Pasting properties of hydroxypropylated starches before or after proteinase treatment

To examine the effect of starch protein on hydroxypropylation, corn (normal and waxy) and potato starches were hydroxypropylated with propylene oxide at two levels (8.3 and 12.3% based on dry basis of starch weight) before or after proteinase (thermolysin) treatment, and then pasting properties of the starches were measured. For normal corn starch, protein appeared to be involved in hydroxypropylation, especially at the higher concentration of reagent (12.3%); the starch hydroxypropylated after proteinase treatment (Enz‐HP) showed less reaction efficiency than that only hydroxypropylated (HP) or proteinase treated starch after hydroxypropylation (HP‐Enz). This suggests a possible reaction between some of the reagent and the starch proteins that exist in the channel and surface of the starch granules. However, not much difference was found with the waxy corn starch, as it contains much lower amounts of amylose and protein than normal corn starch. The potato starch, which has no channels, showed complicated protein effects. For potato starch, a different access of the enzyme and chemical reagents to the granule matrix could be possible.     

Substituent distribution within cross-linked and hydroxypropylated sweet potato starch and potato starch

Revealing the substituents distribution within starch can help to understand the changes of starch properties after modification. The distribution of substituents over cross-linked and hydroxypropylated sweet potato starch was investigated and compared with modified potato starch. The starches were cross-linked with sodium trimetaphosphate and/or hydroxypropylated with propylene oxide. The native and modified starches were gelatinized and hydrolysed by pullulanase, β-amylase, α-amylase and a combination of pullulanase, α-amylase and amyloglucosidase. The hydrolysates were analysed by HPSEC, HPAEC and MALDI-TOF mass spectrometry. Cross-linking had only a slight effect on the enzymatic hydrolysis, where hydroxypropylation evidently limited the enzymatic hydrolysis. The results obtained suggest that the hydroxypropyl substituents are not distributed regularly over the starch chains. Although the average substitution was around 2 hydroxypropyl groups per 10 glucose units, in the enzyme digests of hydroxypropylated starches, oligomer fragments of 10–15 glucose units, carrying 5–8 hydroxypropyl groups, were identified. It is hypothesised that higher levels of substituents are present in the amorphous regions and periphery of clusters of starch granules. This is the first time that the location of hydroxypropyl groups within sweet potato starch has been examined in this detail. Despite significant differences in granule architecture between starches from potato and sweet potato, similar patterns of hydroxypropylation have been found.     

Influence of hydroxypropylation on retrogradation properties of native,defatted and heat-moisture treated potato starches

Recent studies have shown that defatting and heat-moisture treatment cause structural changes within the amorphous and crystalline regions of potato starch. Furthermore, the alkaline reagents (NaOH and Na₂SO₄) used during hydroxypropylation has been shown to cause structural changes within the amorphous and crystalline regions of native, defatted and heat-moisture treated starches. In this study, we have compared (using different techniques) the retrogradation properties of potato starch before and after physical (defatting and heat-moisture treatment), and chemical (alkaline treatment and hydroxypropylation) modification. Turbidity measurements showed that changes in turbidity during storage (4°C for 24 h and then at 40°C for 29 days) of native, defatted and heat-moisture treated gelatinized starch pastes were influenced by the interplay of two factors: (1) interaction between leached starch components (amylose–amylose, amylose–amylopectin, amylose–amylopectin), and (2) interaction between granule remnants and leached amylose and amylopectin. In alkali treated gelatinized native, defatted and heat-moisture treated starch pastes, turbidity changes on storage was influenced by aggregation of granule remnants. Hydroxypropylation decreased the rate and extent of increase in turbidity during storage of native, defatted and heat-moisture treated starches. The change in turbidity during storage of hydroxypropylated starch pastes was influenced by the interplay between: (1) steric effects imposed by hydroxypropyl groups on chain aggregation, (2) aggregation between small granule remnants, and (3) settling of large granule remnants beneath the path of the spectrophotometer beam. Stored gelatinized pastes of native, defatted and heat-moisture treated starches gave a `B' type X-ray pattern. A similar pattern was also observed after alkaline treatment, and hydroxypropylation. However, the X-ray intensity of the strong reflection at 5.2 Å decreased after alkaline treatment and hydroxypropylation. The retrogradation endotherm (monitored by differential scanning calorimetry) occurred after 2 days storage in native, defatted and heat-moisture treated starches. A similar trend was also observed after alkaline treatment. However, the retrogradation endotherm appeared only after 7 days in hydroxypropylated starches. The enthalpy of retrogradation in all starches decreased on alkaline treatment and hydroxypropylation.     

