Abstract
The aim of this study was to characterize the influence of Konjac glucomannan (KGM) on the functional and structural properties of wheat starch. Results showed that KGM significantly decreased the starch hydrolysis rate, with a lower level of rapidly digestible starch (RDS), and a higher content of slowly digestible starch (SDS). Besides, KGM decreased the content of leached amylose, while enhanced the swelling power, water‐holding capacity, freeze‐thaw stability, and paste clarity of wheat starch, which indicated a good improvement on the functional properties. Differential scanning calorimetry (DSC) and X‐ray diffraction patterns (XRD) manifested that the addition of KGM disrupted the original crystalline structures of wheat starch, which may result in the increased hydrolysis rate of starch. Interestingly, this did not consist with the decreased starch hydrolysis rate showed in the study. Moreover, FTIR results showed the existence of the interaction between KGM and starch. The morphological characterization demonstrated that the addition of KGM contributed to a more compact structure of freeze‐dried wheat starch. And KGM inhibited the expansion of starch granules and formed a barrier around the gelatinized starch. Therefore, the barrier around the starch granules and the interaction between KGM and starch were considered to be the important reasons that affected the starch digestibility.
Keywords: crystalline structures, functional properties, Konjac glucomannan, leached amylose, starch hydrolysis rate, wheat starch
Konjac glucomannan decreased the starch hydrolysis rate.Konjac glucomannan changed the chemical structures of wheat starch.Konjac glucomannan formed a physical barrier around starch.
1. INTRODUCTION
Starch is the main nutrition components in the human diet, which widely exist in seed endosperm (Cornell & Eliasson, 2004). The physicochemical and nutritional properties of starch to a large extent determine the starchy food products quality (Maningat & Seib, 2010). Nowadays, various food additives (dietary fiber, polyphenol, enzymes, etc.) are used to improve the functional properties of starch (Han, Cheng, & Qiu, 2013; Matuda, Chevallier, de Alcântara Pessôa Filho, LeBail, & Tadini, 2008; Sun & Miao, 2019). Among these additives, dietary fiber can be used to modify the structural properties of starch, which intimately associated with the gelling and texture properties of starchy foods (Shevkani, Singh, Bajaj, & Kaur, 2017; Wüstenberg, 2015). Thus, adding dietary fiber to starchy food is a good choice for the functional food market.
Konjac glucomannan (KGM) is a kind of dietary fiber extracted from konjac tuber (Amorphophallus konjac K. Koch), which has been widely used as food additives in drinks and foods (Jimenez‐Colmenero, Cofrades, Herrero, Solas, & Ruiz‐Capillas, 2013; Silva, Ferreira, Bruschi, Britten, & Matumoto‐Pintro, 2016; Tatirat, Charoenrein, & Kerr, 2012; Xu, Liao, & Wang, 2012). Many researchers have investigated the influence of KGM on wheat‐based food products. A preliminary study showed that KGM addition could improve the overall quality of noodles made from low‐protein wheat flour through reinforcing the gluten network (Zhou et al., 2013). Further studies described that KGM could interact with gluten proteins via noncovalent interactions (Li, Zhu, Yadav, & Li, 2019; Wang et al., 2017). Moreover, KGM was also reported to affect the rheological and retrogradation properties of starch from different sources, which dependent on the structural compatibility and molecular interactions (Funami et al., 2005; Khanna & Tester, 2006; Yoshimura, Takaya, & Nishinari, 1998). Some researchers revealed the formation of strong hydrogen bonding between pea starch and konjac glucomannan (Chen, Liu, Chen, Chen, & Chang, 2008). However, there are few systematic reports related to the mechanism of KGM on the functional properties of wheat starch. The aim of this study was to characterize the influence of interaction between KGM and wheat starch on the functional and structural properties of wheat starch.
2. MATERIALS AND METHODS
2.1. Materials
Konjac glucomannan was purchased from Wuhan Yangyoudao health industry co., LTD company (Hubei, China). Starch from wheat, α‐amylase Type IX‐A from human saliva (activity 1,000–3,000 units/mg protein), pepsin from porcine gastric mucosa (activity 456 U/mg), amyloglucosidase from aspergillus niger (activity 30–60 units/mg protein), amylose from potato, and 3,5‐Dinitrosalicylic acid and fluorescein 5(6)‐isothiocyanate were purchased from Sigma‐Aldrich Co.
