Effect of sodium nitrite and sodium chloride on growth of lactic acid bacteria.

The effect of NaNO2 and NaCl on the growth of 24 lactic acid bacteria strains isolated from vacuum-packed cooked ring sausages were examined by analyzing different growth parameters with Bioscreen. NaNO2 had a very limited effect on the growth of lactic acid bacteria at 50 and 100 mg/l but at 400 mg/l a more pronounced inhibitory effect was found. Bacterial growth was enhanced by 1-2% (w/v) of added NaCl, while NaCl concentrations above 3% (w/v) had a clear inhibitory effect. Leuconostoc isolates seemed to be more sensitive to sodium nitrite and sodium chloride than homofermentative lactobacilli strains. Among homofermentative lactobacilli, the strains resembling Lactobacillus curvatus were more sensitive to NaCl than those resembling Lactobacillus sake.     

白跗平腹小蜂对主要森林害虫抑制力研究

１９８７～１９９２年连续６年研究结果表明，白跗平腹小蜂Ａｎａｓｔａｔｕｓａｌｂｉｔａｒｓｉｓ对马尾松毛虫Ｄｅｎｄｒｏｌｉｍｕｓｐｕｎｃｔａｔｕｓ、柳杉毛虫Ｄｅｎｄｒｏｌｉｍｕｓｌａｔｉｐｅｎｎｉｓ、水青蛾Ａｃｔｉａｓｓｅｔｅｎｅｎｉｎｇｐｏａｎａ等１３种主要森林害虫卵有较明显的抑制作用。在林间，该蜂对马尾松毛虫第１、２代卵的自然抑制力分别力１６．５５％和２２．２９％，对柳杉毛虫越冬代卵的自然抑制力为２３．４５％；对水青蛾第１、２代卵的抑制力分别力５．４９％和２．６３％；在林间，人为释放白跗平腹小蜂对第１代马尾松毛虫卵的校正抑制力为３３．５％，在室内１２．３～２８℃范围内，每头雌峰对马尾松毛虫、水青蛾和柞蚕剖腹卵的日破坏数（寄生数）分别力１５、１８和２６粒，一生破坏数分别为５６、９１和２０８粒。即使虫卵即将孵化，该峰同样亦能寄生，并羽化出正常的子代白跗平腹小蜂。     

退化草地土壤生化活性研究

通过对三种不同退化程度的退化草地土壤生化活性进行测定和相关性分析，结果表明草地退化后其土壤生化活性受到不同程度的影响，表现为土壤生化活性随着退化程度增高而减小，但差异并非都达到统计学上的显著性，而土壤生化活性间的相关性则显著地与草地退化程度有关，说明退化草地土壤微生物间的协调作用受到显著影响，从而影响土壤氮素和碳素代谢途径。     

蜂胶高生物活性黄酮组分的研究

本文探讨了蜂胶总黄酮中最具活性的黄酮类物质的提取分离、官能结构特征与功能关系、可能的功效,进而提出了如何看待蜂胶总黄酮含量高低的问题.     

银杏幼苗叶片转化酶活性及其动力学

采用波钦诺克XH法研究了田间和室内栽培的银杏幼苗叶片转化酶的活性及其动力学性质。结果表明:银杏幼苗叶片转化酶在pH值5.0、温度55℃时活性最强;该酶的米氏常数为3.7×10-2mol·L-1;室内盆栽的银杏幼苗叶片转化酶的活性显著高于田间栽培的同龄银杏幼苗叶片转化酶的活性。     

植物化学生态学中的克生作用在草业上的表现

为了解植物生化他感作用在草业（田间杂草）中的作用，１９８６－１９８８年通过查阅资料并对我国大部分牧区和农区实地考察，证明，在植间广泛存在着因植物次生代谢产物对微生态环境的改变所引起的植物种内和种间生长发育相互促进和抑制的生化他感作用，其中植物间的克生作用（抑制作用）表现的较为明显，而这种作用与草原退化和农田杂草的蔓延有着密切关系。     