A Study of Native and Chemically Modified Potato Starch. Part II: Digestibility in the Rat Intestinal Tract

The in vivo digestibility of the following chemically modified potato starch derivatives was evaluated in rats; distarch phosphate (DSP), acetyl di-starch phosphate (ADSP) and hydroxypropyl di-starch phosphate (HPDSP). Unmodified potato starch was used as reference. The starches were studied raw and after gelatinization by drum-drying. The extent of in vivo digestion was evaluated through balance experiments in normal rats (apparent digestibility) and in rats treated with an antibiotic drug to suppress hind-gut fermentation (true digestibility). Starch digestibility was calculated from direct measurement of starch in feed and faeces. Three different methods for starch analysis were compared. The apparent digestibility of raw potato starches was low, ranging from 50 (HPDSP) to 84% (ADSP). The true digestibility of gelatinized unmodified potato starch was essentially complete and was not affected to any appreciable extent as a result of cross-linking or acetylation. In contrast, etherification with hydroxypropyl significantly reduced the extent of digestion and absorption to a low level, about 50%, which was not significantly different from that with the corresponding raw material. Thus, the digestibility of the HPDSP derivative was not improved by gelatinization. The maldigested hydroxypropylated starch fraction was only metabolized to a limited degree by the hind-gut microorganisms.     

Synthesis and Characterization of Cross‐linked Carboxymethyl Potato Starch Ether Gels

Hydrogels were synthesized by cross‐linking of potato starch (PS) with dichloroacetic acid (DCA) in the presence of monochloroacetic acid (MCA) to form etherified carboxymethyl starch (CMS) gels, to be used for ultrasonic medical examinations. By etherification cross‐linked CMS‐hydrogels can be produced, that are stable in contrast to the in the long‐term unstable esterified gels, that were presented in the last paper. The rheological benchmarks for the CMS‐hydrogels were set in comparison with synthetic ultrasonic gels. Gels with potato starch contents in the reaction batch ranging from 12.5% to 20% showed the best compliance with the benchmark parameters. The DS values of these CMS‐hydrogels vary from 0.42 to 0.49, increasing with decreasing amount of starch in the reaction mixture. The free swelling capacities (FSC) vary between 77 g/g for the 12.5% PS‐gel and 34 g/g for 20% PS‐gel, the turbidities of the samples being in the range from 14.5 NTU (Nephelometric Turbidity Units) (12.5% PS) up to 20.5 NTU (20% PS). The variation of the PS fraction in the reaction mixture showed that with an increased amount of PS in the reaction batch the number of cross‐links of the CMS‐gels increases, too. At a higher number of cross‐links the swelling capacity is reduced and the concentration needed to form stable hydrogels is greatly increased. Thus a hydrogel of a polymer concentration of 5 mass‐% from a 12.5% PS batch was produced, that showed the best accordance with the rheological benchmark parameters such as gelatinization time, visco‐elastic and pseudoplastic properties and long‐term stability. The ultrasonic pictures taken with this CMS‐gel were not different from those taken with the synthetic gels. This hydrogel was then subjected to long‐term‐stability measurements performed over one year and to rheological temperature cycle tests. The tests showed that the long‐term stability of the gels is sufficient for their use as ultrasonic gel.     

Phase transition of cross-linked and hydroxypropylated corn (Zea mays L.) starches

The thermal behaviors of three chemically modified starches (cross-linked waxy corn, hydroxypropylated regular corn, and hydroxypropylated and oxidized waxy corn) were studied using light microscopy, SEM, DSC, XRD, and HPSEC. During the gelatinization process, molecular and crystalline order losses occurred independently from each other. Oxidation treatment altered the effects of hydroxypropylation on starch gelatinization. Both cross-linking and hydroxypropylation tended to preserve granular crystalline order during initial stages of gelatinization. The crystallinities and X-ray patterns of each starch remained essentially unchanged prior to phase transition.     