2.2. Measurement of in vitro digestibility
Starch digestibility was measured by Englyst, Kingman, and Cummings (1992) with some modifications. Wheat starch 0.2 g was gelatinized in 2 ml distilled water together with KGM (0%, 5%, 10%, and 15%) at 95°C for 20 min. After cooled to room temperature, the starch paste sample was immersed in 10 ml pepsin solution (456 U/mg/100 ml 0.01 M KCl‐HCl buffer, pH 1.2) with continuously oscillated at 37 ℃ for 60 min and volumetric to 25 ml with 0.1 M sodium phosphate buffer (pH = 7.5). Next, the samples were added with 5 ml α‐amylase solution (2 U/mL) and incubated at 37°C for 120 min. Then, 1 ml of the reaction solution was obtained from the mixture system every ten minutes. When the enzyme activity was rapidly inactivated at 95°C for 5 min, 3 ml 0.2 M sodium acetate buffer (pH = 4.75) and 21 μl amyloglucosidase solution (40 U/ml) were added to each removed reaction solution and incubated at 60°C for 50 min. Determination of sugar was obtained by the colorimetric method with 3,5‐Dinitrosalicylic acid. The optical density (OD value) was read at 520 nm, and the content was calculated by the calibration curve plotted for glucose. Starch was calculated as glucose × 0.9. According to the different hydrolysis percentage at each time point, the values for the different levels of starch fractions (RDS, SDS, and RS) were calculated using the following calculations:
where RDS‐rapidly digestible starch, SDS‐slowly digestible starch, RS‐resistant starch, TS‐the total starch content, G20‐starch hydrolysis at 20 min, and G120‐starch hydrolysis at 120 min.
2.3. Leached amylose
Wheat starch 0.1 g together with KGM was added to 1 ml 95% ethanol solution and 9 ml 1 mol/L NaOH solution and gelatinized at 95°C for 10 min, and then, 0.5 ml 1 mol/L acetic acid solution was added to lower the pH (pH ≈ 5.5). The content of amylose leached during gelatinization was obtained by the iodine colorimetry with I2KI solution. The standard curve was made with amylose as a standard substance (Duan, Donner, Liu, Smith, & Ravenelle, 2012).
2.4. Swelling measurement
The swelling test was determined based on a reported method (Lu, Brennan, Serventi, Mason, & Brennan, 2016) with slight modifications. Wheat starch 0.2 g together with KGM (0%, 5%, 10%, and 15%) was immersed in 10 ml deionized water in a centrifuge tube, which was heated at 95 ℃ for 20 min. Then, samples were centrifuged at 3,800 g for 25 min; the sediment was dried and weighed. Swelling ratio was calculated from the weight of sediment divided by the dry weight of samples.
2.5. Water absorption capacity (WAC) measurement
Determination of water absorption capacity (WAC) of starch was according to Nawab, Alam, and Hasnain (2014). About 0.4 g starch sample together with KGM (0%, 5%, 10%, and 15%) was immersed in 10 ml distilled water. After left at room temperature for 30 min, the sample was centrifuged at 4,000 g for 15 min. The wet weight of the starch sample was weighed and dried under standardized conditions. Water absorption (WAC) was calculated as follows:
where, Mm—the weight of wet sediment [g]; M—the dry weight of samples [g].
2.6. Freeze‐thaw stability (FTS) measurement
Freeze‐thaw stability was measured using Wattanachant’ method (Wattanachant, Muhammad, Hashim, & Rahman, 2003). Wheat starch 0.3 g together with KGM (0%, 5%, 10%, and 15%) was immersed in 10 ml deionized water and heated and then froze at −20 ℃ for 24 hr and thawed at room temperature referred as a freeze‐thaw cycle. The thawed sample was centrifuged at 3,800 g for 20 min. The supernatant was eliminated from the sample, then which was freeze and thawed repeatedly for four times. The freeze‐thaw stability was represented as water loss and calculated by the following formula:
where, mm—The weight of starch paste[g]; m—the weight of starch paste precipitation[g].
2.7. Paste clarity measurement
The paste clarity of wheat starch was measured concerning to Waterschoot, Gomand, Fierens, and Delcour (2015). Wheat starch 0.1 g together with KGM (0%, 5%, 10%, and 15%) was immersed in 10 ml deionized water and then stored at refrigerated temperature for a week. The absorbance of the starch samples was read at 650 nm. The conversion relationship between absorbance and transmittance (T) was as follows:
2.8. Differential scanning calorimetry (DSC)
Wheat starch 5 mg together with KGM (0%, 5%, 10%, and 15%) was dissolved and mixed with distilled water in a preweighted aluminum pot and placed at 4°C for 12 hr until the water was completely in equilibrium with the sample. The condition was set to 10°C/min speed heat from 20 ℃ to 120 ℃ in DSC instrument, as a comparison with an empty plate.
