不同pH水平下两种菌根真菌对紫云英生长的影响及其相互作用

设计在不同pH水平（4．3、5．1、5．8、6．8）下两种VA菌根真菌Glomus mosseae和Gigaspora margarita对紫云英Astragalus sinicus进行单接种、混合接种及无接种对照的盆栽实验。对紫云英地上和地下部分生物量、根部侵染率、SDH和ALP酶活进行了检测。实验结果表明：紫云英的生长效应与VA菌根真菌的侵染率及两种酶活成明显相关性。土壤pH升高,单接种Glomus mosseae和混合接种的侵染率也随之升高,而单接种Gigaspora margarita的侵染率呈现出先上升后下降的趋势。本实验设计了特异性扩增Glomus mosseae和Gigaspora margarita的引物gml和gigl,在混合接种实验中,nested PCR扩增结果显示：在低pH水平下（4．3-5．1）大多数根段为Gigaspora margarita所侵染,在高pH水平下（5．8—6．8）Glomus mosseae表现出较强的竞争力,但并没有检测到两种VA真菌存在于同一条侵染根段;对比单接种实验,在低pH水平下,Glomus mosseae显著抑制了Gigaspora margarita的侵染,而在高pH水平下Gigaspora margarita明显促进Glomus mosseae的侵染。     

不同pH水平下两种菌根真菌对紫云英生长的影响及其相互作用

设计在不同pH水平(4.3、5.1、5.8、6.8)下两种VA菌根真菌Glomus mosseae和Gigaspora margarita对紫云英Astragalus sinicus进行单接种、混合接种及无接种对照的盆栽实验.对紫云英地上和地下部分生物量、根部侵染率、SDH和ALP酶活进行了检测.实验结果表明:紫云英的生长效应与VA菌根真菌的侵染率及两种酶活成明显相关性.土壤pH升高,单接种Glomus mosseae和混合接种的侵染率也随之升高,而单接种Gigaspora margarita的侵染率呈现出先上升后下降的趋势.本实验设计了特异性扩增Glomus mosseae和Gigaspora margarita的引物gml和gigl,在混合接种实验中,nested PCR扩增结果显示:在低pH水平下(4.3-5.1)大多数根段为Gigaspora margarita所侵染,在高pH水平下(5.8-6.8)Glomusmosseae表现出较强的竞争力,但并没有检测到两种VA真菌存在于同一条侵染根段;对比单接种实验,在低pH水平下,Glomus mosseae显著抑制了Gigaspora margarita的侵染,而在高pH水平下Gigasporamargarita明显促进Glomus mosseae的侵染.     

丛枝菌根真菌种间差异对柚苗营养生长及矿质含量的影响

在温室盆栽条件下研究了3种AM真菌Gigaspora margarita、Glomus mosseae和Glomus versiforme对长寿沙田柚(Citrus grandis cv. Changshou Shatian You)无菌苗营养生长及矿质含量的影响.结果表明,接种AM真菌的植株均有效地被感染;与对照相比,接种AM真菌能显著促进植株地上和地下部分生长,尤其促进了须根的生长,接种Glomus mosseae处理的主根长度比对照增加了22.7％,侧根数量增加了35.7％,须根数量和总长分别增加了160.8％和103.2％;接种AM真菌显著地提高了叶片的N、P、K、Ca、Mg、Zn、Cu和Mn含量,与对照相比,3种真菌处理的P含量分别增加了46.8％、88.7％和32.3％.3种AM真菌处理中,以接种Glomus mosseae处理营养生长最好,菌根依赖性最大,矿质元素N、P、K、Ca、Zn和Cu的含量最高,其效应顺序为Glomus mosseae＞Gigaspora margarita＞Glomus versiforme,可见,3种AM真菌对长寿沙田柚生长均有正效应,以Glomus mosseae最为显著,为长寿沙田柚适宜的优良菌种（株）.     

