Morphological and physiological comparisons ofHelicobasidium mompa andH. purpureum

Morphological and physiological comparisons were made of sevenHelicobasidium mompa isolates and fourH. purpureum isolates. Colonies of theH. mompa isolates were thin, dense, or hard and dense, and most were pale brown to brown or dark brown, while that of isolate 344c was pinkish. Colonies ofH. purpureum isolates were hard and dense, and their colonies were dark brown. Diameters of hyphae were similar forH. mompa andH. purpureum. Dimensions of conidia and morphology of conidiophores ofH. mompa isolate 344c were close to those ofH. purpureum reported previously.H. mompa isolates grew well at 23°C, 25°C or 27°C, while all isolates ofH. purpureum grew well at 23°C. Growth rates ofH. purpureum isolates was almost the same as those ofH. mompa isolates with slow growth. Polygaracturonase activity at pH 3 was variable among the isolates for bothH. mompa andH. purpureum. Itaconic acid was produced abundantly by three isolates ofH. mompa but not produced by isolate AH130, whereas all isoaltes ofH. purpureum produced a small amount of itaconic acid.     

柊叶和象草波式潜流人工湿地的对比研究

为探索柊叶和象草在人工湿地中的应用及其净化机理,该研究以柊叶和象草为人工湿地植物分别构建了波式潜流人工湿地系统,分析了柊叶和象草波式潜流人工湿地对生活污水中COD_(cr)、TN和TP的净化效果,观察了柊叶和象草两种植物在不同季节的生长状况。结果表明:经过15个月的连续运行,在表面水力负荷约0.3 m·d~(-1)的条件下,柊叶和象草波式潜流人工湿地平均去除率是COD_(cr)分别为66.1%和70.1%,TN分别为60.4%和63.7%,TP分别为74.1%和75.1%。两种植物生长良好,根系发达,象草的地上生物量是柊叶的2.1倍,地下生物量相当;冬季象草生长缓慢,柊叶部分叶片的四周干枯,但二者都不会枯亡。这说明两个人工湿地对COD_(cr)、TN和TP都具有较好的去除效果,但无显著性差异,柊叶和象草能明显提高潜流人工湿地的净化效果。     

Induction of enzymatic scavengers of active oxygen species in rice in response to infection by <Emphasis Type="Italic">Rhizoctonia solani</Emphasis>

Changes in the activities of peroxidase, ascorbate peroxidase, catalase and superoxide dismutase in rice in response to infection by Rhizoctonia solani were studied. A significant increase in peroxidase activity was observed in R. solani-inoculated rice leaf sheaths 1 day after inoculation and the maximum enzyme activity was recorded 3 days after inoculation at which period a 3-fold increase in peroxidase activity was observed compared to the untreated control. Three peroxidase isozymes viz., PO-4, PO-5 and PO-6 were induced in rice upon infection by R. solani. Ascorbate peroxidase and catalase activities significantly increased 1–2 days after inoculation and the maximum enzyme activities were recorded 5 days after inoculation. Superoxide dismutase activity increased significantly 2 days after inoculation and increased progressively, reaching four times the control value at 7 days after inoculation.     

Effect of culture temperature on the heterologous expression of <Emphasis Type="Italic">Pleurotus eryngii</Emphasis> versatile peroxidase in <Emphasis Type="Italic">Aspergillus</Emphasis> hosts

Production of recombinant versatile peroxidase in Aspergillus hosts was optimized through the modification of temperature during bioreactor cultivations. To further this purpose, the cDNA encoding a versatile peroxidase of Pleurotus eryngii was expressed under control of the alcohol dehydrogenase (alcA) promoter of Aspergillus nidulans. A dependence of recombinant peroxidase production on cultivation temperature was found. Lowering the culture temperature from 28 to 19 °C enhanced the level of active peroxidase 5.8-fold and reduced the effective proteolytic activity twofold. Thus, a maximum peroxidase activity of 466 U L^-1 was reached. The same optimization scheme was applied to a recombinant Aspergillus niger that bore the alcohol dehydrogenase regulator (alcR), enabling transformation with the peroxidase cDNA under the same alcA promoter. However, with this strain, the peroxidase activity was not improved, while the effective proteolytic activity was increased between 3- and 11-fold compared to that obtained with A. nidulans.     

