非淀粉多糖酶对奥尼罗非鱼生长及抗菌力的影响

本文旨在研究非淀粉多糖酶对奥尼罗非鱼的生长及其抗菌力的影响。试验选用体重约60 g的奥尼罗非鱼(Oreochromis niloticus×O.aureus)560尾,随机分成4个处理组,每组7个重复,每重复20尾奥尼罗非鱼,分别投喂添加不同梯度的液体酶制剂(0、0.1、0.2和0.4 mL/kg的饲料)。结果表明:(1)非淀粉多糖酶对罗非鱼的特定生长率、饲料转化率等生产性能指标均有显著升高(P<0.05);(2)添加非淀粉多糖酶0.2 mL/kg和0.4 mL/kg显著提高了罗非鱼白细胞的吞噬活性(P<0.05)和血清的杀菌能力(P<0.01),试验组各组织溶菌酶活力也显著增加(P<0.05)。     

饲用复合酶对蛋用种鸡日粮磷的利用和生产性能的影响

本试验旨在研究低磷日粮添加复合酶制剂对蛋用种鸡磷的利用和生产性能的影响。选用972只24周龄罗曼褐父母代种鸡,分为3个处理,每处理6个重复,每重复54只种鸡。采用玉米-豆粕-杂粕型基础饲粮,正对照组含总磷0.55%,非植酸磷0.40%,不加酶;负对照组含总磷0.40%,非植酸磷0.21%,不加酶;试验组含总磷0.40%,非植酸磷0.21%,加酶制剂。试验期18周。结果表明:在低非植酸磷的日粮中添加复合酶,粪便中磷含量极显著低于正对照组(P<0.01);粪便中粗蛋白质含量显著低于正对照组和负对照组(P<0.05);显著改善蛋黃顔色(P<0.05);不影响生产性能、骨骼发育和蛋壳质量。添加200 g/t复合酶替代罗曼褐蛋用种鸡日粮中75%的磷酸氢钙能够降低饲料成本,提高养殖企业的经济效益,对罗曼褐蛋用种鸡生产性能无不利影响。     

A Novel Gelatinase from Marine Flocculibacter collagenilyticus SM1988: Characterization and Potential Application in Collagen Oligopeptide-Rich Hydrolysate Preparation

Although the S8 family in the MEROPS database contains many peptidases, only a few S8 peptidases have been applied in the preparation of bioactive oligopeptides. Bovine bone collagen is a good source for preparing collagen oligopeptides, but has been so far rarely applied in collagen peptide preparation. Here, we characterized a novel S8 gelatinase, Aa2_1884, from marine bacterium Flocculibacter collagenilyticus SM1988^T, and evaluated its potential application in the preparation of collagen oligopeptides from bovine bone collagen. Aa2_1884 is a multimodular S8 peptidase with a distinct domain architecture from other reported peptidases. The recombinant Aa2_1884 over-expressed in Escherichia coli showed high activity toward gelatin and denatured collagens, but no activity toward natural collagens, indicating that Aa2_1884 is a gelatinase. To evaluate the potential of Aa2_1884 in the preparation of collagen oligopeptides from bovine bone collagen, three enzymatic hydrolysis parameters, hydrolysis temperature, hydrolysis time and enzyme-substrate ratio (E/S), were optimized by single factor experiments, and the optimal hydrolysis conditions were determined to be reaction at 60 ℃ for 3 h with an E/S of 400 U/g. Under these conditions, the hydrolysis efficiency of bovine bone collagen by Aa2_1884 reached 95.3%. The resultant hydrolysate contained 97.8% peptides, in which peptides with a molecular weight lower than 1000 Da and 500 Da accounted for 55.1% and 39.5%, respectively, indicating that the hydrolysate was rich in oligopeptides. These results indicate that Aa2_1884 likely has a promising potential application in the preparation of collagen oligopeptide-rich hydrolysate from bovine bone collagen, which may provide a feasible way for the high-value utilization of bovine bone collagen.     

不同植物生长促进剂对香蕉假植大苗培育的调控作用

采用盆栽试验,在香蕉假植大苗培育过程中分别喷施浓度均为20 mg/L的赤霉素、复硝酚钠、胺鲜酯、α-萘乙酸钠等植物生长促进剂,以喷施清水为对照,通过不同处理假植大苗生长、物质累积及生理指标的分析,明确不同植物生长促进剂在香蕉假植大苗调控的作用。结果表明,本试验采用的4种植物生长促进剂对香蕉假植大苗培育的调控作用不同。与对照相比,叶面分别喷施20mg/L赤霉素、复硝酚钠均能有利于香蕉假植大苗假茎高及叶面积增加,提高叶绿素含量及叶绿素a、b含量,且以上两种植物生长促进剂平均提高叶绿素含量26.46%;喷施20mg/Lα-萘乙酸钠能提高假植苗假茎粗,提高干物质累积量16.11%积及吸氮量9.95%,促进氮磷钾养分吸收。叶面喷施赤霉素、复硝酚钠、α-萘乙酸钠和胺鲜酯均能显著提高香蕉假植大苗抗性,平均降低丙二醛含量14.64%、提高脯氨酸含量64.36%和SOD含量16.74%,且赤霉素还能显著提高POD含量82.13%。     