泡囊丛枝（VA）菌根对玉米际磷酸酶活性的影响

以玉米为材料,利用三室隔网培养方法,研究了缺P土壤上施用植酸和卵磷脂时接种几种菌根真菌（Glomus mosseae,Glmous versiformea,Gigaspora margarita)对根际土壤酸性磷酸酶和碱性磷酸酶活性的影响,玉米生长70d后,收获测定距根表不同距离土壤中的磷酸酶活性,结果表明,接种菌根真菌增加了根际土壤酸性和碱性磷酸酶活性,Gigaspora margarita菌根菌的作用大于其它2个菌极菌,不同P源对磷酸酶活性有明显影响。     

接种不同VA菌根真菌对红三中草利用不同磷源的影响

以红三叶草为材料,利用三室隔网培养方法,研究了施用不同磷源条件下,接种VA菌根真菌（Glomus mosseae和Glomus versiforme)对外加有机磷源及土壤有机磷的利用效率,植物生长10周年,测定植株博干物重、含磷量、菌根侵染率及根系长度,结果表明：接种菌根真菌能明显增加植干物重和含磷量。接种条件下无机磷（KH2PO4）对植株生长的促进作用大于有机磷（Na-phytate)处理,接种Glomus versofrorme的作用明显大于接种Glomus mosseae。接种Glomus mosseae,植株对磷酸二氢钾中磷的吸收量明显大于植酸钠,而接种Glomus versiforme时则植株对植酸钠的磷吸收量明显高于磷酸二氢钾。上述结果说明接种两菌种对不同磷源的作用不同,接种Glomus mosseae可提高磷酸二氢钾中磷的利用率,接种Glomus versiforme则可提高对植酸的磷利用率。     

大豆毛状根-VA菌根真菌双重培养体系的建立

以大豆毛状根为宿主,接种VA菌根真菌珠状巨孢囊霉（Gigaspora margarita）,经过3.5个月的双重培养,观察到VA菌根真菌珠状巨孢囊霉对大豆毛状根的侵染,辅助细胞形成,并获得VA菌根真菌成熟孢子,在无菌条件下建立了大豆毛状根-VA菌根真菌双重培养体系,为研究菌根真菌侵染大豆根部形成共生体系及相关分子机制提供了一种有效的研究方法。     

丛枝菌根真菌对牡丹生长及相关生理指标的影响

以采自山东省菏泽牡丹园的牡丹'凤丹'种子为试材,采用盆栽的方法研究了接种丛枝菌根(Arbuscular mycorrhizal,AM)真菌Glomus mosseae、Glomus versiforme和Glomus intraradices对牡丹幼苗生长及生理生化特性的影响.结果表明:(1)不同AM真菌的侵染率不同,并以G.mosseae的侵染率最高,为48.3%;(2)AM真菌能够促进牡丹幼苗生长,接种G.mosseae的植株干重比对照显著提高了69.5%;(3)AM真菌能够提高牡丹的叶绿素、可溶性糖、可溶性蛋白、矿质元素(N、P、K)含量和硝酸还原酶活性,并对可溶性蛋白含量和硝酸还原酶活性的影响达显著水平.(4)植株总干重与菌根侵染率、硝酸还原酶活性、叶绿素含量呈极显著正相关,与可溶性糖、可溶性蛋白含量呈显著正相关.研究发现,G.mosseae是最适宜牡丹接种的优良菌种.     

AMF及Frankie混合接种对沙棘生长效应的研究

报道了丛枝菌根真菌Glomus mosseae和Frankia混合接种对沙棘苗期的接种效应。研究发现,丛枝菌根真菌和Frankia之间存在联合增效作用,混合接种对沙棘苗木具有显的促生长作用,明显优于单接种处理苗木。     

西藏高原天然长芒草地丛枝菌根真菌接种效应

采用草地均匀打孔方法,就草地土壤未消毒条件下接种丛枝菌根（AM）真菌对长芒草(Stipa bungeana)的侵染效应以及对植物生长、吸磷效率、土壤微生物区系等的影响进行研究.结果表明,1)接种处理、不接种处理的菌根效应存在着明显的差异,多数接种处理根围土壤AM真菌孢子密度、菌根侵染率和侵染强度显著提高,但对丛枝丰度的影响相对较低.2)接种后AM真菌孢子密度对菌根侵染率具有极显著影响(r=0.7679**);随菌根侵染率的增加,植株总干物重和吸磷总量均呈极显著提高,r值分别为0.7556**、0.8018**.3)与植株地上部相比,接种AM真菌对提高根系干物重、根系吸磷量和含磷量的促进作用相对较大.4)多数接种处理根际土壤酸性磷酸酶、碱性磷酸酶活性均呈一定程度的提高,根际土壤细菌数量显著增加,真菌、放线菌的数量变化则不甚明显.5)各接种处理对寄主植物的综合侵染效应在总体上呈Glomus mosseae+G. intraradices+Scutellospora calospora＞G. mosseae+G. aggregatum＞Glomus sp.＞G. mosseae＞G. mosseae+ G. etunicatum+G. intraradices+S. erythropa＞G. geosporum的趋势.     