入侵植物飞机草与4种牧草的竞争效应

【背景】飞机草是我国危害最严重的入侵植物之一,目前仍缺乏可持续的控制手段。【方法】运用De Wit取代试验研究法,设置2株·盆-1(42.42株·m~(-2))、4株·盆-1(84.84株·m-2)和8株·盆~(-1)(169.68株·m~(-2))3种密度,分别研究杂交狼尾草、木豆、山毛豆和宽叶雀稗与飞机草的竞争效应,以明确4种牧草对飞机草的替代控制潜力。【结果】3种密度下,杂交狼尾草和木豆均可以显著抑制飞机草的生长,其竞争平衡指数显著大于0,说明杂交狼尾草和木豆的竞争力均大于飞机草;山毛豆和宽叶雀稗的相对产量均显著小于1,其竞争平衡指数均显著小于0,说明山毛豆和宽叶雀稗的竞争力小于飞机草。【结论】杂交狼尾草和木豆可用作飞机草的替代控制植物。     

Active Suppression of EndoPG IV by Ligation of the Pro-Sequence from Stereum purpureum Pro-EndoPG I

We attempted to inactivate endopolygaolacturonase from Stereum purpureum (EndoPG) IV of identical origin by linking the pro-sequence of S. purpureum Pro-EndoPG I to the C-terminus. The recombinant Pro-EndoPG IV, expressed in Escherichia coli, had no polygalacturonase (PG) activity, but activity was acquired after partial degradation of the pro-sequence with V8 protease, as was the case for Pro-EndoPG I. These results indicate that the pro-sequence of Pro-EndoPG I can suppress the PG activity of EndoPG IV.     

Efficacy and environmental fate of Chondrostereum purpureum used as a biological control for red alder (Alnus rubra)

A field trial to assess the ability of Chondrostereum purpureum to limit the resprouting of cut red alder (Alnus rubra) was established in British Columbia, Canada. Overall, 92% of stumps inoculated with C. purpureum died in the first year and 100% were dead by the second year. C. purpureum was thus as effective as the herbicide treatments Carbopaste and liquid glyphosate (12% Vision) and reduced resprouts to zero. Naturally occurring C. purpureum spores colonized about 40% of untreated cut stumps and about 20% of the stumps treated with chemical herbicides. The peak production of C. purpureum basidiocarps occurred about 22 months after the trial was established, with C. purpureum on 66% of treated stumps. The following year, the basidiocarps persisted on 23% of treated stumps. About 600 young red alder trees were cut to act as spore traps 2 years after trial establishment, when the most C. purpureum basidiocarps were present on treated stumps in the trial. These spore-trap trees were subsequently sampled, and PCR markers were used to verify and characterize 43 dikaryotic C. purpureum individuals, none of which were identified as the released isolate 2139. There was little difference in average band-sharing with the applied isolate among pre-trial (37% average) and spore-trap (38% average) populations. There was therefore no evidence that the C. purpureum strain applied inundatively to stumps in this trial was detectable on nontarget trees in the local area or had any measurable impact on the local C. purpureum population.     

A Brominating and Hydroxylating Peroxidase from the Red Alga Cystoclonium purpureum

A particulate enzyme displaying peroxidase activity has been extracted from the red alga Cystoclonium purpureum (Huds.) Batt. The enzyme preparation was shown to contain ferri-protoporphyrin IX through its formation of formic acid hemochromogen with absorption maxima at 399, 402, 555 and 600 nm. The preparation catalyses the formation of 3-bromo-p-hydroxybenzyl alcohol from p-hydroxybenzyl alcohol in the presence of H₂O₂ and NaBr at pH = 5.4. The formation of 3-bromo-p-hydroxybenzyl alcohol was measured by gas chromato-graphy-mass spectrometry. At pH = 6.7, 4,5-di-hydroxybenzyl alcohol was formed. Addition of homogentisic acid stimulated the formation of dihydroxybenzyl alcohol and suppressed the brominating reaction. Iodide inhibits the enzyme. The results are consistent with a two-site model of the enzyme.     

