茅苍术挥发油对三种内生真菌及七种外源真菌的抑菌活性

为了研究宿主植物次级代谢产物对内生真菌生长的抑制作用,以药用植物茅苍术及其内生真菌为材料,采用有机溶剂萃取法提取茅苍术挥发油,应用滤纸片扩散法和平板涂布法研究茅苍术挥发油对茅苍术内生真菌及其他外源真菌的抑菌作用.结果表明: 挥发油对3种内生真菌生长具有抑制作用;对酵母、水霉有很强的抑菌活性;对根霉、犁头霉抑菌作用不明显;对绿色木霉、黑曲霉的产孢具有抑制作用;对疫霉生长无抑制作用.在高浓度挥发油胁迫下,内生真菌菌丝分支增多,分支间距离变短,气生菌丝生长受到抑制.两种内生真菌对挥发油具有代谢转化能力,降低了其主要成分的含量.表明茅苍术挥发油对内生真菌生长具有限制作用,但内生真菌能够通过自身分解代谢适应茅苍术挥发油.     

药用植物内生菌对宿主植物促生作用机制研究进展

植物内生菌是一类能够代谢产生新颖生物分子和多种酶类的重要微生物资源,在农业、植保、制药等领域具有广阔的应用前景。了解内生菌与药用植物间相互关系是当前促进药用植物生长和提升药材品质的重要途径。植物内生菌资源具有丰富的多样性,对宿主植物生长发挥着重要功能,如固氮、溶磷、产生铁载体、分泌植物激素吲哚乙酸(indole-3-acetic acid,IAA)、产生ACC脱氨酶(1-aminocyclopropane-1-carboxylate deaminase)、增强宿主抗逆性、产生次生代谢产物等。本文通过相关文献回顾,聚焦内生菌与药用植物间的关系,着重探讨药用植物内生菌对宿主植物的促生作用机制,展望新技术在植物内生菌研究方面的应用,以便有效利用分子手段阐明内生菌对药用植物的促生长作用,为其在相关领域的应用提供理论参考。     

温郁金内生真菌Chaetomium globosum L18对植物病原菌的抑菌谱及拮抗机理

通过体外培养法,研究了药用植物温郁金内生真菌Chaetomium globosum L18对几种常见的植物病原菌的抑菌谱及其拮抗机理。结果表明,Chaetomium globosum L18对多种植物病原真菌和细菌均有不同程度的抑制作用,具有较广的抑菌谱,但对不同植物病原菌的抑制作用具有显著性差异(P<0.05),抑制率最高可达到92.9%;抑菌机制结果显示,竞争作用和重寄生作用是其主要的拮抗机制之一;发酵产物抑制作用测定发现,内生真菌Chaetomium globosum L18能够分泌产生抗菌物质抑制病原菌菌丝的生长和孢子萌发,可引起病原菌菌丝菌丝膨大成串珠状,分枝增多,分枝顶端膨胀后细胞壁破裂,原生质外溢,产生溶菌作用;使分生孢子萌发畸形,萌发率降低。     

药用植物内生真菌的多样性及生物功能研究进展

药用植物内生真菌资源丰富,其代谢产物常具有抗肿瘤、抗氧化、抑菌等作用,能产生药用植物生长调节物质及与宿主相同或类似的次生代谢产物,从而成为近年来的研究热点。本文对药用植物内生真菌的分离鉴定、多样性、生物活性及生物学功能等方面进行综述,以期为今后筛选及利用有效的药用植物内生真菌奠定基础。     

植物内生菌及其防治植物病害的研究进展

综述了植物内生菌及其防治植物病害的研究进展.植物内生菌分布广,种类多,几乎存在于所有目前已研究过的陆生及水生植物中,目前全世界至少已在80个属290多种禾本科植物中发现有内生真菌,在各种农作物及经济作物中发现的内生细菌已超过120种.感染内生菌的植物宿主往往具有生长快速、抗逆境、抗病害、抗动物危害等优势,比未感染内生菌的植株更具生存竞争力.植物内生菌的防病机理主要表现在通过产生抗生素类,水解酶类,植物生长调节剂和生物碱类物质,与病原菌竞争营养物质,增强宿主植物的抵抗力以及诱导植物产生系统抗性等途径抑制病原菌生长.另外,对植物内生真菌和内生细菌的分离、筛选和检测方法;利用植物内生菌控制植物病害的途径如人工接种内生菌,利用内生菌代谢产生的抗生素以及将内生菌作为基因工程的载体菌等进行了综述.同时,对植物内生菌作为生物防治因子未来发展前景及存在的问题进行了讨论.利用植物内生菌作为生物防治因子进行大田防病,需要考虑它的病理学、生态学和形态学等方面的影响.     

