蛇床子素粉剂对玉米象成虫的杀虫活性及酶活性的影响

研究1.0%蛇床子素(osthole)粉剂对玉米象Sitophilus zeamais Motschusky成虫的杀虫活性及其对玉米象成虫羧酸酯酶、乙酰胆碱酯酶、谷胱甘肽S-转移酶及蛋白质活性的影响。结果表明,1.0%蛇床子素粉剂对玉米象成虫有很好的杀虫活性,处理玉米象成虫3d后,0.8mg/kg以上剂量的蛇床子素粉剂对玉米象成虫的校正死亡率达100%;用0.19mg/kg蛇床子素粉剂处理玉米象成虫2d后,试虫体内乙酰胆碱酯酶、羧酸酯酶和蛋白质活性均表现出受抑制,而谷胱甘肽S-转移酶活性随处理时间的延长整体趋势表现出被诱导。     

β-细辛醚对谷蠹成虫体内四种酶活性的影响

采用石菖蒲Acorus gramineus根茎提取物β-细辛醚对谷蠹Rhizopertha dominica成虫进行拌粮处理,测定β-细辛醚对谷蠹体内乙酰胆碱酯酶、谷胱甘肽S-转移酶、羧酸酯酶和酯酶同工酶的时间效应和剂量效应。结果表明：β-细辛醚对试虫体内4种酶的酶活性均表现出较强的时间效应。LC₅₀（94.49 mg/kg）剂量的β-细辛醚处理后,谷蠹成虫体内乙酰胆碱酯酶和谷胱甘肽S-转移酶活性随处理时间的延长整体表现为抑制作用,对羧酸酯酶和酯酶同工酶则表现诱导增加作用。低剂量（67.5 mg/kg）β-细辛醚对乙酰胆碱酯酶具有显著的诱导作用,但是随着处理剂量的升高,对乙酰胆碱酯酶的活力多数表现为抑制作用。低剂量（≤100.0 mg/kg）β-细辛醚对谷胱甘肽S 转移酶具有诱导作用,而高剂量（≥133.3 mg/kg）β-细辛醚对谷胱甘肽S-转移酶具有抑制作用。β-细辛醚对羧酸酯酶的活性多数表现为诱导作用,提高β-细辛醚的处理剂量可提高羧酸酯酶的活力。不同剂量的β-细辛醚处理对谷蠹酯酶同工酶均具有显著的诱导作用,但诱导效果与处理剂量关系并不显著。     

D染色体组对小麦酯酶同工酶的影响

应用垂直平板聚丙烯酰胺凝胶电泳,分析了灌浆期种子胚乳的酯酶同工酶。结果表明,具有 D 染色体组的节节麦、偏凸山羊草和粗厚山羊草都有1条迁移率相同的 E_(1-1)带。在普通小麦(AABBDD)和二粒系小麦(AABB)的酶谱中,E_(1-1)和 E_(1-2)各自由两条紧密靠近的带构成。这两个种的 E_3区都有5条带。虽然两个种的小麦之间这些带的迁移率没有差异,但是,其活性不同,而且表现出规律性的变化。二粒系和普通小麦之间正反交杂种的酶谱大多倾向于母本类型,表现出 D 染色体组的剂量效应。     