Origin of the main class of repetitive DNA within selected Pennisetum species

In an attempt to identify relationships among genomes of the allotetraploid Pennisetum purpureum Schumach and closely related Pennisetum species with which it can be successfully hybridized, repetitive DNA sequences were examined. Digestion with KpnI revealed two highly repetitive fragments of 140 by and 160 bp. The possibility that these sequences could be used as genome markers was investigated. Average sequences were determined for the 140 by and 160 by KpnI families from P. purpureum and P. squamulatum Fresen. Average sequences (based upon four or five repeats) were determined for the P. glaucum (L.) R. Br. 140 by KpnI family and the diploid P. hohenackeri Hochst. ex Steud. 160 bp KpnI family. The average sequences of the 160 by KpnI families in P. purpureum and P. squamulatum differ by only nine bases. The 140 by KpnI families of the three related species, P. purpureum, P. squamulantum, and P. glaucum are nearly identical, and thus likely represent a recent divergence from a common progenitor or a common genome. Each repetitive sequence may contain internal duplications, which probably diverged following amplification of the original sequence. The 140 by KpnI repeat probably evolved from the 160 by KpnI repeat since the missing 18 by segment is part of the internal duplication that is otherwise conserved in the subrepeats. Tandemly arrayed repetitive sequences in plants are likely to be composed of subrepeats which have been duplicated and amplified.Florida Aqricultural Experiment Station series #R-02758     

Inhibitory effects of microalgae on the activation of hyaluronidase

The inhibitory effects of seven microalgae, Nostoc flagelliforme, Spirulina platensis, Porphyridium purpureum, Rhodosorus marinus,Chlorella pyrenoidosa, Dunaliella salina and Pleurochrysiscarterae on the activation of hyaluronidase were evaluated. Theinhibitory effect of the ethanol-insoluble fraction of each water extract frommicroalgae was stronger than that of the ethanol-soluble fraction. The50% inhibitory concentration (IC₅₀) of the ethanol-insolublefraction of S. platensis, P. purpureum, R. marinus, C.pyrenoidosa, D. salina and P. carterae was 0.15, 0.18, 0.26,0.94, 0.15 and 0.41 mg mL^-1, respectively. The IC₅₀ ofN .flagelliforme was not calculated, because there was no detectableinhibitory effect of this alga. The IC₅₀ of disodium cromoglycate(DSCG) used as the anti-allergic medicine was 0.14 mg mL^-1. The IC₅₀ of S. platensis, P. purpureum and D. salinawere almost the same as that of DSCG. This suggests that theethanol-insoluble fraction of S. platensis, P. purpureum and D. salina might be an anti-allergic substance. The ethanol-insoluble fractionof S. platensis and D. salina was ultrafiltered through a membranehaving a molecular exclusion limit of 20 kDa. The IC₅₀ of theresidue was stronger than that of the filtrate. These results suggest that theanti-allergic substance(s) of these microalgae may be polysaccharides.     

Relationships between peroxidases and in vitro bulbification in garlic (Allium sativum L.)

Summary The relationship between in vitro bulbification and peroxidase activities of garlic (Allium sativum L.) was studied. Two stages could be distinguished during in vitro bulb formation characterized by the peroxidase activity, isoenzymatic patterns especially of the soluble fractions, dry weight, and bulbification index (BI). The first stage, called the morphogenic stage, started after planting until 30d of culture with a maximum soluble peroxidase activity, BI=1–0.5 and low dry weight. At that time axillary buds preformed at the base of the leaves grew and the in vitro bulb was generated. The second stage (filling in and bulb maturation) started when the BI reached 0.5 at 30 d of the ontogenic cycle, as a result of the bulb assimilate accumulation phenomenon. During the morphogenic stage the soluble peroxidase activity was maximum and the zymograms showed higher intensity bands. The second stage presented anodic ionic peroxidases and substantial increase in staining of the anodic covalent peroxidase fraction. The putative role of the different isoforms of peroxidases in relation to the bulbification process is discussed.     