Hydroxypropylated microcrystalline pea starch: optimisation,functional characterisation

Pea starch (PS) appears to be very attractive for the peculiar physicochemical characteristics, which is used for the vermicelli, film‐forming material due to the high amylose content. The aim of this study was to optimise the hydroxypropylation technology parameters of the microcrystalline pea starch based on pea starch as a raw material, hydrochloric acid as an hydrolysis reagent, epoxy propane as an etherisation reagent by the Box–Behnken method. The thermal properties of hydroxypropylated microcrystalline pea starch were characterised by the thermogravimetric analyser and differential scanning calorimeter, respectively. Through the analysis of Design‐Expert software, the regression model and corresponding variances were obtained. In this case, the determination coefficient (R²) was 0.9631. This implied that 96.31% of the variation could be explained by the regression model. The best reaction conditions for preparing the hydroxypropylated microcrystalline pea starch were as follows: reaction temperature 40 °C, reaction time 16 h, amount of epoxy propane 14%, amount of sodium hydroxide 1.2% and amount of anhydrous sodium sulphate 12%. After the microcrystalline pea starch was hydroxypropylated, its peak temperature, melting enthalpy, temperature range of the endothermic peak increased, but its the thermal stability, onset temperature decreased.     

In vitro Digestibility of Hydroxypropylated and Cross-linked Waxy and Non-waxy Rice Starches

In vitro digestibility of hydroxypropylated and cross-linked waxy and non-waxy rice starches was investigated to find the proper resistant starch (RS) assaying method for chemically modified starches. RS and total dietary fiber (TDF) content of hydroxypropylated and cross-linked waxy and non-waxy rice starches were measured using the approved AOAC RS assay procedure (AOAC method 2002.02) and the AOAC TDF assay procedure (AOAC method 985.29). Hydroxypropylation did not alter the RS content of waxy and non-waxy rice starches (less than 1% of RS). Cross-linking also did not change the RS content of waxy and non-waxy rice starches (less than 1% of RS). It is interesting to note that non-RS content decreased with increasing hydroxypropylation (97-80%) and cross-linking (99-95%) in both waxy and non-waxy rice starches. This indicates that some fraction of RS in hydroxypropylated and cross-linked waxy and non-waxy rice starches cannot be measured using approved AOAC RS and TDF assay procedures. Therefore, the RS and TDF assay procedures performed in this study are not appropriate to determine the RS content of chemically modified starch. Further investigation is needed to develop a method to determine the RS content of chemically modified starch.     

Retrogradation of Starch Mixtures Containing Rice Starch

ABSTRACT: Different starches often coexist in food systems. Starch retrogradation is the primary reason for quality deterioration of a food system during storage. This article addresses the retrogradation behaviors of several starch mixtures containing normal rice starch (NRS). Potato starch, tapioca starch, waxy corn starch, hydroxypropylated potato starch, hydroxypropylated tapioca starch, and acetylated tapioca starch were mixed with NRS. Starch suspensions were gelatinized and the relative solid content, (S′) measured by pulsed nuclear magnetic resonance, was used to characterize the retrogradation behavior of starch systems. The retrogradation behaviors of starch mixtures can be divided into two categories according to the additive or non‐additive nature of S′, for which the concept “regional moisture content” was introduced.     

Effects of Potato Fiber and Potato‐Resistant Starch on Biomarkers of Colonic Health in Rats Fed Diets Containing Red Meat

Abstract: The effects of red meat consumption with and without fermentable carbohydrates on indices of large bowel health in rats were examined. Sprague‐Dawley rats were fed cellulose, potato fiber, or potato‐resistant starch diets containing 12% casein for 2 wk, then similar diets containing 25% cooked beef for 6 wk. After week 8, cecal and colonic microbiota composition, fermentation end‐products, colon structure, and colonocyte DNA damage were analyzed. Rats fed potato fiber had lower Bacteroides‐Prevotella‐Porphyromonas group compared to other diet groups. Colonic Bifidobacterium spp. and/or Lactobacillus spp. were higher in potato fiber and potato‐resistant starch diets than in the cellulose diet. Beneficial changes were observed in short‐chain fatty acid concentrations (acetic, butyric, and propionic acids) in rats fed potato fiber compared with rats fed cellulose. Phenol and p‐cresol concentrations were lower in the cecum and colon of rats fed potato fiber. An increase in goblet cells per crypt and longer crypts were found in the colon of rats fed potato fiber and potato‐resistant starch diets. Fermentable carbohydrates had no effect on colonic DNA damage. Dietary combinations of red meat with potato fiber or potato‐resistant starch have distinctive effects in the large bowel. Future studies are essential to examine the efficacy of different types of nondigestible carbohydrates in maintaining colonic health during long‐term consumption of high‐protein diets. Practical Application: Improved understanding of interactions between the food consumed and gut microbiota provides knowledge needed to make healthier food choices for large bowel health. The impact of red meat on large bowel health may be ameliorated by consuming with fermentable dietary fiber, a colonic energy source that produces less harmful by‐products than the microbial breakdown of colonic protein for energy. Developing functional red meat products with fermentable dietary fiber could be one way to promote a healthy and balanced macronutrient diet.     

