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1.
蜜环菌菌索是天麻生长的主要营养来源,而蜜环菌生物种菌索之间可能存在种间相互作用,因此天麻栽培时蜜环菌种的混用可能对天麻的产量产生影响。为揭示我国蜜环菌分类单元间菌索的相互作用,以我国8个蜜环菌分类单元为研究对象,通过研究其共同培养时整体及单侧菌索的生长速率和单位长度内生长尖端个数来研究其菌索间的作用特性。结果表明:两者间相互拮抗的有CBS D-CBS F;仅有一个蜜环菌菌索未受到影响或受到协同作用的有:CBS A-CBS H中的CBS A、CBS F-CBS J中的CBS J、CBS A-CBS F中的CBS A、CBS A-CBS N中的CBS A、CBS F-CBS M中的CBS M、CBS J-CBS M中的CBS M、CBS B-CBS J中的CBS B;组合中两种蜜环菌菌索靠近侧协同生长的有:CBS A-CBS M;组合中对两者靠近的区域具有优势的有:CBS A-CBS B中的CBS B、CBS A-CBS J中的CBS J、CBS B-CBS F中的CBS F、CBS D-CBS H中的CBS H、CBS D-CBS N中的CBS N和CBS F-CBS M中的CBS F。本研究的开展为我国蜜环菌的鉴定、天麻栽培用蜜环菌种的选用提供理论指导。  相似文献   

2.
Cha  Joo Young  Sung  Jae Mo  Igarashi  Tsuneo 《Mycoscience》1994,35(1):39-47
Three intersterility groups ofArmillaria mellea sensu lato were discovered by examining all pairwise combinations of monosporous isolates of basidiomes collected in Hokkaido. One of them, group IV, was identified asA. sinapina by mating it with tester strains. Two new species, groups III and V, were namedA. jezoensis andA. singula, respectively. Their morphological forms and the ecology of their basidiomes are described.  相似文献   

3.
用光学和电子显徽镜研究了生长在木材上的蜜环菌成熟菌索的超微结构。拟薄壁组织中有线粒体、内质网、核、液泡、质膜体、核糖体和典型的桶孔隔膜等。在菌索腔中疏松组织由薄壁菌丝、厚壁菌丝和非细胞衬质物质所组成,这些菌丝除了无隔孔帽的隔孔器和分散的核仁以外,见不到其它普通的细胞器,其最明显的特征是质壁分离和质膜断裂而卷曲,似乎是处在脱水状态。一旦它们进入新的寄主,一些普通细胞器就可出现。所以,可认为这些菌丝是处于休眠状态。对蜜环菌菌索的结构和功能的关系也进行了讨论。  相似文献   

4.
中国蜜环菌的新生物种   总被引:11,自引:0,他引:11  
在调查研究蜜环菌生物种的过程中,先后在东北、华北、华中和西南地区,发现了四个新的中国蜜环菌生物种,CBS F、CBS G、CBS H和CBS I。研究表明,CBS G属于典型的同宗配合种,其余三个为异宗配合。CBS H与CBS C之间存在部分互交可育,比例高达17.8%,在同一个国家的两个种之间出现如此高的互交可育比例还是首次报道。上述三个生物种同欧美的已知蜜环菌种均互交不育,为亚洲特有种。CBS I为无菌环的假蜜环菌A.tabescens (Scop. ) Emel,它与欧洲的假蜜环菌互交可育,属于同种。但同中国其它各生物种互交不育。同时讨论了蜜环菌生物种的群体观点。  相似文献   

5.
Armillaria isolates were collected from a unique forest ecosystem in the Niobrara Valley Preserve in Nebraska, USA, which comprises a glacial and early postglacial refugium in the central plains of North America. The isolates were collected from diverse forest trees representing a unique mixture of forest types. Combined methods of rDNA sequencing and flow cytometric measurements of nuclear DNA content determined that all Armillaria isolates collected from the site were A. gallica.  相似文献   

6.
7.
蜜环菌遗传测定的单孢分离和培养方法   总被引:16,自引:0,他引:16       下载免费PDF全文
从平板中直接分离担子菌萌发孢子的单孢分离方法,主要利用自制的毛细管和显徽玻璃针等简单工具操作。该法简便快速,抗污染,获得单孢率高。同时报道一种改进型的担子菌互交不育性测定用培养基MEJA,与国内外目前常用的SR和MEA培养基相比,增加一项判断标准,使互交不育性和互交可育性的反应更加清晰可靠。  相似文献   