华南象草Pp4CL基因的克隆及其转基因烟草木质素含量分析

为探究华南象草(Pennisetum purpureumcv.Huanan)木质素合成关键酶基因的调控机制,通过同源克隆得到华南象草4-香豆酸:CoA连接酶基因(Pp4CL)的cDNA序列,长度为1 943bp,其中编码区序列1 662bp。Pp4CL蛋白由553个氨基酸组成,分子量为59.57kD,等电点为5.2,属于疏水性蛋白。该蛋白含有AMP结合结构域,属于AFD ClassⅠ超家族。在系统进化分析中,Pp4CL与At4CL1、Os4CL1遗传距离最近,聚为一支。Pp4CL氨基酸序列具有SSGTGLPKGV和GEICIRG等2个保守基序,是典型的植物4CL。构建原核表达载体pGEX-4CL,得到约88kD的Pp4CL-GST融合蛋白,为Pp4CL酶活性测定及Western免疫印迹分析奠定了基础。同时构建植物表达载体pBA-4CL,并通过叶盘法对烟草进行了遗传转化,得到3个转基因阳性株系(OX-9、OX-7、OX-4),它们中叶柄木质素总含量分别比非转基因植株(对照)提高了10.0%、16.2%和94.6%,茎秆基部节木质素总含量分别比对照提高了0.9%、4.0%和13.5%。研究结果表明,Pp4CL蛋白与木质素合成有关,过表达Pp4CL基因能够显著提高植株木质素含量。该研究结果为华南象草木质素改良工作打下了基础,同时也为深入开展牧草分子育种提供了依据。     

Ascorbate-independent electron transfer between cytochromeb 561 and a 27 kDa ascorbate peroxidase of bean hypocotyls

Summary Cytochromeb ₅₆₁ (cytb ₅₆₁) is a trans-membrane cytochrome probably ubiquitous in plant cells. In vitro, it is readily reduced by ascorbate or by juglonol, which in plasma membrane (PM) preparations from plant tissues is efficiently produced by a PM-associated NAD(P)Hquinone reductase activity. In bean hypocotyl PM, juglonol-reduced cytb ₅₆₁ was not oxidized by hydrogen peroxide alone, but hydrogen peroxide led to complete oxidation of the cytochrome in the presence of a peroxidase found in apoplastic extracts of bean hypocotyls. This peroxidase active on cytb ₅₆₁ was purified from the apoplastic extract and identified as an ascorbate peroxidase of the cytosolic type. The identification was based on several grounds, including the ascorbate peroxidase activity (albeit labile), the apparent molecular mass of the subunit of 27 kDa by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, the dimeric native structure, the typical spectral properties of a heme-containing peroxidase, and an N-terminal sequence strongly conserved with cytosolic ascorbate peroxidases of plants. Cytb ₅₆₁ used in the experiments was purified from bean hypocotyl PM and juglonol was enzymatically produced by recombinant NAD(P)H:quinone reductase. It is shown that NADPH, NAD(P)H:quinone reductase, juglone, cytb ₅₆₁, the peroxidase interacting with cytb ₅₆₁, and H₂O₂, in this order, constitute an artificial electron transfer chain in which cytb ₅₆₁ is indirectly reduced by NADPH and indirectly oxidized by H₂O₂.Abbreviations APX ascorbate peroxidase - b ₅₆₁PX cytochrome 6561 peroxidase - CPX coniferol peroxidase - cyt cytochrome - GPX guaia-col peroxidase - IWF intercellular washing fluid - MDHA monodehydroascorbate - PM plasma membrane     

Optimalization of the peroxidase production by tissue cultures of horseradish <Emphasis Type="Italic">in vitro</Emphasis>

Tissue cultures of Armoracia rusticana L., both transformed with Agrobacterium rhizogenes and nontransformed, were screened for peroxidase activity. Most of the derived and tested strains exhibited 20 times higher activity [from 99 to 723 U g⁻¹(d.m.)] than the root of the intact plant [(30 U g⁻¹ (d.m.)]. The highest peroxidase activity was found in tumour culture growing on the medium without growth regulators. The influence of the addition of sugars and heavy metal ions in the medium on peroxidase production was tested. Increase in peroxidase activity was observed after cultivation of horseradish culture with cadmium, cobalt, nickel or lead ions.This work is supported by Grant Agency of Czech Republic Project No. 526/04/0135.     