芦荟内生菌内生哈茨木霉LH-7对植物病原菌的抗性

通过体外培养方法,研究了药用植物库拉索芦荟内生真菌内生哈茨木霉LH-7对9种常见植物病原菌的抑菌谱及其拮抗机理.结果表明： 内生哈茨木霉LH-7 对供试植物病原真菌具有显著的抑制作用(抑制率为62.4%～88.4%),且营养竞争和重寄生是其主要拮抗机制.该菌株的代谢产物中具有能够抑制病原菌生长及孢子萌发的活性物质,其作用可导致病原菌菌丝体生长的畸形、细胞壁破裂、产孢结构发育不健全、孢子形成及萌发率降低,从而有效抑制病原菌的生长和繁殖.
     

枸骨益生菌的筛选及其抑菌作用

采用涂布平板法分离药用植物枸骨可培养内生细菌,采用对峙法和发酵滤液培养法筛选对植物病原菌具高抑制作用的菌株,通过镜检和显微摄影观察处理组菌丝的变化,对16SrDNA PCR产物进行测序和同源性分析菌株的系统发育关系,通过形态、生理生化特征和16SrDNA序列比对确定菌株的分类地位.从枸骨健康植株的根、茎、叶及果实中分离得到85株内生细菌,筛选出对烟草赤星病菌、稻瘟病菌、棉花枯萎病菌等有较强抑菌作用的10株菌,初步鉴定为4属7种.其中,抑菌效果最强的GG78(60.3％)、GG31 (48.1％)、GG3(61.0％)分别属于阴沟肠杆菌、路德维希肠杆菌和蜡样芽孢杆菌.受抑制病原菌菌丝均发生畸形、扭曲,局部膨大形成原生质浓缩球、菌丝基部出现毛发状细分支等现象,可能与内生菌分泌到胞外具有一定抑菌或杀菌作用的代谢物质如抗生素、水解酶类、生物碱等有关.     

芦竹内生真菌F0238对植物病原菌的拮抗作用

从黄海海岸低盐药用植物芦竹(Arundo donax L．)中分离得到木霉属的内生真菌F0238,对其进行拮抗植物病原菌活性及作用机制的试验研究。结果表明F0238发酵液对Botrytis cinerea,Sclerotium rolfsii等8种植物病原菌有强的抑菌活性及抑制孢子萌发作用,且这种作用在发酵原液被稀释了160倍后仍然存在;对峙培养试验表明F0238菌对植物病原菌有很强的拮抗作用,拮抗机制主要为重寄生作用、营养竞争作用及抗生作用等。     

植物内生菌活性代谢产物最新研究进展

内生菌广泛存在于植物组织中,作为一种新型的微生物资源,具有丰富的物种多样性,也是发掘新型天然活性物质的重要途径之一,有些内生菌还能产生与宿主植物相同或相似的活性成分。因此从植物内生菌中挖掘抗菌尤其抗临床耐药菌、抗肿瘤等天然活性产物不仅为新药的研发提供了新的方向,还能在一定程度上解决传统的天然产物药源——药用植物生长缓慢、资源紧缺等问题。从多个角度概述了近年来国内外报道的植物内生菌次生代谢产物及其来源、生物活性等方面的主要成果和最新进展,以期为植物内生菌活性代谢产物的研究提供参考。     

剑叶龙血树内生真菌的分离及体外抑菌活性筛选

为研究剑叶龙血树内生真菌资源多样性,初步探讨和筛选具有抑菌活性的特异性菌株以及进一步开发剑叶龙血树内生真菌的抗菌活性化合物。该文采用植物组织分离法从剑叶龙血树茎和叶中分离内生真菌,对内生真菌进行液体发酵7 d,经乙酸乙酯萃取后制得粗提物,并采用牛津杯扩散法,以10种常见病原菌和5种临床耐药菌为靶标检测其发酵粗提物的抑菌活性,对有较好抑菌活性的内生真菌进行分子鉴定。结果表明:(1)从剑叶龙血树茎、叶中共分离得到345株内生真菌,294株对一种以上指示菌有抑制活性;(2)其中84株内生真菌对5株临床耐药菌均有不同程度的抑制活性,占所分离菌株总数的24.35%,75%的内生真菌对金黄色葡萄球菌有抑制活性。这说明剑叶龙血树中存在多种有抑菌活性的内生真菌,为剑叶龙血树内生菌抗菌活性成分挖掘及新型抗菌药物筛选奠定了基础。     

