High content of (1,3;1,4)-?-d-glucan in barley grains is regarded as an undesirable factor affecting malting potential, brewing yield and feed utilization. Production of thermostable bacterial (1,3;1,4)-?-glucanase in transgenic barley grain or supplementation of exogenous bacterial (1,3;1,4)-?-glucanase has been used to improve malt and feed quality. The aim of the present study was to investigate the effect of over-expression of an endogenous (1,3;1,4)-?-glucanase on ?-glucan content and grain composition in barley. RESULTS A construct containing full-length HvGlb2 cDNA encoding barley (1,3;1,4)-?-glucanase isoenzyme EII under the control of a promoter of barley D-Hordein gene Hor3-1 was introduced into barley cultivar Golden Promise via Agrobacterium-mediated transformation, and transgenic plants were regenerated after hygromycin selection. The T2 generation of proHor3:HvGlb2 transgenic lines showed increased activity of (1,3;1,4)-?-glucanase in grains. Total ?-glucan content was reduced by more than 95.73% in transgenic grains compared with the wild-type control. Meanwhile, over-expression of (1,3;1,4)-?-glucanase led to an increase in 1000-grain weight, which might be due to elevated amounts of starch in the grain. CONCLUSION Manipulating the expression of (1,3;1,4)-?-glucanase EII can control the ?-glucan content in grain with no apparent harmful effects on grain quality of transgenic plants. ? 2016 Society of Chemical Industry
© 2001-2024 Fundación Dialnet · Todos los derechos reservados