Peroxidase activity of selenoprotein GrdB of glycine reductase and stabilisation of its integrity by components of proprotein GrdE from Eubacterium acidaminophilum

The anaerobe Eubacterium acidaminophilum has been shown to contain an uncharacterized peroxidase, which may serve to protect the sensitive selenoproteins in that organism. We purified this peroxidase and found that it was identical with the substrate-specific “protein B”-complex of glycine reductase. The “protein B”-complex consists of the selenocysteine-containing GrdB subunit and two subunits, which derive from the GrdE proprotein. The specific peroxidase activity was 1.7 U (mg protein)⁻¹ with DTT and cumene hydroperoxide as substrates. Immunoprecipitation experiments revealed that GrdB was important for DTT- and NADH-dependent peroxidase activities in crude extracts, whereas the selenoperoxiredoxin PrxU could be depleted without affecting these peroxidase activities. GrdB could be heterologously produced in Escherichia coli with coexpression of selB and selC from E. acidaminophilum for selenocysteine insertion. Although GrdB was sensitive to proteolysis, some full-size protein was present which accounted for a peroxidase activity of about 0.5 U (mg protein)⁻¹ in these extracts. Mutation of the potentially redox-active UxxCxxC motif in GrdB resulted in still significant, but decreased activity. Heterologous GrdB was protected from degradation by full-length GrdE or by GrdE-domains. The GrdB-GrdE interaction was confirmed by copurification of GrdE with Strep-tagged GrdB. The data suggest that GrdE domains serve to stabilise GrdB. Dedicated to Prof. Dr. Gerhard Gottschalk.     

Effect of pH on the stability of Pleurotus eryngii versatile peroxidase during heterologous production in Emericella nidulans

Complementary DNA (cDNA) encoding the new versatile peroxidase from the ligninolytic basidiomycete Pleurotus eryngii has been expressed in the ascomycete Emericella nidulans. In recombinant E. nidulans cultures, the pH reached values as high as 8.3, correlating with a sharp decrease in peroxidase activity. Peroxidase was rapidly inactivated at alkaline pH, but was comparatively stable at acidic pH. The peroxidase inactivation in alkaline buffer could be reversed by adding Ca²⁺ and lowering the pH. However, reactivation did not result after incubating the enzyme in non-buffered E. nidulans cultures that reached pH 7.5. To optimize recombinant peroxidase production, the effect of controlling the pH in E. nidulans bioreactor cultures was studied. An extended growth period, and a significant increase in the recombinant peroxidase level (5.3-fold higher activity than in the bioreactor without pH control) was obtained when the pH was maintained at 6.8, showing that culture pH is an important parameter for recombinant peroxidase production.     

Changes in intracellular localization of peroxidase during Microsporogenesis in Gymnosperms

Cytochemical investigations on peroxidase localization during microsporogenesis inLarix europaea D.C.,Taxus baccata L. andPinus sylvestris L. have revealed striking differences in the localization and activity level of this enzyme linked with the developmental stage. The localization and level of activity of peroxidase, typical of each stage, changed in the course of microsporogenesis in a strictly orderly way, giving a characteristic and stable pattern. The pattern of intracellular peroxidase localization proved to be the same for microsporogenesis of all the gymnosperms in question. It is suggested that the identity of that pattern in plants so phylogenetically distant asTaxus baccata L. andPinus sylvestris L. indicates that peroxidase activity in gymnosperms’ microsporogenesis is connected with the fundamental and genetically well stabilized processes of meiotic cytodifferentiation. Moreover, enhanced peroxidase activity has been found in the sites of callose walls synthesis of dyads and tetrads, which suggests the participation of this enzyme in callose synthesis.     