2.9. X‐ray diffraction (XRD)
The diffraction patterns of freeze‐dried starch samples were determined by X‐ray diffractometer (X'Pert Pro, PANalytical B.V., Almelo, Netherlands) running at 40 kV and 40 mA. Samples were scanned in the range from 10 to 55° (2θ) (Chen, Ren, Zhang, Tong, & Rashed, 2015). The relative crystallinity of starch samples through the analysis of Software JADE 5.0 is calculated from the area of the crystalline peak divided by amounts of all the area of peak (the amorphous and crystalline peak).
2.10. Fourier transform infrared spectroscopy (FTIR)
Wheat starch 5 g together with KGM (0%, 5%, 10%, and 15%) was dissolved in 40 ml of deionized water and stir well and then pasted on 95°C for 20 min. After cooling to room temperature, freeze‐dried starch samples were obtained by vacuum freeze‐drying and pulverized through 100 mesh sieve. The FTIR spectra of four freeze‐dried starch samples were tested at 4,000 ~ 400 cm−1 band. The resulting data were obtained in 64 scans at a resolution of 4 cm−1.
2.11. Particle size analysis
Particle size analysis of freeze‐dried wheat starch samples was evaluated by Malvern laser particle size analyzer (Mastersizer 3,000). The results were expressed in terms of the volume distributions of freeze‐dried wheat starch. The mean particle size parameters were reported as D[4,3] (volume‐weighted mean) and D[3,2] (surface‐weighted mean). Each sample was performed in three replicates.
2.12. Scanning electron microscopy (SEM)
Freeze‐dried wheat starch samples were cut into cubes, and morphological properties of starch/ KGM samples were obtained by a scanning electron microscopy (Sirion 200, FEI, Netherlands) at a voltage of 15 kV. The starch sample was adhered to double‐sided coated carbon tape and fixed on the aluminum frame and then coated with gold–palladium. A meaningful freeze‐dried starch sample images were obtained at 1,200 × magnification.
2.13. Confocal light scanning microscopy (CLSM)
The internal structure of starch granules was investigated by using confocal laser scanning microscopy (CLSM) (Funami et al., 2008). Native wheat starch and mixed samples of wheat starch (5%, 10%, 15% KGM based on the mass of starch) were dissolved in distilled water and heated at 95°C for 20 min to produce gelatinized starch samples. Starch samples were stained at room temperature overnight using 20 μL 2 mg/ml FITC. The samples were observed by using a confocal laser electron microscopy (FLUOVIEW FV3000, OLYMPUS, Japan) under a fluorescence mode by a × 60 oil‐immersed objective lens. A small sample was dropped onto the glass slide. Excitation and emission for FITC were at 488 nm and 525 nm, respectively.
2.14. Statistic analysis
Data in our study were presented as means ± SEM of triplicate. Analysis of variance was used to contrast the significant difference by using one‐way analysis of variance (ANOVA). The significant differences (p < .05) were evaluated and displayed by different letters.
3. RESULTS AND DISCUSSION
3.1. In vitro digestibility
The effects of Konjac glucomannan (KGM) on starch in vitro digestion were investigated. As shown in the Figure 1a, the hydrolysis percentage of native starch at 10 and 120 min were 62.98% and 88.19%, respectively. With the addition of KGM, there was a significant decrease in the rate of starch digestibility. Especially, the mixed sample containing 15% KGM had the most significant reduction at 10 min and 120 min, which the hydrolysis percentages were 22.7% and 64%, respectively. This result was supported by the previous study that the starch digestibility was affected by the presence of apple dietary fibers, inulin, guar gum, and xanthan gum (Bae, Jun, Lee, & Lee, 2016; Brennan, Kuri, & Tudorica, 2004; Roberts, 2011).
The addition of KGM had a positive effect on the content of rapidly digestible starch (RDS), slowly digestible starch (SDS), and resistant starch (RS). As shown in the Figure 1b, the content of RDS was decreased from 65.93% to 33.03% for wheat starch enriched with KGM, while the content of SDS was increased from 22.26% to 31.12%. Also, an increase in RS ranged from 11.81% to 35.85% was observed (Figure 1b). It was worth noting that the addition of 5% KGM showed the highest SDS content. This can be explained by the changed content of digestible starch, which consists of RDS and SDS. Compared with 5% KGM, the content of RS increased more significantly after the addition of 10% and 15% KGM. This result indicated that the content of digestible starch in the addition of 5% KGM was significantly higher than that of 10% and 15% KGM. As the RDS content was decreased regularly by the addition of KGM, it is reasonable that the addition of 5% KGM showed the highest SDS content. Thus, the addition of KGM was beneficial to prevent rapid degradation of starch and reduced postprandial blood sugar.
