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。     

草莓果实的流变特牲及其在贮藏过程中的变化规律

利用自制的应力－应变试验台，对草莓果实的应力－应变特性和蠕变特性进行了测定与研究，建立了草莓果实应力－应变的数学模型，指出了草莓果实的极限屈服点变动范围。同时对草莓在不同贮藏条件下流变特性的变化规律进行了初步的研究，发现草莓的成熟度、贮藏温度及贮藏时间对果实的硬度、屈服应力均有较显著的影响，建立了屈服应力随时间变化的不同阶段的回归方程，可用于预测在相应贮藏条件下的草莓果实的屈服应力。     

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。     

铅胁迫对金丝草生长及生理生化的影响

采用土培方法,探究不同梯度铅胁迫(0、1000、2000和3000 mg·kg^-1)对金丝草生长形态、体内抗氧化系统和渗透调节物质的影响。结果表明:低浓度(1000 mg·kg^-1)处理会诱导金丝草叶片过氧化物酶(POD)活性、可溶性蛋白(SP)含量和根系抗超氧阴离子自由基活力(ASAFR)、可溶性糖(SS)及脯氨酸(Pro)含量增加,使得金丝草植株总抗氧化能力(T-AOC)处于较高水平,促进了金丝草株高、叶长和生物量的增加。随胁迫浓度增加,高浓度(2000~3000 mg·kg^-1)处理下,金丝草叶片和根系丙二醛(MDA)含量迅速增加,株高、叶长、叶面积和生物量下降,生长受到抑制。但金丝草通过增强叶片和根系POD、过氧化氢酶(CAT)活性来抵御过氧化作用,提高可溶性蛋白和可溶性糖含量维持细胞正常运作,增加根系生物量占比来加强根系发育,一定程度适应了高浓度铅胁迫。综上表明,金丝草主要通过叶片和根系不同抗氧化酶差异化响应、提高渗透调节物质含量,提升金丝草植株总抗氧化能力等途径来提高Pb耐性,对Pb污染矿区植物修复有较大潜力。     

山杏种皮黑色素的抗氧化活性

对山杏种皮黑色素的抗氧化活性进行评价.结果表明:山杏种皮黑色素可以显著抑制β-胡萝卜素的氧化褪色,其清除自由基活性具有量效性,清除羟自由基能力与2,6-二叔丁基对甲酚(BHT)无显著差异而高于抗坏血酸(VC),清除超氧阴离子能力超过BHT和VC.山杏种皮黑色素既可以作为氢供体,清除DPPH自由基,但清除能力低于BHT和VC,也可作为电子供体,其还原能力高于BHT和VC.     

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.