改进型气升式反应器能耗的研究

首次研究了操作条件和反应器结构（导流筒直径和静态混合元件数）对改进型气升式反应器功耗的影响。结果表明,优化导流筒结构可以实现节能降耗。曝气量相同时,在导流筒直径为4.0cm,静态混合元件数为39的条件下,改进型反应器的功耗最小,比普通反应器平均降低23.6%。达到相同供氧能力时,在导流筒直径为5.5cm,静态混合元件数为13的条件下,改进型反应器的功耗最小,比普通反应器平均降低43.9%。在改进型反应器中,升流区功耗最大,占70%～80%;底隙区次之,占20%左右;气液分离区最小,小于10%;降流区功耗可以忽略不计。最大体积功耗出现在底隙区。升流区是解决反应器能耗问题的重点。     

人Ⅳ型胶原的提纯及其抗血清制备

采用胃蛋白酶限制性消化,NaCl分级盐析,还原和烷基化反应,纤维素离子交换层析从人胎盘组织分离纯化Ⅳ型胶原.经SDS-PAGE电泳鉴定符合Ⅳ型胶原α肽链电泳带.用纯化的Ⅳ型胶原免疫兔制备出高效价的特异抗血清.     

A rapid enzymatic assay for high-throughput screening of adenosine-producing strains

Adenosine is a major local regulator of tissue function and industrially useful as precursor for the production of medicinal nucleoside substances. High-throughput screening of adenosine overproducers is important for industrial microorganism breeding. An enzymatic assay of adenosine was developed by combined adenosine deaminase (ADA) with indophenol method. The ADA catalyzes the cleavage of adenosine to inosine and NH₃, the latter can be accurately determined by indophenol method. The assay system was optimized to deliver a good performance and could tolerate the addition of inorganic salts and many nutrition components to the assay mixtures. Adenosine could be accurately determined by this assay using 96-well microplates. Spike and recovery tests showed that this assay can accurately and reproducibly determine increases in adenosine in fermentation broth without any pretreatment to remove proteins and potentially interfering low-molecular-weight molecules. This assay was also applied to high-throughput screening for high adenosine-producing strains. The high selectivity and accuracy of the ADA assay provides rapid and high-throughput analysis of adenosine in large numbers of samples.     

生物化学检验技术实验教学与开放式综合实验设计初步效果探讨

目的:探讨生物化学检验技术实验教学(Experimental biochemistry inspection teaching,EBIT)与开放式综合实验设计(Open comprehensive experiment design,OCED)的初步效果,为EBIT教学提供新型选择方案。方法:选择2012届我们所带教医学检验专业的2个班级111例学生作为研究对象,分别归入观察组和对照组,其中观察组56例,对照组55例。对照组EBIT中予以传统的模式,观察组则采用OCED模式。对比两组实验成绩、教学效果的满意度。结果:观察组的合格率显著高于对照组,差异有统计学意义(P<0.05)。观察组对教学效果的满意度显著高于对照组,差异有统计学意义(P<0.05)。结论:OCED方式应用于EBIT过程中,可获得较好的教学效果,值得推荐。     

人为干扰对黑腹滨鹬觅食行为的影响

2003年11月至2004年3月,采用目标动物取样法和人为干扰实验法,于浙江省乐清湾滩涂进行人类活动对黑腹滨鹬(Calidrisalpina)觅食行为影响的研究。取样观察结果表明,在每天沿海堤可观察黑腹滨鹬持续觅食的1h里,96.6%的黑腹滨鹬在35m或更小的距离上通过奔跑或惊飞对人类的活动作出反应;黑腹滨鹬花费90%(人类较多的盐盆滩涂为85%,较少的乐成滩涂为94%)的时间觅食,10%的时间用于避免人类的干扰;人数、人类活动类型对觅食时间具有显著影响,人数、人离黑腹滨鹬的距离、人类活动类型对黑腹滨鹬移动的距离、移动的次数以及黑腹滨鹬对人类靠近的反应均具有显著效应。人为干扰最小接近距离实验结果表明,黑腹滨鹬对人类反应的距离在3～30m;干扰人数为1人时的最小接近距离显著大于2人;人类行走和奔跑的两种活动类型对黑腹滨鹬的最小接近距离没有显著影响。本研究验证了滨鸟觅食区内的人为活动严重影响黑腹滨鹬觅食行为的假设。     