黄荆精油对玉米象的杀虫活性成分、毒力及作用机制

为明确黄荆精油及其主要成分作为储粮保护剂的开发利用价值,采用水蒸气蒸馏法从泰山黄荆Vitex negundo Linn.叶片中提取精油,利用GC-MS技术进行了成分分析鉴定,研究了黄荆精油及其主要成分桉树脑和α-蒎烯对玉米象 Sitophilus zeamais Motschulsky 成虫的毒力及作用机制。结果表明: 黄荆精油中含量大于0.3%的成分有31种,其中石竹烯、桉树脑和α-蒎烯的含量分别为35.97%,8.21%和0.69%。桉树脑、α-蒎烯和黄荆精油对玉米象成虫的综合杀虫毒力都较高,并以桉树脑的毒力最高,LC₅₀为0.7171 g·kg^-1;在2.0 g·kg^-1剂量下,桉树脑、α-蒎烯和黄荆精油对玉米象种群的抑制率分别达100％,85.45％和89.73％;3种药剂对玉米象72 h触杀LC₅₀分别为0.2690,0.7529 和0.2969 mg·cm^-2,毒力都很高;3种药剂在4 g·kg^-1剂量下,对玉米象的驱避率分别为96.49%,84.26％和90.61%,防虫作用大;3种药剂对玉米象72 h的熏蒸LC₅₀分别为14.053, 28.648 和21.429 μL·L^-1,熏蒸杀虫毒力较高,其中以桉树脑的毒力最高。3种药剂对玉米象有干扰呼吸的作用,对离体乙酰胆碱酯酶、过氧化氢酶和羧酸酯酶都有抑制作用。这些结果明黄荆精油及其主要成分的作用机制具有多样性。     

水菖蒲活性物质β-细辛醚对玉米象不同虫态的熏蒸作用

为了确定水菖蒲(Acorus calamus)活性成分β-细辛醚对玉米象Sitophilus zeamais Motschulsky的熏蒸活性,研究β-细辛醚对玉米象不同虫态的熏蒸作用。结果表明:β-细辛醚对玉米象4种虫态都有一定的熏蒸作用,其中对成虫的熏蒸效果最好,其次是卵,幼虫和蛹对β-细辛醚具有较高的耐药性。以质量浓度为200μL/L熏蒸卵120h后,卵的死亡率达到了99.09%。对幼虫和蛹的熏蒸作用不明显。对成虫熏蒸120h后,LC50为17.82μL/L。     

高温对田间小菜蛾DNA损伤及4种抗药性相关酶系活性的抑制

研究了高温对福州上街菜田小菜蛾成虫4种抗药性相关酶系活性的影响。与饲养在25℃下的小菜蛾相比,33．5~C或40℃处理72h导致小菜蛾基因组DNA出现DNA凋亡特征梯度化条带。33~C饲养小菜蛾4、8、12或24h对小菜蛾成虫乙酰胆碱酯酶（AChE）和羧酸酯酶（CarE）活性无显著影响,但33℃饲养小菜蛾12或24h导致小菜蛾成虫谷胱甘肽s转移酶（GSTs）酶活性和细胞色素P450含量显著下降。36℃、24h可导致AChE活性显著下降,36℃、12h和24h可导致CarE活性显著下降,36℃、4h,8h,12h和24h可导致GST活性和细胞色素P450含量显著下降。总体上,高温对CarE、GSTs和细胞色素P450的抑制作用大于对AChE的影响,此外,3CC对AChE、CarE、GSTs酶活性和细胞色素P450含量的抑制作用大于33℃的抑制作用。     

根瘤菌属几种同工酶的研究

本文对根瘤菌属12株不同根瘤菌的过氧化物酶,谷氨酸草酰乙酸转氨酶及酯酶同工酶进行了测定,结果发现:所有菌株的过氧化物酶和谷氨酸草酰乙酸转氨酶均呈阴性。酯酶同工酶酶带数在快生型和慢生型根瘤菌之间存在明显的区别,在YMA培养基上,快生型根瘤菌仅有1—2条,迁移率在0.71—0.98之间变化;而慢生型根瘤菌却有4—6条酶带,迁移率在0.15—0.98之间变化,同一菌株在不同碳源上酯酶同工酶酶带数也发生显著变化。     

