Utilization of alkali-treated grain. 1. Alkali-treated grain in complete diets for steers and lambs

In one experiment, 32 lambs were offered (ad libitum) diets based on whole or NaOH-treated barley, or whole or NaOH-treated oats. The live-weight gains from 17 to 35 kg live weight were 371, 290, 258 and 229 g/day, respectively, while the calculated carcass weight gains were 190, 161, 86 and 118 g/day, respectively. There were large differences in the gut contents at slaughter which were 5.0, 3.3, 9.2 and 3.0 kg for the four diets, respectively.Forty-eight, Hereford-cross steers were allocated to six dietary treatments which consisted of unrestricted access to one of the following diets: NaOH-treated barley; rolled barley; NaOH-treated oats; rolled oats; NaOH-treated wheat; or NaOH-treated maize. The steers were fattened from 325 to 425 kg live weight. The average live weight gains were 1.56, 1.91, 1.37, 1.38, 1.49 and 1.42 kg/day, respectively. The steers receiving rolled barley achieved the greatest live weight gains (P < 0.05). The rumen contents at slaughter were 19.8, 32.2, 24.2, 46.0, 20.8 and 18.4 kg, respectively. Because of differences in gut contents, the only significant differences in carcass weight gain were found for the steers receiving rolled oats, for which carcass gain was lower than that for any other treatment (P < 0.001).Sixteen, Hereford-cross steers were allowed free access to diets containing either NaOH-treated barley alone, or NaOH-treated barley mixed with 10% of chopped straw. The live weight gains from 325 to 425 kg live weight were 1.55 and 1.07 kg/day, and food conversion was 5.7 and 8.4 kg feed/kg gain respectively.     

Demonstration of sequence variations in the promoter region of the human cystatin C gene.

Four point mutations in the promoter region of the human cystatin C gene have been detected by direct sequencing of polymerase chain reaction (PCR) amplified DNA. The four base changes are all localized within a short segment of 85 base pairs. Three cystatin C gene alleles could be defined with respect to these promoter mutations; one with the sequence previously published, one carrying three of the mutations and one with all four base substitutions. Two of the observed mutations are involved in a novel Sst II polymorphism and another generates a new Dde I restriction site. A PCR-based assay for analysis of these Sst II and Dde I sites was designed and used to demonstrate Mendelian inheritance of the polymorphisms as well as to determine the frequencies of the cystatin C gene alleles in the population.