不同阶段猪用颗粒饲料物理性能的对比分析

对某饲料厂不同阶段猪用4种颗粒饲料的物理性能包括直径、长度、硬度、容重、含粉率和耐久性指数（Pellet Durability Index, PDI）等进行测定,对结果进行归类总结并采用统计学的方法参照有关标准进行分析。结果表明,4种颗粒饲料直径在2.87~3.94 mm之间,母猪料直径最大,小猪料最小,两两之间差异显著（P<0.05）,而且随着猪只年龄的增加,颗粒饲料的直径呈递增趋势。颗粒长度在8.62~11.94 mm之间,以大猪料最长,小猪料最短,长径比偏高。颗粒硬度在3.86~6.47 kg之间,以大猪料最大,小猪料最小,中小猪料显著低于大猪料和母猪料（P<0.05）,只有小猪料符合有关要求。颗粒容重在576.7~614.6 g/L之间,母猪料最大,小猪料最小,两两之间差异显著（P<0.05）,与直径呈相同的增减趋势。含粉率以小猪料最大,且只有小猪料与大猪料之间差异显著（P<0.05）。颗粒PDI以大猪料最大,小猪料最小,各阶段猪料的含粉率和PDI均符合有关要求。建议饲料厂家注重颗粒饲料物理性能指标的控制,调整饲料配方和工艺参数,不断改进颗粒饲料的质量。     

Expression of Anti-Lipopolysaccharide Factor Isoform 3 in Chlamydomonas reinhardtii Showing High Antimicrobial Activity

Antimicrobial peptides are a class of proteins with antibacterial functions. In this study, the anti-lipopolysaccharide factor isoform 3 gene (ALFPm3), encoding an antimicrobial peptide from Penaeus monodon with a super activity was expressed in Chlamydomonas reinhardtii, which would develop a microalga strain that can be used for the antimicrobial peptide production. To construct the expression cluster, namely pH2A-Pm3, the codon optimized ALFPm3 gene was fused with the ble reporter by 2A peptide and inserted into pH124 vector. The glass-bead method was performed to transform pH2A-Pm3 into C. reinhardtii CC-849. In addition to 8 μg/mL zeocin resistance selection, the C. reinhardtii transformants were further confirmed by genomic PCR and RT-PCR. Western blot analysis showed that the C. reinhardtii-derived ALFPm3 (cALFPm3) was successfully expressed in C. reinhardtii transformants and accounted for 0.35% of the total soluble protein (TSP). Furthermore, the results of antibacterial assay revealed that the cALFPm3 could significantly inhibit the growth of a variety of bacteria, including both Gram-negative bacteria and Gram-positive bacteria at a concentration of 0.77 μM. Especially, the inhibition could last longer than 24 h, which performed better than ampicillin. Hence, this study successfully developed a transgenic C. reinhardtii strain, which can produce the active ALFPm3 driven from P. monodon, providing a potential strategy to use C. reinhardtii as the cell factory to produce antimicrobial peptides.     

原木灵芝孢子粉和浸膏粉中的牛磺酸

采用热水提取－磺基水杨酸沉淀法进行样品的前处理，利用氨基酸自动分析仪测定供试样品的牛磺酸含量。试验结果表明，原木灵芝孢子粉和破壁孢子粉中牛磺酸含量分别为8．44mg/100g-9.23mg/100g和7．34mg/100g-7.89mg/100g，而灵芝浸膏粉中牛磺酸含量高达140．82mg/100g-157.38mg/100g.     

羔羊全营养代乳粉对羔羊增重影响的试验

为了研究羔羊出生后采取人工饲喂代乳粉溶液的效果，对10日龄羔羊称重，以平均日增重与母乳组比较，用t检验方法检验差异显著性。研究结果显示羔羊平均日增重试验组为0.097-0.126kg，母乳组为0.071-0.113kg，二者没有显著差异。在生产中，代乳粉能替代绵羊母乳饲喂羔羊，对多胎品系羊的推广应用以及解决绵羊缺乳、少乳或无乳问题具有重要意义。     

酮粉法检测泌乳牛尿酮乳酮的应用研究

荷斯坦泌乳牛尿、乳酮体的酮粉法定性试验表明：尿酮阳性率为29．25％，乳酮阳性率为10％。尿、乳阳性牛的血酮、血糖、乳酮、尿酮定量测定表明：酮粉法判定泌乳奶牛亚临床酮病，尿酮阳性反应具有早期、敏感、准确性低的特点。乳酮阳性反应具有准确、敏感性低、方便等特点。二者同时定性检测具有互补作用。     

