4.7 Article

Starch hydroxyalkylation: Physicochemical properties and enzymatic digestibility of native and hydroxypropylated finger millet (Eleusine coracana) starch

Journal

FOOD HYDROCOLLOIDS
Volume 23, Issue 2, Pages 415-425

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.foodhyd.2008.02.013

Keywords

Finger millet starch; Hydroxypropylation; Functional properties; NMR spectroscopy

Funding

  1. Alexander von Humboldt foundation of Germany
  2. Olabisi Onabanjo University, Nigeria

Ask authors/readers for more resources

Starch was isolated from finger millet (Eleusine coracana) and it was etherified with propylene oxide to produce hydroxypropylated derivative. The specific specie used in this study is African finger millet known asjeero. The yield of starch obtained from finger millet on dry weight basis was 52.4%. Progressive increases in molar substitution (MS) were observed as the volume of propylene oxide added to the reaction medium increased. The X-ray pattern of native finger millet starch conforms to the 'A' diffraction pattern characteristics of cereal starches. Prominent peaks were observed at around 2 theta = 15 degrees, 17 degrees, 18 degrees and 23 degrees and weaker peaks at around 2 theta = 20 degrees and 26 degrees. No pronounced differences were observed between the diffractograms of native starch and the hydroxypropyl derivatives. Hydroxypropylation improved the free swelling capacities of the native starch at all temperatures studied (30-90 degrees C). Turbidity of unmodified finger millet starch paste increased progressively as the days of storage increased. Turbidity reduced remarkably after hydroxypropylation and reduction in turbidity was observed as the MS of the modified starches increased. Hydroxypropylation reduced pasting temperature, increased peak viscosity but reduced setback value. In addition, hydroxypropylation reduced percentage syneresis of the unmodified starch. Retrogradation properties monitored with differential scanning calorimetry reveals that starch retrogradation reduced reasonably after hydroxypropylation. Carbon 13 NMR spectroscopy reveals that hydroxypropylation took place predominantly on carbon 6 on the anhydroglucose unit (AGU). (C) 2008 Elsevier Ltd. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available