小桐子枝叶提取物对植物病原真菌的生物活性

采用菌丝生长抑制法,测定了小桐子枝叶6种不同溶剂提取物对小麦赤霉病菌、稻瘟病菌、烟草疫霉菌和辣椒疫霉菌的抑制作用,从中筛选出抑制作用最强的粗提物进行进一步的活性组分分离和抑菌活性测定。结果表明小桐子枝叶的乙醇提取物对4种植物病原菌抑制活性最高,在浓度为0.8 g·L^-1时,小桐子枝叶的乙醇提取物对小麦赤霉病菌、稻瘟病菌、烟草疫霉菌、辣椒疫霉菌菌丝生长抑制率分别为：87.1%、90.3%、86.4%、77.9%,其抗菌活性与农药世高均无显著差异;在小桐子枝叶乙醇提取物的不同溶剂萃取物对稻瘟病菌和烟草疫霉病菌进行生物活性追踪测试中发现,石油醚和水萃取物都具有较好的活性,当浓度为0.8 g·L^-1时,石油醚和水萃取物对两种病菌抑制率都达50%以上。表明小桐子枝叶含有丰富的抗植物病原真菌活性物质,且主要存在于小桐子枝叶乙醇提取物的石油醚相和水相中。     

Only the Complete NADH:Nitrate Reductase Activity is Inhibited by Magnesium, not the Partial Activities

In response to in situ dark modulation, or in vitro ATP preincubationof higher plant nitrate reductase, Mg²⁺ inhibits NADH:nitratereductase activity but not MV:nitrate reductase activity incrude extracts. Also for the purified enzyme the complete NADH:nitratereductase activity is inhibited by Mg²⁺, but not the partialMV:nitrate reductase or Cyt c reductase activities. (Received October 13, 1993; Accepted January 24, 1994)     

Comparative studies on the effects of anions on ATPase and acid phosphatase activities from different sources

The effect of several anions on Mg²⁺-ATPase activity [EC 3.6.1.3 [EC] ]was studied in crude extracts of the following sources: twelvespecies of bacteria, one fungus, one yeast, six species of algae,five higher plant tissues, and two animal tissues. All the materialsexamined exhibited Mg²⁺-ATPase activity at pH 7.5. Except fora few species of bacteria, blue-green alga and etiolated seedlingsof a leguminous plant, Mg²⁺-ATPases of all the materials studiedwere stimulated two- to ten-fold by the addition of Group VIanions such as sulfite, selenite, and chromate. This stimulationseems to be a common characteristic of ATPases of most bacteria,chloroplasts, and mitochondria. On the other hand, the stimulation of acid phosphatase by sulfatewas not observed in any organism other than Thiobacillus thiooxidans. (Received July 27, 1977; )     

The Effects of Irradiance on Uptake and Assimilation of Nitrate by Young Barley Seedlings

The nitrogen economy of barley plants growing in a range ofirradiances from full shade (less than 0·5 W m^–2)to 119 W ^m–2 has been examined by analysing levels oftotal, organic and nitrate nitrogen, and by determining nitratereductase activity in leaf extracts. It has been confirmed thatroot growth is reduced in low irradiances which are also associatedwith a lower level of total nitrogen in the plant, and hencewith a lower uptake of nitrate. In all parts of the plant thelevel of organic nitrogen is higher in high light intensitybut nitrate-nitrogen as a proportion of the total is greatestin low irradiances. In the first leaf accumulation of free nitrateis substantially greater in low irradiances. The data indicate a higher level of nitrate assimilation inhigh irradiances and nitrate reductase activity in leaf extractsis higher in such conditions. When the first leaf is shadednitrate reductase activity falls to undetectable levels afterabout 4 days, but in the case of the second leaf, where thisis shaded, some reductase activity is always found, althoughthis is substantially less than that in unshaded conditions. It is concluded that in vitro rates of nitrate reduction mayover-estimate nitrate assimilation determined as increase inorganic nitrogen.     

