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1.
测定了水稻、玉米和狼尾草花粉在低温(4℃),低湿(RH45%),低温(4℃)高湿(RH90%),高温(35℃),低湿(RH45%)和高温(35℃),高湿(RH90%)4种贮藏条件下的蛋白酶活性,蛋白质含量,游离氨基酸含量的变化,结果表明:在低温高湿条件下,蛋白质降解和游离氨基酸含量上升慢;在高温条件下蛋白质降解快,游离氨基酸含量迅速上升。3种植物花粉中,水稻花粉蛋白酶活性强,在贮藏过程中蛋白质降解速率和游离氨基酸含量上升快:狼尾草花粉蛋白酶活性低,在贮藏过程中蛋白质降解速率和游离氨基酸含量上升慢;玉米花粉的蛋白酶活性、蛋白质降解速率和游离氨基酸含量上升速率居两者之间。  相似文献   

2.
芦笋茎叶游离氨基酸的提取及含量测定   总被引:4,自引:0,他引:4  
通过对芦笋茎叶游离氨基酸提取工艺中温度、提取时间、料液比、乙酸浓度等影响因素的试验分析,确定芦笋茎叶游离氨基酸测定过程中的最佳提取条件为:提取温度60℃;料液比为1:35;提取时间为2.5h;并对芦笋茎叶游离氨基酸含量进行了测定,确定芦笋茎叶游离氨基酸含量为76.54mg/100g。  相似文献   

3.
在浙江温岭沿海逐月采样,显微观察了可口革囊星虫体腔中卵细胞大小组成的周年变化。3—5月,卵径30~90μm的卵细胞占大部分。6月,卵径70~130μm的卵细胞占多数。7月,大部分卵细胞卵径达100μm以上,其中130~150μm的卵细胞约占1/3。8月,卵细胞卵径均在110μm以上,其中130~150μm的卵细胞约占2/3。9月,仍多数卵细胞卵径在110μm以上,130~150μm的卵细胞约占1/3。10月,以110~140μm的卵细胞占多,40μm以下的卵细胞较少,大卵细胞开始退化。11月至翌年2月,随着大型卵细胞的逐渐退化,小型及中型卵细胞逐渐增多,2月仍可见少量未退化的大型卵细胞。分析认为,可口革囊星虫在浙江温岭的繁殖期主要在7—9月。  相似文献   

4.
本实验以灵芝、金耳以及冬虫夏草作为发酵菌种,选用豆浆为基本原料配制培养基,在发酵过程中定时取样并测定其中几种生物活性物质的含量,分析各生物活性物质在发酵过程中的变化。研究结果表明,三种食用真菌发酵豆浆的发酵液中总游离型大豆异黄酮含量在发酵过程中均缓慢上升并分别在发酵72 h、24 h和36 h达到最高,与发酵初期相比分别增加了31.81μg/m L、19.05μg/m L和15.71μg/m L;三种食用真菌发酵液中蛋白质含量随着发酵时间的推移而降低的同时氨基酸含量均有增加,且发酵液中的肽主要是分子量范围在300 Da~1 500 Da之间的具有较高生物活性的小分子肽,发酵液中的必需氨基酸含量以及占总氨基酸含量的比值均有增加。本实验探究了食用真菌发酵豆浆过程中生物活性物质的变化,为日后的富集游离型大豆异黄酮、多肽以及氨基酸等生物活性物质实验提供依据,并为工业化生产提供实践基础。  相似文献   

5.
游离氨基酸是烟叶中的重要化合物,它很大程度上影响着烟叶的品质和风味。为了解不同生长温度对烟叶中游离氨基酸的含量及其代谢的影响,通过人工气候室设置均温18.5℃、23.5℃和28.5℃3个动态气温条件,在烟叶从早期生长至成熟的整个时期进行不同生长温度处理,用分光光度法、气相色谱-质谱法和荧光定量PCR分析,研究了不同生长温度下总游离氨基酸含量和单个游离氨基酸含量的变化规律及对脯氨酸和苯丙氨酸代谢的影响。结果表明,不同生长温度对烟叶生长发育过程中游离氨基酸总量和单一游离氨基酸含量有明显影响。其中,随着烟叶生长发育的进行,所含游离氨基酸含量逐渐下降。在不同生长温度处理下,随生长温度升高总游离氨基酸含量下降;各游离氨基酸含量基本上也随生长温度的升高而降低。对脯氨酸代谢相关酶(P5CS,OAT,ProDH)活性以及苯丙氨酸代谢相关酶(PAL,C4H)活性及其基因表达的定量研究表明,其酶活性和基因表达的变化与含量变化的趋势一致。上述研究结果表明,随着烟叶的生长发育和成熟,其游离氨基酸含量逐渐降低,而较低的生长温度有利于烟叶维持较高的游离氨基酸水平。  相似文献   

