aNDF, NDFd, iNDF, ADL and kd: What have we learned?
aNDF, NDFd, iNDF, ADL and kd: What have we learned?
aNDF, NDFd, iNDF, ADL and kd: What have we learned?
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a reverse-phase column. Ether-linked PCA <strong>and</strong> FA <strong>we</strong>re calculated as the difference<br />
bet<strong>we</strong>en total <strong>and</strong> ester-linked phenolic acids. Phenolic acids <strong>and</strong> respective amounts of<br />
their different linkages <strong>and</strong> lignin types <strong>we</strong>re used in a multiple regression to select<br />
those factors explaining most of the variation in <strong>kd</strong>, 24hr <strong>and</strong> 96hr NDFD.<br />
Since most esterified PCA on lignin are not covalently attached to other cell wall<br />
polymers, they should not directly influence cell wall degradability. Ho<strong>we</strong>ver some cell<br />
wall models show how they can interfere with ferulate-lignin cross linking <strong>and</strong> in some<br />
cases reduce the proportion of lignin bound to cell wall. Figure 2 <strong>and</strong> 3 show the<br />
relationship bet<strong>we</strong>en 24hr NDFD <strong>and</strong> PCA content in NDF <strong>and</strong> ADF residues<br />
respectively. Forage groups demonstrated different relationships for digestibility from<br />
positive to negative in NDF residues. ADF residues <strong>we</strong>re instead characterized by a<br />
consistent negative relationship among all forage groups <strong>and</strong> similar results <strong>we</strong>re<br />
obtained for 96 hr NDFD.<br />
Relationship bet<strong>we</strong>en 24hr <strong>and</strong> 96hr NDFD with esterified FA content in NDF<br />
residues are shown in Figures 4 <strong>and</strong> 5, respectively. Ester-linked FA had generally a<br />
negative relationship except in bmr corn for 24hr <strong>and</strong> positive for 96hr NDFD. Ferulates<br />
primarily form as esters of arabinoxylans <strong>and</strong> later they cross-link through ether linkages<br />
with lignin. So esters of FA should not necessarily limit NDF degradation. This has<br />
probably more to do with the degree of arabinoxylans substitution.<br />
Ether linkage bet<strong>we</strong>en FA <strong>and</strong> lignin has been used a measure of cross-linking<br />
bet<strong>we</strong>en lignin <strong>and</strong> arabinoxylans <strong>and</strong> defined as the most important factor limiting<br />
energy utilization (Casler, 2001). Ho<strong>we</strong>ver in our case <strong>we</strong> <strong>we</strong>re not able to obtain<br />
consistent negative relationship with NDFD. Figure 6 <strong>and</strong> 7 show the relationship for 24<br />
<strong>and</strong> 96 hours respectively with divergent relationship for 24 hr <strong>and</strong> consistent positive<br />
ones for 96 hr NDFD. Negative effect of etherified FA on NDFD has been found in<br />
elongating internodes in maize but not in internodes that had stopped the elongation<br />
process <strong>and</strong> confirms the hypothesis that secondary cell wall development may mask<br />
the negative impact of etherified FA on NDFD. Interestingly also, bmr shows higher<br />
content of etherified FA compared to conventional corn in NDF residues, demonstrating<br />
that etherified FA is not always a good indicator of cross-linking bet<strong>we</strong>en lignin <strong>and</strong><br />
arabinoxylans <strong>and</strong> this was also shown recently by Marita et al. (2003). Ho<strong>we</strong>ver this<br />
relationship changes when ADF residues <strong>we</strong>re analyzed for ether linked FA, showing<br />
how the solubulization or branching of the lignin structure has in this case more<br />
importance than linkages. Acid detergent solution in this case might dissolve those FAs<br />
that only etherified (instead of having <strong>and</strong> ester-ether linkage).<br />
A multiple regression with stepwise selection was run within each forage group using<br />
the independent variables lignin type (<strong>ADL</strong> or Klason lignin) <strong>and</strong> their difference on an<br />
NDF basis <strong>and</strong> phenolic acids with their specific linkages also on an NDF basis. We<br />
wanted to determine how much variation in 24hr <strong>and</strong> 96hr NDFD <strong>and</strong> <strong>kd</strong> was explained<br />
by the above mentioned variables. The procedure was not able to find any significant<br />
variable for the alfalfas (P < 0.10), showing how NDF digestibility cannot be easily<br />
explained in legumes by many of these factors. All the other forage groups reached