黑木耳胞外酶活变化与栽培性状比较的研究

研究了黑木耳10个菌株胞外酶活性及与栽培性状和产量的关系,结果表明,胞外漆酶、多酚氧化酶活性的变化趋势大致相似,酶活与栽培产量呈正相关,相关系数为0.823(7号菌株除外),酶活性相对较高的菌株(3、4、8号),栽培中产量相对较高。纤维素酶活性高峰时间出现较漆酶、多酚氧化酶早,且酶活性高峰出现早的菌株菌丝长速较快。蛋白酶活与栽培产量呈一定负相关性,相关系数为-0.700(6号菌株除外),蛋白酶活最低的3号菌株,栽培产量最高;而活性较高的5、9号菌株栽培产量较低。     

Estradiol stimulated proliferation and differentiation of prostatic stromal cells through regulation of BPH-1 paracrine

AIM: To characterize the effect of estradiol on proliferation, differentiation and extracellular matrix (ECM) accumulation in stromal cells through regulation of BPH-1 paracrine. METHODS: BPH-1 cells were stimulated with different concentrations of estradiol. Conditioned media (CM) were harvested and their effects on stromal cell cultures were tested. Cell proliferation was determined by MTT assay. mRNA of smoothelin, fibronectin, collagen Ⅳ and transforming growth factor β₁(TGF-β₁) were analyzed by real-time RT-PCR. Western blotting was used to determine smooth muscle myosin heavy chain (SMMHC). ELISA and radioimmunoassay were respectively used to measure fibronectin, TGF-β₁ and collagen Ⅳ protein expressions.RESULTS: Estrodiol stimulated the expression and secretion of TGF-β₁ in BPH-1 cells. The proliferation of stromal cells increased when they were cultured with CM harvested from estrogen treated BPH-1 cells. The mRNA levels of collagen Ⅳ and smoothelin increased in stromal cells treated with CM from BPH-1 cells. The results of radioimmunoassay also showed that the collagen Ⅳ protein level up-regulated in the supernatants and cell extracts of CM-treated stromal cells. A neutralizing antibody to TGF-β₁ inhibited the stimulation of collagen Ⅳ and SMMHC by BPH-1 CM. The expression of fibronectin was only marginally changed in stromal cells cultured in the presence of BPH-1 CM. CONCLUSION: The BPH-1 cells increase ECM accumulation and differentiation of stromal cells through TGF-β₁. Estradiol stimulate differentiation of stromal cells by induction of TGF-β₁ expression. Estradiol stimulate proliferation by influencing the factors secreted from prostatic epithelial cells.     

The effects of 17β-estradiol on cardiomyocyte hypertrophy induced by endothelin

AIM:To investigate the effect of 17β-estradiol (E₂) on myocardial hypertrophy induced by endothelin-1(ET-1) and the related mechanism. METHODS:Myocardial cells from neonate rats were cultured in vitro and myocardial hypertrophy model was established with ET-1.The effects of 17β-estradiol on myocardial hypertrophy were observed. The role of ERK1/2 in the effects of 17β-estradiol was also detected. RESULTS:Compared with control group,ET-1 increased cell protein content,cell surface area and ［³H］^-Leucine ［³H］^-Leu) incorporation. Pretreatment with E₂ for 24 h could inhibit the increase in cell protein content,cell surface area and ［³H］^-Leu incorporation induced by ET-1.ET-1 significantly stimulated ERK1/2 activity,which was prevented by pretreatment with E₂.Tamoxifen,estradiol receptor antagonist,partially inhibited the effect of E₂. The ability of ET-1 to stimulate ［³H］^-Leu incorporation was significantly blocked by PD98059,which could enhance the inhibitory effect of E₂ on the increase of ［³H］^-Leu incorporation in cardiomyocytes induced by ET-1.CONCLUSION:E₂ can inhibit cardiomyocyte hypertrophy induced by ET-1. This effect is mediated by estrogen receptor. ERK1/2 signal pathway is closely correlated with the inhibitory effect of E₂ on cardiomyocyte hypertrophy induced by ET-1.     

