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1.
2.
研究了不同提取方法,不同细胞裂解剂和醌还原酶(QR)反应液的培育时间对QR法分析的影响。结果表明,芥蓝组织用磷酸缓冲液(5mmol/LK2HPO4-KH2PO4,1mmol/LEDTA,pH7.6)提取效果良好,与常用的三元试剂提取法效果相当。这种方法简单而有效,优于其他有机溶剂提取法。0.4%乙基苯基聚乙二醇(NP40)可以替代细胞裂解剂——0.8%毛地黄皂苷用于QR分析,且效果良好,QR反应中反应液的培育时间以5 ̄10min为宜。  相似文献   

3.
Jasmonates, including jasmonic acid and its derivatives such as methyl jasmonate (MeJA), are plant growth substances that control various responses. Jasmonates regulate leaf trichome density in dicotyledonous plants, but their effects on the trichome density of monocotyledonous plants, such as those in the Poaceae, remain unclear. In the present study we examined the effects of exogenous MeJA on the trichome density of Rhodes grass, which has three kinds of trichomes: macrohairs, salt glands, and prickles. Exogenous MeJA significantly increased the densities of macrohairs and salt glands on the adaxial and abaxial leaf surfaces and those of prickles on the adaxial leaf surface. Because exogenous MeJA significantly reduced the leaf area, we calculated the number of trichomes per 1000 epidermal cells to eliminate the effects of reduced leaf area. Exogenous MeJA significantly increased the number of macrohairs per 1000 epidermal cells on both adaxial and abaxial leaf surfaces, but it significantly decreased the number of salt glands per 1000 epidermal cells on both surfaces. Exogenous MeJA had no significant effects on the number of prickles per 1000 epidermal cells on either of the leaf surfaces. These results indicate that exogenous MeJA alters the trichome density by affecting leaf area and trichome initiation, and the effects of exogenous MeJA on trichome initiation differ among the various trichome types.  相似文献   

4.
Short-term (2 h) treatment with 10 μM abscisic acid decreased stomatal conductance and net photosynthetic rate, and increased carbonic anhydrase activity in pea seedlings. The treatment with 10 μM methyl jasmonate did not significantly affect these parameters. This revised version was published online in June 2006 with corrections to the Cover Date.  相似文献   

5.
Abstract: The application of enzymatic staining techniques, using tetrazolium dyes, to aldehyde-treated brain sections has revealed the presence of NADPH-diaphorase activity attributed to nitric oxide synthase. When evaluating the specificity of the putative guanylyl cyclase inhibitor LY 83583, a robust and novel staining pattern was noted in epithelial, endothelial, and astrocytic cells when LY 83583 was included in the NADPH-diaphorase histochemical reaction. This LY 83583-dependent staining could be blocked by the NAD(P)H:quinone oxidoreductase inhibitor dicumarol. Based on its quinone structure, we hypothesized that LY 83583 was a substrate for the enzyme NAD(P)H:quinone oxidoreductase. Transfection of human embryonic kidney 293 cells with the rat liver isoform of NAD(P)H:quinone oxidoreductase resulted in robust NADPH- and LY 83583-dependent staining that was completely blocked by dicumarol and was not observed in untransfected cells. Analysis of transfected cell extracts and brain homogenates indicated that LY 83583 was a substrate for NAD(P)H:quinone oxidoreductase, with a K m similar to the well-characterized substrate menadione. Sensitivity of the nitroblue tetrazolium reduction to superoxide dismutase indicated that the reduction of LY 83583 by NAD(P)H:quinone oxidoreductase leads to superoxide generation. The localization of NAD(P)H:quinone oxidoreductase activity to astrocytic cells suggests a role for glia in combating oxidative insults to brain and in activating quinone-like drugs such as LY 83583.  相似文献   

6.
Lazova  G.N.  Kicheva  M.I.  Popova  L.P. 《Photosynthetica》2000,36(4):631-634
Short-term (2 h) treatment with 10 µM abscisic acid decreased stomatal conductance and net photosynthetic rate, and increased carbonic anhydrase activity in pea seedlings. The treatment with 10 µM methyl jasmonate did not significantly affect these parameters.  相似文献   

