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Review

Effect of Rice Processing towards Lower Rapidly Available Glucose (RAG) Favors Idli, a South Indian Fermented Food Suitable for Diabetic Patients

by
Ramachandran Chelliah
1,†,
Sangeeta Chandrashekar
2,†,
Kandasamy Saravanakumar
3,
Sudha Rani Ramakrishnan
4,
Momna Rubab
1,
Eric Banan-Mwine Daliri
1,
Kaliyan Barathikannan
1,
Akanksha Tyagi
1,
Fred Kwame Ofosu
1,
Xiuqin Chen
1,
Se-Hun Kim
1,
Fazle Elahi
1,
Han NaKyeong
1,
Myeong-Hyeon Wang
3,
Vijaykumar Raman
2,*,
Usha Antony
5,* and
Deog-Hwan Oh
1,*
1
Department of Food Science and Biotechnology, College of Agriculture and Life Science, Kangwon National University, Chuncheon 24341, Korea
2
Department of Physiology, Bharath Institute of Higher Education and Research, Chennai 600 073, India
3
Department of Medical Biotechnology, College of Biomedical Sciences, Kangwon National University, Chuncheon 24341, Korea
4
School of Food Science and Biotechnology, Kyungpook National University, Daegu 41566, Korea
5
Department of Biotechnology and food technology, Anna University, Chennai 600 025, India
*
Authors to whom correspondence should be addressed.
These authors contributed equally to this work.
Nutrients 2019, 11(7), 1497; https://doi.org/10.3390/nu11071497
Submission received: 3 May 2019 / Revised: 31 May 2019 / Accepted: 13 June 2019 / Published: 30 June 2019

Abstract

:
The Asian food pattern primarily embraces rice and rice-based products, which mainly comprise 90% starch. Among these various food products, Idli is mostly prepared through fermentation. It has high palatability, and the rapid and highly digestible nature of the food product results in a higher post-glucose level in diabetic patients. A heat-treated Idli rice sample was prepared by roasting parboiled rice at the temperature range of 155 to 165 °C for 65 to 75 s. Idli/rice-based Dokala made from heat-treated rice is better when compared to untreated rice in terms of its microbiological profile and physiochemical properties. The proximate composition of heat-treated parboiled rice Idli/Rice Dokala showed slightly higher values than the untreated parboiled rice Idli/Rice Dokala, which reveals that it has marginally higher nutritive value. Determination of the Rapidly Available Glucose (RAG) and Slowly Available Glucose (SAG) values, SEM analysis, resistant starch analysis, microbial assay, and in vivo studies were performed to determine the glycemic index (GI) and glycemic load in normal and diabetic persons. Sensory analysis also proved that heat-treated Idli/Rice Dokala is superior to untreated based on the color, flavor, appearance, taste, and texture.

1. Introduction

Diabetes has developed into a chronic disease in humans, affecting approximately 200 million adults globally and almost 15 million Americans in 2000. In 2002, the rate of diabetes increased drastically; also, the treatment and medicine productivity costs were raised. Likewise, the incidence of diabetes among U.S. adults has grown to 61%; previously, it was 5% in 1990, and it continuously increased to 8.1% in 2000 [1]. It has been predicted that in 2075, diabetes will affect almost 29 million adults in the United States. The lifetime risk of diabetes based on gender was 32.8% in males and 39.2% in the female population of the United States in 2000 [2]. Moreover, the extreme level of diabetes-affected persons led to an increased death rate, accounting for 71,372 deaths in 2000 [3]. It has been anticipated that an examination for diabetes at 50 years of age will result in increased life expectancy for about 12.5% of males and 15.1% of females [2] (Figure 1).
Famous traditional rice-based Indian foods such as Idli and Dokala are mainly prepared with parboiled rice, which is rich in amylose content, leading to soft and spongy textural characteristics [4]. Fermentation and cooking cause a reduction in oligosaccharides of 40% and result in a reduction in levelness of the product based on the substitution of other grains such as pulses (kidney beans, black gram, broad bean, chickpea, soybean, and lentil); hence, depending on the composition, the starch digestibility—indirectly responsible for our understanding of the context of type 2 diabetes—differs [5]. Several studies have been conducted to understand the blood glucose response based on the carbohydrate content of food products. Usually, blood glucose is quantified based on the glycemic index (GI). Apart from the glycemic index, the resistant starch (RS) content is measured based on starch digestibility. The fabrication of gradually digestible starch (GDS) and RS has been established to alleviate the quantity of blood sugar and to produce aids to human health [6]. The RS level of rice is increased by heat treatment methods, and it has been reported that high-pressure heating (116 °C, 10 min) increased the RS level in raw rice from 6.29% to 14%. Nevertheless, parboiling reduced the RS by 50% in long-grain rice. It appears that heating at higher than 100 °C possibly enhances the RS content. Moist heat treatment (MHT) is a hydrothermal method which changes the physiochemical properties of starch and is mostly performed at a controlled humidity level (lower than 35%) and by heating at 84–140 °C for 15 min to 16 h [7]. It leads to gelatinization of the rice product due to a lower moisture content. Also, changes such as the development of complexes of amylose–lipid (ALC) and lowered enzymatic vulnerability occur during MHT [8]. The quantity of RS in MHT-treated starch leads to breakdown of the granules’ minor structure. The assembly of gradually digestible starch (GDS) and RS has been initiated to regulate the quantity of blood sugar towards better health and welfare [6].

2. Dietary Factors and Type 2 Diabetes

The complex nature of inter-connections between nutrients and nourishment in the diet and the hazard of diabetes and high glucose levels in the blood has been inspected by numerous researchers. The most prominent research indicates that a lifestyle of consuming a high-fat and high-calorie diet leads to type 2 diabetes, but epidemiologic research information has shown that this is relatively unpredictable [9]. Recent studies have revealed that specific food intake based on high glucose content and carbohydrates and an irregular dietary profile [10] leads a person to be more prone to diabetes.

3. Contemporary Perceptions of the Deterrent Levels of Starch/Carbohydrate/Fiber/Fat in Diet

Currently, the emphasis being placed on the glycemic reaction to various carbohydrate-enhanced foods varies from the conventional conviction about basic versus complex carbohydrates in the management of diabetes mellitus [11]. Recently, significant evidence has shown that different carbohydrate-containing foods reveal the same quantity of sugars in chemical analysis but cause wide variation in blood glucose tolerance or response after the ingestion of food.

4. Rice and the Glycemic Index Mechanism

Rice, a staple food in India, is a prime source of carbohydrate, and different varieties are applied as a primary food. However, the GI of rice is higher than that of any other starch-containing food [11]. Rice can be biochemically translated as starch (60%–80%). The digestion of the starch is carried out by the enzymes amylase and amyloglucosidase. Alpha-amylase (1, 4 α D-Glucan-glucanohydrolase) targets outsized polymers of starch at intimate bonds and splits them into short glucose polymers [12]. Amyloglucosidase catalyzes the hydrolysis of the alpha-1, 4 and alpha-1, 6 linkages of starch, producing glucose. During hydrolysis, glucose is removed from the non-reducing end of amylose or amylopectin chains [13,14,15]. The basic hydrolysis rate depends on the type of linkage and chain length: for example, alpha-1, 4 linkages are more readily hydrolyzed than alpha-1, 6 linkages [16]. The amyloglucosidase mechanism focuses on the shorter polymers and splices them off into single glucose units (Figure 2).

