几种添加物对蛋清蛋白热诱导不可逆凝胶性质的影响

以蛋清蛋白为原料,制备热诱导制取不可逆性凝胶,在单因素试验基础上,采用三因素二次正交旋转组合设计研究了三聚磷酸钠(X1)、瓜尔胶(X2)、酪蛋白酸钠(X3)对蛋清蛋白热诱导不可逆性凝胶性质的影响,建立了二次回归模型。结果表明,X12,X22在0.01水平上差异极显著,X32在0.05水平上差异显著;最佳配比为三聚磷酸钠质量分数0.100%,瓜尔胶质量分数0.100%,酪蛋白酸钠质量分数0.250%,此时蛋清蛋白凝胶强度预测值为550 g/cm2,实际值为542 g/cm2,二次正交旋转组合设计法可信度强,具有很好的预测意义。     

利用凝胶扩散法测定刺萼龙葵种子中β-甘露聚糖酶的活性

β-甘露聚糖酶是种子萌发过程中降解胚乳细胞壁的关键酶,明确其活性的动态变化可为揭示杂草种子的休眠萌发机制提供重要依据。以外来杂草刺萼龙葵Solanum rostratum Dunal种子为材料,建立了种子中β-甘露聚糖酶活性的检测方法—凝胶扩散法。利用凝胶扩散法对不同贮存时间及贮存条件下刺萼龙葵种子中β-甘露聚糖酶的活性进行了检测,发现贮存3年以上的种子中该酶的活性为0.03 nmol/(min·mg),显著低于贮存3年以下的种子中的酶活性0.15 nmol/(min·mg),而湿润冷藏的种子中β-甘露聚糖酶的活性为0.12 nmol/(min·mg),显著高于干燥冷藏的种子的酶活性0.02 nmol/(min·mg)。实际应用结果表明,凝胶扩散法综合了传统方法的优势,检测特异性强、灵敏度高、重复性好,可同时检测大量种子样品,具有良好的实用性。     

不同施肥和保水措施对油茶土壤N2O排放的影响

为探究不同施肥和保水措施对油茶土壤N_2O排放的影响,采用静态暗箱-气相色谱法,设置对照(B0CK)、氮肥(N,0.13 g N·kg~(-1))、磷肥(P,0.065 g P·kg~(-1))、氮磷肥(NP,0.13 g N·kg~(-1)+0.065 g P·kg~(-1))、低复合保水材料(生物炭和聚丙烯酰胺,B1,每盆13.65 g炭+1.35 g聚丙烯酰胺)、高复合保水材料(生物炭和聚丙烯酰胺,B2,每盆27.30 g炭+2.70 g聚丙烯酰胺)、低复合保水材料和N(NB1)、高复合保水材料和N(NB2)、低复合保水材料和P(PB1)、高复合保水材料和P(PB2)、低复合保水材料和NP(NPB1)、高复合保水材料和NP(NPB2),共12个处理,进行不同施肥和保水措施下土壤N_2O排放的差异比较。结果表明,N、P添加均显著增加土壤N_2O的累积排放量,NP添加与对照无差异。施加复合保水材料抑制土壤N_2O的排放,随着复合保水材料施用量的增加,土壤N_2O的排放显著降低,与对照相比,B1和B2处理N_2O减排50%以上。N添加条件下,与对照相比,添加复合保水材料NB1、NB2的N_2O累积排放显著降低。P与复合保水材料无交互作用。N、P和复合保水材料对土壤N_2O累积排放量具有显著作用,在NP同施时,与对照相比,添加复合保水材料NPB1、NPB2的N_2O累积排放分别降低了1.18%、30.69%。因此,高复合保水材料类型的施肥措施对减少油茶土壤N_2O排放具有重要意义,从而对缓解全球气候变化具有重要影响。     

紫薯淀粉对小麦淀粉凝胶特性的影响

以小麦淀粉和紫薯淀粉为材料，利用质构仪、核磁共振、动态流变仪和扫描电镜等分析了紫薯淀粉添加量（0～15%）对小麦淀粉凝胶特性的影响。结果表明：紫薯淀粉添加量在0～15%范围内，随着紫薯淀粉添加量的增加，小麦淀粉凝胶的弹性和内聚性显著增加(P < 0.05)，添加量为10%时，变化最明显。混合淀粉凝胶的弹性模量（G′）和粘性模量（G″）随着紫薯淀粉增加而增加，而损耗角正切值（tanδ）呈下降趋势且小于1，表明混合淀粉凝胶的固体性质增强。在冻融循环过程中，与纯小麦淀粉相比, 混合淀粉凝胶的脱水缩合率呈下降趋势，表明紫薯淀粉的添加使小麦淀粉凝胶强度增大，凝胶网络结构变致密，所以水分难以从淀粉凝胶网络结构中析出。低场核磁中的结果显示，紫薯淀粉的添加，使小麦淀粉凝胶中的一部分自由水转化为弱结合水，提高了混合凝胶的持水性；凝胶网络结构扫描结果显示，紫薯淀粉的添加使混合淀粉凝胶的孔洞分布均匀且孔洞变小。综合结果表明，紫薯淀粉可增强小麦淀粉凝胶的网络结构，改善小麦淀粉的凝胶特性。     