Malate: A Possible Source of Error in the NAD Glutamate Dehydrogenase Assay

The effects of externally induced metabolic perturbations areoften studied through changes of the enzyme activity patternsin crude plant extracts. From glutamate dehydrogenase (GDH)it is reported that environmental changes not only influencethe amount of the enzymatic activity, but also the ratio ofthe aminating to the deaminating activities (NADH/NAD⁺ ratio).Using crude cell extracts of suspension cultures of wheat (Triticumaestivum L. cv. Heines Koga II) we find evidence that the pretreatmentof the homogenate directly influences this ratio. Dialysis ofthese crude cell extracts resulted in a 70% loss of the NAD⁺activity, while the NADH activity remained unchanged. The deaminatingactivity in the dialysed extract could be completely restoredupon addition of a dialysable factor which was identified tobe malate. The interference of malate with the glutamate dehydrogenasereaction is caused through the action of malate dehydrogenaseand glutamate oxaloacetate transaminase which are both presentin high activities in the extracts. Only in exhaustively dialysedcell extracts can the proper deaminating GDH activity be determined.The results are discussed in the light of the controversialreports on the variable ratio of the NADH/NAD⁺ activity of GDH. Key words: Glutamate dehydrogenase, malate, NADH/NAD⁺, activity, Triticum aestivum     

不同炮制方法对玉竹提取物得率及体外抗氧化作用的影响

以多糖、总黄酮、醇溶物和水溶物的得率及体外抗氧化活性为考察指标,研究了酒蒸和蜜蒸两种炮制方法对玉竹品质的影响。结果表明：酒蒸炮制玉竹的多糖、醇溶物得率最高,蜜蒸炮制玉竹总黄酮、水溶物的得率最高,比未炮制的玉竹（生品玉竹）中相应成分的得率分别提高了43.86%、29.53%、49.46%和34.66%。将多糖、水溶性浸出物、醇溶性浸出物及总黄酮四者得率相加的和进行比较,蜜蒸最好,蜜蒸为111.069%,酒蒸为107.309%,生品玉竹为80.926%。酒蒸炮制玉竹的多糖、水溶物对DPPH自由基的清除率均高于蜜蒸玉竹和生品玉竹,其DPPH_IC50分别为0.345±0.019和0.441±0.022 mg·mL^-1;蜜蒸炮制玉竹的总黄酮、醇溶物对DPPH自由基的清除率均高于酒蒸玉竹和生品玉竹,其DPPH_IC50分别为0.047±0.011和0.199±0.036 mg·mL^-1;在浓度为1 mg·mL^-1时,蜜蒸玉竹总黄酮对DPPH自由基的清除率最大,为90.29%,超过了浓度为0.05 mg·mL^-1的芦丁和槲皮素标品对DPPH自由基的清除率。两种炮制方法均提高了多糖、水溶物、总黄酮3种提取物的还原能力,但是降低了醇溶物的还原能力。     

蓝莓果渣提取物总酚含量及抗氧化活性研究

研究了蓝莓果渣提取物总酚含量及其抗氧化活性。分别采用水、40%乙醇及纤维素酶辅助乙醇超声提取蓝莓果渣,并用Folin-Ciocalteu试剂对3种提取物的总酚含量进行评估;并采用DPPH清除实验及O2—.清除实验对3种提取物的抗氧化活性进行研究。实验结果表明,纤维素酶辅助超声提取蓝莓果渣的总酚含量最高,可达425.36±15.21 mg GAE.100 g-1DW,远远高于水提物(169.46±9.75 mg GAE.100 g-1DW)及醇提物(218.39±12.54mg GAE.100 g-1DW)中的总酚含量。且纤维素酶辅助乙醇超声提取物对DPPH的清除能力为2.67±0.13 gVc.100 g-1DW,对O—.2的清除能力2.48±0.14 g Vc.100 g-1DW,明显好于醇提物及水提物抗氧化活性。     

L-Tyrosine carboxy-lyase of barley roots

_L-Tyrosine carboxy-lyase (E.C. 4. 1. 1. 25) was isolated fromroots of germinating barley (Hordeum vulgare). The enzyme requirespyridoxal phosphate for maximum activity. The optimum pH foractivity is about 7.0. The enzyme is inhibited by p-chloromercuribenzoateand hydroxylamine at 10^–3 M. Enzyme activity is foundin extracts from young roots, especially from those in earlystages of development, but not in extracts from shoots of thesame plant. Localization and changes in the amounts of _L-tyrosinecarboxy-lyase and aromatic amines in developing barley seedlingswere measured. Participation of carboxy-lyase in the formationof aromatic amines in barley roots is suggested. (Received July 17, 1970; )     

Ethylene: Modification of peroxidase activity and isozyme complement in cotton (Gossypium hirsutum L.)