Evaluation of in vitro alpha-glucosidase inhibitory,antimicrobial, and cytotoxic activities of secondary metabolites from the endophytic fungus,Nigrospora sphaerica,isolated from Helianthus annuus

This study aimed to evaluate alpha-glucosidase inhibition and antimicrobial activity as well as cytotoxic activity of extracts from the endophytic fungus, Nigrospora sp., isolated from leaves of Helianthus annuus, which is widely cultivated for food and used as a medicinal plant. The fungus (TSU-CS003) was identified based on internal transcribed spacer ribosomal DNA sequences and fungal biomass, and fermentation broth was subjected to extraction by solvents (hexane and ethyl acetate). All extracts were tested for their antimicrobial activity, alpha-glucosidase inhibition, and cytotoxicity activity. In addition, the active extract was analyzed by using gas chromatography mass spectrometry (GC-MS) TSU-CS003 was identified as Nigrospora sphaerica. The fermentation broth extract (BE) showed strong antimicrobial activity against Staphylococcus aureus and methicillin-resistant S. aureus (Gram-positive bacteria) with minimum inhibitory concentration (MIC) values in the range of 16–32 μg/mL and a few yeasts with MIC values ranging from 64 to 128 μg/mL, especially Talaromyces marneffei with an MIC value of 4 μg/mL. The effects of BE were observed by SEM. The results showed that this extract affected the cell morphology of T. marneffei. The half-maximal inhibitory concentration (IC50) of BE from alpha-glucosidase inhibition was recorded as 17.25 μg/mL and also showed significant cytotoxicity against A549 human cancer cell lines with an IC50 value of 22.41 μg/mL. Furthermore, BE was analyzed by using GC-MS and divided into three main compounds, including 5-pentyldihydrofuran-2(3H)-one, (Z)-methyl 4-(isobutyryloxy)but-3-enoate, and 2-phenylacetic acid. This was the first report of the endophytic fungus N. sphaerica from H. annuus. It is a potential source of active metabolites, which gave the strong antifungal activity, antioxidant activity, and cytotoxicity to A549 cancer cell lines.     

Aspergillus sp. EA-LJS80的分离及其发酵液提取物七叶皂苷C的生物活性

本研究从陕西留坝紫柏山采集的七叶树Aesculus chinensis根和茎中分离出一株具有高产七叶皂苷C的内生真菌,将其编号为EA-LJS80。利用ITS序列分析鉴定其种属并对其形态进行观察;采用紫外-可见分光光度计进行全波长扫描,确定其最大紫外吸收峰;采用HPLC测定七叶皂苷C的产量;采用滤纸片扩散法研究其发酵液提取物的抑菌活性;采用CCK-8法测定提纯后七叶皂苷对肺腺癌A₅₄₉细胞的增殖抑制率,探究其生物活性。结果显示,该菌株EA-LJS80为曲霉菌属Aspergillus真菌,最大紫外吸收波长为230nm,测得提纯后七叶皂苷C的产量为9.23mg/mL。生物活性实验表明：菌株EA-LJS80的发酵液提取物对大肠杆菌Escherichia coli等4种致病菌有明显的抑菌效果;经CCK-8法测定,提纯后的七叶皂苷对肺腺癌A₅₄₉细胞的增殖有明显的抑制作用。综上所述,菌株EA-LJS80具有产七叶皂苷活性,尤其是七叶皂苷C的产量较高,且其产生的七叶皂苷具有较高的生物活性,这对于改进七叶皂苷生产模式,提高生产效率具有重要意义,同时对于七叶皂苷C的进一步研究有一定的促进作用。     

风信子中抗青霉素内生菌的分离、筛选和活性检测

通过用初筛培养基培养,从风信子叶子中分离出一种抗青霉素的内生菌,进行离体培养和抑菌活性检测。结果表明所筛选的菌株的发酵产物对细菌和真菌均有一定的抑菌活性。其中发酵液提取物对枯草芽孢杆菌有一定的抑菌活性,对苹果干腐病原菌和烟草赤星病原菌的抑菌率分别是94.8%和93.8%,而菌体内的活性物对蜡状芽孢杆菌和枯草芽孢杆菌都有较高的活性,对苹果干腐病原菌、烟草赤星病原菌和苹果轮纹病原菌的抑菌率都在80%以上。     