In vitro expression and inhibition of procoagulant activity produced by bovine alveolar macrophages and peripheral blood cells

Local and systemic activation of coagulation is frequently associated with bacterial sepsis. The coagulopathy is due, at least in part, to expression of tissue factor (TF) by monocytes and macrophages. The purpose of this study was to evaluate the expression of procoagulant activity by bovine alveolar macrophages, leukocytes and platelets, and to determine the relative potency of three chemical inhibitors of TF expression (pentoxifylline, retinoic acid, and cyclosporin A). Bovine alveolar macrophages were stimulated with lipopolysaccharide (LPS) derived from Pasteurella haemolytica or recombinant bovine tumour nervous factor (TNF) and dose- and time-dependent effects on TF expression were studied. LPS and TNF induced TF expression in alveolar macrophages and LPS treatment of whole blood induced TF expression in mononuclear cells. Neutrophils and platelets also expressed procoagulant activity, but this activity was not inhibited by anti-bovine TF monoclonal antibody. Pentoxifylline (40 mol/L), retinoic acid (0.01 mmol/L) and cyclosporin A (0.08 mol/L) inhibited TF expression when added concurrently with LPS or TNF, but not when added 4 h after stimulation. TF mRNA was not detected in unstimulated alveolar macrophages by Northern blot analysis. In contrast, exposure to LPS or TNF for 6 h induced marked expression of TF mRNA, which was inhibited by treatment with pentoxifylline, retinoic acid and cyclosporin A. Expression of TNF by alveolar macrophages stimulated with LPS was also inhibited by these compounds. Our results indicate that procoagulant activity expressed by alveolar macrophages and monocytes is associated with expression of TF, whereas procoagulant activity expressed by neutrophils and platelets is not. The concentrations of pentoxifylline and retinoic acid necessary for inhibition of TF expression in vitro may not be achievable in vivo owing to their toxic effects. However, the in vitro concentration of cyclosporin A that inhibited TF expression did not exceed the plasma concentration observed in humans, and therefore may be useful for inhibition of TF expression in vivo.Abbreviations BAL bronchoalveolar lavage - LPS lipopolysaccharide - cDNA cloned deoxyribonucleic acid - cAMP cyclic adenosine monophosphate - GAPDH glyceraldehyde phosphate dehydrogenase - mRNA messenger ribonucleic acid - TF tissue factor - TNF tumour necrosis factor - DPBS Dulbecco's phosphate-buffered saline     

Serum lipase determination in the dog: a comparison of a titrimetric method with an automated kinetic method

An enzymatic, kinetic method for determining serum lipase activity was evaluated and compared to a standard manual method for use in dogs. The kinetic method was a commercial kit adapted for use on a tandem access clinical chemistry analyzer and utilized a series of coupled enzymatic reactions based on the hydrolysis of 1,2-diglyceride by lipase. The manual method was the Cherry-Crandall technique based on the titration of base against the acid formed by hydrolysis of an olive oil substrate by lipase. The correlation between the two methods was very good (r = 0.94). The reference range for 56 clinically healthy dogs assayed by the kinetic method was 90 to 527 U/L. Diseases associated with a greater than twofold elevation in serum lipase activity as determined by the kinetic method included pancreatitis, gastritis with liver disease, and oliguric renal failure with metabolic acidosis. In some cases, pancreatitis was seen with other clinical problems, such as gastroenteritis, diabetic ketoacidosis, duodenal mass, disseminated intravascular coagulation, and septic peritonitis. Diseases associated with serum lipase activity within the reference range or elevated less than twofold included gastritis, gastric ulcer, cholestasis, phenobarbital-induced hepatopathy, colitis, copper hepatopathy, abdominal hematoma, apocrine gland adenocarcinoma, and thrombocytopenia with pneumonia.