Ethylene increased the peroxidase activity in extracts fromcotton plants (Gossypium hirsutum L.) pre-treated with the gas.The response was greatest in young leaves and plant fractionscontaining petioles and abscission zones. Ethylene also increasedthe peroxidase activity of extracts of cotton cotyledonary nodeexplants pre-treated with the gas. These data parallel someearlier reports on IAA-oxidase activity of ethylene-treatedplants. Disc gel electrophoresis of crude extracts of ethylene-treatedcotton seedlings revealed both quantitative and qualitativechanges in peroxidase isozymes from tissues treated with thegas. The possible functional role of peroxidase increased byethylene treatment is discussed in relation to leaf abscission. ¹ Present address: Department of Agronomy, New Mexico StateUniversity, Las Cruces, New Mexico 88001, U.S.A. (Received March 8, 1972; )     

Occurrence of Methyl (+)-Abscisate as an Artefact of Extraction

Alkaline methanolic extracts of avocado (Persea gratissima)fruit contain large amounts of methyl (+)-abscisate but littleor no (+)-ABA is liberated by alkaline hydrolysis of the aqueoussolution left after extraction of ether-soluble acidic and neutralcompounds. No methyl (+)-abscisate is detectable in acetoneor acidic methanol extracts but (+)-ABA can be released by alkalinehydrolysis of the aqueous solution in these experiments. Itis concluded that methyl (+)-abscisate is an artefact of extractioncaused by the methanolysis of a conjugate in neutral or basicconditions. Reports of neutral inhibitors in plant extractsrequire re-examination because some of the inhibitory activitymay be attributable to methyl (+)-abscisate formed during methanolextraction. (+)-ABA biosynthesised from (±)-[3'-¹⁴C]mevalonolactoneby avocados had a higher specific activity than had the bound(+)-ABA; this suggests that free (+)-ABA is formed first andthe conjugate is derived from this, rather than the reverse.     

Instability of thymidine kinase in plant extracts

Thymidine kinase and phosphotransferase activities were assayedin various plant tissues to examine claims that phosphotransferaseis the dominant phosphorylating mechanism. Results showed thatthymidine kinase is the principal activity in young tissuesand that its apparent absence is due to the relatively highinstability of the enzyme in plant extracts. ¹Present address: Lab. Applicazioni Agricoltura, CSN Casaccia,Roma, Italy. (Received December 5, 1973; )     

A Rapid and Simple Radioassay for Abscisic Acid using 14C-Diazomethane

A simple physical method for measuring abscisic acid concentrationin plant material is described. Abscisic acid in partially purifiedextracts was radiolabelled by reaction with ¹⁴C-diazomethaneto give ¹⁴C-methyl abscisate, which was purified from otherradiolabelled products by thin layer chromatography. Abscisicacid concentration was measured by comparison of the ¹⁴C radioactivityincorporated into plant abscisic acid with that in standard¹⁴-C-methyl abscisate prepared under the same conditions fromknown amounts of pure abscisic acid. Losses of abscisic acidwhich occurred during purification were corrected by measuringthe recovery of ³H-abscisic acid added to initial extracts. Abscisic acid concentration was measured by radioassay and byconventional electron capture-gas chromatography in oat, bean,and turgid or wilted tobacco leaves. Results from the two methodswere closely comparable. Radioassay is as rapid and sensitiveas existing procedures for measuring abscisic acid, but requiresonly simple and inexpensive chromatographic equipment.     

甘草根茎乙醇提取物抗菌活性研究

本实验采用琼脂扩散法和微量肉汤稀释法,研究了甘草根茎乙醇提取物对5种细菌(表皮葡萄球菌、金黄色葡萄球菌、枯草芽孢杆菌、大肠杆菌和绿脓杆菌)和2种真菌(白色念珠菌和黑曲霉)的抗菌活性。结果表明,甘草根茎乙醇提取物对革兰氏阳性菌非常敏感,而对革兰氏阴性菌和真菌不敏感,80%乙醇提取物对革兰氏阳性菌的MIC范围为0.156～0.312 mg·mL^-1,而10%乙醇提取物对革兰氏阳性菌的MIC范围为0.625～1.250 mg·mL^-1,表明甘草根茎抗菌活性成分在高浓度乙醇中溶解度较大,为临床上应用甘草根茎醇提物作为抗菌制剂提供了科学依据。     

DNA Biosynthesis in Chloroplasts: II. DEVELOPMENTAL VARIATION IN TTP INCORPORATION INTO DNA BY PLASTID EXTRACTS

