RA 00048.pdf - OAR@ICRISAT
RA 00048.pdf - OAR@ICRISAT
RA 00048.pdf - OAR@ICRISAT
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Table 1. Percent crude protein, 96 hr in vitro dry matter disappearance (IVDMD) and indigestible protein in<br />
eight sorghum genotypes.<br />
Genotypes<br />
Catechin<br />
equivalent<br />
Crude<br />
protein<br />
96 hr<br />
IVDMD<br />
Indigestible<br />
protein<br />
residue<br />
IS0062<br />
IS0418<br />
IS8165<br />
IS0616<br />
0.29<br />
0.27<br />
4.28<br />
5.93<br />
13.78 94.8a*<br />
12.11 93.1a<br />
11.26 88.8b<br />
14.20 83.0c<br />
1.13<br />
1.62<br />
2.80<br />
4.73<br />
* Means in a column followed by the same letter do not differ significantly at the 0 05 level of probability using Newman-Keul's test.<br />
nols and of the effects of polyphenols on sorghum<br />
grain quality. We will discuss some of his<br />
basic observations on the interactions between<br />
tannins and the nutritional value of sorghum grain<br />
in relation to our own research and to the<br />
scientific literature.<br />
Oswalt first recognized that in vitro dry matter<br />
digestibility (IVDMD) of sorghum grains varied<br />
significantly between genotypes, and that the<br />
catechin equivalent values for tannin content<br />
were negatively correlated with IVDMD as shown<br />
in Table 1 (Schaffert et al. 1974). This was an<br />
extremely important observation because it explained<br />
the discrepancies which had previously<br />
been observed between protein quality and biological<br />
value in rat feeding experiments. Based on<br />
the amino acid composition of sorghum grain, one<br />
would predict that the biological value of any<br />
particular variety of sorghum grain would be<br />
directly proportional to its lysine content. This, in<br />
fact, is true for low-tannin sorghum genotypes.<br />
The data in Figure 1, however, illustrate that lysine<br />
is not the first limiting component of biological<br />
value for a group of high-tannin sorghum lines<br />
from the world collection. There is an important<br />
interaction between tannin content and protein<br />
quality in sorghum which is not found in any of the<br />
other major cereals. Cummings and Axtell (1973)<br />
demonstrated this experimentally by feeding<br />
whole grain and dehulled high-tannin sorghum<br />
grain of IS 8260, as shown in Figure 2. Rat growth<br />
is poor for the whole grain IS 8260, with and<br />
without supplemental lysine. In contrast, denuding<br />
IS 8260 grain improves biological value substantially,<br />
and also allows a significant rat growth<br />
response to the addition of supplemental lysine. A<br />
similar technique was used in this study to<br />
16-<br />
14-<br />
1 2 -<br />
10<br />
8<br />
6<br />
4<br />
2<br />
Low t a n n i n s o r g h u m<br />
H i g h t a n n i n s o r g h u m<br />
0 .20 .22 .24 .26 .28 .30 .32 .34 .36<br />
L y s i n e<br />
Figure 1. Relationship of biological value to<br />
lysine concentration (g/100 g sample)<br />
in high- and low-tannin sorghum lines<br />
from the world collection in a 14-day<br />
weanling rat feeding experiment.<br />
determine the quantitative effects of tannins on<br />
biological value. Using varying proportions of<br />
high-tannin sorghum grain mixed with its dehulled<br />
low-tannin counterpart, we were able to provide<br />
diets containing a range of tannin content that<br />
were essentially isogenic comparisons. Data from<br />
this study are shown in Figure 3.<br />
The protein digestibility and nutritional quality as<br />
measured by rat weight gain are significantly<br />
reduced by increasing levels of tannins in the diet.<br />
We can conclude from Butler's (1982) data that<br />
tannins bind specifically to proline residues in<br />
proteins and thus to the storage proteins (the<br />
prolamines) which are rich in proline but poor in<br />
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