水产调味品鲫鱼汁的研制

随着人们生活水平的提高,对食品质量的要求也在不断的提高,调味品在食品质量中扮演着非常重要的角色。本实验以普通养殖鲫鱼为主要原料,研究水产调味品鲫鱼汁的最佳工艺。通过正交试验和感官评价,最终得到水产调味鲫鱼汁的最佳配方:黄原胶0.04%,鲫鱼汁30%,盐15%,糖5%,谷氨酸钠5%,5′-肌苷酸0.25%,叶黄素0.03%,鱼味香精0.03%,山梨酸钾0.05%,均质压力35MPa。水产调味品鲫鱼汁质地均匀,口感细腻,鱼鲜风味突出,色泽淡黄,气味芬芳,符合人们对于风味和营养的需求,具有广阔的市场前景。     

复合涂膜保鲜剂对番荔枝模拟贮运期间品质的影响

研究大黄与五倍子复合涂膜保鲜剂涂膜对番荔枝模拟贮运期间贮藏品质的影响,明确该保鲜剂的保鲜效果。将保鲜剂涂膜的番荔枝作为处理组、未涂膜的果实作为对照(CK),分别置于加冰的泡沫箱中贮藏20 h模拟当地贮运技术,之后开箱放置于常温下贮藏,考察复合涂膜保鲜剂对番荔枝感官品质及其生理生化的影响。结果表明,与CK组比较,经涂膜处理后番荔枝果实的裂果、烂果、霉果和失重情况明显改善,褐变指数和乙烯释放量显著降低;有效延缓了果实软化,延迟了呼吸高峰第1次出现的时间,抑制呼吸高峰的第2次出现, 可显著降低淀粉酶活性、减缓淀粉转化为可溶性固形物的速度。该保鲜剂可有效延缓番荔枝模拟贮运期间果实的衰老,起到较为理想的保鲜效果。     

热碱致魔芋胶与黄原胶共混凝胶的显微结构与流变规律

【目的】探究魔芋胶与黄原胶混合溶胶体系在碱性条件下的凝胶形成机理与凝胶特性,为魔芋胶与黄原胶相关凝胶食品的开发提供理论依据。【方法】在总多糖浓度约为2.0%的条件下,配制不同黄原胶与魔芋胶比例的混合溶胶体系,添加2.0%的Na₂CO₃,并于90℃条件下恒温处理各溶胶体系2 h,冷却至室温后制得不同黄原胶与魔芋胶配比的复合凝胶。通过测定复合凝胶添加碳酸钠前后的凝胶破裂强度,揭示热碱处理对混合凝胶破裂强度的影响。分别测定去离子水浸泡、2.0%柠檬酸溶液浸泡以及冻融处理后凝胶破裂强度的变化情况,并结合扫描电镜观测凝胶的微观形貌,探究复合凝胶的凝胶特性。此外,通过流变学手段进一步研究黄原胶与魔芋胶复合凝胶网络的形成机制。【结果】在室温（20℃）条件下,非热碱处理的魔芋胶与黄原胶最佳协同比为5﹕5,热碱处理后的魔芋胶与黄原胶最佳协同比增加至7﹕3,原因可能是魔芋胶碱化后分子链上脱去部分乙酰基,形成分子间三维网络结构,但在随后的冷却过程中,与黄原胶协同结合位点减少,因此在达到最大协同比时,需要更多数目的魔芋胶分子参与。此外,经去离子水和2.0%柠檬酸溶液浸泡后,所有凝胶体系的破裂强度都有所降低,其中经过2.0%柠檬酸溶液浸泡后的凝胶破裂强度下降更为明显。冻融处理后,复合凝胶均出现明显的析水现象,魔芋胶比例越高,析水现象越明显。进一步探究魔芋胶与黄原胶共混体系在2.0% Na₂CO₃浓度、90℃条件下的凝胶化过程,发现随黄原胶添加量增加,凝胶化速率呈减小趋势。此外,凝胶弹性模量在90—60℃呈降低趋势,60℃以下逐渐上升。【结论】在90℃条件下碱处理魔芋胶与黄原胶共混体系时,诱导体系形成热不可逆凝胶。当降低该体系的温度时,黄原胶分子在60℃时开始与魔芋胶网络结合,增加了凝胶的弹性模量。当魔芋胶与黄原胶比例为7﹕3时,室温下混合凝胶的破裂强度最大。经去离子水和2.0%柠檬酸溶液浸泡后,凝胶强度均有所降低。魔芋胶与黄原胶形成的复合凝胶在一定条件下可以改善单纯碱法诱导的魔芋胶凝胶析水多、强度差等缺点。     

