细菌解磷能力测定方法的研究*

选择分解有机磷能力较强的 3株细菌和溶解磷矿粉较强的 4株细菌 ,砂培 4周后 ,用不同的方法测定水浸提液中磷的含量。发现不同的细菌解磷能力差异很大 ,细菌在分解磷化合物的同时 ,一部分磷被细菌同化 ,一部分以无机磷酸盐状态贮藏在细菌细胞内。直接测定浸提液中无机磷酸盐的含量 ,将大大低估细菌的解磷能力 ,必须将浸提液消煮 ,才能比较正确地反映细菌分解磷的能力。     

西湖沉积物中解磷菌的分离纯化及其解磷能力

采用有机磷固体培养基和无机磷固体培养基从沉积物中分离出具有解磷能力的菌株,通过平板划线分离纯化后得到6株磷细菌,其中2株为有机P细菌（编号为OP₁、OP₂）,4株为无机磷细菌（编号分别为NOP₁、NOP₂、NOP₃、NOP₄）.测定发现,OP₁、OP₂和NOP₃溶磷能力较强,NOP₄解磷能力较微弱,而NOP₁及NOP₂在分离纯化后失去了解磷能力;菌株OP₁及OP₂具有较强的分解有机磷卵磷脂的能力,接种OP₁、OP₂菌株的培养液中水溶性磷含量分别比对照增加了38.53和64.53倍;接种NOP₃菌株的培养液中磷含量比对照增加了54.06倍.     

杨树根际解无机磷细菌Mp1-Ha4的鉴定及其解磷机理

解无机磷细菌能够溶解土壤中的难溶性磷酸盐,增加土壤有效磷含量,促进植物生长。以一株杨树根际土壤中筛选得到的解无机磷细菌Mp1-Ha4为研究对象,利用分子生物学的方法对该菌株进行鉴定,测定了其对磷酸钙、磷酸铝和磷酸铁的解磷能力,并对该菌株9 d内的磷酸钙溶解动力学进行了研究。结果表明,解无机磷细菌Mp1-Ha4为一株西地西菌Cedecea sp.,其对磷酸钙的溶解能力远强于对磷酸铝和磷酸铁的溶解能力。在NBRIP液体培养基中,该菌株对磷酸钙的溶解能力达到了497.4 mg/L,在其对磷酸钙解磷过程中,培养基pH及可滴定酸度与解磷量分别呈显著负、正相关。高效液相色谱分析显示,该菌株在解磷过程中分泌了大量有机酸,主要包括α-酮戊二酸,酒石酸和苹果酸。分泌有机酸,降低环境pH可能是解无机磷细菌西地西菌(Cedecea sp.)Mp1-Ha4溶解难溶性磷酸盐的主要机制,同时该菌株对磷酸钙的高效溶解作用使其具有较大的研究和应用前景。     

麦田土壤解无机磷细菌的分离、筛选及其解磷效果

通过选择性解磷细菌培养基从麦田土壤中分离、纯化解无机磷细菌,并用钼蓝比色法定量研究磷细菌的解磷效果。结果表明通过选择性平板分离,发现麦田土壤中有15个菌株有解无机磷的作用,根据菌株直径和其解磷圈的大小,确定解磷能力较强的菌株9个;经过进一步分离纯化,选出单一无杂菌的菌株7个。解磷菌株经摇瓶培养后,比色测定培养液中磷的含量,通过比较发现其中5个菌株的解磷效果要显著优于其它两个菌株（P=0.05）。     

一株高效解无机磷细菌BS06的鉴定及其解磷能力分析

【目的】对一株来源于广西甘蔗根际土壤的高效解无机磷细菌BS06的分类和解磷能力进行探讨,以期为解磷微生物在广西甘蔗生产上的开发和应用提供理论依据。【方法】通过形态观察、生理生化测定及16S rRNA基因序列同源性分析,进一步结合种特异的recA基因序列分析对解磷菌BS06进行分类鉴定;通过改变无机磷培养基中的碳源、氮源对菌株解磷能力的影响,分析菌株的解磷特性;通过盆栽试验了解菌株对甘蔗品种粤糖00236、桂糖28磷素吸收的影响。【结果】分类鉴定结果表明菌株BS06属于洋葱伯克霍尔德菌(Burkholderia cepacia);菌株在以乳糖为碳源条件下具有较强的解磷能力,其发酵液中水溶性磷含量为262.71 mg/L;在以硝酸钠为氮源条件下有较强解磷能力,其发酵液中水溶性磷含量达到305.85 mg/L;接种BS06菌株显著促进甘蔗组培苗的生长并提高甘蔗植株的含磷量。【结论】解磷细菌BS06具有较大的开发利用潜力。     