6.
采用生物化学方法测定和分析了河川沙塘鳢(Odontobutis potamophila)胚胎、仔鱼发育过程中蛋白质含量及氨基酸的组成和含量。结果显示,从受精卵开始到孵出后8 d饥饿仔鱼的整个胚胎和仔鱼发育过程中,其总蛋白和总氨基酸含量均呈下降趋势;总的必需氨基酸含量和总的非必需氨基酸含量也一样都呈现出下降趋势;平均含量最高的氨基酸是亮氨酸Leu、赖氨酸Lys、谷氨酸Glu和天冬氨酸Asp。与总氨基酸库相反,游离氨基酸库却呈现出随着发育的进行而不断增长的趋势,这种增长趋势也反映在游离的必需氨基酸和游离的非必需氨基酸含量的变化上,并且平均含量最高的游离氨基酸是赖氨酸Lys、亮氨酸Leu、脯氨酸Pro和谷氨酸Glu。整个发育过程中,游离氨基酸的含量仅占总氨基酸库的很小一部分(在受精卵,仅占0.16%)。由于总蛋白和总氨基酸含量在发育过程中均呈下降趋势,而游离氨基酸含量呈增长趋势,由此可知,在整个胚胎发生过程中,其卵黄蛋白的水解速度大于胚体同化和异化作用对氨基酸的消耗速度。  相似文献   

7.
土鳖虫体内富含蛋白质和氨基酸,是一种重要的药用昆虫。高温对昆虫生命活动产生重要影响。为探明短时高温胁迫对土鳖虫体内蛋白质和氨基酸含量的影响,本试验以中华地鳖Eupolyphaga sinensis Walker 8龄雌若虫为研究对象,通过人工设置29℃、33℃、37℃为高温处理组,以25℃为对照,测定2 h短时高温胁迫对中华地鳖存活率以及体内蛋白质和氨基酸含量的影响。结果表明:29℃、33℃和37℃短时高温处理对中华地鳖存活率无影响,蛋白质含量分别为76.57%±3.29%、79.60%±0.92%、77.00%±0.71%,与对照(84.50%±1.57%)相比均明显下降;短时高温处理后,29℃处理组土鳖虫总氨基酸含量为206.97±7.42 mg/g,6种人体必需的游离氨基酸苏氨酸8.23±0.32 mg/g,甲硫氨酸3.98±0.49 mg/g,异亮氨酸8.27±0.35 mg/g,亮氨酸16.38±0.86 mg/g,苯丙氨酸8.34±0.40 mg/g,以及赖氨酸12.56±0.64 mg/g的含量较对照和33℃、37℃高温处理组均显著升高,表明29℃短时高温处理可显著提高中华地鳖体内人体必需游离氨基酸含量。本研究是国内外对高温胁迫下药用昆虫体内活性成分的首次报道,研究结果将为进一步明确高温对土鳖虫的药用价值的影响,以及为土鳖虫人工养殖条件提供理论依据。  相似文献   

8.
萌发绿豆子叶自然衰老过程中可溶性蛋白质含量一直下降;从衰老开始到衰老前期,总游离氨基酸含量明显上升;但游离氨基酸各组分在子叶衰老期间的变化趋势并不相同。~3H-亮氨酸掺入蛋白质试验和多聚核糖体的相对量及其与总核糖体的比值(P/T)测定都证明在子叶衰老前期有蛋白质的新合成。子叶衰老期间。氨肽酶活性明显降低;而以酪蛋白为底物的蛋白水解酶活性却急剧上升,承担着催化蛋白质降解的主要功能。  相似文献   

