Expression of mosquitocidal crystal protein genes in non‐insecticidal Bacillus thuringiensis subsp. israelensis
Jong Yul Roh, Heung‐Woo Park, Yeon Ho Je, Dong‐Wook Lee, Bo-Hyoung Jin, Hyun-Ji Oh, Sarjeet S. Gill, Sang‐Kee Kang
Abstract
Jong Yul Roh, Heung‐Woo Park, Yeon Ho Je, Dong‐Wook Lee, Bo-Hyoung Jin, Hyun-Ji Oh, Sarjeet S. Gill, Sang‐Kee Kang
Abstract
Bacillus thuringiensis NTB‐1 isolated from soil samples in Korea produces ovoidal parasporal inclusions with proteins of approximately 24–40 kDa in size. Although serological study indicated that the isolate has a flagella (H) antigen identical with subsp. israelensis, it seemed to be non‐insecticidal against Lepidoptera and Coleoptera as well as Diptera. To investigate the activity of non‐insecticidal B. thuringiensis transformed with insecticidal crystal protein genes, cryIVD and cytA genes of B. thuringiensis subsp. morrisoni PG‐14, highly toxic to mosquito larvae, were introduced into the isolate NTB‐1. The expression of mosquitocidal crystal protein genes in NTB‐1 was characterized by SDS–PAGE analysis and electron microscopy. The results showed that crystalline inclusions of host, CryIVD and CytA were stably expressed in the transformant. However, the mosquitocidal activity of transformant was similar to that of B. thuringiensis subsp. kurstaki Cry−B harbouring cryIVD and cytA genes, demonstrating that a synergistic effect by an interaction of both introduced insecticidal and resident non‐insecticidal crystal proteins was not observed.
OpenAlex reports 4 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Bacillus thuringiensis NTB‐1 isolated from soil samples in Korea produces ovoidal parasporal inclusions with proteins of approximately 24–40 kDa in size. Although serological study indicated that the isolate has a flagella (H) antigen identical with subsp. israelensis, it seemed to be non‐insecticidal against Lepidoptera and Coleoptera as well as Diptera. To investigate the activity of non‐insecticidal B. thuringiensis transformed with insecticidal crystal protein genes, cryIVD and cytA genes of B. thuringiensis subsp. morrisoni PG‐14, highly toxic to mosquito larvae, were introduced into the isolate NTB‐1. The expression of mosquitocidal crystal protein genes in NTB‐1 was characterized by SDS–PAGE analysis and electron microscopy. The results showed that crystalline inclusions of host, CryIVD and CytA were stably expressed in the transformant. However, the mosquitocidal activity of transformant was similar to that of B. thuringiensis subsp. kurstaki Cry−B harbouring cryIVD and cytA genes, demonstrating that a synergistic effect by an interaction of both introduced insecticidal and resident non‐insecticidal crystal proteins was not observed.
Key concepts: Bacillus thuringiensis, Bacillales, Bacillaceae, Biology, Microbiology, Lepidoptera genitalia, Gene, Bacteria