鳄鱼血蛋白酶解产物抗氧化特性和血管紧张素转化酶抑制活性研究

研究了鳄鱼血蛋白酶解产物的抗氧化特性和对血管紧张素转化酶（ ACE）的抑制活性。利用木瓜蛋白酶酶解鳄鱼血浆蛋白和血球蛋白,用分光光度法测定了酶解产物的抗氧化能力和用高效液相色谱（ HPLC）测定其ACE的抑制率。结果显示：鳄鱼血浆和血球蛋白酶解产物的亚铁离子螯合能力差异性不显著（ P＞0．05）;在0～5 mg/mL的浓度范围内,血球蛋白酶解产物清除ABTS自由基的能力大于血浆蛋白酶解产物,且在浓度为1 mg/mL时,两者清除ABTS自由基的能力差异性极显著（ P＜0．01）;血浆蛋白酶解产物清除DPPH自由基的能力在0～5 mg/mL的浓度范围内随着蛋白浓度的增加而升高,血球蛋白酶解产物在蛋白浓度为4 mg/mL处达到最大清除率,之后下降;在0～20 mg/mL的浓度范围内,两种酶解产物的还原力随着蛋白浓度的提高显著升高,但两者还原力的差异性不显著（ P＞0．05）;鳄鱼血浆和血球蛋白酶解产物对ACE具有良好的抑制力,其最大抑制率可分别达到75．56％和86．42％。研究表明,鳄鱼血蛋白酶解产物在体外具有抗氧化和抑制ACE的活性。     

热稳定脱脂米糠蛋白质碳水化合物酶-蛋白酶分步提取法酶的筛选和条件优化

热稳定脱脂米糠(HDRB)中蛋白质已严重变性,采用常规方法很难提取其中蛋白质。本研究其目的在于评价不同碳水化合物酶和蛋白质水解酶组合在HDRB蛋白质提取的作用,以及利用响应曲面方法优化蛋白质提取组合条件。结果发现使用果胶酶P-Ⅱ处理HDRB,继后对其残渣进行蛋白酶P处理,蛋白质提取率可达到80%。采用中心成分回归设计进一步对果胶酶P-Ⅱ、蛋白酶P、水糠比、温度、pH、提取时间进行RSM优化,最大蛋白质提取率可达到89%。本研究为合理利用米糠蛋白及利用米糠蛋白制备功能性短肽提供了可靠的方法。     

凝结芽孢杆菌对奥尼罗非鱼消化酶活性、消化率及生长性能的影响

在基础饲料中分别添加不同剂量的凝结芽孢杆菌(Ⅰ:1.0×1011cfu/kg饲料,Ⅱ:3.0×1011cfu/kg饲料,Ⅲ:6.0×1011cfu/kg),室外水族箱中饲养奥尼罗非鱼(Oreochromis niloticus×O.aureus)(34.50±0.25 g),用基础饲料投喂作为对照,每饲料组设三个重复,每水族箱随机放养16尾鱼,投喂率为3%。采用静水饲养以避免各箱之间水的交换。56 d后测定鱼体的生长和消化酶活性。结果显示:不同添加量的凝结芽孢杆菌均能显著提高奥尼罗非鱼胃、肝胰脏和肠道蛋白酶活性(P<0.05),但酶的活性随添加量的提高呈下降趋势。凝结芽孢杆菌的添加对胃、肝胰脏和肠道淀粉酶及脂肪酶活性没有显著影响(P>0.05)。Ⅰ组和Ⅱ组的干物质表观消化率、蛋白质消化率、相对增重率、饵料系数和蛋白质效率均显著高于对照组(P<0.05),而Ⅲ组和对照组之间差异不显著(P>0.05)。结果提示,饲料中添加1.0×1011cfu/kg饲料的凝结芽孢杆菌就能显著促进奥尼罗非鱼的生长和饲料营养物质的利用,满足最佳生长。     

淀粉共生蛋白对淀粉水解的影响

以小麦面粉为原料,研究了淀粉共生蛋白对淀粉酶解性质的影响。对洗淀粉过程中影响蛋白含量的条件进行了单因素试验,用SDS溶液和蛋白酶进一步除去淀粉中的蛋白质成分,然后对制得的含氮量不同的淀粉样品进行酶解。试验结果表明,蛋白酶能有效地去除淀粉共生蛋白,而淀粉共生蛋白有助于淀粉的水解。     

海带粒蜂蜜口服液的研制

以蜂蜜和海带为主要原料开发研制了一款口服液新产品.海带经过浸泡、清洗、切丝、熟化、打浆、打磨、过滤、调pH、酶解、灭酶、调配等工艺处理.通过正交试验得出酶解海带浆的最佳工艺参数为pH4.5、温度50℃、酶用量0.06％、酶解时间2h;通过评价正交试验样品,得出最佳配方为海带粒浆体50％、蜂蜜20％、海藻糖15％、柠檬酸0.2％、β-环糊精0.08％.     

秸秆覆盖对附子氮代谢几种相关酶活性的影响

以江油附子主栽品种为材料,采用随机区组设计,研究了稻草覆盖方式(整草覆盖、切割与粉碎覆盖)和数量对附子硝酸还原酶(NR)、谷草转氨酶(ALT/GOT)和谷丙转氨酶(AST/GPT)等几种氮代谢相关酶活性的影响.结果表明:各覆盖处理的酶活性水平均高于对照组,即秸秆覆盖处理均有效益；不同的秸秆覆盖量间差异性显著,覆盖量为1 kg/m的处理酶活性水平高于覆盖量为0.5 kg/m2和1.5 kg/m2的处理；虽然切割覆盖的酶活性水平高于整草覆盖和粉碎覆盖,但不同覆盖处理间差异性并不显著；切割覆盖1 kg/m2处理的NR、GOT和GPT酶活性水平虽均为最高,但整草覆盖1 kg/m更能够达到较高经济效益的栽培效果；3种酶之间存在较好的正相关性,具有一定的协同作用.     