9.
缩节胺对棉蚜体内能源物质的影响   总被引:1,自引:0,他引:1  
为探究缩节胺对棉蚜体内能源物质的影响,以室内繁殖棉蚜为试材,采用生化酶学方法,测定了缩节胺对棉蚜代谢过程中主要能源物质脂类、蛋白质、总糖、游离氨基酸含量。结果表明:15 mg/L、25 mg/L、35 mg/L、50 mg/L缩节胺处理下的棉蚜体内三油酸甘油酯含量均比对照组低,且处理初期随缩节胺浓度增大,甘油酯含量逐渐下降;总糖、游离氨基酸及蛋白质含量均比对照组高,游离氨基酸含量变化趋势与蛋白质含量变化趋势相似。表明棉蚜受到缩节胺胁迫初期时,棉蚜以消耗体内脂肪能源物质来应对缩节胺对自身的胁迫作用,与此同时,棉蚜体内糖类、游离氨基酸、蛋白质能源物质开始积累,以维持棉蚜正常的生命活动。  相似文献   

10.
氨基酸是海洋有机质尤其是有机氮的重要组分,其地球化学行为活跃,在海洋有机质生物地球化学循环过程中起着重要作用.氨基酸的含量、组成和分布等信息可有效指示有机质的降解状态.本研究系统总结了海洋颗粒物/沉积物中氨基酸的分布特征及影响因素,以及氨基酸对有机质降解程度的指示作用.海洋颗粒物/沉积物氨基酸的主要成分为甘氨酸(Gly)、谷氨酸(Glu)、丙氨酸(Ala)和天冬氨酸(Asp),其含量从近岸到大洋逐渐降低,并随深度增加呈下降趋势组.氨基酸的碳、氮归一化产率()越低,表明有机质%AA-C/TOC,%AA-N/TN)以及基于氨基酸成的降解因子(DI的降解程度越高.基于非蛋白质氨基酸以及)D型氨基酸含量与组成的活性因子(RI)和D型氨基酸与L型氨基酸比值(D/L等指标可以根据细菌对氨基酸的转化作用来指示有机质的降解程度,其中RI值越接近于0,D/L值越高,蛋白质与非蛋白质氨基酸的比值的高Asp/β-Ala和Glu/γ-Aba(氨基丁酸)越小,均表明有机质受到微生物降解和转化程度越.颗粒物/沉积物中氨基酸的迁移转化过程主要受到溶解氧、营养盐水平、有机质来源、沉积环境以及微生物转化等因素的影响.今后应加强颗粒物和沉积物之间的协同效应以及微生物对氨基酸的影响与具体调控机理研究.  相似文献   

11.
A gas chromatographic method for the separation and quantitation of the 20 protein amino acids is described using N-methyl-N(tert.-butyldimethylsilyl)trifluoroacetamide, with 1% tert.-butyldimethylchlorosilane as catalyst, to prepare the tert.-butyldimethylsilyl amino acid derivatives. Alkylsilylation of amino acids proceeds at 140 degrees C in 20 min. The derivatives formed in the one-step reaction are used directly for gas-liquid chromatographic analysis, using a flame-ionization detector, without prior isolation or purification. Complete separation and quantitation of all protein amino acids are readily achieved using a 15-m DB-5 capillary column. Strict linearity extends from less than 15 to about 100 ng for all amino acids except Arg, which has a linear range from 50 to 300 ng. The limits of detection, however, range from one to several hundred nanograms. The method was used to analyze the free amino acid pool in carnation petals.  相似文献   

12.
微波高压罐水解法在氨基酸分析中的应用简报   总被引:1,自引:0,他引:1  
本文报导了采用微波高压罐水解技术快速水解食物蛋白质,并测定其17种氨基酸含量的方法。研制的高压罐具有密闭性、微波穿透性好,耐热、耐压、耐腐蚀等特点。采用该高压罐研究了微波强度及作用时间等条件对氨基酸稳定性的影响,在微波输出功率100W35~45分钟水解了3份食品样品,其氨基酸含量测定结果与传统的110℃22左水解基本相符,17种氨基酸5次平行测定结果CV值均<10%。  相似文献   

13.
Chitosan (Chi), a protein recovery agent for the treatment of aqueous food processing streams, appears to work by mechanical entrapment and electrostatic interaction of chitosan amino groups with anionic groups on proteins. Chitosan effectiveness for recovering soluble proteins from surimi wash water (SWW) is increased by complexation with alginate (Alg) and by adjusting complex concentration and treatment time. Flocculation at 20 degrees C with Chi-Alg at a 0.2 mixing ratio added as 20, 40, 100 and 150 mg/L SWW was aided by 5 min agitation at 130 rpm and then held at the same temperature for 30 min, 1 and 24 h. Turbidity measurements, protein determinations and qualitative FTIR analysis confirmed SWW protein adsorption which depended on Chi-Alg concentration and reaction time while turbidity reduction was affected by concentration only. No differences (p < 0.05) in protein adsorption were found between 1 and 24 h. Using 100 mg Chi-Alg complex/L SWW for 1 h achieved 83% protein adsorption and 97% turbidity reduction.  相似文献   