乙酰化羟丙基淀粉改性次序及程度研究

为确定复合改性对淀粉性质的影响,从而为复合改性淀粉在食品中的应用提供参考。以玉米淀粉为原料,在羟丙基淀粉及乙酰化淀粉2种单一改性淀粉研究的基础上,采用分光光度法确定单一改性淀粉取代度,并以复合取代度为指标,探讨乙酰化羟丙基复合改性淀粉的改性次序及改性程度对复合改性淀粉制备的影响。结果表明:水解作用与空间位阻是影响复合改性效果的重要因素;乙酰化羟丙基复合改性淀粉合理的改性次序应为先羟丙基化后乙酰化,且在一定范围内,乙酰化反应不受羟丙基化程度的影响。     

Hydroxypropylation of pigeon pea (Cajanus cajan) starch: Preparation, functional characterizations and enzymatic digestibility

Hydroxypropyl starch derivatives were prepared from pigeon pea starch (NPPS) which is an unconventional starch source. Functional parameters and characterization of both native and modified starches were carried out. The starch granules appeared oval or elliptical in shape with sizes ranging from 7 to 40 μm in width and 10 − 30 μm in length. Hydroxypropylation did not alter the shape of the starch granules in a pronounced way. Generally, the x-ray diffractograms of native pigeon pea starch showed the “A” pattern. However, slight reductions in the diffraction intensity of starches after modification were observed. At all temperatures studied (30-90 °C), swelling and solubility of hydroxypropylated starches were higher than the NPPS. Progressive increases in swelling capacity and solubility were observed as the molar substitution (MS) increased among the hydroxypropylated starches. Hydroxypropylation reduced starch paste turbidity on storage. Also, studies showed that syneresis reduced after hydroxypropylation. In addition, syneresis reduced as the MS of the hydroxypropyl starches increased. The results indicate that pasting temperature and peak temperature reduced after modification but peak viscosity increased in hydroxypropylated starch derivatives compared with the native starch. Setback reduced in hydroxypropylated starches compared with the native starch. Enthalpy of gelatinization and percentage retrogradation reduced after hydroxypropylation and progressive reductions were observed as the MS increased among the starch derivatives. Hydroxypropylation increased enzymatic digestibility.     

不同变性淀粉对冷冻面团热力学特性的影响

采用差示扫描量热法(DSC)研究4种不同种类变性淀粉对冷冻面团热力学特性(玻璃化转变温度、冰晶融化特性和可冻结水含量)的影响。结果表明,冷冻面团的玻璃化转变温度在-30℃左右,不同变性淀粉对冷冻面团玻璃化转变基本无明显影响;添加5%马铃薯羟丙基淀粉、木薯羟丙基淀粉和木薯醋酸酯淀粉可以显著降低冷冻面团冰晶融化范围,面团中形成的冰晶大小更加均匀;冷冻面团可冻结水含量随着马铃薯醋酸酯淀粉和马铃薯羟丙基淀粉添加量的增加呈降低趋势,添加10%木薯羟丙基淀粉时,面团可冻结水含量显著低于空白组,而木薯醋酸酯淀粉对面团可冻结水含量无显著影响。     

冻融处理对淀粉膜结构、热稳定性、机械性能及物理性质的影响

本实验分别以天然马铃薯淀粉（potato starch,PS）、改性马铃薯淀粉（包括羟丙基二淀粉磷酸酯（hydroxypropyl distarch phosphate,HDP）、醋酸淀粉（acetate starch,AS）和氧化淀粉（oxidized starch,OS））为基材,通过流延法制备可食用淀粉膜,考察冻融处理对膜物理性质、机械性能、阻隔性能、微观结构和热稳定性的影响。X射线衍射结果表明,马铃薯来源的淀粉颗粒具有典型的B型晶体结构,在成膜过程中淀粉结晶度降低,冻融处理后淀粉膜晶体峰强度明显减弱。扫描电子显微镜观察结果显示,冻融处理破坏了淀粉膜的微观结构,其中PS膜上出现明显裂纹,AS膜上出现蜂窝和层状结构,而HDP和OS淀粉膜具有更完整的形态。热重分析结果表明,随着温度的升高,淀粉膜的热重曲线出现4 个质量损失阶段,分别对应水分散失、甘油挥发、淀粉解聚及淀粉分解,而冻融处理对膜热稳定性影响较小。常温条件下,PS膜具有最佳的机械性能,其拉伸强度为2.29 MPa,断裂伸长率为68.82%。在3 个冻融循环后,淀粉膜的拉伸强度至少增加了2 倍,断裂伸长率普遍降低,而溶解度和水蒸气透过率仅有轻微变化。综合考虑不同淀粉膜微观结构、机械性能、水蒸气透过率及水溶性,HDP膜表现出更好的冻融稳定性,可应用于冷冻低水分食品的保藏。     