The spore coat of the bean anthracnose fungus Colletotrichum lindemuthianum is required for adhesion, appressorium development and pathogenicity

The spores (conidia) of the bean anthracnose fungal pathogen, Colletotrichum lindemuthianum, adhere to the aerial parts of plants to initiate the infection process. In previous studies we have shown that the Colletotrichum spores are surrounded by a fibrillar spore coat, comprising several major glycoproteins. Previous evidence showed that a monoclonal antibody (UB20) that recognised these glycoproteins was able to inhibit adhesion of spores to a hydrophobic surface. In this paper we have further studied the role of the spore coat in adhesion, germination and fungal development by studying the effects of UB20 and protease treatment of spores. The latter treatment has previously been shown to remove the spore coat. Spores germinate on glass, polystyrene and water agar, however, appressoria only develop on glass or polystyrene, showing a requirement for a hard surface. Removal of the spore coat with protease inhibits adhesion at 30 min, before the secretion of ECM glycoproteins. Protease treatment also inhibits the development of appressoria and reduces pathogenicity on leaves. Incubation of spores with the MAb UB20 inhibits adhesion at 30 min, but does not affect appressorium formation or pathogenicity. The results suggest that an intact spore coat has two functions; it is required for adhesion to a hydrophobic surface and for the detection of a hard surface necessary for appressorium formation. We suggest that contact with a hard surface, rather than adhesion, is the key event leading to appressorium formation.     

Influence of Sucrose, Mucin and Xanthan Gum on Spore Germination of Ten Different Fungi

Germination of conidia, uredospores and basidiospores of ten diverse fungi were compared in sterile distilled water, 0.5% sucrose, 0.5% mucin and 0.5% xanthan gum. All three compounds generally increased spore germination on cellophane membranes compared to water, but mucin was the most effective. Mucin stimulated significantly more germination than sucrose for 7 of the 10 fungi, and only Aspergillus niger and Colletotrichum gloeosporioides showed greater spore germination in sucrose than in mucin. Sucrose had no effect on uredospore or basidiospore germination, but mucin stimulated germination of these spores. Mucin was more effective than xanthan gum in increasing spore germination for 9 of the 10 fungi. Animal mucin is chemically similar to the natural spore matrix of some fungi and may provide some of the benefits of the spore matrix without the drawback of possible germination inhibitors. Animal mucin may be a useful substitute for the spore matrix in inoculations of a variety of fungi.     

基于Lefkovitch矩阵模型的山酢浆草种群动态分析

依据林下多年生草本植物山酢浆草Oxalis griffithii的形态学特征,将其生活史划分为4个阶段,并根据3种生境下山酢浆草种群的野外调查资料建立了不同种群的Lefkovitch结构矩阵模型,在此基础上预测了山酢浆草种群的动态及其阶段结构的变化;同时,运用敏感度、贡献率指标分析了影响种群动态的关键生活史阶段。结果表明：不同生境下山酢浆草种群的动态发展趋势不尽相同,常绿阔叶林下的种群（MD）呈稳定发展状态,其他2种生境下种群表现出衰退的发展趋势;种群的动态变化过程受个体的生长、残存、萎缩和繁殖等的综合影响;不同生活史阶段对种群动态的影响差异显著,种群动态过程及其发展趋势主要受种群内较大阶段个体的影响。图2表5参19     

最佳线性无偏预测估计种畜育种值（BLUP）可视化计算机程序

应用VB6可视化编程软件，设计较先进的最佳线性无偏预测估计种畜育种值（BLUP法）程序，增强了软件的功能，使其更具易用性、广泛性。     

反应网络的物料平衡一致性校验

通过对反应网络的物料平衡分析，提出了反应网络的物料平衡一致性校验方程，并用于反应网络的数据校正和推测     

闭式Leontief模型为可行的一个实用的判定程序

设Ｔ是某闭式Ｌｅｏｎｔｉｅｆ投入产出模型的投入矩阵，如果有正向量Ｘ使得Ｘ≥ＴＸ，则称该模型为可行的．本文给出闭式Ｌｅｏｎｔｉｅｆ模型是否可行的一个实用的判定程序．