The chemical composition,antifungal, antioxidant and antimutagenicity properties of bioactive compounds from fungal endophytes associated with Thai orchids

Some plant‐derived bioactive compounds produced by fungal endophytes have been proven to have antimicrobial and antioxidant activities. In this study, endophytic fungi were isolated from 20 orchid samples collected in northern Thailand from 12 genera of orchids. In total, 97 isolates were isolated from the leaves (44.3%), stems (40.2%) and flowers (15.5%) of the orchid samples. The antifungal activity was investigated of the endophytic isolates against the plant pathogenic fungi. The results showed that 13 endophytic isolates provided antifungal activities against Fusarium sp., Colletotrichum sp. and Curvularia sp. The endophyte CK F05‐5, which was isolated from the flower part of Dendrobium lindleyi, was chosen for further testing because it the highest level of antifungal activity against Fusarium sp. The isolate CK F05‐5 was identified as Fusarium oxysporum on the basis of its ITS sequences of 5.8 s rRNA, and phytochemical analysis revealed the presence of coumarins. The ethyl acetate extract of CK F05‐5 was examined for its total phenolic content and antioxidant activity using Folin–Ciocalteu's reagent and 2,2‐diphenyl‐1‐picrylhydrazyl (DPPH) radical scavenging assay, respectively. The phenolic content was 160.51 mg of GAE/g of extract, and the free radical scavenging activity was 89.61 µg/ml at the half maximal inhibitory concentration (IC₅₀). The antimutagenic potential of the ethyl acetate extract of CK F05‐5 against Trp‐P‐1 mutagenic substances was determined using the Ames test which revealed that the extract of CK F05‐5 at 10 mg/plate had the highest antimutagenic activity against Trp‐P‐1 (51.2%) and 39.6% for strains TA98 and TA100, respectively. The active compounds present in the acetate extract of CK F05‐5 were examined using GC‐MS analysis, which displayed the presence of gibepyrone A, pyrrolo [1, 2‐a] pyrazine‐1, 4‐dione, hexahydro‐3‐(2‐methylpropyl) and indoleacetic acid as major components. Based on the results, this endophytic fungus contains various bioactive components that have various biological activities. This useful information could help in producing potentially valuable and novel pharmaceutical products.     

Endophytic fungi from the root tubers of medicinal plant Stephania dielsiana and their antimicrobial activity

The adverse effects of chemical synthetic fungicides on agricultural fields and the environment are driving a need to search for safer and less environmentally harmful plant protectants to move toward more sustainable development of agriculture. The endophytic fungal community associated with the medicinal plant Stephania dielsiana, and its potential for providing antimicrobial secondary metabolites were investigated. A total of 26 isolates of endophytic fungi were obtained, and 21 isolates were identified and classified into eight different genera, including Briansuttonomyces, Glomerella, Pleosporales, Diaporthe, Phoma, Penicillium, Periconia and Colletotrichum, and the most frequent endophytic species obtained were Diaporthe phaseolorum, Penicillium sp., Periconia igniari and Colletotrichum sp. The ethyl acetate (EtOAc) extract of the endophytic fungus Diaporthe phaseolorum Stdif6 displayed the most significant antifungal activity against all tested phytopathogens, with EC₅₀ values ranging from 0.0138 to 0.3103 mg/mL. While the EtOAc extract of the endophytic fungus Penicillium sp. Stdif9 exhibited greater potential for antibacterial activity, with the minimum inhibitory concentration (MIC) values against seven bacteria ranging from 1.25 to 6 mg/mL. The remarkable antimicrobial activity of fungal endophytes suggests that fungal endophytes harbored inside the root tubers of S. dielsiana hold great promise as biocontrol agents against a broad spectrum of economically significant pathogens.     