油松菌根际高效解磷钾细菌筛选与鉴定

本研究筛选出油松-褐环乳牛肝菌菌根根际土中高效解磷钾细菌并对其进行种类鉴定。采用平板稀释法自菌根际土中筛选解磷钾细菌,并用钼蓝比色法和原子吸收法分别对其液体培养5 d后的菌株进行解磷能力和解钾能力测定,筛选出高效的解磷钾细菌。同时,对筛选出的菌株进行显微观察、生物学鉴定和16Sr DNA序列分析。通过筛选得出解有机磷细菌P6和解无机磷细菌P15能力较强,其培养液中有效磷浓度分别为283 mg/L和898.5 mg/L,经鉴定P6属于节杆菌属(Arthrobacter sp.),P15为荧光假单胞菌(Pseudomonas fluorescens),以及2株能力较强的解钾细菌K1和K12,其培养液中有效钾浓度分别为21.6 mg/L,19.3 mg/L,经鉴定K1为壤霉菌属(Agromyces cerinus),K12为中华根瘤菌属(Sinorhizobium sp.)。由此可见,油松-褐环乳牛肝菌菌根根际存在高效解磷钾细菌,褐环乳牛肝菌可以通过影响根际解磷钾细菌的种类及能力来改善油松幼苗的根际磷钾营养状况。     

一株寒地高效解无机磷细菌的分离鉴定及拮抗作用

【目的】从北方寒地种植的不同农作物根际土壤中分离高效解磷的细菌,为微生物制剂和磷肥的开发提供适于本地区的优良菌种。【方法】通过初筛和复筛从26株解磷菌中筛选获得一株高效解磷细菌,对其进行生理生化和分子生物学鉴定,同时采用钼蓝比色法测定解磷能力。采用平板对峙法测定拮抗植物病原菌能力。【结果】通过筛选后获得的菌株B51-7经鉴定为伯克霍尔德菌属。菌株在发酵液中可溶性磷含量最高达到832.74 mg/L,同时具有很强的广谱抑菌作用,抑菌率最高为89.71%,可以显著促进水稻生长。【结论】菌株B51-7是一株具有生物防治作用的高效解磷细菌,可应用于生物菌肥和生防制剂中。     

磷尾矿土壤中解磷细菌的筛选及解磷能力的测定

以贵州瓮福磷尾矿土壤为原料,从中分离纯化得到具有较高解磷能力的细菌。利用溶磷圈试验筛选出具有明显溶磷圈的细菌,通过形态学特征、生理生化试验、16S rDNA基因序列分析及系统发育树对其进行初步鉴定。再以磷酸三钙为唯一磷源对筛选所得菌株进行液态培养,探索不同菌株解磷能力与培养液pH值之间的关系,并通过钼锑抗比色法测定3株细菌的最大解磷能力。从分离纯化得到的4株细菌筛选出具有明显溶磷圈的细菌PSB1、PSB3和PSB4,初步鉴定菌株PSB1为普城沙雷氏菌(Serratia plymuthica),PSB3为嗜麦芽窄食单胞菌(Stenotrophomonas maltophilia),PSB4为泡囊短波单胞菌(Brevundimonas vesicularis),最大解磷能力分别为148.87μg/mL、153.84μg/mL和146.76μg/mL。与国内已报道的文献相比,实验筛选所得的3株细菌都是具有较高解磷能力的菌种。菌株PSB1和PSB4培养液中pH值与其解磷能力存在显著的负相关性,而菌株PSB3不存在,其解磷机理还需进一步研究。     

花椒（Zanthoxylum bungeanum）凋落物分解过程中酚酸的释放及其浸提液对土壤化学性质的影响

应用分解网袋法研究了花椒凋落物分解过程中（0、10、30d和60d）酚酸的释放动态及凋落物浸提液对花椒林地土壤化学性质的影响。结果表明：花椒凋落物在分解过程中呈现出明显的毒性动态。凋落物分解的60d中,凋落物残留量在前30d内变化最大,30d后无显著变化;凋落物中酚酸含量随分解时间的延长,呈显著降低的趋势,且在分解10d时,酚酸释放量最大。4个分解动念的凋落物浸提液显著地改变了土壤好气性自生固氮菌、氨化细菌、好气性纤维素分解菌的数量和土壤pH值、酚酸含量、铵态氮、有效磷等化学性质。不同分解时间的凋落物浸提液均造成了土壤pH值的显著升高;分解10d的凋落物浸提液对土壤铵态氮的含量具有显著的降低作用,对土壤好气性自生固氮菌和氨化细菌的生长均具有显著的促进作用,而对好气性纤维素分解菌的生长具有抑制作用;分解60d的凋落物浸提液显著地降低了土壤酚酸含量,对土壤有效磷含量具有显著的升高作用,对好气性自生固氮菌的生长具有抑制作用,而对好气性纤维素分解菌的生长具有促进作用。     