7.
H-rev107 is a member of the HREV107 type II tumor suppressor gene family and acts as a phospholipase to catalyze the release of fatty acids from glycerophospholipid. H-rev107 has been shown to play an important role in fat metabolism in adipocytes through the PGE2/cAMP pathway, but the detailed molecular mechanism underlying H-rev107-mediated lipid degradation has not been studied. In this study, the interaction between H-rev107 and cytochrome P450 reductase (POR), which is involved in hepatic lipid content regulation, was determined by yeast two-hybrid screen and confirmed by using in vitro pull down assays and immunofluorescent staining. The expression of POR in H-rev107-expressing cells enhanced the H-rev107-mediated release of arachidonic acid. However, H-rev107 inhibited POR activity and relieved POR-mediated decreased triglyceride content in HtTA and HeLa cervical cells. The inhibitory effect of H-rev107 will be abolished when POR-expressing cells transfected with PLA2-lacking pH-rev107 or treated with PLA2 inhibitor. Silencing of H-rev107 using siRNA resulted in increased glycerol production and reversion of free fatty acid-mediated growth suppression in Huh7 hepatic cells. In summary, our results revealed that H-rev107 is also involved in lipid accumulation in liver cells through the POR pathway via its PLA2 activity.  相似文献   

8.
The objective of this study was to identify factors which limit leaf nitrate reductase (NR) activity as decline occurs during flowering and beginning seed development in soybean (Glycine max [L.] Merr. cv Clark). Level of NR enzyme activity, level of reductant, and availability of NO3 as substrate were evaluated for field-grown soybean from flowering through leaf senescence. Timing of reproductive development was altered within one genotype by (a) exposure of Clark to an artificially short photoperiod to hasten flowering and podfill, and (b) the use of an early flowering isoline. Nitrogen (N) was soil-applied to selected plots at 500 kilograms per hectare as an additional variable. Stem NO3 concentration and in vivo leaf NR activity were significantly correlated (R2 = 0.69 with nitrate in the assay medium and 0.74 without nitrate in the medium at P = 0.001) across six combinations of reproductive and soil N-treatment. The supply of NO3 from the root to the leaf tissue was the primary limitation to leaf NR activity during flowering and podfill. Levels of NR enzyme and reductant were not limiting to leaf NR activity during this period.  相似文献   

9.
茉莉酸甲酯是植物细胞响应外界刺激产生的重要信号分子,与植物次生代谢物的生物合成有关。本研究考察了茉莉酸甲酯(methyl jasmonate,MeJA)对丹参培养细胞中迷迭香酸(rosmarinic acid,RA)生物合成的影响。结果显示,诱导24h后可显著提高丹参愈伤细胞中RA的积累量及其相关酶(PAL、TAT)的活性,在48h时RA积累量和酶活性达到最大。布洛芬(IBu)处理可抑制MeJA对RA积累量和相关酶活性的促进作用,外源施加MeJA可部分解除IBU对RA合成及其相关酶活性的抑制作用。说明MeJA可以显著促进丹参培养细胞中RA的生物合成,IBU抑制了MeJA合成、PAL和TAT活性,从而导致了RA合成受阻。  相似文献   

10.
茉莉酸甲酯能减缓水分胁迫时期花生幼苗(三叶期)叶片相对合水量的降低,明显提高抗旱性。经过茉莉酸甲酯处理的花生幼苗,在水分胁迫条件下,体内超氧物歧化酶和过氧化氢酶的活性下降程度比未经处理的轻,超氧物歧化酶同工酸酶带数则较多,抗坏血酸含量也较高,以减少雨二醛在叶片中的积累。  相似文献   

11.
Tan  Junping  Han  Muxian  Mao  Dun  Cheng  Shuiyuan  Ye  Jiabao  Liu  Xiaomeng  Zhang  Xian  Zheng  Jiarui  Xu  Feng  Chen  Zexiong  Zhang  Weiwei  Liao  Yongling 《Plant Molecular Biology Reporter》2022,40(1):81-94
Introduction

 Terpene trilactones (TTLs) are one of the main active ingredients of Ginkgo biloba. Owing to TTL’s unique chemical structure, it is difficult to increase TTL content through chemical and biological methods. Studying its regulatory mechanism is important in the G. biloba industry.