球磨-酶解法制备纳米竹纤维的结构表征

采用机械球磨对竹纤维进行预处理,再经纤维素酶水解制备纳米竹纤维。通过光学显微镜(OM)、透射电子显微镜(TEM)、傅立叶红外光谱仪(FTIR)和X射线衍射仪(XRD)对竹纤维的形貌、组成、光谱学性能以及晶体特性进行了表征。实验结果表明:球磨法和酶解法在一定程度上都可以细化竹纤维;球磨预处理有助于竹纤维的酶解过程,且球磨-酶解法制备的纳米竹纤维粒径在100 nm左右;所制备的纳米竹纤维仍然保持竹纤维的基本化学结构,但球磨处理破坏了纤维素的结晶结构,其结晶度由64.15%降低到了38.55%。     

Relation of Japanese <Emphasis Type="Italic">Xanthomonas campestris</Emphasis> pv. <Emphasis Type="Italic">vesicatoria</Emphasis> with worldwide strains revealed with three specific monoclonal antibodies

Strains of Xanthomonas campestris pv. vesicatoria Dye 1978 (Xcv), the causal agent of bacterial spot, have been classified into two groups based on their ability to hydrolyze starch. Three monoclonal antibodies (MAbs), 7AH10, 5HB3, and 4AD2, were produced immunized against the living bacteria and were specific to and could distinguish Xcv strains able or unable to hydrolyze starch (Amy⁺ or Amy^–). The MAb 7AH10, obtained against strain UPB141(Amy^–) reacted in an enzyme-linked immunosorbent assay with all the Amy^– strains (n = 19) and 1 of 11 Amy⁺ strains. Against Xcv 2625, an Amy^– unusual phenotype strain, MAb 5HB3, recognized 97% of our worldwide collection of Xcvs (n = 30). Also against that strain, the MAb 4AD2 reacted with none of the homologous Amy^– phenotypes and with 90% (n = 11) of the heterologous Amy⁺ phenotypes. For all the MAbs, cross reactions with other pathovars or species were less than 4% (n = 67). By assaying a Japanese collection of strains against the three MAbs, the Amy⁺ strains were distinguished from the Amy^– strains, and their relation with other world strains could be demonstrated. All the MAbs reacted with the lipopolysaccharide fraction of the bacterial cell wall during immunoblotting.     

Computational chemistry study of the environmentally important acid-catalyzed hydrolysis of atrazine and related 2-chloro-s-triazines

Many chlorine-containing pesticides, for example 2-chloro-s-triazines, are of great concern both environmentally and toxicologically. As a result, ascertaining or predicting the fate and transport of these compounds in soils and water is of current interest. Transformation pathways for 2-chloro-s-triazines in the environment include dealkylation, dechlorination (hydrolysis), and ring cleavage. This study explored the feasibility of using computational chemistry, specifically the hybrid density functional theory method, B3LYP, to predict hydrolysis trends of atrazine (2-chloro-N4-ethyl-N6-isopropyl-1,3,5-triazine-2,4-diamine) and related 2-chloro-s-triazines to the corresponding 2-hydroxy-s-triazines. Gas-phase energetics are described on the basis of calculations performed at the B3LYP/6-311++G(d,p)//B3LYP/6-31G* level of theory. Calculated free energies of hydrolysis (delta h G298) are nearly the same for simazine (2-chloro-N4,N6-diethyl-1,3,5-triazine-2,4-diamine), atrazine, and propazine (2-chloro-N4,N6-di-isopropyl-1,3,5-triazine-2,4-diamine), suggesting that hydrolysis is not significantly affected by the side-chain amine-nitrogen alkyl substituents. High-energy barriers also suggest that the reactions are not likely to be observed in the gas phase. Aqueous solvation effects were examined by means of self-consistent reaction field methods (SCRF). Molecular structures were optimized at the B3LYP/6-31G* level using the Onsager model, and solvation energies were calculated at the B3LYP/6-311++G(d,p) level using the isodensity surface polarizable continuum model (IPCM). Although the extent of solvent stabilization was greater for cationic species than neutral ones, the full extent of solvation is underestimated, especially for the transition state structures. As a consequence, the calculated hydrolysis barrier for protonated atrazine is exaggerated compared with the experimentally determined one. Overall, the hydrolysis reactions follow a concerted nucleophilic aromatic substitution (SNAr) pathway.     

Purification and properties of β-galactosidase from Tilapia intestine: Digestive enzyme of Tilapia-X

ABSTRACT:   β-galactosidase of the intestine of Tilapia nilotica was purified by ammonium sulfate precipitation, followed by PAPTG-Sepharose 4B affinity chromatography, ethylenediamineetetraacetic acid ion-exchange chromatography, polyexchanger PBE 94 chromatofocusing, and Sephadex G-100 gel filtration. β-galactosidase was found to be a single band when examined by poly-acrylamide gel electrophoresis. The purifications of β-galactosidase were 27-fold from the crude extract. β-galactosidase showed optimum activity at pH 5.0 at 40°C, and was specifically found to be able to hydrolyze p -nitrophenyl β-galactopyranoside. It degrades galactan and agarose, and produces galactose. β-galactosidase was strongly inhibited by Hg²⁺ and PCMB. β-galactosidase is considered to be secreted by the upper and middle parts of the intestine and most of the activity was detected in the intestinal juice.