Molecular Structure of Starches from Cassava Varieties having Different Cooked Root Textures

Starches from 12 cassava varieties with different cooked root texture; i.e. mealy, firm and mealy and firm, were investigated with a particular focus on aspects of molecular structures of amylose and amylopectin. Structural elements of amylopectin were essentially constant in terms of unit chain distributions and chain lengths. All cassava amylopectins displayed two distinct chain length peaks, at DP 40–46 and at DP 11–13, with a shoulder at DP 17–19, and average chain length (CL) of amylopectins was 17–20. A fraction of extra‐long chains in the range of 0.24–1.78% was found. Amylose and amylopectin from four varieties with different textures of cooked root were isolated. Data from C‐chain distributions indicated that the molecular size of amylopectin from M‐hanatee (Hanatee), a locally adapted cassava variety, was 2.5–2.9 times smaller than those of the other varieties. Three of the four amylose samples, except that from M‐hanatee, were very similar in average DP (4120–4390), chain length (530–550) and number of chains (7.1–7.5), and composed of nearly equal numbers of linear and branched molecules. The amylose from the M‐hanatee variety showed a unique characteristic: it had smaller size (2050), shorter chain length (450), fewer chains (4.7) and a higher content of linear fraction (58%), when compared with other amyloses.     

Chain‐length Distribution Profiles of Amylopectin Isolated from Endosperm Starch of Waxy and Low‐amylose Bread Wheat (Triticum aestivum L.) Lines with Common Genetic Background

Large A‐type endosperm starch granules were isolated from near‐isogenic waxy and non‐waxy lines and low‐amylose mutant lines of bread wheat with a common genetic background. The amylose contents of A‐type starch ranged from 2.6% to 23.6%. Amylopectin was isolated by concanavalin A (Con A) precipitation from the isolated starch. The λ_max (range: 532‐538 nm) and blue values at 680 nm (range: 0.026‐0.037) of the iodine‐amylopectin complex were not significantly different among the isolated amylopectins, indicating that amylopectins from non‐waxy and low‐amylose lines did not contain such long chains as amylose or extra‐long chains of amylopectin affecting iodine complex properties. Chain‐length distribution profiles measured by both high‐performance size‐exclusion chromatography (HPSEC) and high‐performance anion‐exchange chromatography (HPAEC) showed that the amylopectin structures of these lines were indistinguishable from each other. Extra‐long chains were not detected in the amylopectins by HPSEC measurement. The side‐chains measured by HPAEC were classified into four groups according to their degree of polymerization (DP), and the proportion of each group were in the following ranges: DP 6‐12, 26.5‐27.5%; DP 13‐24, 43.6‐44.1%; DP 25‐36, 13.6‐14.2%, and DP 37‐60, 11.0‐11.7%. The alleles on the Wx‐D1 locus, i.e., Wx‐D1a, Wx‐D1d, Wx‐D1f, and Wx‐D1g, responsible for granule‐bound starch synthase (GBSS I) biosynthesis had no influence on the properties of iodine‐amylopectin complex and the chain‐length distribution profiles of amylopectin.     

The Effect of Environmental Temperature on Distribution of Unit Chains of Rice Amylopectin

The effects of environmental temperature during the early development of seeds on the structural characteristics of the endosperm starch were investigated using near‐isogenic lines of rice plants (Taichung 65, waxy), grown under temperature controlled conditions. High performance gel permeation chromatography (HPLC) demonstrated that Pseudomonas isoamylase‐debranched amylopectins of rice plants grown at lower temperature (25°C) contain increased amounts of short chains and decreased amounts of long chains as compared with amylopectins obtained from rice plants grown at higher temperature (30°C). By high performance anion exchange chromatography with pulsed amperometric detection (HPAEC‐PAD) of isoamylase‐debranched amylopectins it was detected that the amount of unit chains with degree of polymerization (DP) 6 and 11‐13, in the amylopectin of rice plants grown at lower temperature (25°C) had significantly increased and the amount of unit chains with DP 8, 22‐24 and 29 had significantly decreased, as compared with the amylopectin of rice plants grown at higher temperature (30°C). It was confirmed that the environmental temperature between 5 and 10 d after pollination strongly influenced the structure characteristics of the endosperm starch of rice plants.     