8.
A modified hybridization strategy was used to construct a microsatellite enriched library from DNA of Armillaria ostoyae, a serious root pathogen on pine. Sequence characterization of 19 random clones revealed 12 distinct loci harbouring a repetitive motif. Primer design from the flanking regions allowed for their development as polymerase chain reaction based markers. Polymorphic assessment at both the population and global levels revealed levels of variation useful for genetic studies. The level of cross‐species amplification observed with closely related Armillaria species was high, raising the possible exploitation of these primers across the genus.  相似文献   

9.
用ISSR标记研究高卢蜜环菌系统发生学的尝试   总被引:14,自引:0,他引:14  
用ISSR(Inter-Simple Sequence Repeat)标记对黑龙江省牡丹江地区高卢蜜环菌的系统发生学进行了研究,用6个引物对35个菌株的DNA模板进行扩增。结果表明该地区的35个菌株分属3个不同的发育系,并且3个发育系在地理分布上是交错在一起的。同时表明ISSR标记是研究蜜环菌系统发育关系的理想的分子标记手段。  相似文献   

10.
为提高榛蘑人工栽培中出菇的稳定性,对蜜环菌菌索的生物学特性进行了研究,通过在不同生长时间、环境温度、培养基质的条件下对蜜环菌菌索进行培养。试验发现,菌索会由具有活性的黄色菌索逐渐角质化变成黑色丝状菌索,为保持蜜环菌菌索的活性状态,最佳培养条件:培养时间应控制在1523 d,最佳培养温度为恒温25℃,最佳培养基配方为PDA+麦麸+锯末。  相似文献   

11.
The hyphae of Armillaria mellea Fr. invade the large ceils of Gastrodia elata BI. Through the wall pits of cortical cells. During early stage the plasmalemma of large cell invaginates and the cell wall forms papillary thickenings to restrain the hyphae from invading. When a hypha enters a large cell, it is encircled tightly by the invaginated plasmalemma which is surrounded by a large number of vesicles coated by a unit membrane. As these vesicles fusing with their membranes to the plasmalemma and discharging their contents into the space around the hypha, the space lined by the invaginated plasmalemma enlarges gradually and becomes a digestive vacuole in which a hypha is completely digested. Reaction product form acid phosphatase activities in the vesicles and digestive vacuoles testifies that the vesicles and digestive vacuoles are identical with primary and secondary lysosomes of plant lysosomal system respectively.  相似文献   

12.
对采自北京东灵山地区、黑龙江带岭地区、以及帽儿山地区不同寄主上的15个蜜环菌子实体进行了极性测试和生物种测定。配对培养结果表明15个子实体中共存在着四个生物种,分别命名为ChBSI、ChBSI、ChBSⅢ和ChBSⅣ。除生物种ChBSⅢ的极性不清楚外,其它生物种都是四极性异宗配合的真菌。东灵山菌株中的两个生物种是ChBSⅡ和ChBSⅣ,带岭菌株中的两个生物种是ChBSI和ChBSⅢ,帽儿山菌株是生物种ChBSⅠ。经过中国生物种与欧洲生物种的配对培养,发现生物种ChBSⅣ与Armilariagalica融合。  相似文献   

13.
Sixteen fungal communities were sampled by isolating from 0.5–1 cm diameter roots of living trees and stumps of common oak (Quercus robur). The density of fungi was 1.5–2 times greater in roots from stumps than from living trees. The diversity of fungi was similar in living tree roots and stumps. Some of the fungal species with increased densities in stump roots (e.g. Aspergillus kanagawaensis, Chrysosporium pannorum, Cylindrocarpon destructans, C. didymum, Hormiactis candida, Monodictys lepraria, Mycelium radicis atrovirens, Penicillium daleae, P. janczewskii, and Trichocladium opacum) usually stimulated the growth of rhizomorphs of either Armillaria ostoyae or A. gallica in oak‐wood segments in vitro. Eight of 27 isolates that were studied stimulated the rhizomorph growth in both Armillaria spp. It is presumed that the increase in density of `stimulants' may predispose oak stumps to infection by A. ostoyae and A. gallica.  相似文献   

14.
15.
Phenolic fungicides, which were initially fungicidal to mycelium of Armillaria mellea on the surface of well‐colonised wood billets, eventually stimulated the growth of A. mellea. An extensive growth of rhizomorphs was produced from A. mellea inoculum, which had been exposed to phenolic chemicals for 3 months, compared to few or no rhizomorphs produced from inoculum exposed to water or a suspension of a non‐phenolic fungicide, fenpropidin. Inoculated privet plants grown either in pots or under field conditions were treated with a range of fungicides; fenpropidin, phenyl phenol, cresylic acid or water (control) was applied every 6 months over 21/2 yr. Fenpropidin caused a slightly (but significantly) lower incidence of infection than occurred in untreated plants, but the phenolic fungicides, cresylic acid and phenyl phenol, did not reduce the incidence of infection. The severity of infection (% root circumference colonised at 5 cm depth) was greater following cresylic acid treatments than the other fungicides or water‐treated controls. Use of phenolic fungicides such as cresylic acid for the control of A. mellea may therefore be counter‐productive.  相似文献   

