Isolation of starches from various tubers such as elephant foot yam (NYS), taro (NTS), ginger (NGS), green banana (NBS) and lotus stem (NLS) was carried out for studying various characteristics viz. physicochemical, differential scanning calorimeter (DSC), rapid visco analyzer (RVA), rheological, morphological and colour in order to explore their end use potential. A significant variation was observed in pasting properties of isolated starches. X‐ray diffractometery (XRD) showed a B‐type crystal pattern of banana starch, while yam, taro, ginger and lotus starches had A‐type crystal pattern. Scanning electron microscope (SEM) revealed that taro starch possessed the smallest granule size having cluster pattern while lotus starches have the largest granular size with hemispherical facets having dents or hollows at one end. Thermal properties of isolated starches revealed that NLS had lowest To, Tp, Tc values i.e. 68.3, 72.0 and 76.8°C, respectively. Similarly the lowest gel characteristics such as hardness, gumminess, chewiness and adhesiveness 3.09 g, 1.45, 1.27, 8.42 gs, respectively, were also found in NLS. L* values of NTS and NYS starches were the highest i.e. 93.36, 93.29 with no significant difference whereas the lowest i.e. 89.917 in NGS.
Lotus rhizome starch was isolated and subjected to chemical modification using different levels of oxidation, cross-linking, and dual modifications. Fourier transform infrared (FTIR) and X-ray diffraction analyses confirmed the successful modification of native starch. The carbonyl, carboxyl contents, and degree of cross-linking of modified starch were in the range of 0.03-0.07%, 0.07-0.15%, and 4.31-58.28%, respectively, for oxidized, crosslinked, and dual-modified starches. Amylose content varied from 13.57% to 20.60% for native and modified starches. Swelling power (SP) and solubility were temperature dependent and increased with increase in temperature. Oxidation and dual modification increased solubility, while cross-linking decreased solubility. Paste clarity, degree of crystallinity, and whiteness of starches increased significantly with increase in level of modifications. Peak, breakdown, and setback viscosities of the modified starches decreased with increase in modification. Phase transitions using DSC presented lower enthalpy values for modified starches. Gelatinization temperature increased due to modification whereas scanning electron micrographs revealed that modification altered the starch morphology.
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