Characterization of Physical Properties of Flour and Starch Obtained from Gamma‐Irradiated White Rice

Physical and structural characteristics of rice flour and starch obtained from gamma‐irradiated white rice were determined. Pasting viscosities of the rice flour and starch, analyzed by using a Rapid Visco Analyser, decreased continuously with the increase in irradiation dosage. Differential scanning calorimetry showed that gelatinization onset, peak and conclusion temperatures of rice flour and starch changed slightly but the enthalpy change decreased significantly with increase of irradiation dosage. All irradiated starch displayed an A‐type X‐ray diffraction pattern like the native starch. Gel permeation chromatography showed that the blue value ratio of the first peak (amylopectin) to the second one (amylose) decreased with the increase of the irradiation dosage. The weight‐average molecular weight (M_w) and gyration radius (R_z) of amylopectin analyzed by using HPSEC‐MALLS‐RI (high‐performance size‐exclusion chromatography equipped with multiangle laser‐light scattering and refractive index detector) decreased gradually from 1.48×10⁹ (M_w) and 384.1 nm (R_z) of native rice starch to 2.36×10⁸ (M_w) and 236.8 nm of 9 kGy‐irradiated starch. The branch chain‐length distribution of amylopectins determined by HPAEC‐ENZ‐PAD (high‐performance anion‐exchange chromatography with amyloglucosidase post‐column on‐line reactor and pulsed amperometric detector) showed that gamma irradiation had no significant effect on the amylopectin branch chains with 13≤DP≤24 and 37≤DP, but produced more branch chains with 6≤DP≤12 when the irradiation dosage was less than 9 kGy. It might be deduced that gamma irradiation caused the breakage of the amylopectin chains at the amorphous regions, but had little effects on the crystalline regions of starch granules, especially at low dosage irradiation.     

Chemometric Analysis of the Gelatinization and Pasting Properties of Long‐grain Rice Starches in Relation to Fine Structure

Chemometric tests were carried out to better understand the multidimensional facet of starch fine structure‐relationship concerning gelatinization and pasting properties. With Ward's hierarchical cluster analysis 20 long‐grain rice starch samples were sorted out into three clusters based on similarities in functional properties, particularly, paste peak (PV) and final viscosity (FV). The three clusters (arbitrarily named Clusters A, B, and C) exhibited a pasting profile trend of PV<FV, PV˜FV, and PV>FV, respectively. Cluster A samples were also lower in peak temperature, range and enthalpy of gelatinization, and swelling power. These attributes were associated with higher amylose content (AM), β‐amylolysis limit, and percentage of B1 chains (DP13‐24), but lower amylopectin weight‐average molar mass (M_w) and percentage of A chains (DP6‐12). A 5‐variable linear discriminant function correctly predicted 85% of the Ward's cluster membership of the individual cultivars. The discriminant function included the variables A, B1, and B2 (DP25‐36) chains, average chain length (ACL), and gyration radius (R_z). Fine structure variance was fully explained by a total of nine principal components, with the first three components cumulatively accounting for 74%. The leading variables included in the three rotated components pertained to amylopectin chain length distribution (A, B2, and B3+ or DP≥37 chains, and ACL) and amylopectin molar mass (M_w, R_z, and polydispersity). AM and M_w were loaded most frequently in the 4‐variable, best‐fit linear regression models for predicting gelatinization and pasting properties. A combination of at least two fine structure variables controls the functionality of rice starch.     

Structural modification and characterization of rice starch treated by Thermus aquaticus 4-α-glucanotransferase

Rice starch was modified using Thermus aquaticus 4-α-glucanotransferase (TAαGTase) in this study. The changes in the molecular structure and the effect on the starch retrogradation by TAαGTase treatment were investigated on isolated rice starch. By treating TAαGTase, molecular weight profile of amylopectins shifted to higher elution time from 1.0 × 10⁸ to 2.4 × 10⁷ or 0.8 × 10⁷, depending on the level of enzyme dosage. Meanwhile, there were huge increases in the proportions of content corresponding to amylose size and even smaller molecules. On treating with TAαGTase, short branch chains (DP 1–8) increased, and longer branch chains (>DP 19) increased significantly as well, with a broader distribution up to DP 46 compared to the control rice starch. Amylose content decreased from 30.0 to 21.8–23.7%. This indicated that the amylose could be transferred to the amylopectin branch chain by the disproportionation of TAαGTase, resulting in lowering the amylose content and the formation of amylopectin with a broader branch-chain length distribution. TAαGTase modified rice starch showed that X-ray diffraction pattern of the B-type crystalline even before cold storage, and that a variety of cyclic glucans (DP 5–19) were produced by enzymatic reaction. In particular, the accelerated rate of starch retrogradation was clearly observed compared to the control due to an overall increase in the number of elongated long-branch chains, decrease in the amount of amylose–lipid complex, and the possible synergistic effects of these factors.     

