高磷土壤中丛枝菌根真菌的分离鉴定

【背景】丛枝菌根(arbuscular mycorrhiza,AM)真菌具有广泛的寄主范围、环境适应性和优良的植物促生能力。然而,土壤的高磷水平严重抑制了AM真菌生长及AM形成。【目的】分离鉴定出耐较高有效磷含量的华南土著AM真菌菌株,为菌根学研究工作提供新颖材料。【方法】采用经典形态学和分子系统学方法鉴定高磷土壤中AM真菌。【结果】从有效磷含量为53-131 (平均值±标准差为88.2±17.6) mg/kg的根区土壤中鉴定出7属25种AM真菌,包括无梗囊霉属(Acaulospora) 12种、球囊霉属(Glomus) 7种、隔球囊霉属(Septoglomus) 2种、近明球囊霉属(Claroideoglomus) 1种、根孢囊霉属(Rhizophagus) 1种、硬囊霉属(Sclerocystis) 1种和类球囊霉属(Paraglomus) 1种,其中幼套近明球囊霉(Claroideoglomus etunicatum)和蜜色无梗囊霉(Acaulospora mellea)是优势种。在(87.7±8.0) mg/kg的高磷水平下,AM真菌仍能形成丛枝和泡囊。但当有效磷含量达到(99.7±1.2) mg/kg时,菌根侵染率和丛枝丰度显著下降,但仍能够形成泡囊。【结论】从广州市南沙区有效磷含量为(88.2±17.6) mg/kg的耕地植物根区土壤中,鉴定出具有耐高磷潜力的7属25种AM真菌,幼套近明球囊霉和蜜色无梗囊霉等分离株可作为后续高磷抑制机制解析及耐高磷AM真菌菌剂研发工作的试验菌株。     

西藏高原针茅草地土壤因子对丛枝菌根真菌物种多样性的影响

在对西藏高原北部针茅草地根围土壤中的丛枝菌根(AM)真菌种类分离鉴定基础上,研究了藏北针茅草地的土壤质地、pH、有机质和有效磷含量对AM真菌孢子密度、分离频度、相对多度、重要值、物种多样性指数和均匀度的影响.结果表明: 针茅草地根围土壤中共分离鉴定出AM真菌3属15种,其中,球囊霉属9种、无梗囊霉属6种、盾巨孢囊霉属1种.球囊霉属和无梗囊霉属为藏北针茅草地AM真菌的优势属;近明球囊霉和光壁无梗囊霉为藏北高寒草原针茅属植物根围AM真菌的优势种.不同质地土壤中AM真菌孢子密度、分离频度、相对多度和重要值均表现出球囊霉属＞无梗囊霉属＞盾巨孢囊霉属的趋势;土壤pH值对AM真菌种群组成无明显影响,球囊霉属和无梗囊霉属真菌分离频度、相对多度和重要值随土壤pH升高而增加,盾巨孢囊霉属则呈现相反趋势;不同土壤有机质含量范围内,AM真菌孢子密度等各项指标均呈球囊霉属＞无梗囊霉属＞盾巨孢囊霉属,而AM真菌属的分布没有明显规律;土壤有效磷含量对AM真菌种丰度和孢子密度影响较小.研究区域内AM真菌物种多样性指数和均匀度随着土壤有效磷含量升高而增加.     

荒漠生境油蒿根围AM真菌多样性

为了阐明荒漠生境主要植被油蒿(Artemisia ordosica)根围AM真菌多样性, 2007年8月从毛乌素沙地和腾格里沙漠选取榆林、盐池、研究站和沙坡头4个样地, 按0–10、10–20、20–30、30–40、40–50 cm 5个土层采集油蒿根围土壤样品, 研究了油蒿根围AM真菌物种多样性和生态分布。在分离的4属28种AM真菌中, 球囊霉属(Glomus)16种, 无梗囊霉属(Acaulospora)7种, 盾巨孢囊霉属(Scutellospora)4种, 多孢囊霉属(Diversispora)1种。4个样地的共同优势种为摩西球囊霉(G. mosseae), 共同常见种为双网无梗囊霉(A. bireticulata)和网状球囊霉(G. reticulatum), 共同稀有种为缩球囊霉(G. constrictum)。地球囊霉(G. geosporum)仅出现在盐池, 蜜色无梗囊霉(A. mellea)、帚状球囊霉(G. coremioides)、浅窝无梗囊霉(A. lacunosa)和宽柄球囊霉(G. magnicaule)仅出现在研究站, 黑球囊霉(G. melanosporum)仅出现在榆林。盐池与研究站样地AM真菌种类最多, 榆林样地孢子密度最大, 沙坡头样地种类和孢子密度显著偏低。总体上, 孢子密度、分离频度、相对多度和重要值依Glomus >Acaulospora > Scutellospora> Diversispora呈现显著减小趋势。结果表明, 油蒿与AM真菌之间有良好共生性, 这对进一步利用菌根生物技术维护荒漠生态系统结构的完整性具有重要意义。     

