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109<br />

When such a starch sample is X-rayed, a crystalline V structure<br />

is detected. The alternative for V to appear in this case would include migration<br />

through the granule of<br />

a large amylose molecule and/ or long chain fatty acids. A<br />

second limiting factor would be to locate sufficient material in one place for<br />

crystallite formation. In general, retrograded amylose gives the V-type starch X-ray<br />

diffraction pattern. Early X-ray diffraction analysis of stretched amylose film in the<br />

B-type structure was interpreted in terms of a six-fold single helix structure with a<br />

repeat distance of 10.4 o A (Blackwell et al. 1969). On this basis, it could be postulated<br />

that the mechanism of cross-linking amylose gels was via junction zones of<br />

aggregated single<br />

helices.<br />

Figure<br />

21 X-ray diffraction pattern of native HARS and RS III from 0, 16 and 48-hr<br />

Pullulanase debranching of 75°C preheated HARS for 30 min

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