红壤中VA菌根真菌侵染力及接种效应的研究

本文报道了丘陵地区发育于第四纪红色粘土母质的马尾松林自然植被下红壤、栽种胡枝子的两种侵蚀红壤及花生-油菜轮作的耕作红壤等3种生态条件下的土壤中VA菌根真菌繁殖体数量、种类、侵染势、施用石灰石粉改土和增施磷肥对VA菌根真菌侵染的影响以及VA菌根真菌的接种效应.试验结果表明,3种生态条件下的土壤中VA菌根真菌繁殖体数量和侵染势显然不同:马尾松林自然植被下的红壤中VA菌根真菌繁殖体数量大,侵染迅速;花生-油菜轮作的耕作红壤VA菌根真菌繁殖体数量也大,但侵染缓慢,有明显的滞后期;栽种胡枝子的侵蚀红壤VA菌根真菌繁殖体数量小,侵染力很低.对侵蚀红壤与耕作红壤接种VA菌根真菌,显著提高了VA菌根的侵染率,在适当施用磷肥及施石灰石粉改土后,都能促进VA菌根侵染,从而增加了植物的吸磷量,植物生长量显著提高.     

AM真菌种间差异对枳壳生长及耐热性效应的研究※

用地表球囊霉、莫西球囊霉、珠状巨孢球囊霉及其混合菌剂接种无菌根枳壳幼苗进行盆栽试验,25℃培养4个月,观察对枳壳菌根形成和营养生长的影响,在40℃高温胁迫30d,调查分析菌根枳壳的耐热性。试验结果表明:接种AM真菌的根系形成了20%～80%的菌根侵染率;菌根枳壳的苗高、苗质量、节间长、茎基粗、须根数量和须根长度等营养生长显著增加;叶片中的SOD,POD活性和根系活力显著增强,可溶性蛋白、可溶性糖含量显著升高,叶片中的MDA含量降低,膜透性显著变小,枳壳苗的耐热性显著提高;但是,AM真菌在促进枳壳苗菌根化、营养生长和提高耐热性方面存在着种间差异,地表球囊霉、莫西球囊霉、珠状巨孢球囊霉、混合菌剂与枳壳根系形成丛枝菌根的侵染率依次为20.4%±1.2%、61.8%±3.4%、85.7%±2.7%、83.3%±2.2%,促进枳壳苗营养生长提高枳壳苗耐热能力的AM真菌依次为:地表球囊霉<莫西球囊霉<珠状巨孢球囊霉<混合菌剂,认为珠状巨孢球囊霉和莫西球囊霉是枳壳耐高温胁迫菌根化育苗的重要优良菌种。     

