林木外生菌根真菌彩色豆马勃巢式PCR检测

为探讨林木外生菌根真菌的分子检测方法,利用真菌通用引物ITS1-F/ITS4-B扩增了外生菌根真菌彩色豆马勃的核糖体DNA内转录间隔区并进行了序列测定.通过序列比较,设计了一对彩色豆马勃特异性引物PtF/PtR.利用该对特异性引物与ITS1-F/ITS4-B组合进行巢式PCR,能从供试的彩色豆马勃10个菌株中特异性地扩增出1条347 bp的条带,而供试的其他6个参比菌株未出现扩增产物.经分析,该巢式PCR检测技术的灵敏度可达到10 fg的DNA,是常规PCR检测的1 000倍.利用该技术从马尾松苗木菌根中检测到目的外生菌根真菌.这表明采用本研究设计的特异性引物,利用巢式PCR技术可以灵敏、准确地从林木外生菌根中检测出彩色豆马勃.     

浮游动物DNA宏条形码标志基因比较研究

DNA宏条形码技术作为一种新型生物监测方法,在未来生态环境监测中有巨大的应用潜力。目前,浮游动物DNA宏条形码监测仍在发展阶段,需要首先对其(采样方法、引物选择和数据分析等)进行标准化和调整,然后才能用于常规流域生态监测。其中,如何选择合适的PCR扩增引物是DNA宏条形码生物监测标准化的关键问题之一。本研究比较了COI、18SV9和16S通用引物在浮游动物DNA宏条形码监测中的差异,为初步建立规范化的浮游动物DNA宏条形码监测方法提供技术支撑。结果表明,16S引物对浮游动物具有更好的特异性,其产生的操作分类单元(operational taxonomic unit, OTU)有88.1%属于浮游动物。虽然18SV9引物具有更高的物种覆盖度,不仅能扩增出浮游动物,还能扩增出大量藻类和真菌,但其物种识别敏感性较差,不适合浮游动物物种水平多样性监测。COI引物的浮游动物物种特异性、物种覆盖度和物种识别敏感性都适中,检出的浮游动物物种数量高于18SV9引物和16S引物,更加适合浮游动物DNA宏条形码监测。     

光合细菌PCR检测技术的建立与应用

针对光合细菌传统的菌种鉴定方法和MPN定量方法存在费时、费力和准确性筹的问题,本研究建立了光合细菌特异PCR鉴定技术和实时荧光PCR定量的检测技术.以微生物肥料产品常用的光合细菌沼泽红假单胞菌和类球红细菌作为研究对象,分别依据16S rDNA序列和gyrB序列设计出具有种水平特异性的引物,优化并确定了PCR反应条件,其灵敏度达到100 pg/μL,对6个光合细菌产品鉴定的符合率为100%,结果表明建立的PCR鉴定技术具有特异性、灵敏性和实用性.再根据16S rDNA的保守序列设计了常用光合细菌通用引物,用其对系列稀释的已知菌含量样品的DNA模板进行荧光定量PCR,制作标准曲线.对10个光合细菌样品进行荧光定量PCR法测定,根据与标准曲线比较得出样品中的光合细菌含量,其结果与MPN法的相关系数为0.98,两者具有良好的相天性,结果表明建立的荧光定量PCR法可用于光合细菌的定量检测,并具有高特异性和快速等优点.     

丛枝菌根-植物修复重金属污染土壤研究中的热点

随着菌根研究和植物修复技术的发展,利用丛枝菌根强化重金属污染土壤的植物修复逐渐受到人们的重视。本文系统综述了当前的几个研究热点:(1)菌根植物吸收和转运重金属的分子机制;(2)AM真菌对超富集植物重金属吸收的影响及其机制;(3)AM真菌对转基因植物重金属吸收的影响及其机制;(4)AM真菌与其他土壤生物在植物修复中的复合作用;(5)丛枝菌根与化学螯合剂在植物修复中的复合作用;(6)重金属复合污染土壤的丛枝菌根-植物修复;(7)放射性污染土壤的枝菌根-植物修复;(8)丛枝菌根-植物修复的田间试验研究。在未来的丛枝菌根-植物修复研究中,要筛选优良的宿主植物和与之高效共生的AM真菌,加强相关理论和应用基础研究,并构建高效基因工程菌。     

分子生物学方法在微生物多样性及微生物生态研究中的应用

首先介绍了分子生物学技术在微生物多样性及微生物生态研究中应用的理论基础，以及在此基础上引入的分子生物学技术如：PCR、DNA杂交技术在分子层面上来研究微生物遗传多样性，并结合已有工作积累展望了分子微生物生态研究的发展前景．图2参20     

