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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 />

590

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