A method for increasing resistant starch and dietary fibre in rice
A rice and starch technology, applied in the fields of botanical equipment and methods, biochemical equipment and methods, and applications, which can solve problems such as rising risks
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Embodiment 1
[0059] Example 1: RS Assessment Procedure
[0060] RS content was assessed using the Megazyme kit. The kit was obtained from M / s Megazyme International Ireland Ltd, Bray Business District, Wicklow, Ireland. Duplicate 100 ± 1 mg flour samples were taken in screw cap tubes and gently tapped to ensure that no sample stuck to the tube walls. Add 4 ml of amyloglucosidase (AMG) (3U ml -1) of pancreatic alpha-amylase (3 Ceralpha units / mg, 10 mg / ml). Cap the tube tightly so that it is completely dispersed on a vortex mixer and attached horizontally in a shaking water bath aligned with the direction of motion. Tubes were incubated for 16 hours at 37°C with continuous shaking (200 strokes / min). After incubation, tubes were treated with 4.0 mL of ethanol (99%) under vigorous mixing using a vortex mixer. Thereafter, the tubes were centrifuged at 1,500 xg (approximately 3,000 rpm) for 10 minutes (uncapped). The supernatant was decanted carefully and the pellet was resuspended in 8 ml...
Embodiment 2
[0061] Example 2: Degree of Polymerization of Amylopectin Chains
[0062] Pure starch was isolated from all mutants and wild type according to the method described by Lumdubwong and Seib (2000). The amylopectin chain length distribution of isolated starches was analyzed by fluorophore-assisted capillary electrophoresis (FACE) as described by Morell, Samuel and O'Shea (1998). Isolated starch was debranched (2 h at 37°C) using isoamylase (10 U) and labeled with 1-aminopyrene-3,6,8-trisulfonic acid (APTS). FACE was performed using a P / ACE system 5010 (Beckman Coulter, CA, USA) equipped with a 488 nm laser module. Debranched samples were separated using N-CHO (PVA) capillaries (Beckman Coulter, CA, USA) (50 m ID and 47 cm total length) with precombustion windows. Maltose was used as internal standard. Separation was performed at 10°C for 30 minutes. Based on the migration time of maltose, the degree of polymerization (DP) was assigned to the peak.
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