丙酮酸基对黄原胶/魔芋葡甘聚糖复配体系凝胶特性的影响

为了实现对复配凝胶体系状态的调控,扩展凝胶在食品中的应用,该研究通过酸性热处理调控黄原胶中丙酮酸基含量变化,研究其对黄原胶结构、流变特性及黄原胶(Xanthan Gum)与魔芋葡甘聚糖(Konjac Glucomannan)复配凝胶特性(如溶胶-凝胶转换温度、流变特性等)的影响。研究结果表明;XG螺旋结构随丙酮酸基减少而逐渐紧密,流动性增强,有序无序构象转换温度升高。通过对XG/KGM复配凝胶流变特性的研究发现丙酮酸基含量减少,复配体系的黏度系数减小,似固性减弱,趋向于牛顿流体;且同一角频率下,XG/KGM复配凝胶的储能模量和损耗模量随丙酮酸基的脱除均呈现减小的趋势,但储能模量恒大于损耗模量,损耗因子的正切值恒小于1,呈固体特性。温度扫描表明温度降低,复配体系的储能模量逐渐增大,但其增加的起始温度随丙酮酸基含量减少而降低,且整体呈下降趋势,溶胶-凝胶温度从60℃降至41℃,该研究结果使得溶胶-凝胶的转换温度更接近于口腔温度,为食品产业中"入口即化"特性的研究提供了可能。     

黄原胶-N-乙烯基吡咯烷酮辐射接枝共聚物的制备及结构特性研究

为提高黄原胶分子的应用性能,以60Co-γ为辐射源,对黄原胶和N-乙烯基吡咯烷酮进行共辐射接枝处理,制备黄原胶-N-乙烯基吡咯烷酮共聚物(XG-g-NVP),并研究反应条件对接枝率和单体利用率的影响及共聚物的结构表征。结果表明,当辐射吸收剂量为10k Gy,黄原胶浓度12g·L-1,NVP/XG质量比8∶1,4-甲氧基酚阻聚剂添加量为NVP单体质量的0.01%时,最佳接枝率为543.3%,单体利用率为67.9%。红外光谱表明接枝反应发生在NVP乙烯基部位,扫描电镜图显示共聚物形貌由片层状逐步过渡到颗粒状;XG-g-NVP的抗高温及抗剪切能力相比黄原胶有所提高,且黏度值在高温、高剪切力时仍保持恒定值,因此,改性后的黄原胶结构及热稳定性提高。通过对黄原胶分子接枝改性,使其具备了更多优良的性能,为改性黄原胶的进一步应用奠定了理论基础。     

黄原胶与卡拉胶复配在果冻中的应用研究

采用单因素及正交试验,研究黄原胶和卡拉胶复配制作果冻的工艺和配方。结果表明：黄原胶与卡拉胶按1∶10复配在果冻中的应用较佳,最佳果冻配方为：黄原胶添加量0.1%,卡拉胶添加量1.0%、白砂糖18%、柠檬酸0.10%、青苹果汁3.0%,做出的果冻色泽均匀、半透明,组织状态良好、口感细腻。     

Stability of allophane,allophanic clay,and allophane-halloysite floc in aqueous solutions of an anionic exocellular heteropolysaccharide (Gum Xanthan) from Xanthomonas campestris

Stability of allophane with positive and/or negative charges in the presence of gum xanthan (GX) was mainly investigated at three pH levels. At pH 4.5, allophane showed polymeric iocculation (PFL) at low GX concentrations, and polymeric stabilization (PST) at medium GX concentrations. Flocculated allophane (i.e.p.) at pH 6.5 showed polymeric weak-stabilization (PWST) at extremely low GX concentrations, besides PFL and PST described above. At pH 8.5, allophane did not exhibit any change in stability with GX addition. The PFL and PWST can be regarded as charge neutralization between allophane and GX. Allophanic clay with i.e.p. at pH 10 exhibited both PFL and PST but no PWST, even at pH 8.5. The PWST can be explained by the disintegration of the floc when interparticle attraction was weakened by the adsorption of GX. The lower PWST and PST of allophane-halloysite mutual floc strongly suggested the presence of a more stable arrangement among these dissimilar particles. Stability of crystalline clays was also studied for comparison. The above behavior was analyzed on the basis of (i) the suspended microaggregate of allophane, and (ii) the double-stranded wormlike structure of GX, which was taken in this study as a model substance of anionic microbial polysaccharide.     

