The effect of enzyme treatment on the in vitro fermentation of lucerne incubated with equine faecal inocula

被引:17
|
作者
Murray, JAMD
Longland, AC
Moore-Colyer, MJS
Dunnett, C
机构
[1] Inst Food Res, Inst Grassland & Environm Res, Aberystwyth SY23 3EB, Dyfed, Wales
[2] Univ Wales, Inst Rural Sci, Aberystwyth SY23 3AL, Dyfed, Wales
[3] Univ Edinburgh, Royal Dick Sch Vet Studies, Div Anim Hlth & Welf, Roslin EH25 9RG, Midlothian, Scotland
[4] Dengie Crops Ltd, Maldon CM9 4ND, Essex, England
基金
英国生物技术与生命科学研究理事会;
关键词
enzyme treatment; in vitro fermentation; equine inocula; lucerne;
D O I
10.1079/BJN20051561
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
A series of experiments was conducted to determine the effects of a fibrolytic enzyme preparation (enzyme 1; E1) on the in vitro fermentation of lucerne incubated with equine faecal inocula. In experiment 1, high-temperature-dried (HT) lucerne was treated with five levels of E1 (0 to 2.4 ml/g DM) and incubated at 50 degrees C for 20 h. Samples then received a simulated foregut digestion (SFD) treatment before DM and NSP analysis. In experiment 2, HT lucerne was treated with the same enzyme levels used in experiment 1. Samples were then split into two groups; plus or minus an SFD treatment before in vitro fermentation using an equine faecal inoculum. In experiment 3, fresh and wilted lucerne were treated with the same levels of E1 as experiments 1 and 2, incubated at 50 degrees C for 20 h, then fermented in vitro. For experiment 4, fresh and wilted lucerne were treated with low levels (0 to 0.008 ml/g DM) of E1 before fermentation. E1 significantly (P < 0.05) enhanced DM and NSP losses from HT lucerne following SFD treatment compared with the control. High levels of E1 significantly (P < 0.05) enhanced the rate, but not extent, of fermentation of HT, wilted and fresh lucerne; however, low levels of E1 were ineffective. At higher application levels, E1 appears to have considerable potential to enhance the nutritive value of lucerne for horses. Information on the fermentation kinetics of the substrates was valuable; all end-point measurements showed no effect of enzyme treatment.
引用
收藏
页码:771 / 782
页数:12
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