5. Glycemic Index and Glycemic Load

Relatively less epidemiologic research-based evidence has shown the correlation of carbohydrates with diabetes to be indirectly proportional to high glucose in the blood [17,18,19,20]. However, groups of people consuming low levels of carbohydrate or simple sugars such as monosaccharide or disaccharide show lower incidence of diabetes [20,21,22,23]. An exception, the Iowa Women’s Health Study, indicated that the uptake of fructose or glucose leads to the risk of stimulating type 2 diabetes mellitus [24,25,26]. With the development of the GI in 1980, it was concluded that the relation of carbohydrates with type 2 diabetes depends on the structure [27,28,29]. The GI matches the glucose uptake, which is proportionally equal to the absorption of sugar in one’s daily diet [27]. In general, high glucose and high GI uptake lead to type 2 diabetes [29].
The American Diabetes Association (ADA) endorses the consumption of nutritious food such as fruits, vegetable, cereals, pulses, and dairy products as a healthy food diet for diabetes patients, because lower amounts of carbohydrate lead to lower incidence of diabetes [30]. The ADA specifically shows instructions for estimating the uptake of glucose in blood from the specific level of uptake of carbohydrate in a meal or per day [31]. Numerous factors such as the nature of the sugar; the quantity of fiber, lipid, and protein; the food form; the various methods of preparation; and the significant role of enzyme inhibitors influence the GI of a specific food.
The current research shows that higher-carbohydrate/fiber diets result in a reduction in blood glucose and other beneficial factors towards controlling diabetes, specifically in those with type 2 diabetes mellitus [31,32,33]. Similar foods that possess lower GI correspondingly assist in reducing blood cholesterol and triglyceride points. Such foods constitute the main quota of mono, di, and polysaccharides responsible for diabetes. An extended period of research has indicated that the GI is a valuable concept, and the application of sucrose in a reasonable quantity does not affect glucose control [33]. This is a step towards understanding the difference between starch-enriched diets and carbohydrate-enriched nourishment or monosaccharide versus polysaccharide [32] (Figure 3).

6. The Roles of Rapidly Available Glucose (RAG) and Slowly Available Glucose (SAG) in Diabetic Patients

The final product of the digestion of starch is glucose, which is classified into Rapidly Available Glucose (RAG), Slowly Available Glucose (SAG), Free Glucose (FG), and Total Glucose (TG) [34]. RAG and SAG reflect the rates at which sugars (glucose and starch, including maltodextrins) become available for the absorption in the human gut [29]. RAG is rapidly unrestricted and absorbed (within 30 minutes) and is a key factor of glycemic response, while SAG is unconstrained and absorbed slowly and is not expected to affect the glycemic response. Reduced-GI foods yield a gradual increase in blood sugar (RAG) and are associated with reduced risk of diabetes, cardiovascular disease, and cancer [35]. Foods that are more slowly digested may have metabolic benefits in diabetes because the RAG values for such foods would be low and they would not result in a rapid postprandial increase in glucose level. This is beneficial in the dietary management of diabetic patients (Figure 3).

7. Resistant Starch and Gut Microbiota Modulation

Resistant starch (RS) is well defined as the starch and products of starch degradation that are not absorbed in the small intestine of healthy individuals [38]. RS resists digestion by enzymes in the digestive tract but can be partially broken down in the large intestine by gut bacteria. Carbohydrates are made up of sugars, starches, and fibers (Table 1) [31]. In the colon, they are moderately fermented by gut bacteria in a way similar to digestible fibers. The structure of the human microbiome, altered by comparatively few dietary constituents, has been inspected for various functional potentials of the microbiome, such as an increase in Firmicutes to Bacteroidetes leading to an increase in enzymatic pathways involved in phospholipid metabolism in the gut (Figure 4).
The proportion of amylose and amylopectin, physiochemical form, degree of gelatinization, heat treatments, refrigeration, and storage affect the RS quantity in foods [40,41,42]. RS in nutraceutical-based food processing and manufacturing has drawn attention, leading to wide-ranging inquiry into the influence of RS on the non-digestible sugar component of the diet and its physiological implications. RS may be made up of retrograded starch, physically inaccessible starch, starch–nutrient complexes, chemically modified starch, and starches that are complex due to enzymatic inhibition [43,44]. The RAG and SAG values could be altered by RS formation (Figure 5).
As recorded, there are four types of RS: RS1 is starch which is physically difficult to reach due to the manifestation of rigid cell walls in grains, kernels, or rhizomes. RS2 is native crystalline starch granules that are resistant to enzymatic hydrolysis; for example, the starch in uncooked potatoes, the green variety of banana, and elevated-amylose corn. RS3 is retrograded starch which is cooked followed by cooling for a few hours or longer. RS4 is the chemically changed starches; these are due to cross-linking with substance reagents, ethers, esters, and so forth [45].

8. Resistant Starch (RS), Insulin, Glucose Metabolism, Glycemic Load (GL), and Glycemic Index (GI)

Insulin is considered to be the hormone accountable for the transportation of blood-based glucose from the circulatory system to the muscle and (fat) cells [46]. Avoiding insulin hikes has been observed as the primary feature in managing body weight as this hormone not only stores blood-based glucose in lipid-based cells but additionally blocks the arrival of lipids and their subsequent use for energy. Foods containing RS cause continuous insulin discharge; this causes the eradication of lipids to be elevated in the liver and is ultimately utilized for energy (Figure 6). Accordingly, RS assumes a critical role in the insulin reaction balance and in managing glucose digestion [32,47]. As an outcome, the use of RS-rich nourishment is imperative in the management of body weight and obesity and in diminishing the danger of developing diabetes and other significant illnesses.

9. Fermented Foods—Idli

Fermented foods are often more nutritious than their unfermented counterparts, and they are easily digestible. This is true of naturally fermented legume products; hence, such foods are still produced in India by simple traditional methods [49]. Idli is the most common fermented legume and rice product in South India. Idli is highly digestible and is thus recommended as a food for patients, infants, and older people with impaired digestion [49]. However, diabetic patients are advised to avoid Idli because of its rapid digestibility, which in turn results in a rapid rise in their postprandial blood glucose level. This is detrimental to diabetic patients [50]. The GI of Idli made in the traditional method is as follows, making Idli not suitable for the diabetic diet.

10. Limitations of the Glycemic Index (over 77 ± 2, Considered High) and the Glycemic Load (over 40.04, Considered Hiked) for a Serving Size of 250 g

In order to make Idli suitable for diabetic patients, the digestibility must be reduced to give it lower RAG values [51]. This will result in a lower GI. So far, little work has been published on the development of modified starch products. Therefore, the objective of the present work follows Phase I, which involves the optimization of the heat treatment of rice.

11. Processing Method

In food processing, physio-chemical treatments may meaningfully affect starch ingestion. For grain-based foods, modification based on dampness, condition, and so forth is vital [52]. Starch is a combination of binary forms such as amylose and amylopectin, both of which are polymers of glucose. In terms of human nutrition, starch is by far the most important of the polysaccharides. The range of change is typically estimated from dextrose correspondents, which are crudely the segments of the glycoside bonds in the starch which have been fragmented [52,53].