林火对植物根围丛枝菌根真菌多样性的影响

林火是森林生态系统的一种主要干扰因子,以青岛市三标山林火迹地为研究对象,采集荆条(Vitex negundo)、胡枝子(Lespedeza bicolor)、花木蓝(Indigofera kirilowii)、青花椒(Zanthoxylum schinifolium)和野青茅(Deyeuxia arundinacea)5种优势植物根围土壤,研究不同林火强度对丛枝菌根(AM)真菌多样性的影响。结果表明,AM真菌侵染率和孢子密度随火灾强度的加强而降低;非过火区植物根围土壤中,分离鉴定出AM真菌3属11种,轻度过火区分离鉴定出AM真菌3属10种,中度过火区分离鉴定出AM真菌3属9种,重度过火区分离鉴定出AM真菌3属8种。过火区AM真菌种丰度低于非过火区。过火区和非过火区AM真菌的重要值和优势种不同,非过火区植物根围的优势种是地球囊霉(Glomus geosporum)、台湾球囊霉(G.taiwanensis)、分支巨孢囊霉(Gigaspora ramisporophora)、极大巨孢囊霉(Gi.gigantean)、福摩萨球囊霉(G.formosanum)、悬钩子球囊霉(G.rubiforme)、柯氏无梗囊霉(Acaulospora koskei)和松蜜无梗囊霉(A.thomii);轻度过火区植物根围的优势种是地球囊霉和台湾球囊霉;中度过火区的是台湾球囊霉和地球囊霉(野青茅除外);重度过火区植物根围的优势种是地球囊霉。不同强度的过火区对AM真菌群落组成有不同程度的影响。认为林火降低植物根围土壤中AM真菌多样性。     

茂兰地区白茅丛枝菌根真菌多样性及其对紫花苜蓿的接种效应研究

对贵州省荔波茂兰国家自然保护区内优势草本植物白茅(Imperata cylindrica)根际丛枝菌根(Arbuscular Mycorrhizal,AM)真菌多样性,优势种对紫花苜蓿的接种效应进行研究。结果表明:AM真菌对白茅根系的菌根侵染率为91.3%,白茅根际土壤共分离AM真菌2属35种,其中球囊霉属(Glomus)18种,无梗囊霉属(Acaulos pora)17种,黑球囊霉(Glomus melanosporum)、聚生球囊霉(G.fasciculatum)、红色无梗囊霉(Acaulospora capcicula)为优势AM真菌。以三叶草扩繁优势菌种,接种紫花苜蓿(Medicago sativa),均显著提高了生长量和超氧化物歧化酶(Superoxide dismutase,SOD)、过氧化物酶(Peroxidase,POD)、过氧化氢酶(Catalase,CAT)活性。     

崂山茶区茶树根围AM真菌多样性

为调查崂山茶区土壤中丛枝菌根(AM)真菌资源的分布状况, 于2007年9月从青岛崂山茶区12个茶园采集茶树(Camellia sinensis)根围土样, 采用湿筛倾注–蔗糖离心法分离AM真菌, 测定其物种丰度、频度、孢子密度、相对多度、重要值、多样性指数等。共分离到AM真菌3属22种, 无梗囊霉属(Acaulospora)出现的频度最高, 其次是球囊霉属(Glomus)。AM真菌孢子密度以晓望村茶园最高, 高家村茶园最低; 种丰度以常家村茶园最高; 常家村茶园和万来客茶园的Shannon-Wiener指数显著高于其他茶园。光壁无梗囊霉(Acaulospora laevis)是北崂茶厂、万里江茶园、樱山春茶园、万里江有机茶园、常家村茶园和桑园村茶园的优势种; 波状无梗囊霉(Acaulospora undulata)为万里江有机茶园和万来客茶园的优势种; 隐球囊霉(Glomus occultum)为樱山春茶园、晓望村茶园和万来客茶园的优势种。应用典型相关分析(CCA)对环境因子与崂山茶区AM真菌群落组成的关系进行了分析, 各因子的影响大小依次为: 土壤速效磷含量＞土壤有机质含量＞种植年限＞土壤碱解氮含量＞土壤pH值＞土壤速效钾含量。     