14.
The effect of heating conditions on the crust color formation was investigated during the baking of white bread. The surface temperatures were monitored with thermocouples attached to the inside surface of the loaf pan cover. The trace of the surface color in the L(*)a(*)b(*) color coordinate system is defined as the characteristic coloring curve. The overall baking process was classified into the following four stages based on the characteristic coloring curve: i) pre-heating (surface temperature < 110 °C), ii) Maillard reaction (110-150 °C), iii) caramelization (150-200 °C), and iv) over-baking (surface temperature>200 °C). A linear relationship was observed between the L(*) decrease and the increase in weight loss of a sample at each oven air temperature. The L(*) value appeared to be suitable as an indicator to control the surface color by baking conditions.  相似文献   

15.
The effects of low temperature (5 °C and 12°C) and droughttreatments on leaf soluble protein content and free amino acidcontent have been investigated in four species, which were rankedaccording to chilling-sensitivity: pea (chill-resistant), mungbean (highly chill-sensitive), and tomato and french bean (intermediatechilling-sensitivity). Drought treatment caused a 30–40% decrease in proteinlevels, and in all but the mung bean, a 100–200% increasein free amino acid concentration. Four days chilling at 5°C,85% r.h. caused leaf water content to decrease by almost 50%in the mung bean, but by only approximately 6–7% in theother three species. During this treatment the leaf solubleprotein content decreased in all four species although the decreasewas greatest and most rapid in the mung bean, commencing with8 h of chilling (coinciding closely with the onset of waterloss), and decreasing by over 80% after 4 d. In the chill-sensitivespecies (but not in the pea) the decrease in protein contentwas accompanied by an increase in free amino acid content. However,on a mgg–1 dry wt. basis, this increase was insufficientto account for all the protein lost. When plants of each specieswere chilled at 5°C, 100% r.h., water loss was greatly reducedor prevented and there was no significant decrease in leaf solubleprotein. It is concluded that the protein decrease which occurredat 5°C, 85% r.h., was a response to water loss and not thedirect result of low temperature. However, chilling at 100%r.h. did cause an increase in free amino acid content of thechill-sensitive species, suggesting that this was a direct responseto low temperature. Although drought treatment caused a 6–20 fold increasein free proline content in the leaves of the four species examined,chilling (5°C) and chill-hardening (12°C) caused littlechange in free proline content, indicating that the accumulationof this ‘protective’ amino acid is unlikely to contributeto the effectiveness of the chill-hardening treatment. Key words: Low Temperature, Drought, Leaf soluble protein.content, Amino acids  相似文献   

16.
在纯乙酸溶剂中,以乙酸酐酰化消旋酪氨酸,消旋温度为90℃,L-酪氨酸和乙酸酐的摩尔比为12,每消旋1gL-酪氨酸时,溶剂乙酸的用量为5mL,效果较好。同样的方法应用于L-脯氨酸,L-苏氨酸,L-缬氨酸,L-赖氨酸,L-半胱氨酸等氨基酸,消旋率均可达到100%。  相似文献   

17.
从双胸蚓组织中分离出水解胶原的酶(Ⅰ、Ⅱ、Ⅲ)。其中酶Ⅱ是一不具亚基结构的大分子糖蛋白,酸性氨基酸含量高于碱性氨基酸,缺乏胱氨酸。最适pH6~7,最适温度35~45℃,80℃10分钟酶失活。Ca~(++)、Mg~(++)、Ba~(++)、Mn~(++)促进酶活性,Co~(++)、Hg~(++)、EDTA、巯基化合物及正常人血浆抑制酶活性。胶原酶解产物在PAGE图谱上表现为泳动较快的新带。  相似文献   

