By Henderson W. E.

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1981, 2, 176. A. , 1981, 112, 76. , 1981, 111, 122. , 1981, 27, 198. , 1981, 19, 31. , 1981, 110, 380. Usui, ClhChhActa, 1981, 108,493. Bogin,Experientia, 1980, 36, 370. , 1981, 207, 445. , 1981, 113, 423. , 1981, 19, 139. J. , 1981, 38, 13. , 1981, 91, Q. , 1981, 58, 2800. , 1981, 256, 6657. H. , 1980, 2,65. , 1951, 210, 138. C . , 1981, 124,299. Res. ,1981, 98, 242. , 1981, 209, 299. Qlrcmatogr. , 1981, 210, 487. , 1981, 116, 383. , 1981,,&I 489. Linscheid, J . USA, 1981, 78, 1471. , 1980,2& 1137.

5 The chain conformation is a left-handed, six-fold helix The water with 0-6 in the position Bauche to both 0-5 and C-4. molecules are located inside the helical channel of the amylose and in the interstitial spaces, forming an intensive hydrogen-bonded network. 6 The technique, especially with negative ions, extends mass spectrometry to polymers. The molecular-size distribution of modified corn starch has 22 Carbohydrate Chemistry been determined by size-exclusion chromatography. The high performance liquid chromatography of malto-oligosaccharides has been reported.

13 The reaction seemed to be a strong association with the amylose component since the B-amylolysis limit of the amylose is reduced. The starch-xanthan gum exhibited a pseudoplastic behaviour whereas the starch-guar gum resisted shearing at low shear rates. 74 The role of starch in this process was discussed. ’15 With sterile soil a picloram ester was phytotoxic for 48 days. Unmodified starch esters were hydrolysed at a slower rate than gelatinized starch esters. 76 X-Ray and neutron-diffraction studies on hexa-amylose hexahydrate crystal forms A and B have given an indication of the chain-like and circular arrangement of hydrogen bonds within the molecules.

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