Involvement of Protein Tyrosine Phosphatases BcPtpA and BcPtpB in Regulation of Vegetative Development,Virulence and Multi-Stress Tolerance in Botrytis cinerea

Tyrosine phosphorylation and dephosphorylation have emerged as fundamentally important mechanisms of signal transduction and regulation in eukaryotic cells, governing many processes, but little has been known about their functions in filamentous fungi. In this study, we deleted two putative protein tyrosine phosphatase (PTP) genes (BcPTPA and BcPTPB) in Botrytis cinerea, encoding the orthologs of Saccharomyces cerevisiae Ptp2 and Ptp3, respectively. Although BcPtpA and BcPtpB have opposite functions in conidiation, they are essential for sclerotial formation in B. cinerea. BcPTPA and BcPTPB deletion mutants ΔBcPtpA-10 and ΔBcPtpB-4 showed significantly increased sensitivity to osmotic and oxidative stresses, and to cell wall damaging agents. Inoculation tests showed that both mutants exhibited dramatically decreased virulence on tomato leaves, apples and grapes. In S. cerevisiae, it has been shown that Ptp2 and Ptp3 negatively regulate the high-osmolarity glycerol (HOG) pathway and the cell wall integrity (CWI) pathway. Although both BcPtpA and BcPtpB were able to inactive Hog1 and Mpk1 in S. cerevisiae, in contrast to S. cerevisiae, they positively regulate phosphorylation of BcSak1 (the homologue of Hog1) and BcBmp3 (the homologue of Mpk1) in B. cinerea under stress conditions. These results demonstrated that functions of PTPs in B. cinerea are different from those in S. cerevisiae, and BcPtpA and BcPtpB play important roles in regulation of vegetative development, virulence and in adaptation to oxidative, osmotic and cell-wall damage stresses in B. cinerea.     

Contributions of algalization to rice growth,yield, N attributes and incidence of infestation with the blast fungusPyricularia oryzae under different fungicidal treatments

Inoculation of the Japonica rice, Giza 171, with blue-green algae along with 36 kg N/ha or complete N fertilization by 108 kg N/ha were tested along with blast-controlling fungicides: Kitazin-17, Fuji-one and Beam. The algal inoculum, which containedAnabaena cylindrica, Anabaena oryzae, Nostoc muscorum and Tolypothrix tenuis, was applled as 100 kg soil-based inoculum (90% moisture)/ha 5 days after transplanting. Plant growth, yield, N content and fertilizer-N-use efficiency were increased and the incidence and severity of leaf and neck intection withPyricularia oryzae were decreased by treatment with the fungicides applied with the algae along with 36 kg N/ha inslead of 108 kg N/ha without algae.

---

Résumé On a testé l'inoculation du riz Japonica, Giza 171 avec l'algue bleu-verte, simultanément avec la fertillisation azotée soit à 36 kg N/ha solt complète à 108 kg N/ha et simultanément avec les fongicides Kitazin-17, Fuji-1 et Beam. L'inoculum d'algues, qui contenaltAnabaena cylindrica, Anabaena oryzae, Nostoc muscorum etTolypothrix tenuis, étalt appliqué à raison de 100 kg humides à 90% d'inoculum à base de sol par ha, 5 jours aprés la transplantation. La croissance des plantes, leur rendement, leur contenu azoté ainsi que l'efficience de la fertillisation azotée ont augmenté tandis que l'incidence et la sévérité de l'infection des feullies et du col parPyricularia oryzae ont décru par le traitement aux fongicides appliqué simultanément avec les algues et 36 kg N/ha par rapport au traitement à 108 kg N/ha sans algues.

     

Efficiency of rice fertilization schedules including cyanobacteria under soil application of phosphate and molybdate

Productive tillering, grain and straw yields and N-contents of indica rice IR-28 were increased more by urea fertilizer at 48 or 96 kg N/ha along with Inoculation by cyanobacteria than by using 144 kg N/ha without inoculation. Fertilizer N-use efficiency was increased by the cyanobacteria and decreased with increasing amount of urea fertilizer. Further enhancement was obtained by soil application of calclum superphosphate at 36 kg P₂O₅/ha or sodium molybdate at 1 ppm Mo along with cyanobacteria and/or urea. Application of phosphate, however, slightly diminished the enhancement by molybdate.The author is with the Sakha Agricultural Research Station, Kafr El-Sheikh, Egypt.     