STRUCTURAL ANALYSIS ON THE AMYLOPECTIN OF WAXY-BARLEY LARGE STARCH GRANULES

The hydrolysis of waxy-barley starch by the α-amylase of B. subtilis was followed by gel chromatography on Sepharose CL 6B. A range of intermediate dextrins were initially produced, and at later stages dextrins with a degree of polymerization in the range 100–200 accumulated. Maltohexaose was produced simultaneously from the external chains. The hydrolysis of the amylopectin β-limit dextrin followed a similar pattern, though smaller amounts of the low-molecular weight material were formed. The sizes of the more resistant products in the hydrolysis mixtures suggested that the amylopectin contained two types of unit clusters with d.p. for the β-limit dextrins of 65 and 85. A regular model for the structure of the amylopectin that shows the possible mode of interconnection of the unit clusters is presented .     

Effect of Amylopectin Structure on the Gelatinization and Pasting Properties of Selected Yam (Dioscorea spp.) Starches

This study was aimed at elucidating the decisive structural parameters of amylopectin which govern the gelatinization or pasting behavior of yam starch dispersions, exemplified with four selected yam starches from Dioscorea alata and D. batatas with very similar amylose contents (32.2–34.6%). The results indicated that the yam amylopectins examined showed an average degree of polymerization (DP) of 3469–4474 anhydroglucose units (AGU), average chain length (CL) of 18.8–28.5 AGU, average exterior CL (ECL) of 11.8–16.4 AGU, average interior CL (ICL) of 6.0–11.1 AGU, and a noticeable proportion of extralong (> 100 AGU) and long (40–100 AGU) chains that gave the chain ratio r_(el+l)/s (the weight ratio of extralong and long chains to short chains) of 0.88–1.40. Generally, the yam amylopectin with a lower DP and NC possessed a greater CL, ECL, ICL, and r_(el+l)/s, associating with a higher blue value (BV) and maximal wavelength (λ_max) for their complexes with iodine. D. alata amylopectins exhibited a lower DP, longer chain lengths and greater r_(el+l)/s than the D. batata amylopectins. Statistically, r_(el+l)/s was decisive for the BV and λ_max; while CL and phosphate content were crucial for the gelatinization peak temperature and pasting viscosities of the yam starches examined. The role of swelling power or the volume fraction of dispersed remnants instead in governing the pasting viscosity was also mathematically explored.     

Amylopectin structure of heat–moisture treated starches

The effects of heat–moisture treatment (HMT; moisture content of 25%, at 100°C for 24 h) on starch chain distribution and unit chain distribution of amylopectin in normal rice, waxy rice, normal corn, waxy corn, normal potato, and waxy potato starches were investigated. After HMT, starch chain distribution (amylose and amylopectin responses) of waxy corn and potato starches were identical to those of untreated starches, whereas the chromatographic response of waxy rice starch showed a slight decrease, but with a slight increase in peak tailing. This result indicated that HMT had no (or very limited) effect on the degradation of amylopectins. Analysis of unit chain distribution of amylopectins revealed that waxy characteristics affected the molecular structure of amylopectin in untreated starches, i.e., the CL of normal‐type starches was greater than that of waxy‐type starches. After HMT, the CL and unit chain distribution of all starches were no different than those of untreated starches. The results implied that changes in the physico‐chemical properties of HMT starches would be due to other phenomena rather than the degradation of amylopectin molecular structure. However, the thermal degradation of amylopectin molecules of waxy starches could occur by HMT at higher treatment temperatures (120 and 140°C).     