具有乙酰胆碱酯酶抑制活性的蛇足石杉内生真菌分子鉴定

在马铃薯葡萄糖液体培养基(PDB)、沙氏液体培养基(SDB)和查氏液体培养基(CDB)中发酵培养蛇足石杉内生真菌菌株SF88和LF52,乙酰胆碱酯酶(AChE)抑制活性检测结果表明,菌株SF88和LF52在PDB、SDB和CDB发酵后菌体总生物碱对AChE活性的抑制率分别为45.6%和56.7%、56.3%和68.5%、40.8%和48.3%。对这两株不产孢内生真菌的DNA ITS、18S rDNA、28S rDNA、TUB和RPB进行了测序,系统发育分析表明,SF88和LF52为Phaeosphaeriaceae科中一未知种,为开发生物碱类乙酰胆碱酯酶抑制剂(AChEI)药物提供了新的潜在菌种资源。     

蛇足石杉内生真菌无柄盘菌Pezicula sp. JR14中抑制乙酰胆碱酯酶的次级代谢产物分离

采用形态学及ITS-rDNA序列分析法,对具有抑制乙酰胆碱酯酶活性的蛇足石杉内生菌株JR14进行鉴定,确定为无柄盘菌Pezicula sp.。开展了乙酰胆碱酯酶抑制活性化合物的分离,从Pezicula sp. JR14乙酸乙酯提取物中分离到4个化合物,利用核磁共振及质谱技术将其鉴定为behenic acid (1)、himeic acid B (2)、secalonic acid A (3)和palmitic acid (4)。采用改进的Ellman比色法对分离的化合物进行活性检测,结果表明,himeic acid B (2)具有较强的乙酰胆碱酯酶抑制活性,其IC₅₀为205μg/mL（0.64mmol/L）。     

一株海洋真菌Penicillium sp.QF046的细菌群体感应抑制剂的分离和鉴定

目的:从海洋真菌中筛选得到新型群体感应抑制剂,并对其进行活性评价。方法:首先利用紫色杆菌CV026指示菌株对真菌发酵粗提物进行活性筛选。其次通过18S r DNA序列比对进行菌种鉴定,同时采用硅胶柱色谱、凝胶柱色谱和高效液相色谱等技术并结合活性追踪检测分离纯化的活性化合物,再通过核磁质谱分析确定其结构。最后利用定量测定方法检测其在亚抑菌浓度下对紫色杆菌紫色菌素产量影响以及RT-PCR检测与QS调控相关基因的m RNA表达的影响。结果:从海藻共生菌中筛选到一株具有紫色杆菌群体感应抑制活性的海洋真菌Penicillium sp.QF046,其次级代谢产物中纯化到的活性化合物根据结构鉴定为一种星形曲霉毒素(asteltoxin)。该化合物对于紫色杆菌群体感应抑制浓度低于阳性对照化合物呋喃酮C30,同时抑制了群体感应相关基因m RNA水平的表达。结论:从海洋真菌Penicillium sp.QF046代谢产物中发现了一种抑制紫色杆菌群体感应的星形曲霉毒素,为进一步通过结构改造研发新型抗菌药物提供良好的前体化合物。     

药用植物大戟的快速繁殖研究

以野生大戟为材料,探讨了大戟茎尖扦插繁殖和组织培养等快速繁殖技术的条件。结果表明:大戟茎 尖扦插繁殖,其成活率可以达到88.6%,用含有腋芽的茎在MS培养基上培养,发芽比例可以达到55%;用愈 伤组织诱导生芽,最高可以达到12%。嫩芽在不含激素的1/2MS培养基中培养,生根率达到47.1%。幼苗 接种本源的或同科外源植物5株内生真菌,比较其生长表明,接种大戟来源的两株内生真菌全苗重分别达到 对照的1.51和2.08倍,根重达到对照的2.09和3.68倍,最有利于宿主生长。     

Endophytic fungus <Emphasis Type="Italic">Cladosporium cladosporioides</Emphasis> LF70 from <Emphasis Type="Italic">Huperzia serrata</Emphasis> produces Huperzine A

A strain LF70 endophytic fungus was isolated from the leaves of Huperzia serrata. The fungus was identified as Cladosporium cladosporioides LF70 according to its morphological characteristics and nuclear ribosomal DNA ITS sequence analysis. The strain could produce Huperzine A (HupA) identified through thin layer chromatography (TLC) and high-performance liquid chromatography (HPLC) with authentic HupA. The amount of HupA produced by this endophytic fungus was quantified to be 56.84 μg/L by HPLC, which was higher than that of other reported endophytic fungi, Acremonium sp., Blastomyces sp., and Botrytis sp. Acetylcholinesterase inhibition activity of HupA produced by strain LF70 was also similar to authentic HupA in vitro. Isolation of such a fungus may provide a promising alternative approach to producing HupA, which is used in treating Alzheimer’s disease and preventing further memory degeneration.