Swelling Characteristics of Native and Chemically Modified Wheat Starches as a Function of Heating Temperature and Time

The effects of hydroxypropylation (molar substitution, MS 0.05, 0.12, and 0.18) and cross‐linking (0.03%, 0.1%, and 0.2%) on swelling properties of wheat starch granules at several temperatures and heating times were investigated by laser diffraction particle size analysis. Starch samples were dispersed in water at temperatures ranging from 30 to 90°C, for 1 to 360 min. All starch granules exhibited distinct bimodal size distributions: small B‐granules with mean diameter of 2.3 μm and large A‐granules with mean diameter of 20.4 μm. As temperature increased, the B‐granules swelled more than A‐granules. Swelling of A‐granules sharply increased at 60°C. Swelling was more pronounced with increasing molar substitution of hydroxypropyl groups, while increased swelling was not observed in cross‐linked starches. The dependence of swelling capacity on heating time was different at 60 and 80°C as well as amongst modified starches. As heating time was prolonged, mean granule sizes for native, control, and hydroxypropylated starches at 80°C decreased after reaching maximum size due to loss of granule integrity, while those at 60°C showed no significant change.     

The effect of chemically‐modified resistant starch,RS type‐4, on body weight and blood lipid profiles of high fat diet‐induced obese mice

This study was conducted to investigate the effects of feeding chemically‐modified resistant starch type‐4 (RS4) of normal (NCS) and high‐amylose corn starch (HACS) on weight gain and plasma and liver lipid profiles of mice fed a high‐fat diet (HFD). The experimental four groups were, respectively, fed following diets: A 40% HFD with NCS, HACS, NCS‐ and HACS‐RS4. A normal diet (ND) group of mice fed the standard diet was also used as control. In order to produce RS4 by chemical modification, corn starches were treated with STMP/STPP. Total RS (TRS) and total dietary fiber (TDF) levels of chemically‐modified NCS were 26.4 and 44.0%, respectively, while TRS and TDF levels in chemically‐modified HACS were 78.1 and 78.5%, respectively. Onset gelatinization temperatures of both modified corn starches clearly shifted to higher temperatures after STMP/STPP treatment. At the end of the diet trial, the mice on the HACS diet decreased body weight gain compared to the NCS‐fed mice. Adding NCS‐ and HACS‐RS4 to the diet significantly reduced the weight gain relative to NCS and HACS groups. Both RS4 diets were effective in improving the lipid profile compared to their respective controls. They significantly reduced the level of total lipid and total cholesterol.     

Dynamic rheological properties of rice flour‐starch blends

The dynamic rheological properties of blends of rice flour (RF) with six different commercial starches (sweet potato starch, potato starch, tapioca starch, waxy corn starch, hydroxypropylated potato starch, and hydroxypropylated tapioca starch) were evaluated. The magnitudes of storage modulus (G′) of all blend samples were higher than those of loss modulus (G′′) over most of the frequency range (0.63–62.8 rad · s⁻¹). In general, the dynamic moduli results of all blend samples showed that changes in G′ values were relatively greater than changes in G″ values after adding the starches when compared to RF. tan δ (ratio of G′′/G′) values (0.21–0.22) of the RF‐potato starch and RF‐hydroxypropylated potato starch blends were much lower than those (0.25–0.33) of other blends and RF, indicating that there is a more pronounced synergistic effect on the elastic properties of RF‐starch blend systems in the presence of potato starches.     

