柞蚕肠液理化性质与饲料效率的相关性研究

对柞蚕肠液的理化性质与饲料效率的相关性进行研究的结果表明 :柞蚕肠液对促进蚕体抗病与消化吸收功能有着重要作用 ,平均每头蚕有肠液 1 76mL ,品种间开差为 0 78mL ,相对开差 5 7 80 % ,肠液量越多 ,饲料效率越高 ;柞蚕不同品种肠液pH平均值未发现明显差异 ,但强健好养饲料效率高的品种个体间开差小 ;柞蚕肠液缓冲力除与品种强健性有关外 ,还与品种的饲料效率呈正相关 ,在强健丰产与高饲料效率品种中 ,肠液恢复pH原值所需时间越短 ,饲料效率越高 ,电刺法取出肠液后 ,肠液恢复缓冲力所需时间是恢复其pH原值时间的 1 8倍多 ,同恢复肠液pH原值所需时间长短与品种强健性和饲料效率的关系完全一致。     

赖氨酸修饰对梯棱羊肚菌黑色素结构和理化特性的影响

为了进一步提高梯棱羊肚菌黑色素的提取率及溶解性,本试验采用单因素、Plackett-Burman试验、响应面试验对纤维素酶-超声波协同提取梯棱羊肚菌黑色素的提取工艺进行优化研究。通过赖氨酸修饰,并对修饰前后的梯棱羊肚菌黑色素进行结构表征、理化性质及稳定性研究。结果表明,在NaOH浓度为1.54 mol/L,纤维素酶添加量为20 mg/g,纤维素酶酶解时间为78.6 min,料液比为1:30,酶解温度为40 ℃,超声时间为80 min条件下提取的梯棱羊肚菌黑色素最优。未修饰的梯棱羊肚菌黑色素不溶于水,色价值为480.24,修饰后的黑色素溶解度为1 016 g/L,色价值为1 771.18,比未修饰的黑色素在溶解性、色价值方面均有所提高。此外,在不同的温度、光照、pH条件下,修饰前后的梯棱羊肚菌黑色素均比较稳定。以上研究结果为梯棱羊肚菌黑色素的高效提取及其产品的开发利用奠定了理论基础。     

多花黑麦草品种比较试验

通过对现行生产中常用的4个多花黑麦草品种在昆明地区的物候期、株高、草产量、生长率、净同化率等指标的规定表明,在生长初期,特高的生产性能比其余3个品种都好,但生长一段时间后,邦德的生产性能明显超过特高(P<0.05),抗锈王略高于特高(P>0.05),旺饲的生产性能最差(P<0.05)。因此,邦德是一个在生产中值得推广应用的品种。     

微塑料对双酚A在鲤鱼肠道中累积及生长生理的影响

探明微塑料（MPs）对双酚A （BPA）在鱼类肠道中累积特征及鱼类生长生理的影响,本研究以黄河鲤鱼为模型生物,分析了0.5 μm聚苯乙烯微塑料（PS-MPs）与BPA联合作用下鲤鱼肠道中微塑料及BPA的累积特征、鲤鱼生长及其抗氧化酶活性,以及它们之间的响应关系。结果表明：联合处理下鲤鱼肠道中的PS-MPs含量随时间呈线性增加,且随投加的微塑料浓度增加而增加,而PS-MPs累积速率随时间呈先增加后减小趋势,其中在BPA+PS（L）处理（1 mg·L^-1 BPA+20 μg·L^-1 PS-MPs）下,0.25 d时鲤鱼肠道中PS-MPs累积速率达到峰值（373.81 μg·g^-1·d^-1）,BPA+PS（H）处理（1 mg·L^-1 BPA+100 μg·L^-1 PS-MPs）下,则是在0.125 d达到最高（644.00 μg·g^-1·d^-1）。与单一BPA暴露相比,联合暴露下鲤鱼肠道中BPA累积量增加,与BPA （1 mg·L^-1 BPA）处理相比,BPA+PS （L）和BPA+PS （H）处理下鲤鱼肠道中BPA含量分别提高了6.13%和9.74%,BPA累积速率分别增加了190.01%、373.80%。相较于对照处理,BPA处理和MPs与BPA联合处理均引起鲤鱼肠组织中超氧化物歧化酶（SOD）活性、过氧化氢酶（CAT）活性、还原型谷胱甘肽（GSH）含量、丙二醛（MDA）含量增加,使体质量下降幅度减缓,其中BPA、BPA+PS （L）和BPA+PS （H）处理下鲤鱼体质量（21 d）较对照处理分别下降1.22%、3.90%、4.33%。当微塑料投加量达到100 μg·mL^-1时,联合处理会增加鲤鱼肠道中SOD活性、CAT活性和GSH含量,抑制MDA产生,从而缓解MPs和BPA联合作用对鲤鱼造成的氧化损伤,并且减缓鲤鱼体质量下降。研究表明,微塑料的存在会增加双酚A在鲤鱼肠道中的累积,且两者联合作用对鲤鱼产生了协同毒理效应,导致鲤鱼生长速率减缓,体质量下降。     

Bioactive Peptides from Algae: Traditional and Novel Generation Strategies,Structure-Function Relationships,and Bioinformatics as Predictive Tools for Bioactivity

Over the last decade, algae have been explored as alternative and sustainable protein sources for a balanced diet and more recently, as a potential source of algal-derived bioactive peptides with potential health benefits. This review will focus on the emerging processes for the generation and isolation of bioactive peptides or cryptides from algae, including: (1) pre-treatments of algae for the extraction of protein by physical and biochemical methods; and (2) methods for the generation of bioactive including enzymatic hydrolysis and other emerging methods. To date, the main biological properties of the peptides identified from algae, including anti-hypertensive, antioxidant and anti-proliferative/cytotoxic effects (for this review, anti-proliferative/cytotoxic will be referred to by the term anti-cancer), assayed in vitro and/or in vivo, will also be summarized emphasizing the structure–function relationship and mechanism of action of these peptides. Moreover, the use of in silico methods, such as quantitative structural activity relationships (QSAR) and molecular docking for the identification of specific peptides of bioactive interest from hydrolysates will be described in detail together with the main challenges and opportunities to exploit algae as a source of bioactive peptides.     

