油菜素甾醇对沟叶结缕草长期培养愈伤组织生长和再生的影响

为了维持长期培养植物愈伤组组织的高再生率,以应用于体细胞无性系进行变异筛选.本研究以继代15年的沟叶结缕草[Zoysia matrella(L.)Merr.]胚性愈伤组织为材料,用不同浓度的表油菜素内酯(EBL)处理,研究油菜素甾醇(BR)对其生长和再生的影响,选出可提高长期离体培养愈伤组织生长及再生效率的最优EBL浓...     

Characterization of an Insoluble and Soluble Form of Melanin Produced by Streptomyces cavourensis SV 21, a Sea Cucumber Associated Bacterium

Melanin is a widely distributed and striking dark-colored pigment produced by countless living organisms. Although a wide range of bioactivities have been recognized, there are still major constraints in using melanin for biotechnological applications such as its fragmentary known chemical structure and its insolubility in inorganic and organic solvents. In this study, a bacterial culture of Streptomyces cavourensis SV 21 produced two distinct forms of melanin: (1) a particulate, insoluble form as well as (2) a rarely observed water-soluble form. The here presented novel, acid-free purification protocol of purified particulate melanin (PPM) and purified dissolved melanin (PDM) represents the basis for an in-depth comparison of their physicochemical and biological properties, which were compared to the traditional acid-based precipitation of melanin (AM) and to a synthetic melanin standard (SM). Our data show that the differences in solubility between PDM and PPM in aqueous solutions may be a result of different adjoining cation species, since the soluble PDM polymer is largely composed of Mg²⁺ ions and the insoluble PPM is dominated by Ca²⁺ ions. Furthermore, AM shared most properties with SM, which is likely attributed to a similar, acid-based production protocol. The here presented gentler approach of purifying melanin facilitates a new perspective of an intact form of soluble and insoluble melanin that is less chemical altered and thus closer to its original biological form.     

Isolation and Characterization of a Yellow Xanthophyll Pigment-Producing Marine Bacterium,Erythrobacter sp. SDW2 Strain,in Coastal Seawater

Xanthophylls, a yellow pigment belonging to the carotenoid family, have attracted much attention for industrial applications due to their versatile nature. We report the isolation of a homo xanthophyll pigment-producing marine bacterium, identified as the Erythrobacter sp. SDW2 strain, from coastal seawater. The isolated Erythrobacter sp. SDW2 strain can produce 263 ± 12.9 mg/L (89.7 ± 5.4 mg/g dry cell weight) of yellow xanthophyll pigment from 5 g/L of glucose. Moreover, the xanthophyll pigment produced by the SDW2 strain exhibits remarkable antioxidative activities, confirmed by the DPPH (73.4 ± 1.4%) and ABTS (84.9 ± 0.7%) assays. These results suggest that the yellow xanthophyll pigment-producing Erythrobacter sp. SDW2 strain could be a promising industrial microorganism for producing marine-derived bioactive compounds with potential for foods, cosmetics, and pharmaceuticals.     

耐镉阿氏芽孢杆菌缓解水稻受镉胁迫的研究

为了探究阿氏芽孢杆菌T61缓解水稻受镉胁迫的效应,运用96孔板法、电感耦合等离子体质谱法、比色法测定菌株T61的镉耐受性、镉去除率和植物促生性;利用绿色荧光蛋白标记的T61,观察菌株在水稻上的定殖;利用蘸根法施加T61菌剂,观察其降低水稻籽粒镉积累的效应。结果表明：菌株T61对Cd²⁺的最大耐受浓度达到500 μmol·L^-1;在含镉液体培养基中培养24 h后,菌株T61对Cd²⁺的去除率超过50%。菌株T61可以合成植物促生性物质吲哚乙酸（6.2 μg·mL^-1）和铁载体（46.6 μmol·L^-1）,并具有溶磷能力（37.1 μg·mL^-1）。菌株T61可以在水稻根和茎上定殖。大田条件下,T61菌剂可以降低营养期水稻茎叶丙二醛含量和抗氧化酶活性,并使水稻728B和NX1B籽粒中的镉含量分别降低13.5%和11.2%。研究表明,阿氏芽孢杆菌T61是一株具有植物促生性的耐镉细菌,可以缓解某些水稻品种遭受的镉胁迫,在镉污染稻田的微生物修复方面具有一定的应用前景。     