Results

The effect of exogenous methyl jasmonate (MeJA) on the physiological and molecular mechanism of TTL biosynthesis was studied. These results showed that MeJA treatment could improve the TTL contents, soluble sugar, starch, soluble protein, endogenous hormones (ZT, GA3, IAA, and ABA), antioxidant enzymes (catalase, peroxidase, and superoxide dismutase), and the efficiency of photosynthesis in G. biloba leaves. A total of 100 differentially expressed genes (DEGs) were identified between the control group and MeJA treatment through RNA-seq analysis. The results indicated that exogenous MeJA treatment upregulated the expression levels of the following genes: BMY (beta-amylase) in the starch and sucrose metabolic pathway; PEX7 (peroxin-7) in the peroxisome pathway; psbA (photosystem II reaction center D1 protein), psbC (photosystem II CP43 chlorophyll apoprotein), psaA (photosystem I P700 chlorophyll a apoprotein A1), and petF (photosynthetic electron transport ferredoxin) in the photosynthesis pathway; and CYP450 (Gb-16765) (cytochromeP450).

Conclusions

Exogenous MeJA treatment can promote physiological indexes (photosynthetic efficiency, starch, sucrose, antioxidant enzyme activities, etc.) and then regulating differential genes, thus controlling the synthesis of TTLs.

  相似文献   

12.
通过盆栽试验,研究了外源茉莉酸甲酯(MeJA)处理对低温、干旱和极端高温胁迫下蝴蝶兰幼苗叶绿素荧光参数和抗氧化指标的影响。结果表明,较高浓度的MeJA(150和200μmol·L-1)提高了非生物胁迫下蝴蝶兰幼苗叶片最大光化学效率(Fv/Fm)和实际光化学效率(ΦPSII),降低了叶片相对电导率,还使得超氧化物歧化酶(SOD)、过氧化氢酶(CAT)和过氧化物酶(POD)活性升高,丙二醛(MDA)含量降低。表明MeJA作为一种生物调节剂,一定浓度的处理对蝴蝶兰幼苗抗逆性的提高具有明显效果。  相似文献   

13.
14.
研究了水杨酸(SA)和茉莉酸甲酯(MeJA)处理对丹参(Salvia miltiorrhiza Bunge)幼苗叶片显微结构、叶片光合能力及幼苗中非结构糖积累的影响.结果显示:SA处理增加了丹参幼苗叶片气孔密度;叶肉细胞排列紧密、体积减小,叶肉细胞内叶绿体数目减少,但叶绿体体积增大,叶绿体基粒片层结构的数目增加;叶片中叶绿素a、b含量、叶气孔导度、蒸腾速率以及净光合速率均增加;同时,幼苗根中和叶片中酸性转化酶活性降低,幼苗地上部分蔗糖含量及可溶性糖总量显著高于对照.MeJA处理减少了叶片气孔密度,气孔发育畸形;叶肉细胞间隙增大,栅栏细胞层数减少,叶肉细胞内叶绿体数目减少,叶绿体体积减小,叶绿体基粒片层结构被破坏;叶片中叶绿素a及类胡萝卜素含量、叶片的净光合速率低于对照,叶气孔导度、蒸腾速率增强;同时,幼苗根中及叶中酸性转化酶活性增加,幼苗根中蔗糖含量及可溶性糖总量显著低于对照.可见,SA处理能促进植物叶片显微结构发育,增强叶片光合能力,抑制蔗糖降解并促进蔗糖积累;而MeJA处理则破坏了植物叶片显微结构,降低了叶片光合能力,促进了蔗糖降解并减少蔗糖积累.  相似文献   

15.
Hristova  V.A.  Popova  L.P. 《Photosynthetica》2002,40(4):567-574
Twelve-day-old barley seedlings were supplied with 23 M methyl jasmonate (MeJA) or 10 M paraquat (Pq) via the transpiration stream and kept in the dark for 24 h. Then they were exposed to 100 mol m–2 s–1 PAR and samples were taken 1, 2, 3, and 6 h after irradiation. Treatment of seedlings with MeJA alone resulted in decreased content of chlorophyll (Chl), and net photosynthetic (P N) and transpiration rates. Pq treatment led to a decrease in Chl content and to a very strong inhibition of P N, the effects were manifested by 1 h of irradiation. Pq treatment did not affect the activity of ribulose-1,5 bisphosphate carboxylase (RuBPC, EC 4.1.1.39) but increased the activity of the photorespiratory enzymes phosphoglycolate phosphatase (PGP, EC 3.1.3.18), glycolate oxidase (GO, EC 1.1.3.1), and catalase (EC 1.11.1.6). Pre-treatment of seedlings with MeJA before exposure to Pq fully blocked the inhibitory effect of Pq on photosynthesis and protected against subsequent Pq-induced oxidative damage.  相似文献   