丛枝菌根真菌对植物根尖分生区和根冠细胞的侵染*

一般说来,从枝菌根（ＡＭ）真菌大多数是从植物根系根毛区（成熟区）侵入和扩展的,在显微镜下往往看不到根尖分生区和根冠表皮细胞被ＡＭ真菌侵染的特征。这就很容易给人们造成一种假象,似乎ＡＭ真菌不能侵染根尖分生区和根冠表皮细胞,即它们对ＡＭ真菌是免疫的。然而笔者多次于显微镜下看到ＡＭ真菌侵染根尖分生区和根冠表皮细胞,并形成典型的泡囊、丛枝、菌丝等结构。这一现象导致作者在温室盆栽和大田条件下研究了玫瑰红巨孢囊霉（ Ｇｉｇａｓｐｏｒａ　ｒｏｓｅａ Ｎｉｃｏｌ　＆ Ｓｃｈｅｎｃｋ）、珠状巨孢囊霉（Ｇｉｇａｓｐｏｒａ　ｍａｒｇａｒｉｔａ　Ｂｅｃｋｅｒ　＆　Ｈａｌｌ）、根内球囊霉（Ｇｌｏｍｕｓ　ｏｍｔｒａｒａｄｉｃｅｓ　ｓｃｈｅｎｃｋ　＆　Ｓｍｉｔｈ、摩西球囊霉（Ｇｌｏｍｕｓ ｍｏｓｓｅａｅ （Ｎｉｃｏｌ　＆ Ｇｅｒｄ．） Ｇｅｒｄｅｍａｎｎ　＆ Ｔｒａｐｐｅ）、地表球囊霉（ Ｇｌｏｍｕｓ ｖｅｒｓｉｆｏｒｍｅ（ Ｋａｒｓｔｅｎ）Ｂｅｒｃｈ）和弯丝硬囊霉（ Ｓｃｌｅｒｏｃｙｓｔｉｓ　ｓｉｎｕｏｓａ　Ｇｅｒｄｅｍａｎｎ　＆ Ｂａｋｈｉ）对棉花（Ｇｏｓｓｙｐｉｕｍ　ｈｉｒｓｕｔｕｍ　Ｌ．）、烟草（Ｎｉｃｏｔｉａｎａ　 ｔａｂａｃｕｍ Ｌ．）和白     

Regulation of arbuscular mycorrhizal development by plant host and fungus species in alfalfa

Two cvs of alfalfa ( Medicago sativa L.), Gilboa and Moapa 69, were inoculated in glasshouse pots with three arbuscular mycorrhizal (AM) fungi to investigate the efficacy of mycorrhizas with respect to the extent of colonization and sporulation. Paspalum notatum Flugge also was inoculated to describe fungal parameters on a routine pot culture host. Percentage root length of P. notatum colonized by Glomus mosseae (Nicol. & Gerd.) Gerdemann & Trappe, Glomus intraradices Schenck & Smith, and Gigaspora margarita Becker & Hall increased from 10 to 21 wk, and all fungi sporulated during that period. In alfalfa, only colonization by G. intraradices increased over that time period, and it was the only fungus to sporulate in association with alfalfa at 10 wk. Glomus mosseae did not sporulate after 16–21 wk despite having colonized 30–35% of the root length of both alfalfa cvs. In vitro experiments in which Ri T-DNA-transformed roots of alfalfa were inoculated with AM fungi showed normal mycorrhizal formation by G. intraradices and a hypersensitivity-like response to Gi. margarita . Colonized cells became necrotic, and HPLC analysis indicated increased concentrations of phenolics and isoflavonoids in these root segments. These data strongly support the existence of a degree of specificity between AM fungi and host that might rely on specific biochemical regulatory processes initiated in the host as a result of the attempts at colonization by the fungus.     

Arbuscular mycorrhizal colonization of tomato by Gigaspora and Glomus species in the presence of root flavonoids

The effect of flavonoids isolated from arbuscular mycorrhizal (AM) colonized and noncolonized clover roots on the number of entry points and percentage of root colonization of tomato (Lycopersicum esculentum L.) by Gigaspora rosea, Gi margarita, Glomus mosseae and G. intrarradices symbionts was determined. With fungi of both genera, a correlation between the number of entry points and the percentage of root colonization was found in the presence of some of the tested flavonoids. The flavonoids acacetin and rhamnetin, present in AM clover roots, inhibited the formation of AM penetration structures and the AM colonization of tomato roots, whereas the flavonoid 5,6,7,8,9-hydroxy chalcone, which could not be detected in AM clover root, inhibited both parameters. The flavonoid quercetin, which was present in AM clover roots, stimulated the penetration and root colonization of tomato by Gigaspora. However, the flavonoids 5,6,7,8-hydroxy-4'-methoxy flavone and 3,5,6,7,4'-hydroxy flavone, which was not found in AM clover root, increased the number of entry points and the AM colonization of tomato roots by Gigaspora. These results indicated that flavonoids could be imnplicated in the process of regulation of AM colonization in plant root, but its role is highly complex and depend not only on flavonoids, but also on AM fungal genus or even species.     