苜蓿根系构型及生理特性对干旱复水的响应

为了研究苜蓿根系构型及生理特性对干旱复水后的响应,对肇东苜蓿进行盆栽控水试验.设置正常供水(CK)、轻度干旱(LS)、中度干旱(MS)和重度干旱(SS)4个处理,在干旱处理4周后进行复水,研究各处理间根系构型及生理指标的差异.结果表明:干旱处理对根干重和根尖数有极显著影响(P<0.01),对比根长、根表面积、根体积和根...     

基于生物酶法的酰基化桑椹花青素的制备与特性

为尽可能减少花青素的降解,提高其稳定性,采用生物酶法,对桑椹花青素进行酰基化修饰,并与非酰基化花青素进行对比研究。运用单因素试验筛选脂肪酶、反应溶剂和酰基供体,分析对花青素酰基转化率的影响。确定酰基化反应的优化条件为南极假丝酵母脂肪酶为酰基化催化酶、吡啶为催化反应溶剂、苯甲酸甲酯为酰基供体,酰基化效果最好,转化率最大为13.5%。采用傅里叶红外、高效液相色谱对产物进行分析,经鉴定,酰基化产物为单酰基或多酰基花青素。此外,研究了酰基化对花青素稳定性和抗氧化性的影响。酰基化可提高花青素的热稳定性、光稳定性和耐酸碱稳定性。相同温度下,酰基化花青素保留率提高约5.0%,光照6d后,酰基化花青素的保留率仍高达96.1%。酰基化可以显著增加花青素体外抗氧化性,增强DPPH自由基清除能力,总还原能力比非酰基化花青素提高30%,金属离子螯合能力高达90%。酰基化花青素肿瘤细胞活性抑制率可达81%,而非酰基化花青素仅为50%。该研究为花青素稳定性提高和性能改善提供参考的理论依据。     

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。     

饲料溶菌酶添加水平对氨氮应激下吉富罗非鱼血清生化指标、抗菌性能和肝脏抗氧化能力的影响

为研究氨氮应激下溶菌酶对吉富罗非鱼血清生化指标、抗菌性能及肝脏抗氧化能力的影响,用6种不同溶菌酶添加水平(0、18、36、54、72和90 mg/kg)的饲料(分别记为L0、L18、L36、L54、L72和L90)饲喂初始均重为(11.35±0.08)g的罗非鱼60 d,之后应用氯化铵进行24 h氨氮应激实验。结果显示:1应激后,各组鱼的血清生化指标在组间存在较大差异(P0.05),不同溶菌酶添加水平下的鱼体对氨氮应激产生了不同的响应机制。L54组鱼主要通过激发免疫系统并调节蛋白质代谢来抵抗氨氮浓度突变;L72和L90组鱼主要通过调节高密度脂蛋白和低密度脂蛋白、胆固醇和甘油三酯之间的动态变化来缓解氨氮对机体的应激。2血清抗菌实验表明,L54和L72组鱼对大肠杆菌、金黄色葡萄球菌和嗜水气单胞菌的抑制能力最大,且显著高于对照组(P0.05);L36~L90组对溶藻弧菌的抑制作用显著高于对照组和L18组(P0.05);各溶菌酶添加组的鱼对枯草芽孢杆菌具有不同程度的保护作用。3应激后肝脏的超氧化物歧化酶、谷胱甘肽过氧化物酶和过氧化氢酶活性随溶菌酶添加水平的增加总体呈现先升后降的变化趋势,L54组显著高于对照组(P0.05);各添加组丙二醛含量均显著低于对照组(P0.05)。研究表明,54和72mg/kg溶菌酶添加水平对氨氮应激下吉富罗非鱼的血清生化指标、抗菌活性和肝脏抗氧化指标产生了最积极有效的调控,能够增强鱼体的抗应激能力。     