中药药效物质的研究方法

中药药效物质的研究是中药现代化研究的核心,科学阐明中药临床治疗的物质基础,是中药药效学研究的最终目标。现阶段中药药效物质基础研究方法主要有化学分离分析、生物色谱法和虚拟筛选等方法。本文对现有中药药效物质基础的几种研究方法进行了分类,并对其特点进行了介绍。     

基于“无废理念”的纺织服装工业区绿色化改造模式研究

通过对中国工业区,特别是纺织服装工业区"产废"情况的梳理,明确针对污染严重,经济效益不高的工业区进行改造的必要性。为实现对纺织服装工业区绿色化改造,从"无废理念"出发,重点研究纺织服装工业区绿色化改造的可实施路径。在研究方法上将纺织服装工业区作为研究整体,基于可持续发展思想,构建纺织服装工业区经济、社会、环境复合生态系统,运用层次分析法,选取对于该类工业园区具有代表性的经济、社会、环境指标进行评价,通过评价后总的分值,结合生命周期规律,将需要改造的纺织服装工业区进行初步筛选。同时,利用经济、社会、环境各子系统的分值,对具体改造模式加以判别。文章通过对纺织服装工业区不可持续性的内涵挖掘,将工业区绿色化改造模式与改造内容建立关联,可以通过产业绿色化改造和建成空间绿色化改造,来实现工业园区的升级与转型,进而实现可持续发展。最后,根据模式判别结果,针对不同模式在产业与建成空间的不同特征,提出相应的绿色化改造方法和政策建议。在结论中总结基于"无废理念"纺织服装工业区绿色化改造与可持续发展的辩证关系。此方法适用于其他类型的工业区改造模式判别,以促进工业区的可持续发展。     

Anti-atherosclerosis effect of H2S donors based on nicotinic acid and chlorfibrate structures

Based on the structures of nicotinic acid and chlorfibrate, a series of new H₂S donors were synthesized and their anti-atherosclerosis activities using Ox-LDL RAW 264.6 cells as model were evaluated. The release test showed that all the compounds could release H₂S effectively and showed low cytotoxicity. In the bioactivity experiments, compounds 1, 3, 9 and 14 increased the survival rate of HUVEC cells treated by ox-LDL; among four compounds, compounds 1 and 3 displayed higher activity than the others. In the foam cell model, compounds 1 and 3 were found to inhibit the formation of foam cells and significantly reduced the content of TC and FC in foam cells. They had more obvious effects on lipid reduction than those of nicotinic acid and chlorfibrate. In anti-oxidation, compounds 1 and 3 significantly reduced ROS and MDA and increased the expression level of SOD, whereas the precursor compounds, niacin and chlorfibrate had little antioxidant effect. In addition, both compounds also inhibited the inflammatory response in foam cells, with reducing pro-inflammatory factor TNF-α and increasing anti-inflammatory cytokine IL-10. WB assay showed that the tested compounds inhibited the expression levels PI3K, Akt and NF-κb proteins. In conclusion, the compounds as H₂S donors could protect HUVEC cells from damage and inhibit the formation of foam cells by inhibiting PI3K/Akt/NF-κb signal pathway. All these suggest the compounds have potential to be candidate for anti-atherosclerosis medicines.     

Involvement of FgERG4 in ergosterol biosynthesis,vegetative differentiation and virulence in Fusarium graminearum

The ergosterol biosynthesis pathway is well understood in Saccharomyces cerevisiae, but currently little is known about the pathway in plant‐pathogenic fungi. In this study, we characterized the Fusarium graminearum FgERG4 gene encoding sterol C‐24 reductase, which catalyses the conversion of ergosta‐5,7,22,24‐tetraenol to ergosterol in the final step of ergosterol biosynthesis. The FgERG4 deletion mutant ΔFgErg4‐2 failed to synthesize ergosterol. The mutant exhibited a significant decrease in mycelial growth and conidiation, and produced abnormal conidia. In addition, the mutant showed increased sensitivity to metal cations and to various cell stresses. Surprisingly, mycelia of ΔFgErg4‐2 revealed increased resistance to cell wall‐degrading enzymes. Fungicide sensitivity tests revealed that ΔFgErg4‐2 showed increased resistance to various sterol biosynthesis inhibitors (SBIs), which is consistent with the over‐expression of SBI target genes in the mutant. ΔFgErg4‐2 was impaired dramatically in virulence, although it was able to successfully colonize flowering wheat head and tomato, which is in agreement with the observation that the mutant produces a significantly lower level of trichothecene mycotoxins than does the wild‐type progenitor. All of these phenotypic defects of ΔFgErg4‐2 were complemented by the reintroduction of a full‐length FgERG4 gene. In addition, FgERG4 partially rescued the defect of ergosterol biosynthesis in the Saccharomyces cerevisiae ERG4 deletion mutant. Taken together, the results of this study indicate that FgERG4 plays a crucial role in ergosterol biosynthesis, vegetative differentiation and virulence in the filamentous fungus F. graminearum.