浙南山区杨梅大棚促早栽培技术研究

本研究选择‘东魁’杨梅为试验材料,以露地栽培为对照,研究大棚设施促早栽培对‘东魁’杨梅的物候期、产量、品质、效益的影响效应。经过3年的试验,通过对‘东魁’杨梅物候期的记载,产量、效益的统计,单果质量、可溶性固形物、总糖、总酸、钾含量、Vc含量等质量指标的检测,综合分析结果表明,东魁杨梅大棚栽培促早、提质、增效效果显著。本研究对优化和推广杨梅大棚促早栽培技术具有重要意义,对山区农民增收提供示范案例。     

山西谷子品种主要农艺性状的相关和主成分分析

为了明确山西谷子品种主要农艺性状间的关系,采用相关分析和主成分分析方法对11个山西谷子品种的10个农艺性状进行分析。结果表明：农艺性状的变异范围为1.94%~13.39%,各农艺性状的变异程度由大到小依次为单穗重、穗粒重、产量、穗长、株高、千粒重、出苗期—抽穗期天数、抽穗期—成熟期天数、出谷率、生育期。抽穗期—成熟期天数、单穗重、穗粒重、千粒重、出谷率等5个性状指标与产量呈正相关,其中,抽穗期—成熟期天数与产量呈显著正相关(P<0.05),出苗期—抽穗期天数与抽穗期—成熟期天数呈极显著负相关(P<0.01),出苗期—抽穗期天数与生育期呈极显著正相关(P<0.01)。在所有的主成分分析中,主要集中在前3个主成分,其累积贡献率达75.20%。在对高产品种综合性状评价和选育过程中,穗粒重是提高产量的关键,但同时也应注重对其他性状的综合考虑,注重选择单穗重偏高、株高偏低、生育期、穗长和出谷率适中的材料。     

江苏地区小麦赤霉病菌种群检测与抗药性分析

本研究旨在检测江苏地区小麦赤霉病菌的种群组成与对传统杀菌剂单剂的抗性严重度。以江苏溧阳、通州和盐城地区小麦赤霉病菌子囊孢子为试材,鉴定其优势种群,检测对多菌灵、戊唑醇和咪鲜胺的抗性。结果表明：江苏地区小麦赤霉病菌株中全部检测到亚细亚镰孢,是绝对优势种群;禾谷镰孢占比最高是溧阳地区的14%,最低是通州地区的8%,平均占比为11.33%,显著低于亚细亚镰孢占比;江苏地区小麦赤霉病菌对多菌灵的抗性频率介于26.3%~54.5%;未检测到戊唑醇和咪鲜胺具有抗性的赤霉菌株。综上,江苏地区小麦赤霉病菌优势种群是亚细亚镰孢,其对多菌灵单剂已产生严重抗性,未发现对戊唑醇和咪鲜胺产生抗性。     

棉花“保险+期货”模式助力南疆主产棉区脱贫攻坚

通过解析棉花“保险+期货”模式的运行机制、优势及存在的不足,并提出了发展优质棉“订单生产+保险+期货”模式和引入银行、基金等信贷机构的建议,期望对南疆主产棉区贫困棉农增收致富、助力脱贫攻坚提供有益探索。     

Identifying and Characterizing a Novel Peritrophic Matrix Protein (MdPM-17) Associated With Antibacterial Response From the Housefly,Musca domestica (Diptera: Muscidae)

Peritrophic matrix/membrane (PM) critically prevents the midgut of insects from external invasion by microbes. The proteins in the peritrophic membrane are its major structural components. Additionally, they determine the formation and function of this membrane. However, the role of PM proteins in immune regulation is unclear. Herein, we isolated a novel PM protein (MdPM-17) from Musca domestica larvae. Further, the function of MdPM-17 in regulating host innate immunity was identified. Results showed that the cDNA of MdPM-17 full is 635 bp in length. Moreover, it consists of a 477-bp open reading frame encoding 158 amino acid residues. These amino acid residues are composed of two Chitin-binding type-2 domain (ChtBD2) and 19 amino acids as a signal peptide. Moreover, tissue distribution analysis indicates that MdPM-17 was enriched expressed in midgut, and moderate levels in the fat body, foregut, and malpighian tubule. Notably, MdPM-17 recombinant protein showed high chitin-binding capacity, thus belongs to the Class III PM protein group. MdPM-17 protein silencing via RNA interference resulted in the expression of antimicrobial peptide (defensin, cecropins, and diptericin) genes, and this occurred after oral inoculation with exogenous microbes Escherichia coli (Enterobacteriales:Enterobacteriaceae), Staphylococcus aureus (Bacillales:Staphylococcaceae), and Candida albicans (Endomycetales:Saccharomycetaceae)). Therefore, all the antimicrobial peptide (AMP) gene expression levels are high in MdPM-17-depleted larvae during microbial infection compared to controls. Consequently, these findings indicate that MdPM-17 protein is associated with the antibacterial response from the housefly.