Metabolic Profiling and In Vitro Assessment of the Biological Activities of the Ethyl Acetate Extract of Penicillium chrysogenum “Endozoic of Cliona sp. Marine Sponge” from the Red Sea (Egypt)

Marine sponge-derived endozoic fungi have been gaining increasing importance as promising sources of numerous and unique bioactive compounds. This study investigates the phytochemical profile and biological activities of the ethyl acetate extract of Penicillium chrysogenum derived from Cliona sp. sponge. Thirty-six compounds were tentatively identified from P. chrysogenum ethyl acetate extract along with the kojic acid (KA) isolation. The UPLC-ESI-MS/MS positive ionization mode was used to analyze and identify the extract constituents while 1D and 2D NMR spectroscopy were used for kojic acid (KA) structure confirmation. The antimicrobial, antioxidant, and cytotoxic activities were assessed in vitro. Both the extract and kojic acid showed potent antibacterial activity against Staphylococcus aureus and Pseudomonas aeruginosa with MIC 250 ± 0.82 µg/mL. Interestingly, the extract showed strong antifungal activity against Candida albicans and Cryptococcus neoformans with MIC 93.75 ± 0.55 and 19.53 ± 0.48 µg/mL, respectively. Furthermore, KA showed the same potency against Fusarium oxysporum and Cryptococcus neoformans with MIC 39.06 ± 0.85 and 39.06 ± 0.98 µg/mL, respectively. Ultimately, KA showed strong antioxidant activity with IC₅₀ 33.7 ± 0.8 µg/mL. Moreover, the extract and KA showed strong cytotoxic activity against colon carcinoma (with IC₅₀ 22.6 ± 0.8 and 23.4 ± 1.4 µg/mL, respectively) and human larynx carcinoma (with equal IC₅₀ 30.8 ± 1.3 and ± 2.1 µg/mL, respectively), respectively. The current study represents the first insights into the phytochemical profile and biological properties of P. chrysoenum ethyl acetate extract, which could be a promising source of valuable secondary metabolites with potent biological potentials.     

外源阿魏酸抑制鲜切苹果褐变机制研究

苹果在鲜切过程中易因遭受机械损伤而引发褐变,严重影响其感官品质、风味和商品价值。采用不同浓度外源阿魏酸溶液对鲜切‘红富士’苹果进行浸泡处理,以研究其抑制鲜切苹果褐变的机制。结果表明：1、5、8、10 g/L 的阿魏酸浸泡处理均能有效抑制鲜切苹果褐变,10 g/L 阿魏酸浸泡处理10 min 对鲜切苹果褐变的抑制效果最优;10 g/L 阿魏酸处理显著提高了鲜切苹果超氧化物歧化酶（SOD）活性及1,1-二苯基-2-三硝基苯肼（DPPH）自由基、2,2-联氨-双-3-乙基苯并噻唑啉-6-磺酸（ABTS）阳离子自由基的清除率,抑制了贮藏后期多酚氧化酶（PPO）活性,降低了表儿茶素等单一酚的含量,提高了对香豆酸的含量;添加5 mg/mL 表儿茶素会促进苹果浆液褐变,而添加5、10、20、40 mg/mL 对香豆酸均能抑制苹果浆液褐变。综上所述,外源阿魏酸处理可通过提高SOD 活性、抗氧化能力、内源褐变抑制物含量以及降低褐变底物含量来减轻鲜切苹果褐变。     

黄芪多糖的超声波-闪式协同提取工艺优化及抗氧化活性研究

以黄芪为原料,采用超声波-闪式协同提取黄芪多糖。以黄芪多糖得率为评价指标,采用单因素试验和正交试验,确定最佳提取工艺。结果表明,超声波提取最佳工艺条件为：料液比1∶30（g/mL）,超声温度70 ℃,超声时间40 min,超声波功率500 W,在此条件下,黄芪多糖得率为7.11%;在对超声波提取工艺优化的基础上,协同闪式提取,最佳闪式提取工艺参数为：提取次数3 次,闪提时间100 s,提取电压160 V,在此条件下,黄芪多糖得率为11.03%;体外抗氧化活性试验结果表明：当黄芪多糖质量浓度为1.0 mg/mL 时,其对1,1-二苯基-2-三硝基苯肼（1,1-diphenyl-2-picrylhydrazyl,DPPH）自由基和2,2-联氨-双-3-乙基苯并噻唑啉-6-磺酸（2,2’-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid),ABTS）阳离子自由基的清除率分别为66.27%和58.27%。本研究获得了黄芪多糖的最佳提取方法,得到的黄芪多糖具有较强的抗氧化作用。该方法可为黄芪多糖的提取及开发应用提供参考。     

宁波苦丁有效成分提取方法的比较及其抗氧化活性的研究

采用水蒸气蒸馏法(SDE)、乙醇法(EE)、超声波法(UWE)、微波法(MAE)和超临界CO2萃取法(SCDE)提取宁波苦丁有效成分,得率分别为:0.048%、0.011%、0.631%、0.522%和0.935%,毛细管GC-MS法分别鉴定出10、9、12、9和20种成分,体外抗氧化活性测试均显示了抗氧化结果,活性强度依次为:超临界CO2萃取法＞超声波法＞水蒸气蒸馏法＞乙醇法＞微波法.