西双版纳地区龙脑香科植物AM真菌的初步研究

 对云南省西双版纳地区17种龙脑香科树种根系丛枝菌根（Arbuscular mycorrhiza, AM）真菌的定居情况进行了调查,并对根围土壤中AM真菌进行了分离和鉴定。结果表明,调查根样均有不同程度的菌根感染,感染率最高可达40%,调查揭示了西双版纳地区龙脑香科植物在自然条件下可形成丛枝菌根。初步从龙脑香科植物根际土壤中分离、鉴定出32种AM真菌,隶属于无梗囊霉属（Acaulospora）、球囊霉属（Glomus）、原囊霉属（Achaeospora）、拟球囊霉属（Paraglomus）和盾巨孢囊霉属（Scutellospora）,其中,无梗囊霉属和球囊霉属真菌为西双版纳地区龙脑香科植物AM真菌优势类群。     

接种AM真菌对喜树幼苗生长及光合特性的影响

 喜树(Camptotheca acuminata)是我国特有的多年生亚热带落叶阔叶树种, 因其次生代谢产物喜树碱具有良好的抗肿瘤活性而备受关注。通过温室盆栽接种试验, 观察了3属6种丛枝菌根(AM)真菌木薯球囊霉(Glomus manihot)、地表球囊霉(G. versiforme)、透光球囊霉(G. diaphanum)、蜜色无梗囊霉(Acaulospora mellea)、光壁无梗囊霉(A. laevis)和弯丝硬囊霉(Sclerocystis sinuosa)对喜树幼苗生长及光合特性的影响。结果表明, 除地表球囊霉外, 其余菌根幼苗生物量显著高于无菌根幼苗, 蜜色无梗囊霉、弯丝硬囊霉和透光球囊霉的菌根幼苗生物量分别达到无菌根幼苗的1.6倍、1.4倍和1.3倍。与无菌根幼苗相比, 蜜色无梗囊霉菌根幼苗叶片的净光合速率(P_n)、气孔导度(G_s)和蒸腾速率(T_r)均有显著提高, 而胞间CO₂浓度(C_i)与气孔限制值(L_s)则变化不明显。接种透光球囊霉、蜜色无梗囊霉、光壁无梗囊霉和弯丝硬囊霉的喜树幼苗叶片叶绿素a含量、总叶绿素含量、叶绿素a/b和类胡萝卜素含量均显著高于无菌根幼苗, 而叶绿素b含量只有木薯球囊霉和弯丝硬囊霉菌根幼苗显著高于无菌根幼苗。接种AM真菌对喜树幼苗叶片叶绿素荧光参数影响较小, 只有透光球囊霉菌根幼苗叶片的最大光能转换效率(F_v/F_m)显著高于无菌根幼苗, 接种木薯球囊霉和弯丝硬囊霉的喜树幼苗的PSⅡ有效光化学量子产量(EQY)显著高于无菌根幼苗, 弯丝硬囊霉菌根幼苗的光化学淬灭(qP)显著高于无菌根幼苗, 非光化学淬灭(NPQ)则显著低于无菌根幼苗。     

泰山丛枝菌根真菌群落结构特征

2007年对泰山植被根围内丛枝菌根(arbuscular mycorrhiza,AM)真菌群落组成、数量、分布及其与植物多样性的关系进行了研究。从泰山傲徕峰、黑龙潭库区等样地共分离出4属16种AM真菌:球囊霉属Glomus 9种、无梗囊霉属Acaulospora 4种、巨孢囊霉属Gigaspora 2种和盾巨孢囊霉属Scutellospora1种。其中,球囊霉属Glomus及聚球囊霉Glomus fasciculatum的孢子密度、相对多度、分布频度和重要值均最高,分别为泰山植被区根围内AM真菌优势属和优势种。各样地之间Sorenson相似系数在0.60和0.85之间。植被数量与孢子密度(r=0.80,p0.01)、植物种的丰富度与AM真菌种的丰富度(r=0.77,p0.01)以及与孢子密度(r=0.59,p0.01)均呈极显著正相关关系。研究结果表明植物多样性对于提高AM真菌多样性发挥极为重要的作用。     