Effect of inorganic electrolytes on the stability of allophane in aqueous solutions of anionic xanthan polysaccharide

The polymeric (a) weak-stabilization (PWST), (b) floccelation (PFL), and (c) stabilization (PST) of ailophane with the anionic xanthan (GX) polysaccharide (He and Horikawa 1996a, b: Soil Sci. Plant Nutr., 42, 603-612, 637-644) were investigated further with respect to the effect of 1-1, 2-1, and 1-2 electrolytes (MA). At pH 4.5, the PST was (i) high in 0.1 mM NaCl, MgCl₂, ZnCl₂, and PbCl₂ solutions, whereas (ii) considerably low in 100 mM NaCl, 0.1 mM Na₂SO₄ and NaH₂PO₄ solutions, respectively. At pH 6.5 (i.e.p.), the flocculated ailophane showed (i) a very low PWST in 0.01 mM NaCl, MgCl₂, and Na₂SO₄ solutions, and also (ii) a low PST in 0.01 mM MA except for NaH₂PO₄. In 0.01 mM PbCl₂ and NaH₂PO₄ solutions, ailophane was well dispersed, respectively, and marked PFL and PST were observed with further addition of xanthan. The changes and decrease of PWST and PST were discussed in relation to the iocculation of ailophane due to the (a) effect of MA on the diffuse double layer of the particles, (b) specific adsorption of phosphate and lead ions on the surface, and (c) weakening of the repulsive force between anionic GX chains by MA.     

Adsorption of xanthan polymer on allophane and effect on the changes in colloidal stability of allophane by heavy metal ions

The influence of divalent cations at concentrations of 10^-6.0 to 10^-4.0 M on the colloidal stability of partially deflocculated allophane by gum xanthan (GX) polysaccharide at pH 6.5 was investigated at two GX concentrations. Experiment in the presence of 10^-2.0 g L^-1 GX showed that the stability decreased by the addition of divalent cations and the effect of the decrease due to the cationic species was evident in a higher concentration range, i.e., 10^-5.0 to 10^-4.0 M. The order of the effect was Pb >Zn > Cd > Mg. Experiment in a 10^-4.5 g L^-1 GX solution revealed that (i) the stability increased by the addition of heavy metal cations at 10^-5.0 M (the order of the effect was Pb > Zn > Cd) and decreased at a concentration above 10^-4.5 M, (ii) whereas the stability decreased by the addition of Mg ion. The striking difference in the stability behavior due to the difference between the two GX-concentrations was attributed to the (i) degree of GX-adsorption (and hence negative charge from the carboxyl group in GX) onto allophane based on the electrophoretic mobility, (ii) complexation of heavy metal cations by organic ligand (carboxyl group) in GX which was adsorbed onto allophane, and (iii) surface complexation by heavy metal cations and hydroxyl groups on allophane. The results were discussed in relation to the characteristics of the particles of allophane, viz., (i) polymer-coated soft particles, and (ii) semi-soft particles on which the rigid (hard) surface of allophane substantially remained.     

Rheology of concentrated xanthan gum solutions: Steady shear flow behavior

Using a strain-controlled rheometer, the steady shear flow properties of aqueous xanthan gum solutions of different concentrations were measured over a wide range of shear rates. In this article, both the shear rate and concentration dependencies of steady shear flow behavior are reported from the experimentally obtained data. The viscous behavior is quantitatively discussed using a well-known power law type flow equation with a special emphasis on its importance in industrial processing and actual usage. In addition, several inelastic-viscoplastic flow models including a yield stress parameter are employed to make a quantitative evaluation of the steady shear flow behavior, and then the applicability of these models is also examined in detail. Finally, the elastic nature is explained with a brief comment on its practical significance. Main results obtained from this study can be summarized as follows: (1) Concentrated xanthan gum solutions exhibit a finite magnitude of yield stress. This may come from the fact that a large number of hydrogen bonds in the helix structure result in a stable configuration that can show a resistance to flow. (2) Concentrated xanthan gum solutions show a marked non-Newtonian shear-thinning behavior which is well described by a power law flow equation and may be interpreted in terms of the conformational status of the polymer molecules under the influence of shear flow. This rheological feature enhances sensory qualities in food, pharmaceutical, and cosmetic products and guarantees a high degree of mixability, pumpability, and pourability during their processing and/or actual use. (3) The Herschel-Bulkley, Mizrahi-Berk, and Heinz-Casson models are all applicable and have equivalent ability to describe the steady shear flow behavior of concentrated xanthan gum solutions, whereas both the Bingham and Casson models do not give a good applicability. (4) Concentrated xanthan gum solutions exhibit a quite important elastic flow behavior which acts as a significant factor for many industrial applications such as food, pharmaceutical, and cosmetic manufacturing processes.