Granule‐bound SSIIa Protein Content and its Relationship with Amylopectin Structure and Gelatinization Temperature of Rice Starch

Starch characteristics such as gelatinization properties determine the quality of various products of rice. The eating, cooking and processing qualities of rice are a function of the gelatinization of rice starch. The gelatinization temperature (GT) of rice is controlled by the starch synthase IIa (SSIIa) gene. In the present study, the amount of the starch‐associated SSIIa protein and its relationship with amylopectin structure and GT were investigated. The results indicated that the starch associated SSIIa protein content was positively correlated with GT and level of amylopectin chains with degree of polymerization 12‐24 (DP12‐24), and negatively correlated with the fraction of chains with DP6‐11 and short chain ratio (SCR), i.e. DP6‐11/DP12‐24 (P<0.001). GT was also negatively correlated with DP6‐11 SCR, and positively correlated with DP12‐24. The SSIIa protein content and amylopectin structure showed significant difference between the two SSIIa single nucleotide polymorphisms (SNPs, i.e. guanine‐cytosine/thymine‐thymine (GC/TT)) groups. Rice with GC and TT SNPs had average SSIIa protein contents of 1.076 and 0.681, respectively. Rice with the GC SNPs displayed a lower amount of chains with DP6‐11 and more chains with DP 12‐24 than those with TT SNPs. A mechanism is postulated to explain how SSIIa could determine the distribution of amylopectin side‐chains, which affects the gelatinization temperature of rice starch.     

Starch Biosynthesis. I. The Size Distributions of Amylose and Amylopectin and Their Relationships to the Biosynthesis of Starch

Equations for the size distributions of both linear and branched polymers were applied to debranched amylopectin, linear amylose, and branched amylose polymers. The experimental size distribution of linear amylose corresponds to the broad size distribution of an A–B condensation polymer, whereas that of debranched amylopectin linear chains corresponds to the much narrower Poisson size distribution. These dramatic differences illustrate that different types of enzymes synthesize the linear chains of amylose as compared to those of amylopectin. These results support the previously proposed mechanism. The polymodal behavior of debranched amylopectin is due to the existance of individual Poisson-type polymers created by tier structures in a statistically formed precursor glycogen. Equations were developed which enable the calculation of the percentages of these individual Poisson polymers. When applied to the differences between shx and Bomi barley amylopectins, it is concluded that both studies agree that two different short, inner tier, A-chains exist, where the longer chain is located in the more external third tier in the amylopectins. In amylose, three different polymers exist: A linear amylose A–B type condensation polymer, a branched amylose which behaves as a statistical A–R–B₂ type polymer, and an intermediate, non-statistically branched amylose polymer.     

A review of malting and malt processing for whisky distillation

This paper encompasses a re‐evaluation of published literature and data regarding wort attenuation in malt distilleries raising questions and discussing how the conventional wisdom has changed over time and what questions still need to be answered. Current knowledge is summarized in the following four points: (a) Under normal malting conditions, starch granules are partially degraded by a combination of α‐amylase and α‐glucosidase. This complex can open up the granule at specific sites on the surface and create characteristic ‘pin‐hole’ lesions, which may be widened by secondary hydrolysis by α‐ and β‐amylase, limit dextrinase and α‐glucosidase (maltase). (b) All of these diastatic enzymes can survive mild kilning, probably by forming heat stable complexes on and within the starch granules and can continue a complete degradation of starch when mashed at ambient temperatures with glucose as the end product. (c) At normal mashing temperatures, starch granules gelatinize and dissolve with a concomitant rapid degradation to glucose, maltose, maltotriose and dextrins ranging from degree of polymerization (DP) 4 to > DP20. If there is immediate wort boiling after run‐off, this is the final composition of starch derived carbohydrates according to the conventional paradigm. (d) All malt worts also contain a small amount of panose, isopanose as well as glucosyl maltodextrins, based on a core of 6₂‐α‐glucosyl maltose (panose) or 6‐α‐maltosyl glucose (isopanose), which are remnants of the α‐amylase/glucosidase degradation of granular starch. These dextrins are resistant to the action of debranching enzymes and their concentration may vary between 4 and 8% of the malt extract, depending on the degree of modification of the host starch granules. They may be created at the active sites of this enzyme complex when the granule is gelatinized. In a conventional mash of unboiled distilling wort, the spectrum of wort dextrins produced from gelatinized starch is reduced to true ‘limit’ dextrins of DP4–8 by continued α‐amylolysis during early fermentation. These dextrins will contain side chains of either maltose or maltotriose residues surrounding the α‐1,6‐glucosidic linkage and can be debranched by limit dextrinase during late fermentation, leaving only the above glucosyl maltodextrins dextrins in the spent wash. Copyright © 2016 The Institute of Brewing & Distilling     

Chain Length Distribution of Amylopectins of Double- and Triple-Mutants Containing the Waxy Gene in the Inbred Oh43 Maize Background