3.2. Effects of KGM on leached amylose ratio, swelling power, and water‐holding capacity of wheat starch
As shown in the Figure 2a, the leached amylose ratio of native wheat starch and the mixed samples were 30%, 27.62%, 21.31%, and 11.23%, respectively. Compared with the control sample, the addition of 10% and 15% KGM significantly decreased the leached amylose ratio, while the addition of 5% KGM showed no significant influence. During gelatinization processing, the orderly arrangement of amylose and amylopectin in wheat starch granules was destroyed. The amylose that leached out of the starch granules is similar to the KGM in structure, which makes it could dissolve in the hydrophilic colloid (Chen et al., 2008). The lower level of leached amylose suggested that the KGM may have formed a barrier around the starch that preventing the diffusion of amylose during the gelatinization (Funami et al., 2005). Besides, the barrier around the starch granules reduced the area of contact between starch and enzymes, causing the increasing of RS content (Dupuis, Liu, & Yada, 2014). Moreover, the leached amylose would interact with KGM that led to the formation of KGM–amylose complex, which might generate more SDS (Nawab et al., 2014).
Compared with native wheat starch, the addition of KGM significantly improved the swelling power from 11.73 to 17.66 g/g (Figure 2b), and the water‐holding capacity increased from 0.86 to 7.73 g/g (Figure 2c). This did not consist of the results of previous studies that hydrocolloids inhibited the swelling and starch gelatinization (Chen et al., 2017; Zhang et al., 2018). The increased swelling power and water‐holding capacity of the KGM–starch mixtures may be due to the structural properties of the KGM. Konjac glucomannan is a nonionic polysaccharide hydrophilic colloid, consisting mainly of hydroxyl groups and the acetyl groups (Silva et al., 2016). Due to the hydroxyl groups, KGM competed with starch for water molecules, which inhibited the expansion of wheat starch. On the other hand, hydrated KGM molecules expanded rapidly and could cause a change in conformation, thereby resulting in the increased swelling power and water‐holding capacity of the KGM–starch mixtures.
3.3. Effects of KGM on freeze‐thaw stability and paste clarity of wheat starch
Freeze‐thaw stability is detected to understand the ability of frozen wheat starch with KGM addition to retaining their shape and texture after thawing. As shown in the Figure 3a, the water loss after the first cycle was 72.35% and increased to 89.68% after the fourth freeze‐thaw cycle. The water loss of 5%, 10%, and 15% Konjac glucomannan/starch mixed samples after the first freeze‐thaw cycle was 64.44%, 62.02%, and 60.26%, while after the fourth freeze‐thaw cycle, the water loss was 84.55%, 77.33%, and 69.35%, respectively. The addition of KGM significantly reduced water loss during the freeze‐thaw process. A lower water loss means better water retention and a lower rate of retrogradation (Ye et al., 2018). This result indicated that KGM could inhibit the retrogradation of wheat starch gel and enhance freeze‐thaw stability.
Paste clarity determines the appearance and use of starch products (Yadav, Kumar, & Yadav, 2016). As shown in Figure 3b, the transmittance of wheat starch decreased gradually with the extension of time. In a short period (1st), there was no significant change in transparency among the samples. From the 3rd day to the 7th day of the experiment, the transmittance was significantly increased in wheat starch added with 10% and 15% KGM. The increased transmittance indicated the less retrogradation of wheat starch (Fukuzawa, Ogawa, Nakagawa, & Adachi, 2016). Also, this result was supported by the reduced amylose which detected above, as lower amylose starches are easily dispersed (Singh, Kaur, Sandhu, Kaur, & Nishinari, 2006; Yamamori, 2009).
3.4. Effects of KGM on the chemical structure of wheat starch
As can be seen in the Figure 4, all starch samples had only one endothermic peak (a single Tp), indicating the good compatibility between KGM and wheat starch. The onset temperature (To) and the endothermic peak (Tp) were not significantly affected by the addition of KGM, while the gelatinization enthalpy (ΔH) decreased from 4.771 to 1.401 J/g, respectively. The enthalpy change (ΔH) was a reflection of the formation of ordered structures (Wang, Li, Copeland, Niu, & Wang, 2015). Thus, the decrease in gelatinization enthalpy (ΔH) demonstrated the disruption of crystalline structures on wheat starch caused by KGM (Singh, Singh, Kaur, Sodhi, & Gill, 2003; Wang, et al., 2017). The effect on the gelatinization enthalpy (ΔH) was not consistent with previous studies of polysaccharides (e.g., HPMC, CMC, xanthan gum, apple pectin, tea polysaccharide) (Singh, Singh, Isono, & Noda, 2010; Zhou, Wang, Zhang, Du, & Zhou, 2008). This may be due to the different polysaccharide structure and physical properties (Funami et al., 2005).
