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2009 Proceedings of the Cornell Nutrition Conference For Feed ...

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Estimating Thermal Damage in <strong>Feed</strong>s: The Furosine Procedure<br />

Furosine analysis has been used for over 40 years as an indicator <strong>of</strong> <strong>the</strong>rmal<br />

damage in foods (Erbersdobler and Somoza, 2007). ε-N-deoxyfructosyl-L-lysine is <strong>the</strong><br />

major Amadori compound formed during <strong>the</strong> early Maillard reaction (Figure 2). Upon<br />

acid hydrolysis, ε-N-deoxyfructosyl-L-lysine is released in a constant ratio <strong>of</strong> 50% lysine,<br />

30% furosine, 20% pyridosine, and 10% o<strong>the</strong>r compounds (Mauron, 1990). Therefore,<br />

<strong>the</strong> amount <strong>of</strong> furosine measured after acid hydrolysis can be used to calculate %<br />

blocked lysine according to <strong>the</strong> following equation (Mauron, 1990):<br />

% blocked lysine = (3.1 furosine x 100)<br />

[total lysine + (1.86*furosine)]<br />

The acid hydrolysis procedure used in furosine analysis is identical to that used in AA<br />

analysis <strong>of</strong> feeds. Therefore, <strong>the</strong> furosine assay is attractive because furosine and AA<br />

content <strong>of</strong> feeds can all be determined with one procedure. Pahm et al. (2008) used <strong>the</strong><br />

furosine procedure to estimate blocked Lys content <strong>of</strong> 33 DDGS samples, and <strong>the</strong><br />

average blocked Lys content <strong>of</strong> <strong>the</strong> samples was 16% with a coefficient <strong>of</strong> variation <strong>of</strong><br />

7%. Pahm et al. (2008) also reported that blocked Lys was correlated with standardized<br />

ileal Lys digestibility in swine (R 2 = 0.66). Boucher et al. (<strong>2009</strong>b) determined <strong>the</strong><br />

furosine content <strong>of</strong> 16 rumen undegraded residue (RUR) samples: 3 samples <strong>of</strong><br />

soybean meal (SBM), 3 samples <strong>of</strong> expeller SBM (SoyPlus ® ), 5 samples <strong>of</strong> DDGS, and<br />

5 samples <strong>of</strong> fish meal (FM). One <strong>of</strong> <strong>the</strong> SBM, SoyPlus, and DDGS samples were<br />

heated additionally in <strong>the</strong> laboratory oven to intentionally depress digestibility <strong>of</strong> RUP-<br />

Lys. Of <strong>the</strong> 16 samples analyzed, only 9 samples contained furosine, and only <strong>the</strong> 4<br />

unheated DDGS samples contained appreciable amounts <strong>of</strong> furosine (Table 1). Blocked<br />

RUP-Lys was calculated from <strong>the</strong> furosine and Lys concentrations <strong>of</strong> <strong>the</strong> RUR<br />

according to <strong>the</strong> above equation. The same 16 RUR samples were previously fed to<br />

cecectomized roosters to determine digestibility <strong>of</strong> RUP-Lys in vivo. Results <strong>of</strong> <strong>the</strong><br />

experiment indicated that blocked RUP-Lys determined via <strong>the</strong> furosine method was<br />

negatively correlated with standardized RUP-Lys digestibility (R 2 = 0.94; Y = 88.43–<br />

0.89X; P < 0.001, n = 9).<br />

Estimating Thermal Damage in <strong>Feed</strong>s: The Homoarginine Procedure<br />

Homoarginine is an amino acid that is not found in nature. Homoarginine is formed<br />

by <strong>the</strong> reaction <strong>of</strong> <strong>the</strong> epsilon-amino group <strong>of</strong> Lys (<strong>the</strong> NH3 group on <strong>the</strong> side chain) with<br />

O-methylisourea. If <strong>the</strong> epsilon-amino group <strong>of</strong> Lys is bound to ano<strong>the</strong>r compound, such<br />

as a reducing sugar, <strong>the</strong>n homoarginine does not form. Determining <strong>the</strong> amount <strong>of</strong><br />

homoarginine and Lys after <strong>the</strong> reaction with O-methylisourea allows for <strong>the</strong><br />

determination <strong>of</strong> <strong>the</strong> reactive Lys content <strong>of</strong> a feed, or <strong>the</strong> amount <strong>of</strong> Lys in which <strong>the</strong><br />

epsilon-amino group is not bound to ano<strong>the</strong>r compound.<br />

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