12. Physical Treatment

Moisture–heat action has been generally considered a main strategy for altering starch yet heat treatment of starch in a dehydrated environment has been rarely examined. One exemption is pyrodextrin creation by the treatment of starch at high temperatures [54]. Dextrins can be fashioned from starch based on enzymes like amylases by ingestion inside the human body and during malting, squashing, or by applying a high temperature under acidic conditions (pyrolysis or roasting) [55]. It has been claimed that heating starch or flour at >100 °C, preferably for numerous hours, produces functionality equal to that obtained by chemical cross-linking [56]. The rice assortment-based heat discharge process is a novel system for gelatinizing crude starch (Figure 7). It exploits warmed air to substitute for steam when preparing rice under high-temperature fluidization over a brief period. The dextrin shape is difficult to denaturalize and simple to store in contrast with that created by conventional aquatic-based steaming [57].

13. Microstructure of Rice Grains

Eliasson et al. [57] reported that dehydrated warming could be used as an alternative procedure to the biochemical alteration commercially applied to starches of different origins. Starch under thermo-treatment at 100 °C generated a well-designed equivalent to that obtained by chemical cross-networking by increasing the resistance to thickness (viscosity) breakdown and by shortening the glued structure [59]. Mild heat can be used to change the physical abilities of starch [54,55,56,57]. Moist heat treatment (MHT), which involves heating at a controlled humidity level, is a mono process applied to substantially alter starches and rice flours [57]. Eliasson et al. [57] observed that the physical and chemical properties of starches were radically altered after MHT [52,59]. Enhanced RS contents and reduced enzyme vulnerability of starches may be accomplished by different time/temperature treatments; this has been shown previously for starches of different botanical origin and with varying amylose/amylopectin ratios [48,60,61,62,63,64,65,66,67,68]. Dehydrated heating (130 °C) of waxy corn starch expanded the GDS content. Among the temperatures utilized, 130 °C was found to increase the SDS content [69] (Table 2).

14. Glycemic Index

The GI concept was initially developed to categorize diverse sources of sugars and starch-rich foods in the diet based on their influence on postprandial glycemia [70,71,72,73]. Reduced-GI foods are known to produce less postprandial hyperglycemia and hyperinsulinemia than high-GI foods [67,73]. The GL helps quantify the distinct effect of a food product with readily obtainable carbohydrate. In other words, the GL is more practical than the GI of food items in terms of measuring glucose in the circulation [GL = (GI × dietary carbohydrate of serving)/100] (Table 3).
An ADA spot report on nourishment concluded that the application of GI and GL would possibly give greater advantage in regulating diabetes based on total carbohydrate [30]. Additionally, the ADA stated that the data are not adequate to permit a decision on whether low-GL foods reduce the risk of diabetes; however, the ingestion of reduced-GI foods that are high in iron and fiber fortified is recommended [30]. An elevated association exists between the degree of in vitro glucose increase from starch-rich nourishments, centered on pancreatic and digestive enzymes, and the glycemic response in vivo [74]. Numerous dietary factors are directly proportional to glycemic and insulin responses, the carbohydrate (monosaccharide, disaccharide, and polysaccharide) uptake and ingestion rate, and the rate of secretion of digestive enzymes [48,66,67,68]. The rate of breakdown of nutrients differs relative to the physiochemical properties of the food [72,73,74].
Table 3 indicates the hydrolysis index (HI) and assessed GI values of the processed rice samples. Overall, the HI was enhanced with an increase in the degree of cooking of the rice (R < MH < CC), while the enhancement of MH and CC for non-homogenized samples was not statistically significant. Chung, Lim, and Lim [8] reported an absence of variation in starch hydrolysis of sticky rice for samples of diverse gelatinization grades.

15. Rapidly Available Glucose (RAG) and Slowly Available Glucose (SAG)

The glycemic sugar fraction, which is captured in the small intestine, is defined as the quantity of carbohydrate and starch excluding Resistant Starch (RS). The sugar fraction can be subdivided into Readily Available Glucose (RAG) and Slowly Available Glucose (SAG), and in vitro analysis reflects the likely degree of absorption of glucose in the small intestine. Analytical procedures have been developed to characterize foods and reflect their expected biological uptake. The values of RAG and SAG were determined in hydrolyzed foods by enzymes amyloglucosidase and amylase at 20 minutes and 120 minutes of an in vitro carbohydrate digestion method, respectively, by modifying the method by Eliasson [57]. The RAG index was confirmed as a forecaster of the potential glycemic response obtained from the digestion of these food items. The hypothesis is that the RAG fraction is rapidly (within 20 minutes) released and absorbed and is the major concern of the glycemic reaction. The SAG fraction is unconstrained and absorbed slowly and is not anticipated to affect the glycemic response. The in vitro RAG of foods could imitate the glycemic reaction [59]. Fredriksson indicated that in vitro estimation of the carbohydrate ingestion rate is correlated with the glycemic response in human study; this demonstrates that in vitro carbohydrate ingestion can be a valuable model to estimate the biotic response of a carbohydrate-based meal while also being a simple and inexpensive method [69].

16. Processing Method and Resistant Starch

In food processing, physio-chemical treatments may profoundly affect starch indigestibility. For cereal foods, modifications in humidity, thermal conditions, etc., have been verified [52]. Starch is a combination of binary factors such as amylose and amylopectin, both of which are polymers of glucose. In terms of human nourishment, starch is by far the most significant of the polysaccharides. The level of adaptation is typically estimated from dextrose correspondents, which are coarsely the segments of the glycoside bonds in the starch which have been broken [56]. Resistant starch (RS) is considered one of the three types of dietary fiber, along with the carbohydrate that is digested in the small intestine, and that which reaches the large intestine undigested [69].
Further bacterial fermentation leads to the production of volatile fatty acids. This has been observed in the majority of carbohydrate-enriched foods. Consumption of natural RS by humans has been indicated to result in a reduced glycemic response in healthy individuals [35], decreased glycemic response in diabetes, and increased insulin sensitivity in healthy individuals [35,38,75] (Table 4).
An important association was detected when the percentage of rapid carbohydrate ingestion and the Lente carbohydrate assimilation percentage were interrelated with the GI of the food consumed, but only when a single rapid carbohydrate absorption rate was considered. These outcomes validate this as a beneficial, simple, and low-cost method to evaluate the biotic response of high-carbohydrate foods [68,69].

17. Conclusions

The review showed that a slight amendment to rice treatment can modify the physiochemical properties of rice. This rice provides bulk, that is, to satiety, but most is not absorbed and it does not lead to an increase in blood glucose level. By the additional effect of fiber and further effects as discussed, overall and Low-density lipoprotein (LDL) dietary fat was reduced. The process is economically affordable and not expensive. The only disadvantage is minor differences in taste and the raised fuel rate required for heating the rice. Based on this review, it was concluded that the thermal treatment of rice is a better method for increasing the resistant starch content, which, in turn, may be useful for diabetes patients. Hence, heat treatment of rice is preferred for the preparation of low-GI Idli and other rice-based food products.

Author Contributions

Designing the outline of the Review manuscript, Visualization, Conceptualization – (R.C., S.C., V.R., U.A., D.-H.O. Dietary Factors and Type 2 Diabetes – K.B., A.T. - Writing – review & editing. Contemporary Perceptions towards the Deterrent Level of Starch/Carbohydrate/Fiber/Fat in Diet Rice and Glycemic Index Mechanism – M.R., E.B.-M.D.- Writing – review & editing. Glycemic Index and Glycemic Load, Role of Rag and Sag on Diabetic Patients – K.S., S.R.R. - Writing – review & editing. Resistant Starch on Gut Microbiota Modulation, R.C., K.S Insulin, Glucose Metabolism, GL and GI, Fermented Foods – Idli – F.K.O., X.C., S.-H.K., F.E., H.N.– review & editing. Limitation of Glycemic Index, Processing Method, Physical Treatment, Microstructure of Rice Grains – R.C., S.C., K.S – review & editing. Glycemic Index, Rapidly Available Glucose (RAG) and Slowly Available Glucose (SAG), Processing Method and Resistant Starch – R.C., S.R.R., S.C., K.S., K.B., M.-H.W.