光/暗对玉米叶片果糖-6-磷酸激酶-2和果糖-2,6-二磷酸酯酶活力的影响

比较了照光和黑暗条件下玉米叶片果糖—6—磷酸激酶—2(PFK-2)和果糖—2,6—二磷酸酯酶(FBPase-2)的活力变化。当玉米植株从暗中转入光下后,其叶片PFK—2的活力随光照时间的延长而逐渐降低,而FBPase-2活力变化不明显;从光下转入暗后叶片PFK-2活力明显上升,FBPase-2活力仍无明显变化;其PFK-2/FBPase-2比值在光处理时下降,暗处理时上升。同时叶片中果糖—2,6—二磷酸的含量与PFK-2/FBPase-2活力比值的变化趋势一致。连续光照 20 h,PFK-2活力持续下降,表明PFK-2的光钝化现象与玉米植株的昼夜节律变化无关。     

三种瘤背豆象幼虫酯酶同工酶的比较研究

本研究采用聚丙烯酰胺凝胶垂直板型电泳法 ,分析了 3种瘤背豆象属豆象 :绿豆象 Callosobruchuschinensis L.、灰豆象 C.phaseoli ( Gyllenhal)、鹰嘴豆象 C.analis ( Fabricius)幼虫的酯酶同工酶。从酶谱的酶带数、迁移率、酶活性强弱 (酶带染色深浅 )、酶含量 (酶带宽窄 )等方面的比较发现 ,3种瘤背豆象属豆象幼虫的酯酶同工酶酶谱具有明显的差异。由此探讨利用酯酶同工酶电泳法鉴别豆象的可能性     

乌桕梓油和桕脂的脂肪酸组成研究

运用色谱-质谱分析方法,鉴定乌桕梓油和桕脂的脂肪酸成分.分析结果,野生乌桕和栽培乌桕在脂肪酸组成上相同;梓油除了含常见的亚麻酸、亚油酸、油酸、棕榈酸和硬脂酸之外,还含有不常见的2,4-癸二烯酸和8-羟基-5,6-辛二烯酸;桕脂含棕榈酸、油酸、硬脂酸和亚油酸.两者的主要差异在于蜡质层厚度和核的大小及其油脂含量的不同.     

甲酸乙酯及甲酸对离体玉米象乙酰胆碱酯酶及酯酶活性的影响

研究甲酸乙酯和甲酸对离体玉米象Sitophilus zeamais（Motschulsky）酯酶和乙酰胆碱酯酶（AChE）的抑制作用,结果表明甲酸乙酯对离体的玉米象酯酶和AChE没有抑制作用,并且甲酸对玉米象酯酶和AChE的抑制中浓度远远高于甲酸乙酯对玉米象的致死中浓度,说明甲酸对玉米象这两种酶的抑制作用不是甲酸乙酯杀虫的主要机理。     

Proteolytic activity of arginine esterase from dog seminal plasma towards actin and other structural proteins. Comparison with trypsin and kallikrein

At equimolar ratio of enzyme/substrate, actin, tropomyosin, fibronectin and myosin were extensively hydrolyzed during an incubation of one hour at 37 degrees C. Dog serum albumin, ovalbumin, bovine gamma-globulin and human prostatic acid phosphatase were not hydrolyzed. The activity of arginine esterase towards actin at pHs 6.5, 7.1 and 7.6 was respectively 60, 74 and 84% of the one found at optimum pH 8.2. The cleavage products of actin by arginine esterase and trypsin were similar although trypsin activity was 5000-fold higher. Kallikrein produced a major fragment of actin not observed with arginine esterase and trypsin. It is concluded that arginine esterase has a low trypsin-like activity towards structural proteins and that this activity may have a physiological significance.     