Comparison of protein profiles and enzymes in non-mycorrhizal and mycorrhizal roots of Pennisetum pedicellatum

Pennisetum pedicellatum plants were inoculated with Glomus mosseae, G. aggregatum and Gigaspora margarita. There were both quantitative and qualitative changes in the protein pattern of inoculated plants. Gi. margarita induced increase in protein in the plants. Acid phosphatase, alkaline phosphatase, superoxide dismutase and chitinase activities were high at the beginning of infection, but declined as the infection advanced. Gi. margarita was an efficient fungus in enhancing enzyme activity and proteins in roots compared with G. mosseae and G. aggregatum. Protein profile revealed the presence of 12 peaks in mycorrhizal plants compared with 8 in nonmycorrhizal plants.     

山东省不同植被区内野生植物根围AM菌的生态分布

ＡＭ菌是土壤习居菌 ,生态适应性强 ,可发生在各种生态环境。寄主范围也十分广泛 ,除少量植物如莎草科、苋科、灯心草科、藜科、石竹科等 2 0余科植物不能或不易形成ＡＭ外 ,大多数植物包括苔藓、蕨类、裸子植物、被子植物都能被菌根菌侵染。当前人们十分重视对野生植物上ＡＭ菌的调查[3 ,4 ,1 0 ,1 1 ,1 4 ]。研究发现 ,野生植物上可能有比栽培作物更多的ＡＭ菌种类[1 ]。我国野生植物资源丰富 ,开发和利用野生寄主植物上的ＡＭ菌潜力巨大。由于ＡＭ菌对寄主植物的选择性及对环境条件的适应性不同 ,或进化过程中的历史原因 ,造成了自然生态…     

Characterization of root colonization profiles by a microcosm community of arbuscular mycorrhizal fungi using 25S rDNA-targeted nested PCR

The aim of the present work was to study colonization patterns in roots by different arbuscular mycorrhizal fungi developing from a mixed community in soil. As different fungi cannot be distinguished with certainty in planta on the basis of fungal structures, taxon-discriminating molecular probes were developed. The 5' end of the large ribosomal subunit containing the variable domains D1 and D2 was amplified by PCR from Glomus mosseae (BEG12), G. intraradices (LPA8), Gigaspora rosea (BEG9) and Scutellospora castanea (BEG1) using newly designed eukaryote-specific primers. Sequences of the amplification products showed high interspecies variability and PCR taxon-discriminating primers were designed to distinguish between each of these four fungi. A nested PCR, using universal eukaryotic primers for the first amplification and taxon-discriminating primers for the second, was performed on individual trypan blue-stained mycorrhizal root fragments of onion and leek, and root colonization by four fungi inoculated together in a microcosm experiment was estimated. More than one fungus was detected in the majority of root fragments and all four fungi frequently co-existed within the same root fragment. Root colonization by G. mosseae and G. intraradices was similar from individual and mixed inoculum, whilst the frequency of S. castanea and Gig. rosea increased in the presence of the two Glomus species, suggesting that synergistic interactions may exist between some arbuscular mycorrhizal fungi.     

Colonization of roots by arbuscular mycorrhizal fungi using different sources of inoculum

Arbuscular mycorrhizal fungi (AMF) form a number of different infective propagules that are used to form new mycorrhizal associations. These are spores, extraradical hyphae and infected roots. However, not all fungi are equally capable of colonizing roots with all of the above-mentioned propagules and there is conflicting evidence of major differences in colonization strategy between members of the Glomineae and Gigasporineae. In this study, we tested the abilities of eight fungal species from four different genera to colonize roots using three different types of inoculum. Glomus and Acaulospora isolates colonized from all inoculum types, whereas Gigaspora and Scutellospora isolates colonized mainly from spores and to a limited degree from root fragments. Extraradical hyphae were not suitable propagules for the species of Gigaspora and Scutellospora tested. This indicates that AMF have different colonization strategies and that this is largely differentiated at the suborder level. It is unclear why there is such a difference among the fungi in inoculum types. Future research should examine differences in the anatomy and physiology to discern a mechanism for such differences in life-history strategies.