18.
【目的】分析低温驯化后水椰八角铁甲Octodonta nipae体内各种生理活性物质含量的变化,为揭示水椰八角铁甲耐寒机制提供理论基础。【方法】以25℃处理为对照,将水椰八角铁甲各虫态于12.5, 15, 17.5和20℃驯化处理10 d后,比较其体内的游离水、蛋白质、氨基酸、粗脂肪、甘油和可溶性糖原等生理活性物质含量的变化。【结果】低温驯化显著影响铁甲体内上述物质的含量水平。低温驯化能提高该铁甲体内甘油和游离氨基酸的含量,降低游离水、蛋白质、粗脂肪、可溶性糖原的含量。与对照相比,12.5℃驯化对该铁甲各虫态体内游离水含量存在显著影响(P<0.01);经12.5, 15, 17.5和20.0℃驯化后,该铁甲各虫态体内蛋白质、粗脂肪含量与对照相比均存在显著差异(P<0.01);经125,150和175℃驯化后,该铁甲各虫态体内游离氨基酸含量与对照存在显著差异(P<0.01);经12.5,15.0,17.5和20℃驯化后,该铁甲各虫态(2龄幼虫除外)体内甘油含量与对照相比存在显著差异(P<0.01);12.5, 15.0, 17.5和20℃驯化对除2龄幼虫、蛹和成虫外的铁甲其他各虫态体内可溶性糖原含量存在显著影响。经15.0℃驯化处理后铁甲各虫态体内平均甘油含量最高,比对照25℃的平均甘油含量高出约9.4倍,而经12.5℃驯化处理的虫体内的平均甘油含量仅增加3.5倍。【结论】低温驯化对水椰八角铁甲体内相关生理活性物质含量的影响效能是有限的;水椰八角铁甲可以根据不良的环境条件调节最佳的生理状况,以适应未来的环境和达到最强的适应性。  相似文献   

19.
In order to probe the structural and functional properties of a central region of apolipoprotein A-I (apoA-I), we engineered mutants of the mature form of the protein and expressed them using the baculovirus/insect cell expression system. The mutations which targeted the region of apoA-I between amino acids 140 and 150 included: (i) deletion of the region 140-150 (apoA-I(Delta140-150)); (ii) substitution of arginine 149 with valine (apoA-I(R149V)); (iii) substitution of proline 143 with alanine (apoA-I(P143A)); (iv) deletion of region 63-73 (apoA-I(Delta63-73)), which has structural properties similar to 140-150; and (v) a chimeric protein substituting amino acids 140-150 with amino acids 63-73 (apoA-I(140-150 --> 63-73)). The efficiencies of synthesis were vastly different for the various mutants as follows: apoA-I(R149V) > apoA-I(140-150 --> 63-73) > apoA-I(Delta63-73) > apoA-I(P143A) > apoA-I > apoA-I(Delta140-150). About 50% of the synthesized wild type and all apoA-I mutants was retained in the cells. During expression of apoA-I(R149V) an unusual spontaneous recombination occurred. In addition to the expected mutant, another form of apoA-I with an apparent M(r) of 36K was produced which consisted of a duplication of the amino-terminal end of apoA-I, from the prepeptide through to amino acid 62, linked to the original pre-apoA-I(R149V) sequence via a 4-amino-acid linker. Despite the fact that this form of apoA-I carries two prepeptides and consequently two cleavage sites, there was little, if any, cleavage at the internal cleavage site. During expression, less than 20% of this mutant was retained in the cells. These results demonstrate that at least in the model of insect cells, the efficiency of apoA-I synthesis, processing, and secretion depends on apoA-I secondary structure and/or folding.  相似文献   

20.
黄连ISSR反应条件优化的研究   总被引:12,自引:2,他引:10  
以黄连(味连,Coptis Chinensis Franch.)基因组DNA为模板,通过单因子、双因子实验研究了ISSR反应体系中主要成分(Mg2+、dNTP、引物、模板、Taq DNA聚合酶)以及热循环参数(退火温度、循环数、变性时间、退火时间、延伸时间)对扩增结果的影响,并找出各自的最适条件,建立了适合黄连ISSR分析的反应体系和扩增程序,即在25μL反应体系中,内含1×PCR buffer、1.5mmol·L-1 Mg2+、200μmol·L-1 dNTP、0.3 μmol·L-1引物、40 ng模板、1 U TaqDNA聚合酶。扩增程序为94℃预变性5 min,然后进行35个循环:94℃变性30 s,(据不同引物的退火温度)复性1 min,72℃延伸1.5 min,循环结束后72℃延伸7 min,-4℃保存。这一优化系统的建立为今后利用ISSR标记技术进行黄连鉴定及种质遗传多样性分析提供了一个标准化程序。  相似文献   

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