Characterization and the developmental role of plasma juvenile hormone esterase in the adult cabbage looper,Trichoplusia ni

Juvenile hormone (JH) esterase was characterized from the plasma of adult females of the cabbage looper, Trichoplusia ni, and compared with that present in 4th and 5th instar larvae. Ester hydrolysis was the principal route of JH metabolism. Gel filtration of plasma resolved a single peak of JH esterase which was distinct from that of the α-naphthyl acetate (α-NA) esterase activity. The JH esterase apparent molecular weight was 62,000 in prepupae and virgin, female adults and 69,000 in 2-day-old 4th instar larvae. Broad range isoelectric focusing of plasma of prepupae and adults resolved a major peak of activity at pH 5.5 with a minor peak of activity at pH 6.1 and in 4th instar larvae at pH 5.45 and 5.8, respectively. By this method JH esterase was resolved from the α-NA esterase activity. The plasma of prepupae and adults metabolized JH I at about twice the rate of JH III. JH esterase activity from adult plasma was more stable than the α-NA esterase activity. Adult JH esterase activity was insensitive to inhibition by O,O-diisopropyl phosphorofluoridate in contrast to that of the α-NA esterase activity. Mated females oviposited 8 times more eggs than virgin females to 10 days after emergence. The total haemolymph protein content of virgin females remained high throughout the period of study whereas mated females showed a significant decline beginning on day 4. JH esterase activity remained unchanged in virgins whereas it declined drastically in mated females. The α-NA esterase activity declined to low levels shortly after emergence in both groups. JH and α-NA esterase activity was not affected by the application of the juvenoid, (RS)-methoprene. The present study provides evidence of a functional role for JH esterase in JH metabolism and reproduction in adult T. ni. JH esterases in the adult were identical to that of prepupae by the methods described above.     

Isolation and partial characterization of rat urinary esterase A2

An enzyme, esterase A2, which hydrolyzes tosyl-arginine methyl ester was isolated from the urine of female, inbred, Dahl-salt-resistant rats using DEAE-Sephadex ion-exchange, aprotinin-agarose affinity and molecular sieve column chromatography. The purest preparation obtained showed four closely migrating bands on polyacrylamide gel electrophoresis. All four bands of the esterase A2 preparation had enzyme activity since all were stainable on zymograms using N-acetyl-L-methionine alpha-naphthyl ester as substrate. Three of these four bands showed decreased electrophoretic mobility following treatment with neuraminidase, indicating that variable sialic acid content accounts for part of the microheterogeneity. The preparation of esterase A2 used was free of rat urinary kallikrein as shown by radioimmunoassay, electrophoretic and isoelectric focusing experiments. The relative kinin-generating ability of rat urinary kallikrein and esterase A2 was highly dependent on the assay used. Using canine plasma as a source of kininogen and the rat uterus to bioassay kinins, esterase A2 was 47% as active as kallikrein; using pure bovine low-molecular-weight kininogen and a radioimmunoassay to measure generated kinins, esterase A2 was only 6% as active as kallikrein. Esterase activity of A2 was activated non-specifically by proteins and detergents. Esterase A2 was 50% inhibited by an 8-fold molar excess of aprotinin and by a 26.5-fold molar excess of soybean trypsin inhibitor, but ovomucoid inhibitor was not inhibitory.     

Studies of esterase 6 in Drosophila melanogaster. I. The genetics of a posttranslational modification

A locus has been found, an allele of which causes a modification of some allozymes of the enzyme esterase 6 in Drosophila melanogaster. There are two alleles of this locus, one of which is dominant to the other and results in increased electrophoretic mobility of affected allozymes. The locus responsible has been mapped to 3-56.7 on the standard genetic map (Est-6 is at 3-36.8). Of 13 other enzyme systems analyzed, only leucine aminopeptidase is affected by the modifier locus. Neuraminidase incubations of homogenates altered the electrophoretic mobility of esterase 6 allozymes, but the mobility differences found are not large enough to conclude that esterase 6 is sialylated.This work was supported by NIH Grant No. GM23706 and PHS Grant SO7RR7031 to Rollin C. Richmond and by NIH Genetics Training Grant No. 82 to Indiana University.     