Four obvious crystalline diffraction peaks at 2θ close to 15°, 17°, 18°, and 22° were showed in the wheat starch system, which displayed a typical A‐type XRD crystal structure (Figure 5). With the addition of KGM, the crystalline diffraction peaks at 15° disappeared gradually, and the relative crystallinity values of wheat starch containing different concentrations of KGM were 20.34%, 20.13%, 9.01%, and 12.10%, respectively. The decreased crystallinity values indicated that the addition of KGM destroyed the original crystalline domains of wheat starch (Chen et al., 2008). This result was supported by the DSC analysis showed above. The crystallite disruption could facilitate rapid enzymatic hydrolysis (Zhang et al., 2018). Thus, the decreased crystallinity domains caused by Konjac glucomannan may increase the hydrolysis rate of starch. Interestingly, this did not consist with the decreased starch hydrolysis rate showed in the study. Therefore, the barrier around the starch granules and the interaction between KGM and amylose were confirmed to be the important reasons that influenced the starch digestibility, which discussed in the leached amylose experiments.
To evaluate the interaction between KGM and wheat starch, the functional groups of the native wheat starch and the mixture were analyzed (Figure 6). It can be seen that the adsorption peaks at 1639 cm−1, which attributed to the C = O groups, were increased with the addition of KGM, confirming the good compatibility between KGM and wheat starch (Li, Li, Geng, Song, & Wu, 2017). Also, the absorption peaks at approximately 3,435 and 2,929 cm−1, which attributed to the vibration of O‐H stretching and the C‐H deformation of the glucose unit, were significantly enhanced with the addition of KGM. This phenomenon demonstrated the occurrence of the hydrogen bond between KGM and starch (Yuan, Wang, & Mu, 2018).
3.5. Effects of KGM on the average particle diameter
For all starch samples, KGM addition led to an increased content of large particles of freeze‐dried wheat starch (Figure 7a). The surface‐weighted mean diameter D[3,2] of all starch samples was 20.05, 24.37, 29.46, and 36.69 μm, while the volume‐weighted mean diameter D[4,3] of all starch samples was 60.32, 60.51, 68.88, and 76.63 μm, respectively (Figure 7b, c). As we can see from Figure 7c, the addition of 10% and 15% KGM significantly increased the droplet size D[4,3], while the addition of 5% KGM showed no significant increase. This trend was in agreement with the changes in the leached amylose ratio and paste clarity (Figures 2a and 3b). Thus, the increase in the large particles of freeze‐dried wheat starch may be due to the improved gelatinizing structure of starch, which caused by the interaction between KGM and starch molecules.
3.6. Effects of KGM on the morphological characterization of wheat starch
The morphological characterization of freeze‐dried wheat starch samples found that all the starch granules had been broken and a gel network structure was formed after gelatinization (Figure 8a–d). A more regular and lamellar structure was clearly shown on the surface of wheat starch with KGM addition of 5%, 10%, and 15% compared with the native wheat starch. The results suggested that KGM interacted with starch and contributed to a more compact starch structure.
Further morphological characterization of gelatinized starch was performed through confocal laser scanning microscopy (CLSM). During gelatinization, starch granules persist as highly swollen fragile forms, commonly termed granule “ghosts” (Debet & Gidley, 2007). The swollen starch granules were observed on the CLSM images. As can be seen, the starch ghost gradually decreased with the addition of KGM, while natural wheat starch expanded significantly after gelatinization (Figure 8). This result showed that KGM competed with starch for water molecules, inhibited the expansion of starch granules, and formed a barrier around starch to reduce the area of contact between starch and digestive enzymes.
4. CONCLUSION
Konjac glucomannan significantly decreased the starch hydrolysis rate, reduced the content of RDS, and increased the content of SDS and RS and thus slowed down the release of glucose from starch and reduced postprandial blood sugar. The lower level of leached amylose suggested that the KGM may have formed a barrier around the starch, which prevented the diffusion of amylose during the gelatinization. And the leached amylose would interact with KGM that led to the formation of KGM–amylose complex. Due to the strong hydrophilic ability, KGM increased the swelling power and water‐holding capacity of the KGM–starch mixtures. Besides, KGM was identified to enhanced freeze‐thaw stability and paste clarity of wheat starch. All these findings demonstrated that KGM improved the functional properties of starch. It was confirmed by the results of the chemical structures and morphologies characterization, the barrier around the starch granules and the interaction between the leached amylose and KGM were responsible for the reduced starch digestibility.
CONFLICT OF INTEREST
There is none potential conflict between authors and others that bias our work.
ETHICAL APPROVAL
This study does not involve any human or animal testing.
ACKNOWLEDGMENTS
The work was supported by the National Natural Science Foundation of China (31901700) and Natural Science Foundation of Hubei Province (2017CFB196).
Zhang L, Zeng L, Wang X, He J, Wang Q. The influence of Konjac glucomannan on the functional and structural properties of wheat starch. Food Sci Nutr. 2020;8:2959–2967. 10.1002/fsn3.1598
Ling Zhang and Lirong Zeng contributed equally to this work.