Influence of modified starches on properties of gluten-free dough and bread. Part I: Rheological and thermal properties of gluten-free dough

The aim of this study was to analyze the influence of chemically modified starches (HDP and ADA) and high amylose corn starch (HACS) on the rheological and thermal properties of gluten-free dough based on corn and potato starches with pectin and guar gum. The results indicate that the dough with the addition of modified starch behaves as weak gel, the value of storage modulus G′ significantly depends on the frequency and the values of tan δ = G″/G′ range from 0.32 to 0.49. Significant influence of hydroxypropylated distarch phosphate (HDP) on the viscoelastic properties of dough was observed. The share of modified starch in the system caused a decrease of the instantaneous and viscoelastic compliance. It also influenced the retardation time and zero shear viscosity. The application of modified starches (HDP and ADA) for dough preparation did not have much impact on the pasting characteristics. However, significant reduction of the onset and end viscosities were found for high amylose starch (HACS). Thermograms obtained for individual dough systems were characterized by the presence of two peaks, associated with the existence of two different starches in the system. No significant effect of modified starch on the onset temperature (T_O) and only a slight effect of HACS starch on gelatinization enthalpy were observed. However, the level of addition of individual starch affected peak and end (T_E) temperatures, depending on the type of preparation.     

The Reactivity of Porcine Pancreatic alpha-Amylase Towards Native,Defatted and Heat-moisture Treated Potato Starches Before and After Hydroxypropylation

Potato starch was defatted (hot 75% n-propanol) and heat-moisture treated (100°C, 30% moisture) for various time intervals. The results showed that the above treatments increased the susceptibility of potato starch granules (heat-moisture treated > defatted) towards hydrolysis by porcine pancreatic α-amylase. These differences can be accounted for by the structural changes that occur within the amorphous and crystalline regions of the starch granule during defatting and heat-moisture treatment. Native, defatted (7 h) and heat-moisture treated (100°C, 30% moisture, 16 h) potato starches were hydroxypropylated (to different levels of molar substitution [MS]) with propylene oxide (2 → 20 %). The results showed that the alkaline reagents (NaOH and Na₂SO₄) used during hydroxypropylation increased the susceptibility of the above starches (native > defatted > heat-moisture treated) towards hydrolysis by α-amylase. Addition of propylene oxide to alkali treated starches, further enhanced their susceptibility, towards α-amylase. However, granule susceptibility towards α-amylase did not increase exponentially with increase in MS. The extent of hydrolysis began to decrease at MS levels of 0.29 (native), 0.28 (heat-moisture treated) and 0,26 (defatted).     

Quality and safety evaluation of genetically modified potatoes spunta with Cry V gene: compositional analysis, determination of some toxins, antinutrients compounds and feeding study in rats

The aim of this study was to evaluate the composition, nutritional and toxicology safety of GM potato Spunta lines compared to that of conventional potato Spunta. Compositional analyses were conducted to measure the proximate chemical composition with references to 14 components, total solid, protein, lipid, crude fibre, ash, carbohydrate, starch, reducing sugar, nonreducing sugar, sodium, calcium, potassium, phosphorus, and ascorbic acid. Some toxins and anti-nutrients compounds were determined. Feeding study of GM potatoes line (G2 and G3) in rats were done for 30 days. Four groups of albino rats were used for studying the effect and the safety assessment of GM potatoes Spunta G2 and G3. Group (I) was fed on control basal diet, group (II) was fed on control diet plus 30% freeze-dried nongenetically modified potato Spunta, group (III) was fed on control diet plus 30% freeze-dried genetically modified potato Spunta, and group (IV) was fed on control diet plus 30% freeze-dried genetically modified potato Spunta GMO G3. There were no significant differences between GM potatoes G2, G3, and Spunta control potato line in the proximate chemical composition. The levels of glycoalkaloids in transgenic potato tubers and nontransgenic were determined and there were also no significant differences between the GM potatoes and conventional potato line, the levels were in agreement with a safety level recommended by FAO/WHO (200 mg/ kg) for acute toxicity. Protease inhibitor activity and total phenol were estimated and no significant differences between the GM potatoes line and conventional potato Spunta line were found. During the period tested, rats in each group (I, II, III, IV) grew well without marked differences in appearance. No statistical difference were found in food intake, daily body weight gain and feed efficiency. But there is a slightly significant difference in finally body weight between the control group and experimental groups. No significant difference were found in serum biochemical value between each groups, and also between relative organs weight (liver, spleen, heart, kidney, testes). From these results, it can be concluded that the GM potatoes Spunta line (G2 and G3) with Cry V gene are confirmed to have nearly the composition and biochemical characteristics as non-GM potato Spunta.