Starch granules were isolated from mature kernels of double- and triple-mutant combinations of the waxy (wx) gene with other starchmodifying genes in the inbred Oh43 maize background. The amylose content and the distribution of unit chain-length of amylopectin were determined by enzymatic-chromatographic methods. Starches of the mutants containing the wx gene comprised 100% amylopectin. Amylopectin of the amylose-extender;waxy (ae wx) mutant had an increased proportion of long B chains and decreased proportion of short B chains, compared with wx amylopectin, whereas amylopectin of the dull;waxy (du wx) mutant had a decreased proportion of long B chains and an increased proportion of short B chains. Therefore, the ae wx and du wx mutants amylopectins were novel. The A:B chain ratios for amylopectins examined, namely for ae wx, amylose-extender;waxy;floury-2 (ae wx fl₂), amylose-extender;waxy;sugary-1 (ae wx su₁), amylose-extender;waxy;sugary-2 (ae wx su₂), brittle-1;waxy (bt₁wx). dull;waxy (du wx), and sugary-2;waxy (su₂wx) amylopectins, were in a range of 1.1 to 1.4 and similar to the wx amylopectin. Thus, starches of double-mutant combinations of the wx gene with other starch-modifying genes are good sources for elucidating the fine structure of amylopectin, in regards to long- and short-B chains, which is affected by a single recessive gene coupled with the wx gene.     

Starch Biosynthesis. II. The Statistical Model for Amylopectin and Its Precursor Plant Glycogen

A modified Meyer model as well as a model containing all possible randomly branched structures (a statistical model) were used for both a precursor glycogen and its amylopectin and were modified by placing short A-chains into the interior part of the structure and thus eliminating some of the longer chains. Debranching of the exterior A-chains of the glycogen model produced amylopectin plus 25% amylose with the assumption that only those A-chains removed from the glycogen were converted into amylose. A comparison of the debranched amylopectin model with debranched wheat and barley amylopectins showed the polymodal behavior of debranched amylopectins can be duplicated with a model system that has inner A-chains and a Poisson size distribution. Branching of external chains of glycogen without chain extension after synthesis has stopped plus inner A-chains can explain the increase (from glycogen to amylopectin) in the A/B chain ratio, the existance of cluster structures, and the observed decrease in branching (8% to 4%) in going from dent, waxy and sweet corn glycogens to their respective amylopectins (or 6.3% to 2.0% for glycogen to amylopectin in ae corn). Disperseable (as in waxy) or indispersable high molecular weight aggregates may be due to different amylopectin-protein complexes.     

Physicochemical Characteristics of Starches from Unripe Fruits of Mango and Banana

Mango and banana starches were isolated from unripe fruits and their morphology; thermal and pasting properties; molar mass and chain length distribution were determined. Mango starch granules were spherical or dome‐shaped and split, while banana starch had elongated granules with a lenticular shape. Amylopectin of both fruit starches had a lower molar mass than maize starch amylopectin; however, mango amylopectin had the highest gyration radius. Banana amylopectin showed the lowest percentage of short chains [degree of polymerization (DP) 6–12] and the highest level of long chains (DP ≥ 37); mango amylopectin presented the highest fraction of short chains, but the level of longest chains was intermediate between those of banana and maize amylopectins. Banana starch presented the highest average gelatinization temperature followed by mango starch and maize starch had the lowest value; a similar pattern was found for the gelatinization enthalpy. The two fruit starches had a lower pasting temperature than maize starch, but the former samples showed higher peak and final viscosities than maize starch. Structural differences identified in the fruit starches explain their physicochemical characteristics such as thermal and pasting behavior.     

The Influences of Chain Length of Amylopectin on Resistant Starch in Rice (Oryza sativa L.)

Amylopectin is the principle component of starch. To elucidate the relationships between amylopectin and resistant starch content, six rice mutants with altered fine structure of amylopectin were selected for comparative studies with the primary wild type and two types of amylose‐extender (ae) mutants. Significant differences in resistant starch content were observed among mutants with similarity or differences in amylose levels. Mutants high in resistant starch had significantly increased proportions of short amylopectin chains with DP≤12, decreased levels of intermediate chains with size of 13≤DP≤36, and decreased fractions of long chains with DP≥37. Additionally, there was a mutant different to ae, which was characterized by an increased level of short chains with 8≤DP≤12 and 13≤DP≤24, and a decreased proportion of long chains with DP≥37. The increased contents of short chains with 8≤DP≤12 and decreased of intermediate and long chains with 24≤DP were clearly associated with the increase of resistant starch in rice.     