REFERENCES
- Bae, I. Y. , Jun, Y. J. , Lee, S. Y. , & Lee, H. G. (2016). Characterization of apple dietary fibers influencing the in vitro starch digestibility of wheat flour gel. LWT ‐ Food Science and Technology, 65, 158–163. [Google Scholar]
- Brennan, C. S. , Kuri, V. , & Tudorica, C. M. (2004). Inulin‐enriched pasta: Effects on textural properties and starch degradation. Food Chemistry, 86(2), 189–193. 10.1016/j.foodchem.2003.08.034 [DOI] [Google Scholar]
- Chen, J. , Liu, C. , Chen, Y. , Chen, Y. , & Chang, P. R. (2008). Structural characterization and properties of starch/konjac glucomannan blend films. Carbohydrate Polymers, 74(4), 946–952. 10.1016/j.carbpol.2008.05.021 [DOI] [Google Scholar]
- Chen, L. , Ren, F. , Zhang, Z. , Tong, Q. , & Rashed, M. M. A. (2015). Effect of pullulan onthe short‐term and long‐term retrogradation of rice starch. Carbohydrate Polymers, 115, 415–421. [DOI] [PubMed] [Google Scholar]
- Chen, L. , Tian, Y. Q. , Zhang, Z. P. , Tong, Q. , Sun, B. , Rashed, M. M. A. , & Jin, Z. (2017). Effect of pullulan on the digestible, crystalline and morphological characteristics of rice starch. Food Hydrocolloids, 63, 383–390. 10.1016/j.foodhyd.2016.09.021 [DOI] [Google Scholar]
- Cornell, H. , & Eliasson, A. C. (2004). The functionality of wheat starch. Starch in Food, 211–240. [Google Scholar]
- Debet, M. R. , & Gidley, M. J. (2007). Why do gelatinized starch granules not dissolve completely? Roles for amylose, protein, and lipid in granule“ghost” integrity. Journal of Agricultural and Food Chemistry, 55, 4752–4760. 10.1021/jf070004o [DOI] [PubMed] [Google Scholar]
- Duan, D. X. , Donner, E. , Liu, Q. , Smith, D. C. , & Ravenelle, F. (2012). Potentiometric titration for determination of amylose content of starch ‐a comparison with colorimetric method. Food Chemistry, 130(4), 1142–1145. 10.1016/j.foodchem.2011.07.138 [DOI] [Google Scholar]
- Dupuis, J. H. , Liu, Q. , & Yada, R. Y. (2014). Methodologies for increasing the resistant starch content of food starches: A review. Comprehensive Reviews in Food Science and Food Safety, 13(6), 1219–1234. 10.1111/1541-4337.12104 [DOI] [Google Scholar]
- Englyst, H. N. , Kingman, S. M. , & Cummings, J. H. (1992). Classification and measurement of nutritionally important starch fractions. European Journal of Clinical Nutrition (United Kingdom), 46(Suppl 2), S33. [PubMed] [Google Scholar]
- Fukuzawa, S. , Ogawa, T. , Nakagawa, K. , & Adachi, S. (2016). Kinetics on the turbidity change of wheat starch during its retrogradation. Bioscience Biotechnology and Biochemistry, 80(8), 1–6. [DOI] [PubMed] [Google Scholar]
- Funami, T. , Kataoka, Y. , Omoto, T. , Goto, Y. , Asai, I. , & Nishinari, K. (2005). Effects of non‐ionic polysaccharides on the gelatinization and retrogradation behavior of wheat starch. Food Hydrocolloids, 19(1), 1–13. 10.1016/j.foodhyd.2004.04.024 [DOI] [Google Scholar]
- Funami, T. , Nakauma, M. , Noda, S. Ishihara, S. , Asai, I. , Inouchi, N. , & Nishinari, K. (2008). Effects of some anionic polysaccharides on the gelatinization and retrogradation behaviors of wheat starch: Soybean‐soluble polysaccharide and gum arabic. Food Hydrocolloids, 22(8), 1528–1540. 10.1016/j.foodhyd.2007.10.008 [DOI] [Google Scholar]
- Han, L. , Cheng, Y. , & Qiu, S. (2013). The effects of vital wheat gluten and transglutaminase on the thermomechanical and dynamic rheological properties of buckwheat dough. Food and Bioprocess Technology, 6, 561–569. 10.1007/s11947-011-0738-9 [DOI] [Google Scholar]
- Jimenez‐Colmenero, F. , Cofrades, S. , Herrero, A. M. , Solas, M. T. , & Ruiz‐Capillas, C. (2013). Konjac gel for use as potential fat analogue for healthier meat product development: Effect of chilled and frozen storage. Food Hydrocolloids, 30(1), 351–357. 10.1016/j.foodhyd.2012.06.015 [DOI] [Google Scholar]