Funding

This research was funded by [National Research Foundation of Korea (NRF)] grant number [2018007551]” and Brain Korea (BK) 21 Plus Project [Grant No. 22A20153713433].

Acknowledgments

This work was supported by the Korea Research Fellowship Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, in Young Researchers Program [2018007551]; Brain Korea (BK) 21 Plus Project [Grant No. 22A20153713433] Funded by the Korean Government, Republic of Korea.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Geiss, L.S.; Wang, J.; Cheng, Y.J.; Thompson, T.J.; Barker, L.; Li, Y.; Gregg, E.W. Prevalence and incidence trends for diagnosed diabetes among adults aged 20 to 79 years, United States, 1980–2012. JAMA 2014, 312, 1218–1226. [Google Scholar] [CrossRef] [PubMed]
  2. Narayan, K.V.; Boyle, J.P.; Thompson, T.J.; Sorensen, S.W.; Williamson, D.F. Lifetime risk for diabetes mellitus in the United States. JAMA 2003, 290, 1884–1890. [Google Scholar] [CrossRef] [PubMed]
  3. Jones, K.E.; Yan, Y.; Colditz, G.A.; Herrick, C.J. Prenatal counseling on type 2 diabetes risk, exercise, and nutrition affects the likelihood of postpartum diabetes screening after gestational diabetes. J. Perinatol. 2018, 38, 315. [Google Scholar] [CrossRef] [PubMed]
  4. Rani, P.; Kumar, A.; Purohit, S.R.; Rao, P.S. Impact of fermentation and extrusion processing on physicochemical, sensory and bioactive properties of rice-black gram mixed flour. LWT 2018, 89, 155–163. [Google Scholar] [CrossRef]
  5. Rani, M.; Amane, D.; Ananthanarayan, L. Impact of partial replacement of rice with other selected cereals on idli batter fermentation and idli characteristics. J. Food Sci. Technol. 2019, 56, 1192–1201. [Google Scholar] [CrossRef]
  6. Lehmann, U.; Robin, F. Slowly digestible starch–its structure and health implications: A review. Trends Food Sci. Technol. 2007, 18, 346–355. [Google Scholar] [CrossRef]
  7. Arns, B.; Bartz, J.; Radunz, M.; do Evangelho, J.A.; Pinto, V.Z.; da Rosa Zavareze, E.; Dias, A.R.G. Impact of heat-moisture treatment on rice starch, applied directly in grain paddy rice or in isolated starch. Lwt-Food Sci. Technol. 2015, 60, 708–713. [Google Scholar] [CrossRef] [Green Version]
  8. Chung, H.J.; Liu, Q.; Hoover, R. Impact of annealing and heat-moisture treatment on rapidly digestible, slowly digestible and resistant starch levels in native and gelatinized corn, pea and lentil starches. Carbohydr. Polym. 2009, 75, 436–447. [Google Scholar] [CrossRef]
  9. Hu, F.B.; Van Dam, R.M.; Liu, S. Diet and risk of type II diabetes: The role of types of fat and carbohydrate. Diabetologia 2001, 44, 805–817. [Google Scholar] [CrossRef]
  10. Ley, S.H.; Hamdy, O.; Mohan, V.; Hu, F.B. Prevention and management of type 2 diabetes: Dietary components and nutritional strategies. Lancet 2014, 383, 1999–2007. [Google Scholar] [CrossRef]
  11. Brennan, C.S. Dietary fibre, glycaemic response, and diabetes. Mol. Nutr. Food Res. 2005, 49, 560–570. [Google Scholar] [CrossRef] [PubMed]
  12. Hoover, R.; Zhou, Y. In vitro and in vivo hydrolysis of legume starches by α-amylase and resistant starch formation in legumes—A review. Carbohydr. Polym. 2003, 54, 401–417. [Google Scholar] [CrossRef]
  13. Gangoiti, J.; Pijning, T.; Dijkhuizen, L. Biotechnological potential of novel glycoside hydrolase family 70 enzymes synthesizing α-glucans from starch and sucrose. Biotechnol. Adv. 2018, 36, 196–207. [Google Scholar] [CrossRef] [PubMed]
  14. Donlao, N.; Matsushita, Y.; Ogawa, Y. Influence of postharvest drying conditions on resistant starch content and quality of non-waxy long-grain rice (Oryza sativa L.). Drying Technol. 2018, 36, 952–964. [Google Scholar] [CrossRef]
  15. Lin, A.H.M.; Lee, B.H.; Chang, W.J. Small intestine mucosal α-glucosidase: A missing feature of in vitro starch digestibility. Food Hydrocoll. 2016, 53, 163–171. [Google Scholar] [CrossRef]
  16. Ashwar, B.A.; Gani, A.; Shah, A.; Wani, I.A.; Masoodi, F.A. Preparation, of resistant starch—A review. Starch-Stärke 2016, 68, 287–301. [Google Scholar] [CrossRef]
  17. Miao, M.; Jiang, B.; Jin, Z.; BeMiller, J.N. Microbial Starch-Converting Enzymes: Recent Insights and Perspectives. Comp. Rev. Food Sci. Food Saf. 2018, 17, 1238–1260. [Google Scholar] [CrossRef] [Green Version]
  18. Palacios, O.M.; Kramer, M.; Maki, K.C. Diet and prevention of type 2 diabetes mellitus: Beyond weight loss and exercise. Expert Rev. Endocrinol. Metab. 2019, 14, 1–12. [Google Scholar]
  19. Willett, W.; Manson, J.; Liu, S. Glycemic index, glycemic load, and risk of type 2 diabetes. Am. J. Clin. Nutr. 2002, 76, 274S–280S. [Google Scholar] [CrossRef] [Green Version]
  20. Liu, S.; Willett, W.C.; Stampfer, M.J.; Hu, F.B.; Franz, M.; Sampson, L.; Hennekens, C.H.; Manson, J.E. A prospective study of dietary glycemic load, carbohydrate intake, and risk of coronary heart disease in US women. Am. J. Clin. Nutr. 2000, 71, 1455–1461. [Google Scholar] [CrossRef] [Green Version]
  21. Chiu, S.; Mulligan, K.; Schwarz, J.M. Dietary carbohydrates and fatty liver disease: De novo lipogenesis. Curr. Opin. Clin. Nutr. Metab. Care 2018, 21, 277–282. [Google Scholar] [CrossRef] [PubMed]
  22. Chandler-Laney, P.C.; Schneider, C.R.; Gower, B.A.; Granger, W.M.; Mancuso, M.S.; Biggio, J.R. Association of late-night carbohydrate intake with glucose tolerance among pregnant A frican A merican women. Matern. Child Nutr. 2016, 12, 688–698. [Google Scholar] [CrossRef] [PubMed]
  23. Huang, M.; Quddus, A.; Stinson, L.; Shikany, J.M.; Howard, B.V.; Kutob, R.M.; Lu, B.; Manson, J.E.; Eaton, C.B. Artificially sweetened beverages, sugar-sweetened beverages, plain water, and incident diabetes mellitus in postmenopausal women: The prospective Women’s Health Initiative observational study. Am. J. Clin. Nutr. 2017, 106, 614–622. [Google Scholar] [CrossRef] [PubMed]
  24. Sami, W.; Ansari, T.; Butt, N.S.; Ab Hamid, M.R. Effect of diet on type 2 diabetes mellitus: A review. Int. J. Health Sci. 2017, 11, 65. [Google Scholar]
  25. Yu, Z.; Ley, S.H.; Sun, Q.; Hu, F.B.; Malik, V.S. Cross-sectional association between sugar-sweetened beverage intake and cardiometabolic biomarkers in US women. Br. J. Nutr. 2018, 119, 570–580. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Lamothe, L.M.; Lê, K.A.; Samra, R.A.; Roger, O.; Green, H.; Macé, K. The scientific basis for healthful carbohydrate profile. Crit. Rev. Food Sci. Nutr. 2019, 59, 1058–1070. [Google Scholar] [CrossRef] [PubMed]
  27. Lovegrove, A.; Edwards, C.H.; De Noni, I.; Patel, H.; El, S.N.; Grassby, T.; Zielke, C.; Ulmius, M.; Nilsson, L.; Butterworth, P.J.; et al. Role of polysaccharides in food, digestion, and health. Crit. Rev. Food Sci. Nutr. 2017, 57, 237–253. [Google Scholar] [CrossRef]
  28. Sardá, F.A.H.; Giuntini, E.B.; Nazare, J.A.; Koenig, D.; Bahia, L.R.; Lajolo, F.M.; Menezes, E.W.D. Effectiveness of carbohydrates as a functional ingredient in glycemic control. Food Sci. Technol. 2018, 38, 561–576. [Google Scholar] [CrossRef] [Green Version]
  29. Young-Hyman, D.; De Groot, M.; Hill-Briggs, F.; Gonzalez, J.S.; Hood, K.; Peyrot, M. Psychosocial care for people with diabetes: A position statement of the American Diabetes Association. Diabetes Care 2016, 39, 2126–2140. [Google Scholar] [CrossRef]