VA菌根菌剂的生产及其接种潜力的测定

VA菌很是由球囊霉目的结合菌与植物根组织形成的一类共生联合体，在农林业生产中具有巨大的应用前景．众多研究表明，VA菌根真菌是一种亟待开发利用的微生物资源．本文详细介绍了VA菌根真菌的繁殖方法，探讨了VA菌根菌剂的生产途径；文中还讨论了测定菌剂接种潜力的评价方法，重点介绍了最或然数测定法．     

分子标记技术在石斛属植物中的应用研究进展

石斛作为一种名贵中药,近年来受到国内外研究人员的重视.本文对RFLP技术、位点特异性PCR、RAPD技术、AP-PCR技术、AFLP技术、ISSR技术、SRAP技术、DNA序列分析、基因芯片技术等DNA分子标记技术的基本原理和特点作了简要介绍,DNA分子标记技术为石斛类药材的鉴别提供了更加有效、可靠的鉴定方法.综述了近年来上述分子标记技术在石斛属植物中的应用研究进展,总结了这些技术在中药材鉴定中的地位,并对其发展前景做出了展望.     

非纯培养物细菌蛋白酶DNA片段的克隆与表达

为了构建更多的蛋白酶基因工程菌,以及进行蛋白酶基因的直接进化研究,从非纯培养细菌总DNA中扩增各种编码蛋白酶的DNA片段.根据MEROPS和GenBank数据库中的枯草杆菌类蛋白酶的编码区和成熟肽编码序列设计并合成了10条引物.富集培养胞外蛋白酶产生菌并提取了12个总DNA样品,分别用每对引物在降落PCR (TouchdownPCR, TD-PCR)条件下进行蛋白酶编码序列的扩增.选择了19个长800 ~1 200 bp的扩增片段测序,其结果为: 8个是蛋白酶DNA片段,它们应属于4种不同的蛋白酶基因序列;同一对引物扩增到的基因序列差异性可达到32%,说明只使用基于已知序列的PCR方法从混合菌中获得新蛋白酶基因是可行的.将克隆到的1个与碱性蛋白酶E (GenBank No.AJ539133)的编码区99%相似的蛋白酶DNA片段插入pTWIN1载体,在大肠杆菌ER2566中进行表达.结果表明,表达的成熟蛋白酶可分泌到培养基中,能在牛奶平板上产生水解圈,对大肠杆菌有致死作用.图5表3参14     

黑斑蛙Dmrt1基因的克隆及在不同组织中的表达

Dmrt基因家族是新近发现的一个与性别决定相关的基因家族,该家族成员都含有一个新的具有DNA结合能力的保守基序——DM结构域.本文采用简并PCR技术,扩增并克隆了黑斑蛙基因组中的DM结构域,经序列分析,获得了Dmrt家族成员rnDmrt1;进一步根据获得的rnDmrt1序列,设计一对特异引物,采用RT-PCR技术对成蛙不同组织Dmrt1基因的表达进行了研究.结果发现,rnDmrt1只在精巢中特异表达,在卵巢、脑、肝、心、肾及肌肉组织中无表达,显示Dmrt1基因在性别决定和分化中有重要功能. 图4参9     

松材线虫PCR标准化阳性对照构建及检测体系的建立

建立了松材线虫PCR检测标准化阳性对照及特异性强的PCR检测体系.根据松材线虫rDNA-ITS区和BxPe12基因的特异基因序列设计引物,并从中筛选出一对特异引物cqubs01/cquba01,该引物能从松材线虫特异性扩增出196 bp片段,而不能对其他种类线虫进行扩增.基于优化PCR反应体系和反应程序,稳定的检测体系得以建立,检测灵敏度为100 ps/μL.以松材线虫基因组DNA为模板,以上述特异引物进行PCR扩增,将纯化后的PCR产物与PMD18-T载体连接之后转入大肠杆菌中,筛选出阳性克隆进行测序验证,最终获得了松材线虫的无害化阳性对照,建立了松材线虫标准化阳性对照的PCR检测体系.对来自于不同地区的12批次近100个样品进行了实际检测验证,其结果与实际发生情况一致,说明本检测体系稳定可靠.图3表2参8     