16.
Wang  Junwei  Mao  Shuxiang  Xu  Haoran  Wu  Qi  Liang  Mantian  Yuan  Yiming  Liu  Mingyue  Huang  Ke  Wu  Qiuyun 《Plant Molecular Biology Reporter》2020,38(1):62-74
Plant Molecular Biology Reporter - The effects of S and Se treatment on cabbage, especially the interactions of S and Se metabolism with the biosynthesis of glucosinolate (GSL), including...  相似文献   

17.
Nitrate reductase activity in the leaves of a number of plants after transfer from light to dark was assayed both by in vivo and in vitro methods. The initial activity persisted during the dark phase for a considerable length of time and declined gradually. After exposure to light again, the NR activity increased rapidly. The possibility of nitrate assimilation in complete darkness is discussed.  相似文献   

18.
The ester and lactone fraction possessing the most attractive aroma was separated from the aroma concentrate of Ceylon flavory tea by silica-gel column chromatography and analyzed by GC-MS.

Methyl 2-(cis-2′-pentenyl)-cyclopentanone-3-acetate(methyl jasmonate), 5-(cis-2′-pentenyl)-5-pentanolide (jasmine lactone), 2,3-dimethyl-2-nonen-4-olide, 4-octanolide, 4-nonanolide and 5-decanolide were newly identified as the constituents of tes aroma. Former two compounds seemed to carry a major share of aroma character of Ceylon flavory tea.  相似文献   

19.
The effect of methyl jasmonate (JA-Me) on the induction of gum was studied in relation to the action of ethylene in peach (Prunus persica Batsch cv. Benishimizu) shoots. JA-Me applied at concentrations of 0.1–2.5% (w/w) in lanolin paste to current growing or older shoots substantially induced gums 3 days after treatment. The amount of gums exuded increased depending on the dose of JA-Me. Ethephon (2-chloroethyl- phosphonic acid) at 1 or 2% (w/w) in lanolin induced gum and strongly enhanced the promoting effect of JA-Me on gum formation. JA-Me also induced anthocyanin accumulation in current growing shoots, but ethephon did not. Anthocyanin accumulation in response to JA-Me at a concentration of 10 mg/liter or higher was observed also in the cut shoots of peach. Ethephon (100 mg/liter) substantially inhibited anthocyanin accumulation induced by JA-Me. These facts suggest that JA-Me plays an important role in gum formation as well as ethylene and in anthocyanin accumulation and that these processes are not necessarily accompanied by each other in peach shoots. Received January 26, 1998; accepted March 4, 1998  相似文献   

20.
Berger S  Bell E  Mullet JE 《Plant physiology》1996,111(2):525-531
Jasmonates are plant signal molecules that are derived from lipids through the action of lipoxygenase. Jasmonates regulate gene expression during plant development and in response to water deficit, wounding, and pathogen elicitors. The signal transduction chain that mediates jasmonate action was investigated by isolating and studying two methyl jasmonate (MeJA)-insensitive mutants of Arabidopsis thaliana. The recessive mutants, jin1 and jin4, are nonallelic and neither corresponds to coi1, a previously identified MeJA-insensitive mutant. Both mutants showed reduced sensitivity to MeJA-mediated root growth inhibition as well as reduced MeJA induction of AtVsp in leaves. Expression of AtVsp in flowers was not altered in the mutants. Furthermore, MeJA modulation of the jasmonate-responsive lipoxygenase and phenylalanine ammonia lyase genes was not altered in the mutants. jin4 plants exhibited increased sensitivity to abscisic acid in seed germination assays, whereas jin1 plants showed wild-type sensitivity. Neither mutant showed altered sensitivity to ethylene in hypocotyl growth inhibition assays. jin1 and jin4 identify genes that modulate the response of AtVsp to MeJA in leaves of A. thaliana.  相似文献   

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