  30. Inzucchi, S.E.; Bergenstal, R.M.; Buse, J.B.; Diamant, M.; Ferrannini, E.; Nauck, M.; Peters, A.L.; Tsapas, A.; Wender, R.; Matthews, D.R. Management of hyperglycemia in type 2 diabetes, 2015: A patient-centered approach: Update to a position statement of the American Diabetes Association and the European Association for the Study of Diabetes. Diabetes Care 2015, 38, 140–149. [Google Scholar] [CrossRef]
  31. McMacken, M.; Shah, S. A plant-based diet for the prevention and treatment of type 2 diabetes. J. Geriatr. Cardiol. 2017, 14, 342. [Google Scholar] [PubMed]
  32. Dyson, P.; McArdle, P.; Mellor, D.; Guess, N. James Lind Alliance research priorities: What role do carbohydrates, fats and proteins have in the management of Type 2 diabetes, and are there risks and benefits associated with particular approaches? Diabet. Med. 2018. [Google Scholar] [CrossRef] [PubMed]
  33. Haase, N.U. The In Vitro Digestibility of Carbohydrates in Boiled and Processed Potatoes. Potato Res. 2015, 58, 91–102. [Google Scholar] [CrossRef]
  34. Sloth, B.; Krog-Mikkelsen, I.; Flint, A.; Tetens, I.; Björck, I.; Vinoy, S.; Elmståhl, H.; Astrup, A.; Lang, V.; Raben, A. No difference in body weight decrease between a low glycemic index and high glycemic index diet but reduced LDL cholesterol after 10 wk adlibutum intake of the low glycemic index. Am. J. Clin. Nutr. 2004, 80, 337–347. [Google Scholar] [CrossRef] [PubMed]
  35. EURESTA. European Flair-concerted Action on Resistant Starch; Newsletter IV, September; Human Nutrition Department, Wageningen Agriculture University: Wageningen, The Netherlands, 1993; p. 2. [Google Scholar]
  36. Tobaruela, E.D.C.; Santos, A.D.O.; de Almeida-Muradian, L.B.; Araujo, E.D.S.; Lajolo, F.M.; Menezes, E.W. Application of dietary fiber method AOAC 2011.25 in fruit and comparison with AOAC 991.43 method. Food Chem. 2018, 238, 87–93. [Google Scholar] [CrossRef] [PubMed]
  37. Perera, A.; Meda, V.; Tyler, R.T. Resistant starch: A review of analytical protocols for determining resistant starch and of factors affecting the resistant starch content of foods. Food Res. Int. 2010, 43, 1959–1974. [Google Scholar] [CrossRef]
  38. Tovar, J. Bioavailability of Starch in Processed Legumes. Importance of Physical Inaccessibility and Retrogradation. SC. Ph.D. Thesis, Department of Applied Nutrition and Food Chemistry, University of Lund, Scania, Sweden, 1992. [Google Scholar]
  39. Tamura, M.; Singh, J.; Kaur, L.; Ogawa, Y. Impact of the degree of cooking on starch digestibility of rice—An in vitro study. Food Chem. 2016, 191, 98–104. [Google Scholar] [CrossRef] [PubMed]
  40. Tan, L.; Kong, L. Starch-guest inclusion complexes: Formation, structure, and enzymatic digestion. Crit. Rev. Food Sci. Nutr. 2019, 1–11. [Google Scholar] [CrossRef] [PubMed]
  41. Jyothsna, E.; Hymavathi, T.V. Resistant starch: Importance, categories, food sources and physiological effects. J. Pharmacogn. Phytochem. 2017, 6, 67–69. [Google Scholar]
  42. Saura-Calixto, F.; Abia, R. Resistant starch: An indigestible fraction of foods. Grasas Y Aceites 1991, 3, 239–242. [Google Scholar] [CrossRef]
  43. Englyst, H.N.; Macfarlane, G.T. Breakdown of resistant starch and readily digestible starch by human gut bacteria. J. Sci. Food Agric. 1986, 37, 699–706. [Google Scholar] [CrossRef]
  44. Björck, I.; Granfeldt, Y.; Liljeberg, H.; Tovar, J.; Asp, N.-G. Food properties affecting the digestion and absorption of carbohydrates. Am. J. Clin. Nutr. 1994, 59, 699S–705S. [Google Scholar] [CrossRef] [PubMed]
  45. Ferrannini, E.; Iozzo, P.; Virtanen, K.A.; Honka, M.J.; Bucci, M.; Nuutila, P. Adipose tissue and skeletal muscle insulin-mediated glucose uptake in insulin resistance: Role of blood flow and diabetes. Am. J. Clin. Nutr. 2018, 108, 749–758. [Google Scholar] [CrossRef]
  46. Wagenmakers, A.J.; Strauss, J.A.; Shepherd, S.O.; Keske, M.A.; Cocks, M. Increased muscle blood supply and transendothelial nutrient and insulin transport induced by food intake and exercise: Effect of obesity and ageing. J. Physiol. 2016, 594, 2207–2222. [Google Scholar] [CrossRef] [PubMed]
  47. Mandhania, M.H.; Paul, D.; Suryavanshi, M.V.; Sharma, L.; Chowdhury, S.; Diwanay, S.S.; Diwanay, S.S.; Shouche, Y.S.; Patole, M.S. Diversity and Succession of Microbiota during Fermentation of the Traditional Indian Food Idli. Appl. Environ. Microbial. 2019, 85, 00368-19. [Google Scholar] [CrossRef] [PubMed]
  48. Englyst, H.N.; Kingman, S.M.; Cummings, J.H. Classification and measurement of nutritionally important resistant starch fractions. Eur. J. Clin. Nutr. 1992, 46 (Suppl. 2), S33–S50. [Google Scholar]
  49. Chelliah, R.; Ramakrishnan, S.R.; Premkumar, D.; Antony, U. Accelerated fermentation of Idli batter using Eleusinecoracana and Pennisetumglaucum. J. Food Sci. Technol. 2017, 54, 2626–2637. [Google Scholar] [CrossRef]
  50. Sharma, D. Studies on Utilization of Gudmar (Gymnemasylvestre) Leaf Extract as Antidiabetic in Fennel Rts Beverage. Ph.D. Thesis, Vasantrao Naik Marathwada Krishi Vidyapeeth, Parbhani, India, 2017. [Google Scholar]
  51. De Pilli, T.; Alessandrino, O. Effects of different cooking technologies on biopolymers modifications of cereal-based foods: Impact on nutritional and quality characteristics review. Crit. Rev. Food Sci. Nutr. 2018, 30, 1–10. [Google Scholar] [CrossRef]
  52. Heiniö, R.L.; Noort, M.W.J.; Katina, K.; Alam, S.A.; Sozer, N.; De Kock, H.L.; Hersleth, M.; Poutanen, K. Sensory characteristics of wholegrain and bran-rich cereal foods—A review. Trends Food Sci. Technol. 2016, 47, 25–38. [Google Scholar] [CrossRef]
  53. Goelema, J.O.; Spreeuwenberg, M.A.M.; Hof, G.; van der Poel, A.F.B.; Tamminga, S. Effect of pressure toasting on the rumen degradability and intestinal digestibility of whole and broken peas, lupins and faba beans and a mixture of these feedstuffs. Anim. Feed Sci. Technol. 1998, 76, 35–50. [Google Scholar] [CrossRef]
  54. Mukherjee, S.K.; Albury, M.N.; Pederson, C.S.; Van Veen, A.G.; Steinkraus, K.H. Role of Leuconostocmesenteroides in leavening the Batter of Idli, a Fermented Food of India. Appl. Microbiol. 1965, 13, 227–231. [Google Scholar] [PubMed]
  55. Lorenz, K.; Kulp, K. Physico-chemical properties of defatted heat-moisture treated starches. Starch/Stärke 1983, 35, 123–129. [Google Scholar] [CrossRef]
  56. Takahashi, T.; Miura, M.; Ohisa, N.; Mori, K.; Kobayashi, S. Heat Treatments of Milled Rice and Properties of the Flours. Cereal Chem. 2005, 82, 228–232. [Google Scholar] [CrossRef]
  57. Eliasson, A.C. Starch: Physicochemical and functional aspects. In Carbohydrates in Food, 3rd ed.; CRC Press: Boca Raton, FL, USA, 2017; pp. 501–600. [Google Scholar]
  58. Chelliah, R. Anna University: Chennai, India, Unpublished work. 2017.
  59. Caplice, E.; Fitzgerald, G.F. Food fermentations: Role of microorganisms in food production and preservation. Int. J. Food Microbial. 1999, 50, 131–149. [Google Scholar] [CrossRef]
  60. Goddard, M.S.; Young, G.; Marcus, R. The effect of amylose content on insulin and glucose response to ingested rice. Am. J. Clin. Nutr. 1984, 39, 388–392. [Google Scholar] [CrossRef]
  61. Collar, C.; Armero, E. Functional and Thermal Behaviours of Heat-Moisture-Treated Starch-Rich Wheat-Based Blended Matrices: Impact of Treatment of Non-wheat Flours. Food Biopro. Technol. 2019, 1–14. [Google Scholar] [CrossRef]
  62. Sajilata, M.G.; Singhal, R.S.; Kulkarni, P.R. Resistant Starch—A Review. Compr. Rev. Food Sci. Food Saf. 2006, 5, 1–17. [Google Scholar] [CrossRef]