- Khanna, S. , & Tester, R. F. (2006). Influence of purified konjac glucomannan on the gelatinisation and retrogradation properties of maize and potato starches. Food Hydrocolloids, 20(5), 567–576. 10.1016/j.foodhyd.2005.05.004 [DOI] [Google Scholar]
- Li, J. , Li, B. , Geng, P. , Song, A. X. , & Wu, J. Y. (2017). Ultrasonic degradation kinetics and rheological profifiles of a food polysaccharide (konjac glucomannan) in water. Food Hydrocolloids, 70, 14–19. [Google Scholar]
- Li, J. X. , Zhu, Y. P. , Yadav, M. P. , & Li, J. L. (2019). Effect of various hydrocolloids on the physical and fermentation properties of dough. Food Chemistry, 271, 165–173. 10.1016/j.foodchem.2018.07.192 [DOI] [PubMed] [Google Scholar]
- Lu, X. , Brennan, M. A. , Serventi, L. , Mason, S. , & Brennan, C. S. (2016). How the inclusion of mushroom powder can affect the physicochemical characteristics of pasta. International Journal of Food Science & Technology, 51(11), 2433–2439. 10.1111/ijfs.13246 [DOI] [Google Scholar]
- Maningat, C. C. , & Seib, P. A. (2010). Understanding the physicochemical and functional properties of wheat starch in various foods. Cereal Chemistry, 87(4), 1007210812–1007210314. 10.1094/CCHEM-87-4-0305 [DOI] [Google Scholar]
- Matuda, T. G. , Chevallier, S. , de Alcântara Pessôa Filho, P. , LeBail, A. , & Tadini, C. C. (2008). Impact of guar and xanthan hydrocolloids on proofifing and calorimetric parameters of frozen bread dough. Journal of Cereal Science, 48, 741–746. [Google Scholar]
- Nawab, A. , Alam, F. , & Hasnain, A. (2014). Functional properties of cowpea (vigna unguiculata) starch as modified by guar, pectin, and xanthan gums. Starch ‐ Stärke, 66(9–10), 832–840. [Google Scholar]
- Roberts, K. T. (2011). The physiological and rheological effects of foods supplemented with guar gum. Food Research International, 44(5). 10.1016/j.foodres.2011.01.065 [DOI] [Google Scholar]
- Shevkani, K. , Singh, N. , Bajaj, R. , & Kaur, A. (2017). Wheat starch production, structure, functionality and applications‐a review. International Journal of Food Science & Technology, 52, 38–58. 10.1111/ijfs.13266 [DOI] [Google Scholar]
- Silva, D. F. D. , Ferreira, S. B. D. S. , Bruschi, M. L. , Britten, M. , & Matumoto‐Pintro, P. T. (2016). Effect of commercial konjac glucomannan and konjac flours on textural, rheological and microstructural properties of low fat processed cheese. Food Hydrocolloids, 60, 308–316. 10.1016/j.foodhyd.2016.03.034 [DOI] [Google Scholar]
- Singh, N. , Kaur, L. , Sandhu, K. S. , Kaur, J. , & Nishinari, K. (2006). Relationships between physicochemical, morphological, thermal, rheological properties of rice starches. Food Hydrocolloids, 20(4), 532–542. 10.1016/j.foodhyd.2005.05.003 [DOI] [Google Scholar]
- Singh, N. , Singh, J. , Kaur, L. , Sodhi, N. S. , & Gill, B. S. (2003). Morphological, thermal and rheological properties of starches from different botanical sources. Food Chemistry, 81(2), 219–231. 10.1016/S0308-8146(02)00416-8 [DOI] [Google Scholar]
- Singh, S. , Singh, N. , Isono, N. , & Noda, T. (2010). Relationship of granule size distribution and amylopectin structure with pasting, thermal, and retrogradation properties in wheat starch. Journal of Agricultural and Food Chemistry, 58(2), 1180–1188. 10.1021/jf902753f [DOI] [PubMed] [Google Scholar]
- Sun, L. J. , & Miao, M. (2019). Dietary polyphenols modulate starch digestion and glycaemic level: A review. Critical Reviews in Food Science and Nutrition, 10.1080/10408398.2018.1544883 [DOI] [PubMed] [Google Scholar]
- Tatirat, O. , Charoenrein, S. , & Kerr, W. L. (2012). Physicochemical properties of extrusion‐modified konjac glucomannan. Carbohydrate Polymers, 87(2), 1545–1551. 10.1016/j.carbpol.2011.09.052 [DOI] [Google Scholar]
