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Genetic Transformation of Crops for Resistance to Insect Pests 229<br />

Rice<br />

Expression of the potato trypsin inhibitor gene confers resistance to insect pests in rice<br />

(Duan et al., 1996). Constitutive expression of CpTi increases resistance to C. suppressalis<br />

and Sesamia inferens (Walker) in rice (Xu et al., 1996). A synthetic gene (mwti11b) coding for<br />

a winged bean trypsin inhibitor (WTI-11B) signifi cantly retarded the larval growth of<br />

C. suppressalis in rice (Mochizuki et al., 1999). Accumulation of Kunitz type SBTI in rice also<br />

confers resistance to the brown planthopper, Nilaparvata lugens (Stal) (Lee et al., 1999).<br />

Wheat<br />

The Angoumois grain moth, Sitotroga cerealella (Oliver), is one of the major storage pests of<br />

cereals, and no antibiotic resistance in wheat against this insect has been identifi ed to date.<br />

Characterization of the midgut proteases of S. cerealella larvae revealed that the major<br />

digestive proteases were trypsin-like and alpha-chymotrypsin-like serine proteases<br />

(Shukle and Wu, 2003). The potential value of naturally occurring plant protease inhibitors<br />

as resistance factors for S. cerealella has been assessed in bioassays using artifi cial seeds<br />

prepared by freeze-drying a fl our paste in Tefl on moulds and then coating the seeds with<br />

gelatin. Soybean trypsin inhibitor (Kunitz inhibitor) had an adverse effect on the development<br />

of the insect and suggested that protease inhibitors might serve as a transgenic<br />

resistance factor (Shukle and Wu, 2003). A signifi cant reduction in survival rate of the<br />

Angoumois grain moth, S. cerealella has been observed on transgenic wheat seeds expressing<br />

the trypsin inhibitor from barley (Altpeter et al., 1999). However, it did not have a<br />

signifi cant protective effect against leaf-feeding insects.<br />

Sugarcane<br />

Transgenic sugarcane plants expressing potato proteinase inhibitor II have shown<br />

increased antibiosis to larvae of sugarcane grubs, Antitrogus consanguineus (Blackburn)<br />

(Nutt et al., 1999). Antitrogus consanguineus larvae feeding for six weeks on transgenic<br />

plants carrying the potato proteinase inhibitor II gene gained only 4.2% of the weight of<br />

grubs feeding on nontransgenic control plants (Nutt et al., 2001).<br />

Vegetables<br />

The CpTi gene in cabbage, B. oleracea var capitata (cultivars Yingchun and Jingfeng), has<br />

shown resistance to P. rapae (Fang et al., 1997). However, adults of Psylliodes chrysocephala<br />

(L.) feed identically on leaf discs from control or transformed plants of oilseed rape expressing<br />

constitutively the cysteine proteinase inhibitor, oryzacystatin I (OCI) (Western et al.,<br />

1998). Trypsin inhibitor gene from sweet potato expressed in Taiwan caulifl ower, B. oleracea<br />

var. botrytis, showed resistance to insects (L.C. Ding, Yeh, and Wang, 1998). CpTI gene<br />

and nptII gene were introduced into Brassica campestris L. ssp. chinensis. The insect resistance<br />

of the transgenic plants was maintained in the progeny (She et al., 2000). Modifi ed<br />

CpTi gene (sck) has been successfully transferred into Chinese cabbage, B. campestris subsp.<br />

pekinensis cultivars (GP 11 and Zhongbai 4) (G.D. Yang et al., 2002). The resistance of the<br />

transgenic plants to P. rapae was observed in laboratory and fi eld conditions. A trypsin<br />

inhibitor from Indian mustard, Brassica juncea (L.) Czern. (BjTi, a precursor of a 2S seed<br />

storage protein), showed a soybean trypsin inhibitor active site-like motif (GPFRI ) at the<br />

expected processing site (Mandal et al., 2002). The BjTi is a thermostable Kunitz-type

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