  63. Lawal, O.S.; Adebowale, K.O. An Assessment of Changes in Thermal and Physico-Chemical Parameters of Jack Bean (Canavaliaensiformis) Starch Following Hydrothermal Modifications; European Food Research and Technology Zeitschriftfür Lebensmittel- Untersuchung und -Forschung A; Springer: Berlin/Heidelberg, Germany, 2005. [Google Scholar]
  64. Theurer, C.B. Grain processing effects on starch utilization by ruminants. J. Anim. Sci. 1986, 63, 1649–1662. [Google Scholar] [CrossRef]
  65. Gunaratne, A. Heat-Moisture Treatment of Starch. In Physical Modifications of Starch; Springer: Singapore, 2018; pp. 15–36. [Google Scholar] [CrossRef]
  66. Berry, C.S. Resistant starch: Formation and measurement of starch that survives exhaustive digestion with amylolytic enzymes during the determination of dietary fibre. J. Cereal Sci. 1986, 4, 301–314. [Google Scholar] [CrossRef]
  67. Fredriksson, H.; Bjo¨rck, I.; Andersson, R.; Liljeberg, H.; Silverio, J.; Eliasson, A.C.; Åmana, P. Studies on alpha-amylase degradation of retrograded starch gels from waxy maize and high-amylopectin potato. Carbohydr. Polym. 2000, 43, 81–87. [Google Scholar] [CrossRef]
  68. Silverio, J.; Fredriksson, H.; Andersson, R.; Eliasson, A.C.; Aman, P. The effect of temperature cycling on the amylopectin retrogradation of starches with different amylopectin unit-chain length distribution. Carbohydr. Polym. 2000, 42, 175–184. [Google Scholar] [CrossRef]
  69. Eliasson, A.C.; Gudmundsson, M. Starch: Physicochemical and functional aspects. In Carbohydrates in Food; Eliasson, A.C., Ed.; Dekker: New York, NY, USA, 1996; pp. 431–503. [Google Scholar]
  70. Franco, C.M.L.; Ciacco, C.F.; Tavares, D.Q. Effect of heat-moist treatment on enzymatic susceptibility. Starke/Starch 1995, 47, 223–228. [Google Scholar]
  71. Han, J.-A.; BeMiller, J.N. Preparation and physical characteristics of slowly digesting modiWed food starches. J. Carbpol. 2007, 67, 366–374. [Google Scholar]
  72. Jenkins, D.J.A.; Jerkins, A.L.; Kendall, C.W.C.; Augustine, L.; Vuksan, V. Dietary fiber, carbohydrate metabolism, and chronic disease. In Advanced Dietary Fiber Technology; McCleary, B.V., Prosky, L., Eds.; Iowa State University Press: Ames, IA, USA, 2001; pp. 162–167. [Google Scholar]
  73. Guraya, H.S.; James, C.; Champagne, E.T. Effect of enzyme concentration and storage temperature on the formation of slowly digestible starch from cooked debranched rice starch. Starch/Stärke 2001, 53, 131–139. [Google Scholar] [CrossRef]
  74. Englyst, K.N.; Englyst, H.N.; Hudson, G.J.; Cole, T.J.; Cumming, J.H. Rapidly available glucose in foods: An in vitro measurement that reflects the glycemic responses. Am. J. Clin. Nutr. 1999, 69, 448–454. [Google Scholar] [CrossRef] [PubMed]
  75. Han, J.A.; Lim, S.T. Effect of presoaking on textural, thermal, and digestive properties of cooked brown rice. Cereal Chem. 2009, 86, 100–105. [Google Scholar] [CrossRef]
  76. Kim, J.H.; Tanhehco, E.J.; Ng, P.K.W. Effect of extrusion conditions on resistant starch formation from pastry wheat flour. Food Chem. 2006, 99, 718–723. [Google Scholar] [CrossRef]
  77. Koksel, H.; Masatcioglu, T.; Kahraman, K.; Ozturk, S.; Basman, A. Improving effect of lyophilization on functional properties of resistant starch preparations formed by acid hydrolysis and heat treatment. J. Cereal Sci. 2008, 47, 275–282. [Google Scholar] [CrossRef]
  78. Zhao, X.H.; Lin, Y. The impact of coupled acid or pullulanasedebranching on the formation of resistant starch from maize starch with autoclaving–cooling cycles. Eur. Food Res. Technol. 2009, 230, 179. [Google Scholar] [CrossRef]
  79. Goñi, I.; Garcia-Diz, L.; Mañas, E.; Saura-Calixto, F. Analysis of resistant starch: A method for foods and food products. Food Chem. 1996, 56, 445–449. [Google Scholar] [CrossRef]
Figure 1. Development of cereal-based products for diabetes patients.
Figure 1. Development of cereal-based products for diabetes patients.
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Figure 2. Digestive enzymes secreted by different organs contribute to the digestion of foods in humans. The digestive system, an extension of the environment into the body, also stores mucus, acid, bicarbonate, and salts to enable hydrolysis of foods and absorption of nutrients essential for life.
Figure 2. Digestive enzymes secreted by different organs contribute to the digestion of foods in humans. The digestive system, an extension of the environment into the body, also stores mucus, acid, bicarbonate, and salts to enable hydrolysis of foods and absorption of nutrients essential for life.
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Figure 3. The procedure used by Goñi et al. [36] and Perera [37] for the determination of resistant starch (RS) in food. Copyright obtained from Perera et al. [37].
Figure 3. The procedure used by Goñi et al. [36] and Perera [37] for the determination of resistant starch (RS) in food. Copyright obtained from Perera et al. [37].
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Figure 4. Summary of distinguished enzymes, subsequent pathways, particular species, and specific metabolites that are expressively obstructed through a high resistant starch (HRS) diet. Blue arrows/frames, increased with HRS; orange frames, decreased with HRS; black arrows, not detected or not increased with HRS over baseline; green arrows/frames, increased with low resistant starch (LRS). 1, starch and metabolism of sucrose; 2, glucose to pyruvate leads to glycolysis pathway; 3, 3-oxoacyl-(acyl carrier protein) synthase; 4, acetyltransferase-based acetyl-CoA; 5, 3-hydroxyacyl-CoA dehydrogenase; 6, enoyl-CoA hydratase; 7, carrier protein enoyl-(acyl) reductase (NADH); 8, acetate transferase CoA; 9, butyrate kinase; 10, synthase citrate; 11, hydrataseaconitate; 12 and 13, dehydrogenase isocitrate; 14, Ferredoxin oxidoreductase-2-ketoglutarate; 15, CoA-synthetase-succinyl; 16, fumaratereductase/succinate dehydrogenase; 17, fumaratehydratase; 18, dehydrogenase malate; 19, human enzymes.
Figure 4. Summary of distinguished enzymes, subsequent pathways, particular species, and specific metabolites that are expressively obstructed through a high resistant starch (HRS) diet. Blue arrows/frames, increased with HRS; orange frames, decreased with HRS; black arrows, not detected or not increased with HRS over baseline; green arrows/frames, increased with low resistant starch (LRS). 1, starch and metabolism of sucrose; 2, glucose to pyruvate leads to glycolysis pathway; 3, 3-oxoacyl-(acyl carrier protein) synthase; 4, acetyltransferase-based acetyl-CoA; 5, 3-hydroxyacyl-CoA dehydrogenase; 6, enoyl-CoA hydratase; 7, carrier protein enoyl-(acyl) reductase (NADH); 8, acetate transferase CoA; 9, butyrate kinase; 10, synthase citrate; 11, hydrataseaconitate; 12 and 13, dehydrogenase isocitrate; 14, Ferredoxin oxidoreductase-2-ketoglutarate; 15, CoA-synthetase-succinyl; 16, fumaratereductase/succinate dehydrogenase; 17, fumaratehydratase; 18, dehydrogenase malate; 19, human enzymes.
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Figure 5. Important steps according to the protocol by Englyst et al. [43] towards determining enzyme-resistant starch (RS3). The manifestation of an immune enzyme fraction of starch in foods during the measurement of non-starch polysaccharides in foods. Copyright obtained from Perera et al. [37].