盐胁迫对雨生红球藻虾青素累积、虾青素合成相关酶基因表达和抗氧化指标的影响

为探讨盐胁迫对雨生红球藻(Haematococcus pluvialis)虾青素合成的影响与机理,以及雨生红球藻各抗氧化机制之间的关系,本研究采用生化和分子生物学方法研究了不同浓度(0.04 mol/L、0.08 mol/L、0.12 mol/L和0.16 mol/L)和不同时间(3 d、6 d和9 d)的盐(Na Cl)胁迫对雨生红球藻生长、虾青素积累、番茄红素β-环化酶(Lcy)、β-胡萝卜素羟化酶(Crt R-B)和β-胡萝卜素酮化酶(Bkt)基因表达、超氧化物歧化酶(SOD)、过氧化氢酶(CAT)和谷胱甘肽过氧化物酶(GSH-Px)的活性以及丙二醛(MDA)含量的影响。结果表明,各胁迫时间的雨生红球藻的密度均随着盐胁迫浓度的增加而不断下降,在盐胁迫的第9天,雨生红球藻的死亡率和孢子比例均随着盐胁迫浓度的增加而不断升高;雨生红球藻虾青素含量、Lcy、Crt R-B和Bkt基因表达量均随着盐胁迫浓度和时间的增加而不断提高;雨生红球藻SOD、CAT和GSH-Px活性以及MDA含量在不同浓度和不同时间的盐胁迫下与对照组(0.00 mol/L Na Cl)相比均升高,且在不同时间的0.12 mol/L Na Cl胁迫下与对照组相比均显著升高(P0.05);雨生红球藻虾青素含量、Lcy、Crt R-B和Bkt基因表达量在盐胁迫的早期(第3天)和中期(第6天)阶段较低,在盐胁迫的后期(第9天)阶段较高,而SOD、CAT和GSH-Px活性以及MDA含量在盐胁迫的早期和中期阶段较高,在盐胁迫的后期阶段较低。实验结果说明了适当浓度和时间的盐胁迫能促进雨生红球藻累积虾青素,雨生红球藻在盐胁迫下主要是通过提高虾青素合成相关酶基因的转录水平来促进虾青素的合成,其虾青素和抗氧化酶的抗氧化活性可能互为补充,共同保护雨生红球藻免受盐胁迫的氧化损伤。     

Changes in the Quality of Refined Fish Oil in an Accelerated Storage Study

ABSTRACT

The aim of this study was to prepare the refined oil derived from Sardinella longiceps by a step-wise procedure of degumming, bleaching, and deodorization. The refined sardine oil showed greater susceptibility toward oxidation than the crude oil, but the addition of ethyl acetate fractions of the red seaweeds Hypnea musciformis, Kappaphycus alvarezii, and Jania rubens with great antioxidant potential significantly increased the oxidative stability of the refined oil. The refined oil supplemented with the ethyl acetate fraction of these seaweeds indicated more noteworthy oxidative stability indices (≥ 0. 51 h) than α-tocopherol. The induction time was greater for refined oil added with H. musciformis (1.26 h) than butylated hydroxytoluene (1.04 h) and α-tocopherol (0.4 h). No traces of aromatic (δ 6.7–7.5 ppm), hydroperoxides, and aldehydes (δ 9–10 ppm) in the ¹H-NMR spectra of the refined oil supplemented with seaweed extracts at the baseline and after the accelerated storage study demonstrated that the seaweed extracts were able to prevent the formation of secondary oxidation products in the unsaturated system during storage. This study demonstrated the potential of seaweeds as natural alternatives to the synthetic antioxidants to prevent the rancidity of the refined fish for use in food and pharmaceutical industries.