外源NO及反向调控PEG胁迫下苜蓿萌发种子抗氧化酶及其同工酶动态的研究

以紫花苜蓿为材料,用一氧化氮供体硝普钠(SNP)及一氧化氮清除剂c-PTIO对苜蓿种子进行浸种处理,采用分光光度法和同工酶电泳技术来研究外源NO及反向调控对PEG胁迫下紫花苜蓿抗氧化酶活性及其同工酶的影响,并探讨NO调控苜蓿种子耐旱性的生理机制。结果表明:PEG胁迫下外施0.1 mmol·L^-1 SNP,第6天时较PEG处理POD活性降低了32.72%;第4天时SOD、CAT活性较PEG处理升高了10.48%、23.60%,有效缓解了PEG对紫花苜蓿萌发中种子的氧化损伤,提高其抗氧化能力。PEG胁迫下添加 c-PTIO抑制了苜蓿萌发期的抗氧化系统活性。从同工酶的谱带数量和强弱来看,POD同工酶各区带活力均随PEG胁迫时间的延长而增加,在第2天酶带只有1条,而第4天酶带呈现9条;SOD和CAT同工酶表达量变化不显著,但酶带强弱有一定变化,S3酶带随处理时间的延长表达量逐渐减弱;CAT同工酶谱带则一直保持2条带,无明显强弱变化。因此,外源NO在PEG胁迫下紫花苜蓿萌发中抗氧化酶快速响应并在维护氧自由基代谢平衡中起重要保护作用。     

垂叶榕瘿花发育特性的初步研究

研究榕属植物瘿花发育特性是理解榕树/榕小蜂协同进化内在机制的重要内容。本文解析了垂叶榕隐头花序伴随瘿花发育的 5 个发育时期，采用同工酶电泳的方法比较了瘿花与正常雌花同工酶（包括过氧化物酶、过氧化氢酶、淀粉酶和酯酶）谱带的差异，采用扫描电镜对比了瘿花壁与授粉后雌花子房壁的差异。结果表明，瘿花被榕小蜂产卵以后，至少启动了一个与消除过氧化物有关的酶；而且，瘿花子房壁结构疏松，内含物小而少，雌花子房壁结构致密且内含物多而大，说明瘿花发育所消耗的营养物质大于正常雌花发育的消耗。研究结果支持造瘿生物汇集营养与植物防御行为的互利假说。     

干制羊肉基因组DNA不同提取方法的比较

为了研究干制加工羊肉基因组DNA的最佳提取方法,本试验采用传统酚-氯仿法、磁珠法、改良CTAB法、离心柱法分别提取干制处理后的羊肉基因组DNA,并对4种方法提取的羊肉基因组DNA浓度、纯度、完整性以及提取所需时间、PCR扩增效果等进行比较。结果表明,采用磁珠法提取DNA的效果更好,DNA浓度为118.87 ng·μL^-1,A₂₆₀/A₂₈₀值为1.89,而且此方法具有提取时间短、效率高、污染小等特点。本研究结果为干制加工羊肉基因组DNA的大批量提取和检测提供了参考依据。     

An improved method for extraction of sorghum polymeric protein complexes

A method for fractionating sorghum proteins using extraction solvents and techniques designed to obtain polymeric protein structures (especially disulfide linked) was developed. Extraction and separation conditions were optimized in terms of completeness of protein extraction, sample stability, and analytical resolution. After pre-extraction of albumins and globulins, a 3-step sequential procedure involving no reducing agents was applied to ground whole sorghum flour. The three fractions obtained represented proportionally different protein polymer contents and molecular weight distribution as evidenced by comparative size exclusion chromatography. Protein composition also varied among the extracts with differences in kafirin composition and non-kafirin proteins detected in the fractions by RP-HPLC and SDS-PAGE analysis. The ability to quantify and further characterize sorghum polymeric protein complexes will be useful for additional studies linking protein structures with functionality and digestibility and variations for these properties within diverse sorghum germplasm.     

Impact of ethanol,succinic acid,and the combination thereof at levels produced during sponge fermentation on hard wheat,soft wheat,and durum wheat farinograph rheology

The sponge and dough mixing process is one of the most common in the world, yet the mechanistic understanding of this process has yet to be sufficiently explored. In this study, aqueous solutions of ethanol, succinic acid, and their combination were prepared at concentrations intended to replicate fermentation times of 3, 4 and 6 h. These solutions were added to a farinograph mixer to make dough using hard wheat, soft wheat, and durum wheat flour. The results indicate that these yeast metabolites (ethanol, succinic acid) impact the mixing resistance, peak mixing value, and dough mixing stability in each of the flour types, likely primarily affected by the ratios of gliadin to glutenin and LMW glutenin in each flour type. Results suggest a stabilizing non-covalent interaction imparted by gliadin at peak mixing time, a stabilizing effect of HMW glutenin during break down, and synergistic effects of ethanol and succinic acid that leads to a faster rate of breakdown in later stages of mixing. It also suggests an increase in mixing resistance when acidulants are added to durum wheat dough. Taken together, this study adds new insights on the sponge and dough mixing process in a way that has not previously been conducted.