Preservation of protein in wilted lucerne using formic,sulphuric or trichloroacetic acid

A laboratory-scale experiment was conducted with lucerne (Medicago sativa) to determine the effects of acid treatment on proteolysis during ensiling and during subsequent in vitro ruminal protein incubations. Lucerne 300 g dry matter (DM) kg^?1 forage] was either untreated (control) or treated with sulphuric, formic or trichloroacetic acid (a protein precipitant that stops enzyme activity) at levels sufficient to adjust immediately forage pH to 4·0, then conserved as either silage or hay. Time-course data indicated that non-protein nitrogen (N) formation was 70–90% complete after 1 d of fermentation in the silo. Non-protein N concentrations (g kg^?1 total N) were 177 at ensiling and increased to 567 (control), 426 (sulphuric), 398 (formic) and 263 (trichloroacetic) after 60 d of ensiling. Because non-protein N in silage treated with formic and sulphuric acids was nearly three times greater than that in silage treated with trichloroacetic acid, it is clear that the typical acid treatments only slow proteolysis and do not destroy protease activity during ensiling. The ruminal protein degradation rate of conserved forages was slower than that of fresh-cut forage that was preserved with dry ice immediately after cutting. The degradation rate of all acid-treated forages was similar, indicating a consistent effect on ruminal degradation regardless of method of preservation. There was a clear effect of acid treatment on reducing the rate and extent of ruminal degradation of protein in lucerne hay.