纤维板表面粉末涂料的涂饰工艺

研究一种在纤维板表面进行粉末涂装再转移印花的新工艺.结果表明:纤维板粉末涂装基材预处理采用预热干燥,表面砂光,控制含水率为6%～8%;喷涂上粉量为333.33～388.89 g·m-2;固化条件为180 ℃,15～25 min.采用干燥箱中热转移方式,转移印花温度为(160±10)℃,时间15～20 min.按GB/T 4893-85和GB/T1733-79测试涂膜性能,涂膜附着力等级为2级,耐磨性等级为1级,耐水性合格,耐液性等级为1级.图1表4参9     

降低人造板热压机液压系统油液污染的探讨

车间粉尘与湖湿空气是人造板热压机液压系统油液外界污染的主要原因，通过构筑封闭式泵房，增设辅助油箱，改变没箱底部结构，设置排污，排水装置，可有效降低人造板热压机液压系统油液污染，改善液压系统性能，提高压机工作效率。     

Expression of a recombinant crustacean hyperglycemic hormone of the kuruma prawn Penaeus japonicus in methylotrophic yeast Pichia pastoris

ABSTRACT:   Until now, six crustacean hyperglycemic hormones (CHH) designated Pej-SGP-I, -II, -III, -V, -VI and -VII have been characterized in the kuruma prawn Penaeus japonicus . All CHH consist of 72 amino acid residues and have an amidated carboxyl (C)-terminus. In the present study, we expressed Pej-SGP-III in methylotrophic yeast Pichia pastoris in order to obtain a large quantity of recombinant CHH possessing biological activity. A cDNA encoding Pej-SGP-III that had been previously cloned was processed by polymerase chain reaction (PCR) and the resulting product was ligated into an expression vector. Pichia pastoris was transformed with this vector after which a recombinant Pej-SGP-III was expressed having an additional amino acid residue (glycine) at the C-terminus (rPej-SGP-III-Gly), a form considered to be a putative precursor of this hormone. rPej-SGP-III-Gly secreted into the culture medium was purified by reversed-phase HPLC, and amidated using a peptidylglycine alpha-amidating enzyme. The amidated rPej-SGP-III (rPej-SGP-III) showed hyperglycemic activity in in vivo bioassay almost comparable to that of the natural Pej-SGP-III. rPej-SGP-III thus obtained will be a useful tool not only for its physiological study but also for the determination of its 3-D structure.     

A review of antimicrobial peptides: defensins and related cationic peptides

Cationic antimicrobial peptides are present throughout the plant and animal kingdoms and bear striking structural and functional similarities across species lines. They provide primitive, nonspecific means of combating a variety of bacteria, fungi, enveloped viruses, and protozoa. Some are also cytotoxic against host cells, including neoplastic cells. Cationic antimicrobial peptides may play various roles in inflammation and tissue repair. Antimicrobial peptides are found in epithelial tissues regularly exposed to microbial attack as well as in cells whose primary function is defense against potential pathogens. They constitute an important part of the nonoxidative antimicrobial arsenal of leukocytes. They are preformed and/or readily synthesized when the cells are stimulated by exposure to pathogens. They exert their effects directly by inserting into membranes of target cells and forming ion channels which increase membrane permeability; however, antimicrobial peptides can also act as opsonins to facilitate phagocytosis. Resistance to defensins is a virulence factor for organisms such as Salmonella sp. The study of cationic antimicrobial peptides is increasing our understanding of innate immunity, inflammation, and the pathogenesis of genetic diseases such as specific granule disease in humans. Therapeutic applications of antimicrobial peptides are currently under investigation.     

Evaluation of a radioimmunoassay for type III procollagen peptide in the dog

Type III procollagen peptide (P-3-P) is a serum marker for hepatic fibrosis in humans. The utility of a commercially available radioimmunoassay for P-3-P was evaluated in the dog. The specificity of the assay was assessed by polyacrylamide gel electrophoresis (PAGE) of canine serum and purified bovine P-3-P, followed by Western immunoblotting with rabbit aniti-P-3-P serum. The sensitivity was assessed by performing the radioimmunoassay on dilutions of sera from 22 dogs. Polyacrylamide gel electrophoresis of purified bovine P-3-P and sera from two dogs suspected of having elevated P-3-P concentrations revealed no homologous bands of staining. Western immunoblotting showed marked cross-reactivity of the high antisera concentrations with several components of the serum proteins, but none corresponding to the purified P-3-P. All tested sera from dogs had minimal competitive binding with radiolabeled P-3-P in the radioimmunoassay. Dilution curves of dog sera did not parallel either the standard curve or the dilution curve of a known test human serum. There were no statistically different P-3-P concentrations in any of the groups of dogs studied. It was concluded that currently available radioimmunoassay kits for the measurement of P-3-P in the human are not applicable in the dog. Seemingly, the structure or metabolism of canine P-3-P may vary significantly from that of the bovine or human, limiting the sensitivity and specificity of this assay in the dog.