极旱荒漠植物对AM真菌物种多样性的影响

2015年7月在甘肃安西极旱荒漠国家级自然保护区采集膜果麻黄Ephedra przewalskii、红砂Reaumuria songarica、合头草Sympegma regelii、泡泡刺Nitraria sphaerocarpa和珍珠猪毛菜Salsola passerine 5种典型荒漠植物根区土壤样品,分析了植物种类对arbuscular mycorrhiza(AM)真菌群落组成和生态分布的影响。在分离的7属45种AM真菌中包括无梗囊霉属Acaulospora 17种,球囊霉属Glomus 13种,这两属是5种植物共同优势属;盾巨孢囊霉属Scutellospora 5种,管柄囊霉属Funneliformis 4种,根内根生囊霉属Rhizophagus 3种,近明囊霉属Claroideoglomus 2种,多孢囊霉属Diversispora1种。主成分分析研究说明5种植物根区AM真菌群落组成和物种多样性差异显著。结果表明,植物种类对AM真菌群落组成和分布特征影响显著。     

A preliminary survey of the arbuscular mycorrhizal status of grassland plants in southern Tibet

We report for the first time the arbuscular mycorrhizal (AM) status of native plant species and AM fungal diversity in the grasslands of southern Tibet. A total of 51 soil samples were collected from the rhizospheres of the dominant plant species, and AM fungal structures were observed in 18 (82%) of 22 plant species examined. Vesicles and aseptate hyphae were the structures most frequently observed in the plant roots. After trap culture for 5 months, 25 AM fungal taxa were identified in the soil samples collected, of which nine belonged to Glomus, ten to Acaulospora, one to Entrophospora and five to Scutellospora. The frequency of occurrence of different genera and species varied greatly. Glomus was the dominant genus, and the most frequent and abundant species was Glomus mosseae. Over the whole sampling area, spore density in the rhizosphere soil of different host plant species ranged from 2 to 66 per 20 g air-dried soil. Overall AM fungal species richness was 2.10 and species diversity was 2.35. AM fungal diversity was also compared among the four different land use types (farmland and normal, disturbed and highly disturbed montane scrub grassland). Spore densities in the farmland and normal grassland were much higher than in the grasslands that had been degraded to varying degrees. The species richness in normal grassland was the highest of the four land use types examined. Species diversity varied from 1.99 to 0.94 and was highest in normal grassland, intermediate in degraded grassland and farmland, and lowest in the highly disturbed grassland.     

Arbuscular mycorrhizal and dark septate endophyte fungal associations in South Indian grasses

We examined arbuscular mycorrhizal (AM) and dark septate endophyte (DSE) fungal association in 50 south Indian grasses from four different sites. AM fungal diversity was also compared among the different sites. Forty-four of the 50 grasses examined had AM association and dual association with DSE fungi occurred in 25 grasses. We report for the first time AM and DSE fungal status in 23 and 27 grasses respectively. Arum-type AM morphology was the dominant occurring in 21 grasses with typical Paris-type colonization occurring in 6 grasses. AM morphology is reported for the first time in 35 grasses. Over the different sites, spore density in the soil ranged from 5–22 per 100 g air-dried soil. Spores of 11 AM fungal taxa were isolated from the soil samples of grasses of which nine belonged to Glomus, one to Acaulospora and one to Scutellospora. No significant relationship existed between AM fungal colonization and spore numbers. Species richness was high in site II and Glomus aggregatum, Glomus viscosum and Glomus mosseae were most frequent species at different sites. Overall species diversity indices (Simpson index, Shannon-Weaver index, species equitability index) differed significantly between sites.     

