排序方式: 共有6条查询结果,搜索用时 15 毫秒
1
1.
Juan D. Rejón Agnieszka Zienkiewicz María Isabel Rodríguez-García Antonio J. Castro 《Annals of botany》2012,110(5):1035-1045
Background and Aims
A pollen grain contains a number of esterases, many of which are released upon contact with the stigma surface. However, the identity and function of most of these esterases remain unknown. In this work, esterases from olive pollen during its germination were identifided and functionally characterized.Methods
The esterolytic capacity of olive (Olea europaea) pollen was examined using in vitro and in-gel enzymatic assays with different enzyme substrates. The functional analysis of pollen esterases was achieved by inhibition assays by using specific inhibitors. The cellular localization of esterase activities was performed using histochemical methods.Key Results
Olive pollen showed high levels of non-specific esterase activity, which remained steady after hydration and germination. Up to 20 esterolytic bands were identified on polyacrylamide gels. All the inhibitors decreased pollen germinability, but only diisopropyl fluorophosphate (DIFP) hampered pollen tube growth. Non-specific esterase activity is localized on the surface of oil bodies (OBs) and small vesicles, in the pollen intine and in the callose layer of the pollen tube wall. Acetylcholinesterase (AChE) activity was mostly observed in the apertures, exine and pollen coat, and attached to the pollen tube wall surface and to small cytoplasmic vesicles.Conclusions
In this work, for the first time a systematic functional characterization of esterase enzymes in pollen from a plant species with wet stigma has been carried out. Olive pollen esterases belong to four different functional groups: carboxylesterases, acetylesterases, AChEs and lipases. The cellular localization of esterase activity indicates that the intine is a putative storage site for esterolytic enzymes in olive pollen. Based on inhibition assays and cellular localization of enzymatic activities, it can be concluded that these enzymes are likely to be involved in pollen germination, and pollen tube growth and penetration of the stigma. 相似文献2.
Existence of Two Acetylcholinesterases in the Mosquito Culex pipiens (Diptera: Culicidae) 总被引:4,自引:0,他引:4
Denis Bourguet Michel Raymond Didier Fournier †Colin A. Malcolm ‡Jean-Pierre Toutant ‡§ Martine Arpagaus 《Journal of neurochemistry》1996,67(5):2115-2123
Abstract: Two acetylcholinesterases (AChEs), AChE1 and AChE2, differing in substrate specificity and in some aspects of inhibitor sensitivity, have been characterized in the mosquito Culex pipiens . The results of ultracentrifugation in sucrose gradients and nondenaturing gel electrophoresis of AChE activity peak fractions show that each AChE is present as two molecular forms: one amphiphilic dimer possessing a glycolipid anchor and one hydrophilic dimer that does not interact with nondenaturing detergents. Treatment by phosphatidylinositol-specific phospholipase C converts each type of amphiphilic dimer into the corresponding hydrophilic dimer. Molecular forms of AChE1 have a lower electrophoretic mobility than those of AChE2. However, amphiphilic dimers and hydrophilic dimers have similar sedimentation coefficients (5.5S and 6.5S, respectively). AChE1 and AChE2 dimers, amphiphilic or hydrophilic, resist dithiothreitol reduction under conditions that allow reduction of Drosophila AChE dimers. In the insecticide-susceptible strain S-LAB, AChE1 is inhibited by 5 × 10−4 M propoxur (a carbamate insecticide), whereas AChE2 is resistant. All animals are killed by this concentration of propoxur, indicating that only AChE1 fulfills the physiological function of neurotransmitter hydrolysis at synapses. In the insecticide-resistant strain, MSE, there is no mortality after exposure to 5 × 10−4 M propoxur: AChE2 sensitivity to propoxur is unchanged, whereas AChE1 is now resistant to 5 × 10−4 M propoxur. The possibility that AChE1 and AChE2 are products of tissue-specific posttranslational modifications of a single gene is discussed, but we suggest, based on recent results obtained at the molecular level in mosquitoes, that they are encoded by two different genes. 相似文献
3.
硫丹对斑马鱼的毒性效应 总被引:7,自引:1,他引:6
硫丹是一种有机氯杀虫剂,广泛应用于谷物、蔬菜、水果、茶叶等害虫的防治.然而,在杀灭害虫、提高农业产量的同时,硫丹对水生生物的生存构成威胁.为了丰富水生生物毒理学资料,评价硫丹对水生生物健康生长的风险,本文采用传统毒理学方法,在室内静态环境条件下,研究了硫丹对斑马鱼(Dardo rerio)的毒性效应.结果显示24 h、48 h、72 h、96 h半数致死浓度(LG50)分别为4.24 μg/L、2.49 μg/L、1.77μg/L、1.62 μg/L.在亚慢性实验条件下,硫丹对肝和脑组织中的超氧化物歧化酶及乙酰胆碱酯酶有显著影响.硫丹对斑马鱼超氧化物歧化酶活性具有促进效应,在0.17~0.74μg/L范围内对乙酰胆碱酯酶具有抑制效应. 相似文献
4.
The aminoglycoside antibiotics such as neomycin, gentamicin, kanamycin and streptomycin stimulated the purified enzyme phosphatidylinositol-specific phospholipases C from Bacillus thuringiensis at pH 5.5. The involvement of net positive charge of aminoglycoside antibiotics (AA) on phosphatidylinositol-specific phospholipases C activation was probed by modifying the carboxyl group of Asp and Glu present in the enzyme by 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (EDAC). Intrinsic Trp fluorescence of EDAC modified and unmodified PI-PLC in the presence of AA confirmed the interaction of AA with side chain carboxyl group of aspartic and glutamic acid of the enzyme. Thus, the possible interaction of aminoglycoside antibiotics with phosphatidylinositol-specific phospholipases C is predicted to be mediated through the aspartic and glutamic acid residue(s) of the protein. 相似文献
5.
T.?PalvannanEmail author R.?Boopathy 《World journal of microbiology & biotechnology》2005,21(8-9):1393-1399
Summary Response surface methodology was employed in optimizing the nutrient levels needed towards the optimal production of phosphatidylinositol-specific
phospholipase C enzyme by Bacillus thuringiensis serovar. kurstaki. A 23 factorial central composite experimental design was used. The multiple regression equation, relating the enzyme activity
to the nutrient medium, was used to find the optimum values of glucose, peptone and dipotassium hydrogen phosphate. The optimum
values of these variables for maximal enzyme production were found to be: glucose, 6.5 g l−1; peptone, 5.38 g l−1 and dipotassium hydrogen phosphate, 6.36 g l−1 with the predicted enzyme activity of 0.96 U ml−1. 相似文献
6.
Summary Few studies on screening of the enzyme phosphatidylinositol-specific phospholipase C (PI-PLC) have been reported. Here we
present a simple potato-based medium to elaborate large quantities of extracellular PI-PLC from Bacillus thuringiensis serovar. kurstaki. The enzyme activity (1.75 U/ml) was found to be maximum in the potato-extract medium supplemented with sucrose and mineral
salts with a specific activity of 3.88 U/mg protein. 相似文献
1