Zymograms and histochemistry of non-specific esterase in the salivary glands

Summary Zymogramic analysis of esterase in the mouse, rat and guinea-pig salivary glands was undertaken and demonstrated species and organ specificities of esterase with electrophoretic method. Salivary glands esterase was classified into A, B and C types based on the electrophoretic mobility. Mouse submandibular gland had the most complicated pattern, while guinea-pig showed the simpliest patterns which was devoid of B type of esterase. Rat salivary glands exhibited rather regular patterns. Similar zymogram patterns were obtained with many kinds of ester compounds, that is simple and substituted naphthol esters and indoxyl derivatives. The tests of inhibition and activation for esterase activity was obtained. Histochemical properties applied to inhibitor test in the esterase zymogram patterns showed no marked differences between ducts and acini.     

Developmental genetics of the esterase isozymes of Fundulus heteroclitus

The ontogeny of the esterase isozymes of the teleost, Fundulus heteroclitus, has been investigated. One group of esterase isozymes is present at all stages of development, whereas other esterase isozymes only very gradually appear at later stages of development, or abruptly appear at such dramatic developmental events as hatching. The ontogeny of these isozyme patterns is interpreted as the expression of differential regulation of separate esterase genes. The general pattern of teleost esterase gene activation is similar to that reported for birds and mammals. Allelic variation was detected at two of the esterase loci. On the basis of electrophoretic mobility, substrate specificity, inhibitor specificity, genetic variation, and ontogeny of esterases, there appear to be at least 15 different esterase isozymes, which constitute 6–8 groups, each of which is probably encoded in one or more genetic loci.This study was supported by NSF Grant GB 544OX to Professor C. L. Markert and an NSF Graduate Fellowship to G. S. Whitt.     

Biochemistry of differentiation of mouse trophoblast: esterase

In the first half of pregnancy, patterns of esterase activity, as well as electrophoretic esterase isozyme profiles of trophoblast (fetal placenta) homogenates can be distinguished from those of other embryonic tissues and from those of the decidua (maternal placenta). Two electrophoretic bands of esterase activity are found in trophoblast but not embryo proper; one is of maternal origin. Both bands are found in ectopic pregnancies containing mainly giant cells, and at least one is present in preimplantation late morulae and blastocysts. Blastocysts cultured in modified Eagle medium containing dialysed serum give rise mainly to trophoblast-like growths, and under these conditions, the esterase profile is predominantly trophoblast-like. Embryos cultured from the two-cell stage or viable blastocysts which have been unable to hatch from their zona pellucidae also produce trophoblast-like esterase. Unmodified Eagle medium supplemented with heat-inactivated serum allows the proliferation of cells that appear to derive from the inner cell mass. Under these conditions, the esterase profiles closely resemble those of the yolk sac and embryo proper, even after 3 weeks in culture.     

Pregnancy-associated esterase in sera of baboons

Baboon serum samples were resolved by starch gel electrophoresis and polyacrylamide gradient gel electrophoresis and stained with naphthol substrates for esterase activity. An esterase that hydrolyzed alpha-naphthyl butyrate in preference to alpha-naphthyl acetate was found in very high activities in some individuals but not others. It migrated just cathodal of the albumin band in starch gels. In polyacrylamide gradient gels, it co-migrated with albumin and had an apparent molecular weight of approximately 65,000 daltons. Electrophoretic analysis by gel electrophoresis of random serum samples from male and female baboons indicated that this esterase was present only in the sera of pregnant baboons. Further investigation of serial samples collected from carefully monitored baboons confirmed that the amount of activity of this esterase was correlated with stage of pregnancy. Therefore, it was named pregnancy esterase (PE). PE was detectable by gel electrophoresis and chromogenic staining techniques as early as day 30 of pregnancy; its activity gradually increased with progressive pregnancy and reached maximum activity near full term (182 days). Soon after parturition, the activity of PE decreased rapidly and was not detected in maternal sera by day 14 postpartum. No evidence of PE was detected in sera of pregnant humans.