Chain Length Distribution of Amylopectins of Several Single Mutants and the Normal Counterpart,and Sugary-1 Phytoglycogen in Maize (Zea mays L.)

β-Limit dextrins of starches of normal (nonmutant), amylose-extender (ae), dull (du), sugary-2 (su₂) and waxy (wx) maize, and phytoglycogen of sugar-1 (su₁) maize were prepared. The β-limit dextrins were successively debranched by isoamylase and pullulanase, and followed by quantitative gel-filtration. The ratio of A to B chains for the ae starch appeared to be high and that for su₁ phytoglycogen was low. The ratio of short B to long B chains for the du starch was high and that for the ae starch appeared to be low. The phytoglycogen did not contain long B chains. The unit chain-length distribution of amylopectins of the normal, wx, and su₂ starches were similar. Fine structures of maize amylopectins and su₁ phytoglycogen were modeled and described.     

The Fine Structure of Corn Starches of Various Amylose-Percentage: Waxy,Normal and Amylomaize

The fine structure of high-amylose corn starches has been studied after dispersion of the starch and fractionation into their components amylose and amylopectin. The resulting amylopectin fraction reported in the literature possesses anomalous properties with regard to the waxy and normal amylopectin. However, the experimental results obtained by different authors for determining the structure lead to controversal explanations. Therefore, using an enzymic method, which permits the direct examination of the constitutive chains of the starch, the fine structure of the amylopectin of an amylomaize starch (64% amylose) has been investigated and compared with those of waxy and normal starches. The pullulanase – debranched chains are fractionated by gel permeation and their linearity are checked under the action of β-amylase. The inner chains of the amylopectin fraction are studied after debranching of the β-limit dextrins. The results show the identity between amylopectins from waxy and normal starches. The amylopectin fraction of amylomaize has its own structure with longer inner chains than those of waxy-maize amylopectin.     

DEXTRINS IN BREWING

The dextrins in beer exhibit a characteristic wavy distribution with respect to their molecular weight, so that these dextrins seem to fall into distinct groups. These groups of dextrins (I, II, III and IV corresponding to DP 5–10, DP 11–16, DP 17–21 and DP 22–27) have been isolated by gel-chromatography on Bio-Gel P-2. Debranching of the megalosaccharides in Groups II, III and IV by means of pullulanase shows that they contain two, three and four α-1,6 linkages respectively. The dextrins in Group I are either linear or singly-branched. The distribution patterns of the constituent, linear maltosaccharides have been determined and some likely structures for the multiply-branched dextrins are suggested. The results indicate that the majority of the α-1,6 linkages in amylopectin survive the brewing process; 25% of the α-1,6 linkages show up as singly-branched oligosaccharides and at least 35% as multiply-branched megalosaccharides of DP 11–30. With respect to the fine structure of amylopectin, the implication is that although the average interior chain length is about 6 glucose units, at least 35% of the α-1,6 linkages occur in densely branched clusters (pairs, triplets, quadruplets, etc.), the interior chain length of which is about 3 glucose units. This in turn offers an explanation of the wavy distribution of the dextrins in wort and beer.     

6种不同种类直支链淀粉相互混合对其回生的影响

目的 研究6种不同种类直支链淀粉相互混合对其回生的影响。方法 将玉米淀粉、甘薯淀粉、木薯淀粉、马铃薯淀粉、糯米淀粉、小麦淀粉等6种不同种类直支链淀粉分离出来, 然后两两混合, 研究不同直支链混合对其回生率的影响。 结果 马铃薯支链淀粉与甘薯支链淀粉以2:8(m:m)混合回生率最低, 为60.0%, 玉米支链淀粉与木薯支链淀粉以8:2(m:m)混合回生率最低为52.6%, 小麦支链淀粉与糯米支链淀粉以8:2(m:m)混合回生率最低为51.2%, 甘薯支链淀粉与小麦支链淀粉以1:1(m:m)混合回生率最低为53.7%。木薯支链淀粉与小麦直链淀粉以1:1(m:m)混合时所得淀粉回生率最大, 达到了92.0%, 混合淀粉回生后X射线晶型为B型。结论 不同种类直支链淀粉混合对其回生率影响很大, 食品加工中尽量不要混合使用木薯支链淀粉与小麦直链淀粉。