16.
蜜环菌生物种及鉴定方法研究进展   总被引:1,自引:0,他引:1  
门金鑫  邢晓科  郭顺星 《菌物学报》2016,35(11):1281-1302
蜜环菌属真菌是一类重要的大型真菌,在全世界范围广泛分布。该属中有些种是重要的林木病原菌,有些种则具有很高的食药用价值。由于蜜环菌属真菌形态差异并不明显,缺乏分类特征,该属的分类和鉴定一直是大型真菌的研究热点。自从生物种的概念提出之后,蜜环菌的分类鉴定取得了突破性的进展,目前全球范围内已报道的蜜环菌生物种近40种;而对蜜环菌生物种的鉴定方法则包括了最初的形态学鉴定以及近些年发展起来的分子生物学鉴定方法。本文对当前世界范围内已经鉴定的蜜环菌生物种进行了梳理,并对蜜环菌生物种的鉴定方法的研究进展进行了综述,旨在为蜜环菌的研究提供参考。  相似文献   

17.
从大兴安岭和长白山采集到30号蜜环菌(Armillaria mellea)标本,选其中有代表性的10个号的担子果获得单孢株。交配试验表明每一担子果都具有双因子异宗配合系。不同子实体交配型之间交配结果表明,在大兴安岭和长白山地区蜜环菌目前至少存在5个生物种,分别称为生物种A、B、C、D和E。将这5个生物种的单孢菌种与欧洲5个蜜环菌生物种的单孢菌株进行配合,生物种B与欧洲A.gallica,生物种E与欧洲A.ostoyae亲和交配,因此将生物种B和E分别定为A.gallica和A.ostoyae。生物种A、C和D则不与任何欧洲生物种交配。  相似文献   

18.
用电镜技术比较研究了天麻球茎皮层细胞和中柱细胞对蜜环菌侵染的反应,皮层细胞在蜜环菌菌丝的刺渺下能产生囊状结构,然后这些小囊将入侵的菌丝包围和消化,而中柱细胞则不能,上述两种细胞在功能上的主要差别就在于此。  相似文献   

19.
一种优化的蜜环菌分离与纯化方法   总被引:1,自引:1,他引:0  
从分离材料的采集、蜜环菌索的室内培养条件、培养基的改良和分离技术的优化4个方面对前人的蜜环菌分离方法进行了系统的完善和改进。结果表明:采用蜜环菌生长良好的木本植物组织为分离材料,在15℃保湿的条件下培养可以得到健壮的菌索;按玉米粉:黄豆粉:蔗糖:水=6:1:1:26的质量比例制作的培养基不仅能满足蜜环菌生长的营养需求,而且对于其他杂菌具有明显的阻滞作用,有助于菌株纯化;分离前对菌索表面进行适当干燥可显著提高分离的成功率。  相似文献   

20.
Aims: To study the optimization of submerged culture conditions for exopolysaccharide (EPS) production by Armillaria mellea in shake‐flask cultures and also to evaluate the performance of an optimized culture medium in a 5‐l stirred tank fermenter. Methods and Results: Shake flask cultures for EPS optimal nutritional production contained having the following composition (in g l?1): glucose 40, yeast extract 3, KH2PO4 4 and MgSO4 2 at an optimal temperature of 22°C and an initial of pH 4·0. The optimal culture medium was then cultivated in a 5‐l stirred tank fermenter at 1 vvm (volume of aeration per volume of bioreactor per min) aeration rate, 150 rev min?1 agitation speed, controlled pH 4·0 and 22°C. In the optimal culture medium, the maximum EPS production in a 5‐l stirred tank fermenter was 588 mg l?1, c. twice as great as that in the basal medium. The maximum productivity for EPS (Qp) and product yield (YP/S) were 42·02 mg l?1 d?1 and 26·89 mg g?1, respectively. Conclusions: The optimal culture conditions we proposed in this study enhanced the EPS production of A. mellea from submerged cultures. Significance and Impact of the Study: The optimal culturing conditions we have found will be a suitable starting point for a scale‐up of the fermentation process, helping to develop the production of related medicines and health foods from A. mellea.  相似文献   

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