Figure 5. Important steps according to the protocol by Englyst et al. [43] towards determining enzyme-resistant starch (RS3). The manifestation of an immune enzyme fraction of starch in foods during the measurement of non-starch polysaccharides in foods. Copyright obtained from Perera et al. [37].
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Figure 6. Instantaneous procedure for the determination of total starch (TS) as per Englyst et al. [48]. The freely available glucose (FG) and total glucose (TG) matters were defined by quantifying the total starch content of the sample. Copyright was obtained from Perera et al. [37].
Figure 6. Instantaneous procedure for the determination of total starch (TS) as per Englyst et al. [48]. The freely available glucose (FG) and total glucose (TG) matters were defined by quantifying the total starch content of the sample. Copyright was obtained from Perera et al. [37].
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Figure 7. Transmission electron microscopic images indicate the effect of heat treatment on the prepared Idli rice product compared with the control Idli (No Heat Treatment) [58]. (a) The fine particle size of raw rice (Magnification at 100 μm); (b) heat-treated rice particles with increased starch content (Magnification at 100 μm); (c) the rough surfaces of the raw rice particles (Magnification at 200 μm); (d) heat-treated rice particles with increased starch show smooth surfaces (Magnification at 200 μm).
Figure 7. Transmission electron microscopic images indicate the effect of heat treatment on the prepared Idli rice product compared with the control Idli (No Heat Treatment) [58]. (a) The fine particle size of raw rice (Magnification at 100 μm); (b) heat-treated rice particles with increased starch content (Magnification at 100 μm); (c) the rough surfaces of the raw rice particles (Magnification at 200 μm); (d) heat-treated rice particles with increased starch show smooth surfaces (Magnification at 200 μm).
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Table 1. Estimated total dietary fiber, total starch, and resistant starch of some nourishment sources (g/100 g as eaten).
Table 1. Estimated total dietary fiber, total starch, and resistant starch of some nourishment sources (g/100 g as eaten).
SourceTotal StarchTotal Dietary FiberResistant Starch
Legumes
Red beans42.436.224.4
Pulses53.233.125.3
Vigna unguiculata (Peas)53.632.617.5
Cereal grains
Barley (Hordeum vulgare)55.21718.3
Corn Starch77.519.325.7
Arborio rice95.21.214.2
Wheat50.417.213.2
Oats43.237.27.2
Flours
Corn84.22.311.3
Wheat68.512.61.4
Rice86.35.41.5
Potato812.71.6
Grain-based food products
Spaghetti73.95.73.1
Rolled oats56.410.38.2
Cereal products
Crisp bread67.2N/A1.4
White bread46.3N/A1.6
Granary bread44.6N/A6.2
Extruded oat cereal57.1N/A0.5
Puffed wheat cereal67.7N/A1.5
Oat porridge9.2N/A0.4
Cooked spaghettiN/AN/A2.7
Cooked riceN/AN/A3.8
Potato products
Boiled potatoesN/AN/A2.1
Chips29.1N/A4.5
Mashed potatoesN/AN/A2.1
Quantification of total starch, total dietary fiber, and resistant starch levels in diverse raw food material and expressed in terms of percentage. Copyright obtained from Tamura et al. [39].
Table 2. Preparation of resistant starch in starch-rich products by different treatments.
Table 2. Preparation of resistant starch in starch-rich products by different treatments.
Starch SourceTreatmentResistant Starch (%)Reference
Rice starchesNative6.1–10.4
Heat–moisture treatment (HMT)18.3–23.1
Acid and HMT30.1–38
CornNative4.3[48]
Autoclaving24–31
a-amylase and pullulanase58.83[8]
Partial acid hydrolysis followed by HMT63.2[8]
Potato starchRaw75
Wheat starchCross-linking with sodium trimetaphosphate sodium tripolyphosphate, epichlorohydrinandphosphoryl chloride 75.2–85.3
[8]
phosphorylation
Bean starchAcetylation
Estimation of resistant starch levels in diverse food materials based on different processing methods and expressed in terms of percentage. Copyright obtained from Tamura et al. [39].
Table 3. The percentage of starch hydrolysis, hydrolysis index (HI), and estimated glycemic index (EGI) for homogenized and non-homogenized heated rice samples with different degrees of heating during a virtual in vitro ingestion process.
Table 3. The percentage of starch hydrolysis, hydrolysis index (HI), and estimated glycemic index (EGI) for homogenized and non-homogenized heated rice samples with different degrees of heating during a virtual in vitro ingestion process.
C∞ (%)k × 10−2 (min−1)HIeGI
HomogenizedR41.0 ± 3.7 c4.51 ± 0.54 b39.3 ± 2.5 d61.3 ± 1.4 d
MH69.0 ± 4.6 ab19.11 ± 1.26 a78.0 ± 5.1 b82.5 ± 2.8 b
CC78.1 ± 1.0 a22.25 ± 6.94 a88.5 ± 2.1 a88.3 ± 1.1 a
Non-HomogenizedR8.6 ± 1.4 d3.07 ± 0.52 b8.1 ± 1.0 e43.8 ± 0.4 e
MH63.2 ± 9.1 b3.03 ± 0.49 b54.1 ± 4.8 c69.4 ± 2.6 c
CC66.3 ± 2.2 b3.28 ± 0.67 b58.4 ± 3.1 c71.8 ± 1.7 c
Different letters in the same column indicate significant differences (p < 0.05) (n = 3). R, raw; MH, moderately heated; CC, completely cooked; C∞, equilibrium starch hydrolysis percentage; k, kinetic constant. Copyright obtained from Tamura et al. [39].
Table 4. Resistant starch level in cereal starches after processing.
Table 4. Resistant starch level in cereal starches after processing.
Starch SourceTreatmentRSMethod of RS AnalysisReference
Japonica brown ricePre-soaking in water at 30 or 40 °C to reach 25% humidity + heated30.2–30.4%[48][8]
Pre-soaked in water at 20 or 45 °C to reach 30% humidity + heated21.7–27.9%
Waxy riceNatural waxy rice starch10.30%[48][76]
Gelatinized starch3.00%
Ascetically gelatinized starch at 60 °C for 5 min8.60%
Partially gelatinized starch at 70 °C for 5 min7.70%
Pastry wheat flourExtracted at 20% humidity; 150/200/250 rpm; 40–120 °C; stored at 4 °C/0 days0.48–0.52%Megazyme® assay [77]
Extruded at 20% humidity; 150/200/250 rpm; 40–120 °C; stored at 4 °C/7–14 days1.21–1.35%
Extracted at 40% humidity; 150/200/250 rpm; 40–120 °C; stored at 4 °C/0 days0.63–0.67%
Extracted at 40% humidity; 150/200/250 rpm; 40–120 °C; stored at 4 °C/7–14 days1.52–1.86%
Extracted at 60% humidity; 150/200/250 rpm; 40–120 °C; stored at 4 °C/0 days2.54–2.65%
Extracted at 60% humidity; 150/200/250 rpm; 40–120 °C; stored at 4 °C/7–14 days3.55–4.25%
CornAcid modified with 1.64 M HCl at 40 °C for 4 h + gelatinized + sterilized at 121 °C for15 min + freeze dried5%AOAC 991.43 [36] [78]
Acid reformed with 1.64 M Hydrochloric acid at 40 °C for 4 h + gelatinized + sterilized at 121°C for15 min + Stored at 95 °C for 48 h + freeze dried12%
CornNormal corn starch19.70%modified as per [79][76]
Galvanized with high moisture for 24 h at 50 °C18.30%
Moist–heat management (30% moisture + 24 h at ambient temperature + 120 °C for 24 h)16.90%
Galvanized with high humidity for 24 h at 50 °C + Moist–heat treatment (30% humidity + 24 h ambient temperature + 120 °C for 24 h)17.30%
Moist–heat treatment (30% moisture + 24 h ambient temperature + 120 °C for 24 h) + annealed with excess water for 24 h at 50 °C19.70%
High-amylose cornSterilized at 121 °C + Stored at 4 °C for 24 h (repeated twice)30%[36][36]
Sterilized at 121 °C + Stored at 4 °C for 24 h (repeated twice) + hydrolyzed with 0.1 M organic acid39%
Resistant starch levels in different cereal-based starches after processing and expressed in terms of percentage. Copyright obtained from Tamura et al. [39].

