĞLU

Endogenous heat shock protein GroEL of A. actinomycetemcomitans preferentially targets primary human CD8+ T cells

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A new entomopathogenic nematode species from Turkey, Steinernema websteri (Rhabditida: Steinernematidae), and its virulence

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In vitro antiproliferative/cytotoxic activity of 2,3'-biindole against various cancer cell lines

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E-microsatellite markers for some naturally occurring Salvia species in the Mediterranean region

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Cytotoxic effects of various lactic acid bacteria on Caco-2 cells

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