- Wang, K. , Wu, K. , Xiao, M. Kuang, Y. , Corke, H. , Ni, X. , & Jiang, F. (2017). Structural characterization and properties of konjac glucomannan and zein blend films. International Journal of Biological Macromolecules, 105, 1096–1104. 10.1016/j.ijbiomac.2017.07.127 [DOI] [PubMed] [Google Scholar]
- Wang, S. J. , Li, C. L. , Copeland, L. , Niu, Q. , & Wang, S. (2015). Starch retrogradation: A comprehensive review. Comprehensive Reviews in Food Science and Food Safety, 14, 568–585. 10.1111/1541-4337.12143 [DOI] [Google Scholar]
- Wang, Y. , Chen, Y. , Zhou, Y. , Nirasawa, S. , Tatsumi, M. , Li, X. , Cheng, Y. (2017). Effects of konjac glucomannan on heat‐induced changes of wheat gluten structure. Food Chemistry, 229, 409–416. 10.1016/j.foodchem.2017.02.056 [DOI] [PubMed] [Google Scholar]
- Waterschoot, J. , Gomand, S. V. , Fierens, E. , & Delcour, J. A. (2015). Production, structure, physicochemical and functional properties of maize, cassava, wheat, potato and rice starches. Starch ‐ Stärke, 67(1–2), 14–29. [Google Scholar]
- Wattanachant, S. , Muhammad, K. , Hashim, D. M. , & Rahman, R. A. (2003). Effect of crosslinking reagents and hydroxypropylation levels on dual‐modified sago starch properties. Food Chemistry, 80(4), 463–471. 10.1016/S0308-8146(02)00314-X [DOI] [Google Scholar]
- Wüstenberg, T. (2015). General overview of food hydrocolloids. Cellulose and Cellulose Derivatives in the Food Industry Fundamentals and Applications, 1–68. [Google Scholar]
- Xu, D. Y. , Liao, Z. F. , & Wang, H. (2012). Preparation and characterization of konjac glucomannan gel. Applied Mechanics & Materials, 117–119, 1374–1376. [Google Scholar]
- Yadav, R. B. , Kumar, N. , & Yadav, B. S. (2016). Characterization of banana, potato, and rice starch blends for their physicochemical and pasting properties. Cogent Food & Agriculture, 2(1), 1127873 10.1080/23311932.2015.1127873 [DOI] [Google Scholar]
- Yamamori, M. (2009). Amylose content and starch properties generated by five variantwxalleles for granule‐bound starch synthase in common wheat (Triticum aestivum L.). Euphytica, 165(3), 607–614. 10.1007/s10681-008-9793-3 [DOI] [Google Scholar]
- Ye, J. , Yang, R. , Liu, C. , Luo, S. , Chen, J. , Hu, X. , Wu, J. (2018). Improvement in freeze‐thaw stability of rice starch gel by inulin and its mechanism. Food Chemistry, 268, 324–333. 10.1016/j.foodchem.2018.06.086 [DOI] [PubMed] [Google Scholar]
- Yoshimura, M. , Takaya, T. , & Nishinari, K. (1998). Rheological studies on mixtures of corn starch and konjac‐glucomannan. Carbohydrate Polymers, 35(1), 71–79. 10.1016/S0144-8617(97)00232-4 [DOI] [Google Scholar]
- Yuan, Y. , Wang, L. , Mu, R. J. , Gong, J. , Wang, Y. , Li, Y. , … Wu, C. (2018). Effects of konjac glucomannan on the structure, properties, and drug release characteristics of agarose hydrogels. Carbohydrate Polymers, 190, 196–203. 10.1016/j.carbpol.2018.02.049 [DOI] [PubMed] [Google Scholar]
- Zhang, B. , Bai, B. , Pan, Y. , Li, X.‐M. , Cheng, J.‐S. , & Chen, H.‐Q. (2018). Effects of pectin with different molecular weight on gelatinization behavior, textural properties, retrogradation and in vitro digestibility of corn starch. Food Chemistry, 264, 58–63. 10.1016/j.foodchem.2018.05.011 [DOI] [PubMed] [Google Scholar]
- Zhou, Y. , Cao, H. , Hou, M. , Nirasawa, S. , Tatsumi, E. , Foster, T. J. , & Cheng, Y. (2013). Effect of konjac glucomannan on physical and sensory properties of noodles made from low‐protein wheat flour. Food Research International, 51(2), 879–885. 10.1016/j.foodres.2013.02.002 [DOI] [Google Scholar]
- Zhou, Y. , Wang, D. , Zhang, L. , Du, X. , & Zhou, X. (2008). Effect of polysaccharides on gelatinization and retrogradation of wheat starch. Food Hydrocolloids, 22(4), 505–512. 10.1016/j.foodhyd.2007.01.010 [DOI] [Google Scholar]