The diversity of arbuscular mycorrhizal fungi in the subtropical forest of Huangshan (Yellow Mountain), East-Central China

The world heritage of Huangshan is located in the east-central China. In order to obtain a better overview of biodiversity in Huangshan, we investigated the diversity of arbuscular mycorrhizal fungi in the soil of Huangshan. Forty-two rhizosphere soil samples were collected and 989 arbuscular mycorrhizal fungal spore samples were obtained using the wet-sieving method. Twenty-five species of arbuscular mycorrhizal fungi were identified from the collections. The species were of the genera Acaulospora (6 species), Entrophospora (1 species), Glomus (16 species) and Scutellospora (2 species). Acaulospora and Glomus were dominant at the study site. The arbuscular mycorrhizal fungi spore density ranged from 45 to 3,250 per 100 g soil (average 839), and the species richness of arbuscular mycorrhizal fungi ranged from 1 to 9 (average 4.2) per soil sample. Shannon–Wiener index and Simpson’s index were calculated to evaluate the arbuscular mycorrhizal fungal diversity. The diversity of arbuscular mycorrhizal fungal community in the subtropical forest of Huangshan may be the result of mutual selection between arbuscular mycorrhizal fungi and the ecological environment.     

Field response of mycorrhizal and nonmycorrhizal Medicago sativa var. local in the F1 generation

Seeds were collected from plants of Medicago sativa var. local inoculated with Glomus macrocarpum and G. fasciculatum separately in pot experiments. These seeds were sown in garden soil and the percentage germination, general health and yield of subsequent plants (the F1 generation) were studied. The percentage germination was highest in seeds of G. macrocarpum-inoculated parents followed by those inoculated with G. fasciculatum; seeds of uninoculated parent plants showed the lowest germination. Vegetative yield of the progeny decreased in the order of plants inoculated with G. fasciculatum, with G. macrocarpum, and uninoculated. On the other hand, reproductive yield was highest for plants whose parents were inoculated with G. macrocarpum, followed by G. fascicullatum, and lowest for seeds of uninoculated parent plants.     

Arbuscular mycorrhizal fungi associated with common pteridophytes in Dujiangyan,southwest China

The colonization and diversity of arbuscular mycorrhizal (AM) fungi associated with common pteridophytes were investigated in Dujiangyan, southwest China. Of the 34 species of ferns from 16 families collected, 31 were colonized by AM fungi. The mean percentage root length colonized was 15%, ranging from 0 to 47%. Nineteen species formed Paris-type and 10 intermediate-type AM. In two ferns, only rare intercellular non-septate hyphae or vesicles were observed in the roots and AM type could not be determined. Of the 40 AM fungal taxa belonging to five genera isolated from rooting-zone soils, 32 belonged to Glomus, five to Acaulospora, one to Archaeospora, one to Entrophospora, and one to Gigaspora. Acaulospora and Glomus were the dominant genera and Glomus versiforme was the most common species. The average AM spore density was 213 per 100 g air-dried soil and the average species richness was 3.7 AM species per soil sample. There was no correlation between spore density and percentage root length colonized by AM fungi.     

Host-related variability in arbuscular mycorrhizal fungal structures in roots of <Emphasis Type="Italic">Hedera rhombea</Emphasis>, <Emphasis Type="Italic">Rubus parvifolius</Emphasis>, and <Emphasis Type="Italic">Rosa multiflora</Emphasis> under controlled conditions

The arbuscular mycorrhizal (AM) morphology of three host plant species inoculated with single and mixed fungal culture and the distribution of AM fungal species in roots of the hosts treated with a mixed culture of AM fungi were determined. The aim was to investigate the effect of host plants and AM fungi on AM morphology of coexisting plant species. Noncolonized rooted cuttings of Hedera rhombea (Miq) Bean, Rubus parvifolius L., and Rosa multiflora Thunb. were inoculated with five fungal species as single and mixed culture inocula. The fungal species used were Gigaspora rosea and Scutellospora erythropa, previously isolated from H. rhombea; Acaulospora longula and Glomus etunicatum from R. parvifolius; and Glomus claroideum from both plant species. A few hyphal and arbusculate coils were seen in the mixed culture-inoculated roots of R. parvifolius; all fungal treatments produced this Paris-type AM in H. rhombea and Arum-type AM in R. parvifolius, and R. multiflora indicates that AM morphology is strongly controlled by the identity of the host plants used in this study. AM fungal rDNA was extracted separately from roots of each replicate plant species inoculated with the mixed fungal culture, amplified, cloned, sequenced, and analyzed to determine the AM fungal species and their respective proportions in roots of each plant species. Glomus etunicatum and G. claroideum of the family Glomaceae generally occurred more frequently in R. parvifolius and R. multiflora, which form Arum-types, whereas S. erythropa, of the family Gigasporaceae, was the most frequently detected species in H. rhombea, which produced Paris-type AM. Although the genotype of the plant species used appears to determine the AM morphologies formed, there was preferential association between the hosts and AM fungal inoculants.     

