Midgut juice of Plutella xylostella highly resistant to Bacillus thuringiensis Cry1Ac contains a three times larger amount of glucosinolate sulfatase which binds to Cry1Ac compared to that of susceptible strain

被引:10
|
作者
Yamazaki, Takanori [1 ]
Ishikawa, Toshiki [1 ]
Pandian, Ganesh N. [1 ]
Okazaki, Keiichi [1 ]
Haginoya, Kohsuke [1 ]
Tachikawa, Yuka [1 ]
Mitsui, Toshiaki [1 ]
Miyamoto, Kazuhisa [2 ]
Angusthanasombat, Chanan [3 ]
Hori, Hidetaka [1 ]
机构
[1] Niigata Univ, Grad Sch Sci & Technol, Niigata 9502181, Japan
[2] Natl Inst Agrobiol Sci, Tsukuba, Ibaraki 3058634, Japan
[3] Mahidol Univ, Inst Mol Biosci, Nakhon Pathom 73170, Thailand
关键词
Bacillus thuringiensis; Cry1Ac resistant; N-acetylgalactosamine; Glucosinolate sulfatase; Plutella xylostella midgut juice; BRUSH-BORDER MEMBRANE; DIAMONDBACK MOTH; DELTA-ENDOTOXIN; MANDUCA-SEXTA; N-ACETYLGALACTOSAMINE; TRANSGENIC CROPS; TOXIN BINDING; AMINOPEPTIDASE; LEPIDOPTERA; RECEPTORS;
D O I
10.1016/j.pestbp.2011.09.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Midgut juice of Plutella xylostella strain PXR which is resistant to Cry1Ac was biochemically characterized relative to the susceptible PXS strain. The midgut juice of PXR (PXR-Juice) was shown to process Cry1Ac protoxin to 60 kDa active toxin with the same processing pattern as that of juice from PXS (PXS-Juice) in SOS-PAGE. PXS larvae which were given the Cry1Ac toxin pre-processed with PXR-Juice were killed with the same rate as that with Cry1Ac pre-activated by trypsin. PXR-Juice was found to contain three times larger amount of 66 kDa protein (P66) than PXS-Juice and the N-terminal amino acid sequence of P66 was matched to that of glucosinolate sulfatase in data base search. The protein band of P66 was coincided with the band of p-nitro phenyl sulfatase activity in zymogram. P66 purified to homogeneity in SOS-PAGE bound to Cry1Ac and soybean agglutinin, and K-D for Cry1Ac was estimated to be 718 nM with surface plasmon resonance analysis. Using purified sulfatase, K-m and V-max were estimated and involvement of the enzyme in the PXR resistance was discussed. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:125 / 131
页数:7
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