The strawberry (Fragaria · ananassa Duchesne) plant is an octoploid vegetative propagated plant, and its cultivation is labour intensive in comparison with other plants propagated from seeds. The aims of this study were to develop an inbred line from octoploid strawberry and to generate an F 1 hybrid cultivar through the combination of inbred lines. All inbred lines were obtained through selfing using five cultivars. Inbred lines were produced by selecting the best individuals for further inbreeding from each of the previous generations. Plant vigour and yield in inbred lines were low compared with the original cultivar, but completely recovered in the F 1 hybrid. Breeding of inbred lines in octoploid strawberry can be achieved if individuals showing inbreeding depression are eliminated and vigorous individuals are selected, resulting in a strong heterosis of F 1 hybrids through crossing between inbred lines.
A putative bgl operon of Pectobacterium carotovorum subsp. carotovorum LY34 (Pcc LY34) was isolated. Sequence analysis of the 5,557 bp cloned DNA fragment (accession no. AY542524) showed three open reading frames (bglT, bglP, and bglB) predicted to encode 287, 633, and 468 amino acid proteins respectively. BglT and BglP ORFs show high similarity to that of the Pectobacterium chrysanthemi ArbG antiterminator and ArbF permease respectively. Also, the latter contains most residues important for phosphotransferase activity. The amino acid sequence of BglB showed high similarity to various beta-glucosidases and is a member of glycosyl hydrolase family 1. The purified BglB enzyme hydrolyzed salicin, arbutin, pNPG, and MUG. The molecular weight of the enzyme was estimated to be 53,000 Da by SDS-PAGE. The purified beta-glucosidase exhibited maximal activity at pH 7.0 and 40 degrees C, and its activity was enhanced in the presence of Mg(2+). Two glutamate residues (Glu(173) and Glu(362)) were found to be essential for enzyme activity.
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