Incorporation of [³H]TTP into DNA by pea chloroplast extractswas highly dependent on the age of the tissue from which plastidswere prepared. Catalytic activity was greatest in samples from6- to 9-d-old plants; preparations from more mature tissueswere much less effective. Moreover, activity was 3 to 10 timesgreater in younger tissues regardless of whether chlorophyll,protein or plastid number was used as the index of comparison.Enzymes from the first (oldest), second, third, and fourth (youngest)leaves of the same plants were also studied. Again, activitywas 4 to 10 times greater in samples from the youngest tissues.When plastid extracts from older leaves were mixed with thosefrom younger tissues, they did not reduce synthesis. Thus, thedecline in activity does not appear to be due to the productionof an inhibitor during plant development. One explanation forthese data is that enzymes of ctDNA replication, such as DNApolymerase, vary in activity during leaf development; thereforechanges in enzyme levels may be an important factor in controllingchloroplast DNA replication during development. We have alsoexamined the incorporation of [³H]TTP into DNA by isolated intactpea chloroplasts; in general, labelled TTP was less readilyincorporated into chloroplast DNA than was [³H]thymidine. Key words: Chloroplast DNA replication, chloroplast DNA polymerase     

Direct Transfer of Plasmid DNA from Intact Yeast Spheroplasts into Plant Protoplasts

We developed a polyethylene glycol (PEG)-mediated direct DNAtransfer method from intact Saccharomyces cerevisiae spheroplastsinto Arabidopsis thaliana protoplasts. To monitor the DNA transferfrom yeast to plant cells, ß-glucuronidase (GUS) reportergene in which a plant intron was inserted was used as a reporter.This intron-GUS reporter gene on a 2µm-based plasmid vectorwas not expressed in yeast transformants, while it expressedGUS activity when the plasmid DNA was introduced into plantcells. When a mixture of 1 x 10⁸ of S. cerevisiae spheroplastsharboring the plasmid and 2 x 10⁶ of A. thaliana protoplastswas treated with PEG and high pH-high Ca²⁺ solution (0.4 M mannitol,50 mM CaCl₂, 50 mM glycine-NaOH pH 10.5), GUS activity was detectedin the extract of the plant cells after a three-day culture.The GUS activity was higher than that of a reconstitution experimentin which the mixture of 1 x 10⁸ of S. cerevisiae spheroplastswhich did not carry the reporter gene, 2 x 10⁶ of A. thalianaprotoplasts and the same amount of the reporter plasmid DNAas that contained in 1 x 10⁸ of S. cerevisiae spheroplasts,was treated with PEG and high pH-high Ca²⁺ solution. Moreover,the GUS gene expression was resistant to micrococcal nucleasetreatment before and during PEG treatment. From these results,we concluded that plasmid DNA can be directly transferred fromintact yeast spheroplasts to plant protoplasts by a nuclease-resistantprocess, possibly by the cell fusion. ²Deceased on September 15, 1992.     

Presence of a Na+-activated ATPase in the Plasma Membrane of the Marine Raphidophycean Heterosigma akashiwo

Highly purified plasma membranes were isolated from Heterosigmaakashiwo cells, a marine raphidophycean unicellular biflagellate,by the silica microbead method, and the ATPase activity of themembranes was characterized. The ionic requirements and spectrumof effective inhibitors enable us to identify a novel Na⁺-activatedATPase in the plasma membrane of this organism. Furthermore,we detected two phosphorylated intermediate forms of ATPases,with molecular weights of 150 kDa and 95 kDa as judged by acidSDS-polyacrylamide gel electrophoresis of extracts of isolatedplasma membrane. The 150 kDa intermediate was phosphorylated in the presenceof both Mg²⁺ and Na⁺, while the 95 kDa intermediate was phosphorylatedin the presence of Mg²⁺ alone. Both were dephosphorylated inthe presence of monovalent cations. These results indicate thatthe former intermediate was a Na⁺-activated ATPase, similarto Na⁺,K⁺-ATPases from animals, and the latter was similar toH⁺,K⁺-ATPases from higher plants. The physiological significanceof the two kinds of ATPase in the plasma membrane of marinealgae. (Received March 15, 1989; Accepted June 23, 1989)     

The Distribution of 14C-labelled Assimilates in Young Apple Trees as Influenced by Doses of Supplementary Nitrogen: II. Soluble Carbohydrates and Amino Acids

Methanol extracts of young MM.104 apple trees fed ¹⁴CO₂ viaa single leaf were fractionated to compare ¹⁴C activity in totalsoluble sugar and amino acid components. ¹⁴C activity in aminoacids increased after the supply of ammonium nitrate to thesoil in plants where ¹⁴C labelled carbohydrates were presentin the roots. Estimates of specific carbon activity gave lowervalues for the amino acid carbon than the general value fortotal soluble carbohydrates. The fractionation of subsequentmethanol extracts of MM.104 roots has shown that sucrose hadlower specific activity than other components. Although thelevels of activity would accord with sucrose being a substratefor amino acid synthesis, an alternative explanation for theobserved results involving a cyclical system for transferringnitrogen is postulated.     