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Chelliah, R.; Chandrashekar, S.; Saravanakumar, K.; Ramakrishnan, S.R.; Rubab, M.; Daliri, E.B.-M.; Barathikannan, K.; Tyagi, A.; Kwame Ofosu, F.; Chen, X.; et al. Effect of Rice Processing towards Lower Rapidly Available Glucose (RAG) Favors Idli, a South Indian Fermented Food Suitable for Diabetic Patients. Nutrients 2019, 11, 1497. https://doi.org/10.3390/nu11071497

AMA Style

Chelliah R, Chandrashekar S, Saravanakumar K, Ramakrishnan SR, Rubab M, Daliri EB-M, Barathikannan K, Tyagi A, Kwame Ofosu F, Chen X, et al. Effect of Rice Processing towards Lower Rapidly Available Glucose (RAG) Favors Idli, a South Indian Fermented Food Suitable for Diabetic Patients. Nutrients. 2019; 11(7):1497. https://doi.org/10.3390/nu11071497

Chicago/Turabian Style

Chelliah, Ramachandran, Sangeeta Chandrashekar, Kandasamy Saravanakumar, Sudha Rani Ramakrishnan, Momna Rubab, Eric Banan-Mwine Daliri, Kaliyan Barathikannan, Akanksha Tyagi, Fred Kwame Ofosu, Xiuqin Chen, and et al. 2019. "Effect of Rice Processing towards Lower Rapidly Available Glucose (RAG) Favors Idli, a South Indian Fermented Food Suitable for Diabetic Patients" Nutrients 11, no. 7: 1497. https://doi.org/10.3390/nu11071497

APA Style

Chelliah, R., Chandrashekar, S., Saravanakumar, K., Ramakrishnan, S. R., Rubab, M., Daliri, E. B. -M., Barathikannan, K., Tyagi, A., Kwame Ofosu, F., Chen, X., Kim, S. -H., Elahi, F., NaKyeong, H., Wang, M. -H., Raman, V., Antony, U., & Oh, D. -H. (2019). Effect of Rice Processing towards Lower Rapidly Available Glucose (RAG) Favors Idli, a South Indian Fermented Food Suitable for Diabetic Patients. Nutrients, 11(7), 1497. https://doi.org/10.3390/nu11071497

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