菌根真菌对土壤有机污染物的生物降解

利用土壤真菌和植物的结合体菌根真菌修复土壤,尤其是修复有机污染的根际土壤.正作为一个新的研究方向开始受到广泛关注。菌根真菌作为土壤真菌的一种,与放线菌和细菌等微生物相比,对土壤中有机污染具有更大的忍耐能力.并且能将许多持久性有机污染物(POPs)做为碳源来获取能量。文章通过总结近20年菌根真菌与土壤有机污染物关系的研究,列出了43种能分解POPs的菌根真菌,并探讨了菌根真菌通过直接分解和共代谢的方式降解土壤有机污染物的可能性,为进一步研究菌根真菌生物降解土壤中持久性有机污染物,利用菌根植物生物修复有机污染土壤提供信息。     

丛枝菌根对土壤-植物系统中重金属迁移转化的影响

丛枝菌根真菌(arbuscular mycorrhizal fungi, AMF)是一类在自然和农业生态系统中广泛存在并能与多数陆生植物形成共生关系的土壤真菌,在重金属污染土壤中对宿主植物的生长及吸收累积重金属具有重要影响,因而对污染土壤的生物修复具有潜在应用价值。以重金属从根际土壤进入植物并在植物体内再分配过程为主线,介绍丛枝菌根在这一过程中对重金属环境行为,特别是根际土壤中重金属赋存形态及植物吸收重金属的影响。最后,对丛枝菌根影响植物重金属耐性机制研究前沿和菌根修复技术的应用前景进行展望。     

Quantifying dispersal and establishment limitation in a population of an epiphytic lichen

Dispersal is a process critical for the dynamics and persistence of metapopulations, but it is difficult to quantify. It has been suggested that the old-forest lichen Lobaria pulmonaria is limited by insufficient dispersal ability. We analyzed 240 DNA extracts derived from snow samples by a L. pulmonaria-specific real-time PCR (polymerase chain reaction) assay of the ITS (internal transcribed spacer) region allowing for the discrimination among propagules originating from a single, isolated source tree or propagules originating from other locations. Samples that were detected as positives by real-time PCR were additionally genotyped for five L. pulmonaria microsatellite loci. Both molecular approaches demonstrated substantial dispersal from other than local sources. In a landscape approach, we additionally analyzed 240 snow samples with real-time PCR of ITS and detected propagules not only in forests where L. pulmonaria was present, but also in large unforested pasture areas and in forest patches where L. pulmonaria was not found. Monitoring of soredia of L. pulmonaria transplanted to maple bark after two vegetation periods showed high variance in growth among forest stands, but no significant differences among different transplantation treatments. Hence, it is probably not dispersal limitation that hinders colonization in the old-forest lichen L. pulmonaria, but ecological constraints at the stand level that can result in establishment limitation. Our study exemplifies that care has to be taken to adequately separate the effects of dispersal limitation from a limitation of establishment.     

The impact of tillage practices on arbuscular mycorrhizal fungal diversity in subtropical crops.

Arbuscular mycorrhizal fungi (AMF) are a main component of soil microbiota in most agrosystems. As obligately mutualistic symbionts, they colonize the roots of the majority of plants, including crop plants. We used molecular techniques to investigate how different tillage systems (moldboard, shred-bedding, subsoil-bedding, and no tillage) can influence the AM fungal community colonizing maize, bean, and sorghum roots in an experimental site located in northern Tamaulipas, Mexico. Roots from 36 plants were analyzed using AM fungal-specific primers to partially amplify the small subunit (SSU) of the ribosomal DNA genes. More than 880 clones were screened for restriction fragment length polymorphism (RFLP) variation, and 173 of these were sequenced. Ten AM fungal types were identified and clustered into three AM fungal families: Gigasporaceae, Glomaceae, and Paraglomaceae. Glomus was the dominating taxon in all the samples. Four of the 10 identified types were distinct from any previously published sequences and could correspond to either known unsequenced species or unknown species. The fungal diversity was low in the four agriculture management systems, but the multidimensional scaling (MDS) analysis and log-linear-saturated model indicated that the composition of the AMF community was significantly affected by the tillage system. In conclusion, since some fungal types were treatment specific, agricultural practices could directly or indirectly influence AM biodiversity.     