Arbuscular mycorrhiza of Arnica montana under field conditions—conventional and molecular studies

Two distinct populations of Arnica montana, an endangered medicinal plant, were studied under field conditions. The material was investigated using microscopic and molecular methods. The analyzed plants were always found to be mycorrhizal. Nineteen arbuscular mycorrhizal fungal DNA sequences were obtained from the roots. They were related to Glomus Group A, but most did not match any known species. Some showed a degree of similarity to fungi colonizing liverworts. Conventional analysis of spores isolated from soil samples allowed to identify different fungal taxa: Glomus macrocarpum, Glomus mosseae, Acaulospora lacunosa, and Scutellospora dipurpurescens. Their spores were also isolated from trap cultures.     

The diversity of arbuscular mycorrhizas of selected Australian Fabaceae

Abstract

Members of the Australian native perennial Fabaceae have been little explored with regard to their root biology and the role played by arbuscular mycorrhizal (AM) fungi in their establishment, nutrition and long-term health. The ultimate goal of our research is to determine the dependency of native perennial legumes on their co-evolved AM fungi and conversely, the impact of AM fungal species in agricultural fields on the productivity of sown native perennial legume pastures. In this paper we investigate the colonisation morphology in roots and the AMF, identified by spores extracted from rhizosphere soil, from three replicate plots of each of the native legumes, Cullen australasicum, C. tenax and Lotus australis and the exotic legumes L. pedunculatus and Medicago sativa. The plants were grown in an agricultural field. The level and density of colonisation by AM fungi, and the frequency of intraradical and extraradical hyphae, arbuscules, intraradical spores and hyphal coils all differed between host plants and did not consistently differ between native and exotic species. However, there were strong similarities between species in the same genus. The three dominant species of AM fungi in rhizosphere soil also differed with host plant, but one fungus (Glomus mosseae) was always the most dominant. Sub-dominant AM species were the same between species in the same genus. No consistent differences in dominant spores were observed between the exotic and native Fabaceae species. Our results suggest that plant host influences the mycorrhizal community in the rhizosphere soil and that structural and functional differences in the symbiosis may occur at the plant genus level, not the species level or due to provenance.     

Bacterial effects on arbuscular mycorrhizal fungi and mycorrhiza development as influenced by the bacteria, fungi, and host plant

Bacterial strains from mycorrhizal roots (three belonging to Comamonadaceae and one to Oxalobacteraceae) and from non-mycorrhizal roots (two belonging to Comamonadaceae) of Medicago truncatula and two reference strains (Collimonas fungivorans Ter331 and Pseudomonas fluorescens C7R12) were tested for their effect on the in vitro saprophytic growth of Glomus mosseae BEG12 and on its colonization of M. truncatula roots. Only the Oxalobacteraceae strain, isolated from barrel medic mycorrhizal roots, and the reference strain P. fluorescens C7R12 promoted both the saprophytic growth and root colonization of G. mosseae BEG12, indicating that they acted as mycorrhiza helper bacteria. Greatest effects were achieved by P. fluorescens C7R12 and its influence on the saprophytic growth of G. mosseae was compared to that on Gigaspora rosea BEG9 to determine if the bacterial stimulation was fungal specific. This fungal specificity, together with plant specificity, was finally evaluated by comparing bacterial effects on arbuscular mycorrhizal symbiosis when each of the fungal species was inoculated to two different plant species (M. truncatula and Lycopersicon esculentum). The results obtained showed that promotion of saprophytic growth by P. fluorescens C7R12 was expressed in vitro towards G. mosseae but not towards G. rosea. Bacterial promotion of mycorhization was also expressed towards G. mosseae, but not G. rosea, in roots of M. truncatula and L. esculentum. Taken together, results indicated that enhancement of arbuscular mycorrhiza development was only induced by a limited number of bacteria, promotion by the most efficient bacterial strain being fungal and not plant specific.