The Distribution of 14C-Labelled Assimilates in Young Apple Trees as Influenced by Doses of Supplementary Nitrogen: I. Total 14C Radioactivity in Extracts

Rooted shoots of apple rootstock MM.104 were grown in soil andsupplied with doses of ammonium nitrate at different stagesof shoot extension growth. ¹⁴CO₂ was supplied in associationwith the supplementary nitrogen via the largest healthy leafnear the base of the current season's shoot. Samples from thevarious regions of the plants were extracted, giving methanolicsolutions (containing principally sugars and soluble resources)and T.C.A. extracts (containing principally hydrolysis productsof available polysaccharides). These were counted for total¹⁴C activity using liquid scintillation spectrometry. Around90 per cent of the activity was present in the methanolic extracts.Virtually no ¹⁴C activity was transferred to the root regionbefore shoot extension was under way whereas up to 45 per centof the translocated activity occurred in the roots during andafter the main period of shoot extension. Nitrogen uptake hadbeen confined to these later stages but no influence of nitrogensupply on the gross distribution of ¹⁴C outside the source leafwas detected.     

ATP Synthesis in Cell-Free Extracts of Peanut (Arachis hypogaea L.) Seeds

Cell-free extracts of peanut (Arachis hypogaea L., cv. Shulamit)seeds, incubated with various substrates, synthesized ATP. Significantsynthesis occurred in the presence of AMP + PEP, NADH₂ + PEPand NAD + PEP. When the activities were examined in extractsprepared with 0.3 M mannitol, the rates were 0.6, 0.1 and 0.04nmol min^–1 mg^–1 protein, respectively. The activitiesunder such conditions were linear with time up to 90 min incubationat 30 °C. In the presence of PEP + NADH₂ there was a higherspecific activity in extracts from non-dormant seeds than fromdormant seeds. No such difference was found when PEP + AMP orNAD + PEP was used as the substrate. The temperature dependenceof the activity showed a relatively high energy of activation(Ea) for AMP + PEP and a low one if NADH₂ + PEP or NAD + PEPwas used as substrate. In buffer extracts of seeds ATP was synthesizedin the presence of the above-mentioned substrate combinationsbut the rate of activity exhibited a lag phase at the earlytime of incubation, after which higher rates of activities (ascompared with mannitol extracts) were obtained. The activitieswere Co⁺-dependent, with a K_m of about 0.7 mM. In the bufferextracts relatively high activities of adenylate kinase (EC2.7.4.3 [EC] (AK) and pyruvate kinase (EC 2.7.1.50 [EC] ) (PK) were found.AK was stimulated by ethephon (ethylene). This effect is temperature-dependentand occurs in both directions: in the presence of ADP (ATP +AMP) as well as if ATP + AMP is used as substrate to synthesizeADP. PK is Co⁺-dependent, and unaffected by ethephon. Both activitieswere stimulated by malonate. Key words: Adenylate Kinase, Arachis hypogaea, ATP synthesis, Peanut, Pyruvate kinase, Seed     

Requirement of Manganese for Electron Donation of Hydrogen Peroxide in Photosystem II Reaction Center Complex

Mn²⁺ was required for the electron donating reaction from H₂O₂,but not for that from diphenylcarbazide (DPC), in the PS IIreaction center complex which was prepared from spinach chloroplastsby Triton X-100 extraction. The reaction center complex showeda high activity of 2,6-dichloroindophenol (DCIP) photoreductionin the presence of DPC, but a low activity with H₂O₂. The H₂O₂-supportedDCIP photoreduction was suppressed by EDTA and enhanced by asmall amount of Mn²⁺. Ca²⁺ and Mg²⁺ could not replace Mn²⁺.The activation by Mn²⁺ and its binding showed two binding sitesof Mn²⁺ in the reaction center complex, with high (1.5?10⁷ M^–1)and low (1 ? 10⁶ M^–1) binding constants. (Received November 8, 1986; Accepted April 10, 1987)