土壤和地下水中多环芳烃生物降解研究进展

多环芳烃是一类普遍存在于环境中的难降解的危险性"三致"有机污染物。受污染的土壤和地下水中的多环芳烃,生物降解是其归宿的主要途径。研究表明,对于土壤中低分子量多环芳烃类化合物,微生物一般以唯一碳源方式代谢;而大多数细菌和真菌对四环或四环以上的多环芳烃的降解作用一般以共代谢方式开始。文章重点论述了多环芳烃的来源、降解多环芳烃的微生物、生物降解机理、影响生物降解的因素以及生物修复方法。认为今后的研究方向是高分子量多环芳烃的降解机理与降解途径,基因工程技术在多环芳烃生物降解方面的应用,以及生物表面活性剂产生的机理及其在实际处理中的应用等。     

Novel weapons: invasive plant suppresses fungal mutualists in America but not in its native Europe

Why some invasive plant species transmogrify from weak competitors at home to strong competitors abroad remains one of the most elusive questions in ecology. Some evidence suggests that disproportionately high densities of some invaders are due to the release of biochemicals that are novel, and therefore harmful, to naive organisms in their new range. So far, such evidence has been restricted to the direct phytotoxic effects of plants on other plants. Here we found that one of North America's most aggressive invaders of undisturbed forest understories, Alliaria petiolata (garlic mustard) and a plant that inhibits mycorrhizal fungal mutualists of North American native plants, has far stronger inhibitory effects on mycorrhizas in invaded North American soils than on mycorrhizas in European soils where A. petiolata is native. This antifungal effect appears to be due to specific flavonoid fractions in A. petiolata extracts. Furthermore, we found that suppression of North American mycorrhizal fungi by A. petiolata corresponds with severe inhibition of North American plant species that rely on these fungi, whereas congeneric European plants are weakly affected. These results indicate that phytochemicals, benign to resistant mycorrhizal symbionts in the home range, may be lethal to na?ve native mutualists in the introduced range and indirectly suppress the plants that rely on them.     

Distinct mycorrhizal communities on new and established hosts in a transitional tropical plant community

The extent to which interspecific plants share mycorrhizal fungal communities depends on the specificity of the symbiosis. For tropical forest tree seedlings, colonization by mycorrhizal fungi associated with established vegetation could have important consequences for survival and growth. I used a novel molecular technique to assess the potential for sharing of mycorrhizas in forest and pasture in southern Costa Rica, by identifying arbuscular mycorrhizal (AM) fungi in roots of the forest canopy tree species Terminalia amazonia, pasture grasses Urochloa ruziziensis and U. decumbens, and seedlings of T. amazonia planted into experimental reforestation plots. I tested the hypotheses that experimental seedlings were colonized either by the AM fungal community of the forest T. amazonia (suggesting host specificity) or of Urochloa (suggesting absence of specificity/importance of local environment). After two years, pasture-grown T. amazonia seedlings were colonized by neither community, but rather by a species of Glomus that was rarely observed on the other plants. These results suggest that conspecific seedlings planted into existing vegetation generate a distinct mycorrhizal community that may influence competitive interactions and the relative costs and benefits of the AM fungal symbiosis at early stages in the life cycle of tropical trees.     

Predominance of clade D <Emphasis Type="Italic">Symbiodinium</Emphasis> in shallow-water reef-building corals off Kish and Larak Islands (Persian Gulf,Iran)

Scleractinian coral species harbour communities of photosynthetic taxa of the genus Symbiodinium. As many as eight genetic clades (A, B, C, D, E, F, G and H) of Symbiodinium have been discovered using molecular biology. These clades may differ from each other in their physiology, and thus influence the ecological distribution and resilience of their host corals to environmental stresses. Corals of the Persian Gulf are normally subject to extreme environmental conditions including high salinity and seasonal variation in temperature. This study is the first to use molecular techniques to identify the Symbiodinium of the Iranian coral reefs to the level of phylogenetic clades. Samples of eight coral species were collected at two different depths from the eastern part of Kish Island in the northern Persian Gulf, and Larak Island in the Strait of Hormuz. Partial 28S nuclear ribosomal (nr) DNA of Symbiodinium (D1/D2 domains) were amplified by polymerase chain reaction (PCR). PCR products were analyzed using single stranded conformational polymorphism and phylogenetic analyses of the LSU DNA sequences from a subset of the samples. The results showed that Symbiodinium populations were generally uniform among and within the populations of eight coral species studied, and there are at least two clades of Symbiodinium from Kish and Larak islands. Clade D was detected from eight of the coral species while clade C was found in two of species only (one species hosted two clades simultaneously). The dominance of clade D might be explained by high temperatures or the extreme temperature variation, typical of the Persian Gulf. Publication of this article was held up owing to technical problems. The publisher apologizes sincerely for this lengthy delay.