N-Acetylcysteine ameliorates lipopolysaccharide-induced organ damage in conscious rats

Lipopolysaccharide is strongly associated with septic shock, leading to multiple organ failure. It can activate monocytes and macrophages to release proinflammatory mediators such as tumor necrosis factor- (TNF-), interleukin-1 (IL-1), and nitric oxide (NO). The present experiments were designed to induce endotoxin shock by an intravenous injection ofKlebsiella pneumoniae lipopolysaccharide (LPS, 10 mg/kg) in conscious rats. Arterial pressure and heart rate (HR) were continuously monitored for 48 h after LPS administration. N-Acetyl-cysteine was used to study its effects on organ damage. Biochemical substances were measured to reflect organ functions. Biochemical factors included blood urea nitrogen (BUN), creatinine (Cre), lactic dehydrogenase (LDH), creatine phosphokinase (CPK), aspartate transferase (GOT), alanine transferase (GPT), TNF-, IL-1, methyl guanidine (MG), and nitrites/nitrates. LPS caused significant increases in blood BUN, Cre, LDH, CPK, GOT, GPT, TNF-, IL-1, MG levels, and HR, as well as a decrease in mean arterial pressure and an elevation of nitrites/nitrates. N-Acetylcysteine suppressed the release of TNF-, IL-1, and MG, but enhanced NO production. These actions ameliorate LPS-induced organ damage in conscious rats. The beneficial effects may suggest a potential chemopreventive effect of this compound in sepsis prevention and treatment.     

Weak cell cycle dependency but strong distortive effects of transfection with Lipofectamine 2000 in near‐physiologically synchronized cell culture

Previously, we reported a method to generate and validate cell cycle‐synchronized cultures of multiple mammalian suspension cell lines under near‐physiological conditions. This method was applied to elucidate the putative interdependencies of the cell cycle and recombinant protein expression in the human producer cell line HEK293s using Lipofectamine 2000 and the reporter plasmid pcDNA3.3 enhanced green fluorescent protein, destabilized using PEST sequence. A population‐resolved modeling approach was applied to quantitatively assess putative variations of cell cycle dependent expression rates based on the obtained experimental data. We could not confirm results published earlier by other groups, based on nonphysiological synchronization attempts, reporting transfection efficiency being strongly dependent on the cell cycle phase at transfection time point. On the other hand, it is demonstrated that transfection and protein expression distort the progression of the cell cycle.     

Knockdown of phosphotyrosyl phosphatase activator induces apoptosis via mitochondrial pathway and the attenuation by simultaneous tau hyperphosphorylation

Phosphotyrosyl phosphatase activator (PTPA) is decreased in the brains of Alzheimer's disease (AD) and the AD transgenic mouse models. Here, we investigated whether down‐regulation of PTPA affects cell viability and the underlying mechanisms. We found that PTPA was located in the integral membrane of mitochondria, and knockdown of PTPA induced cell apoptosis in HEK293 and N2a cell lines. PTPA knockdown decreased mitochondrial membrane potential and induced Bax translocation into the mitochondria with a simultaneous release of Cyt C, activation of caspase‐3, cleavage of poly (DNA ribose) polymerase (PARP), and decrease in Bcl‐xl and Bcl‐2 protein levels. Over‐expression of Protein phosphatase 2A (PP2A) catalytic subunit (PP2A_C) did not rescue the apoptosis induced by PTPA knockdown, and PTPA knockdown did not affect the level of and their phosphorylation of mitogen‐activated protein kinases (MAPKs), indicating that PP2A and MAPKs were not involved in the apoptosis induced by PTPA knockdown. In the cells with over‐expression of tau, PTPA knockdown induced PP2A inhibition and tau hyperphosphorylation but did not cause significant cell death. These data suggest that PTPA deficit causes apoptotic cell death through mitochondrial pathway and simultaneous tau hyperphosphorylation attenuates the PTPA‐induced cell death.