Revision of Phymatolithon purpureum (Hapalidiales,Rhodophyta) based on ultrastructural and molecular data

ABSTRACT

To elucidate the taxonomy and phylogeny of Phymatolithon purpureum (P. Crouan & H. Crouan) Woelkerling & L.M. Irvine, we observed the type specimens and fresh samples using SEM (ultra-morphology) and analysed DNA sequences. Phymatolithon purpureum was originally described as Lithothamnion purpureum P. Crouan & H. Crouan from Mingant, Brittany, France. Our molecular phylogenetic analyses using psbA and COI–5P regions placed our collections from Ireland, UK and France in a clade with ‘P. borealis W.H. Adey, J.J. Hernandez-Kantun & P.W. Gabrielson (MH252286)’ from Iceland and ‘uncultured Corallinales (GQ917711 and GQ917512)’ from Roscoff, Brittany, France, near the type locality of P. purpureum. We show that P. purpureum is conspecific with P. borealis and P. polymorphum f. papillatum (Foslie) Foslie based on morphology and molecular data. Also, although P. purpureum has been often confused with P. laevigatum (Foslie) Foslie because of their similar morphology (e.g. smooth surface and sunken tetra/bisporangial conceptacles), our molecular phylogenetic analyses indicate that P. purpureum and P. laevigatum are sister taxa. Our sequences from lectotype material of P. laevigatum and syntype material of Lithothamnion emboloides Heydrich are identical.     

Ca2+ and Mg2+ ions counteract the reduction by fosetyl-Al (aluminum tris[ethyl phosphonate]) of peroxidase activity from suspension-cultured grapevine cells

Grapevine (Vitis vinifera cv. Monastrell) cell suspension cultures were treated with 1.5 mM fosetyl-Al, a frequently used systemic fungicide for grapevine diseases caused by oomycetes. These cells showed a reduction in the level of peroxidase activity secreted into the culture media when compared to non-treated cells, the effect being mainly related to a decrease in the level of the basic B₁ peroxidase isozyme. The effect of fosetyl-Al on peroxidase was analogous to that observed with the Ca²⁺-channel blockers Co²⁺, Cd²⁺ and La³⁺, and was counteracted by Ca²⁺ ions, but was not reversed when the Ca²⁺-ionophore A23187 was added to the culture media. Moreover, the effect of fosetyl-Al on peroxidase activity and peroxidase isozymes was also partially reversed by Mg²⁺ ions but not by Sr²⁺, and was accentuated by Ba²⁺ ions. These results suggested that Ca²⁺ and Mg²⁺ ions specifically overcome the inhibitory effect of fosetyl-Al on peroxidase. In this context, an apoplastic Ca²⁺/Mg²⁺-displacement hypothesis is proposed for the mechanism of action of fosetyl-Al on peroxidase from grapevine cells.     

Relationship between peroxidase activity and the amount of fully N-methylated compounds in bean plants infected by Pseudomonas savastanoi pv. phaseolicola

Changes in the level of endogenous formaldehyde (HCHO), some N-methylated compounds (choline and trigonelline) and peroxidase activity were examined in the leaves of bean genotypes (Phaseolus vulgaris L.) with different disease-sensitivity during ontogenesis in the stressfree condition and after natural infection by Pseudomonas savastanoi pv. phaseolicola (until the appearance of lesions). HCHO, as its dimedone adduct, and fully N-methylated compounds were determined by overpressured layer chromatography (OPLC) in different developmental stages and in the infected leaves/leaf discs. Peroxidase activity was measured by a spectrophotometric method. HCHO level decreased with ageing of the primary leaf and accordingly in the leaves at different developmental stages, then increased again in both cases due to the demethylation and methylation processes. Concentration of choline and trigonelline as potential HCHO generators decreased considerably while peroxidase activity increased with ageing of the plants. Comparing the symptomless and the Pseudomonas infected leaf discs (with watersoaked lesions) we found a decrease in the level of HCHO, choline and trigonelline and there was detectable increase in the peroxidase activity in the infected leaf tissues. Our findings are in accordance with previously published results that peroxidases play an important role in oxidative demethylation processes. Our hypothesis is that the high level of HCHO in the old leaves can originate from methylated components as the result of peroxidase activity and this high level may lead to the old leaf being resistant to pathogen. This conclusion is supported by the fact that the leaves of susceptible bean genotypes became resistant to Pseudomonas while growing older.