一些细菌和真菌的解磷能力及其机理初探

4株细菌和8株真菌培养6天后,发现培养液中有机酸含量大幅度增加,PH大幅度地下降,磷的含量大幅度增加,真菌比细菌表现出更强的溶解磷矿粉的能力,不同的微生物分泌有机酸的数量和种类差别很大,菌分泌的有机酸种类比细菌要多。但是,培养液中有机酸总量与解磷量之间并不存在显的相关性。     

青稞根腐病对根际土壤微生物及酶活性的影响

选取甘肃省卓尼县青稞种植区为研究地点,调查青稞根腐病的发病情况,并分别采集其健康植株和发病株根际的土壤,对比分析其土壤微生物生物量(碳、氮、磷)、微生物数量(细菌、真菌、放线菌)以及过氧化氢酶、蔗糖酶、脲酶、碱性磷酸酶、纤维素酶5种酶活性。结果发现,研究区10个采样点均有青稞根腐病的发生,发病率在5%—20%之间,不同地点发病率不同。根腐病的发生,会显著影响青稞根际微生物生物量,导致微生物生物量碳、氮、磷的含量发生变化,其中微生物生物量氮和磷含量整体降低,且不同采样点微生物量不同。土壤微生物数量总体呈现细菌放线菌真菌的趋势,但不同微生物对根腐病发病的响应不同,细菌和放线菌数量因根腐病的发生而减少,真菌的数量则增多;不同采样点土壤微生物数量不相同,细菌和真菌呈现区域性特征,放线菌的数量不呈现地域性。根腐病的发生还造成土壤酶活性的改变,其中蔗糖酶、脲酶、磷酸酶的含量因根腐病的发生而降低,而纤维素酶则升高,过氧化氢酶的变化没有规律。总而言之,根腐病的发生会使青稞根际土壤微生物组成发生改变,碳、氮、磷等物质代谢受到抑制,而能量代谢发生紊乱。因此,研究和防治青稞根腐病就必须重视土壤微生物及土壤酶的作用。     

On the track of natural transformation in soil

Abstract The understanding of microbial gene transfer including how bacteria acquire and disseminate genes in natural environments will provide data on the role of horizontal transfer in evolution. This understanding has been stimulated in recent years by concern about the impact of genetically engineered microorganisms on natural environments. This prospect has increased interest in determining the regulatory mechanisms of indigenous microbial populations as well as detecting genetic interactions between bacteria introduced into soil and the indigenous microflora. This paper will review the strategies developed to demonstrate whether the different steps required by natural bacterial transformation (the uptake of naked DNA by competent bacteria) could actually occur in soil. This will include a review on the release of DNA from microbial cells by passive or active mechanisms, its persistence by adsorption of extracellular DNA onto major soil components such as sand or clay minerals and the uptake of DNA by competent bacteria.     

Effect of wetland plants and bacterial inoculation on dissipation of phenanthrene

This study attempts to evaluate the capacity of wetland plants' ability to dissipate phenanthrene (PHE) under waterlogged conditions. The results indicate that Typha latifolia and Vetiveria zizanioides may efficiently degrade PHE, and were much more effective when under combined plant cultivation with the inoculation of Pseudomonas frederiksbergensis (ATCC BAA-257) . Concentrations of PHE declined from 200 to less than 52 mg kg^?1 in all treatments with plant cultivation. At the end of the experimental period, PHE was undetectable in combined plant cultivation in the presence of bacteria inoculation. Microbial biomass C(carbon), N(nitrogen), and P(phosphate) were significantly different (p < 0.05) in the presence and absence of bacteria inoculation with bacteria inoculation significantly (p < 0.05) increased microbial biomass P. The presence of bacteria inoculation and different plant species significantly (p < 0.05) decreased the PHE concentrations in the microcosms. The inoculation of bacteria and release of exudates from plant roots further enhanced the dissipation of PHE in sand. Concentrations of citric and malic acids were decreased up to 69% in bacteria-inoculated treatments, showing large citric and malic acids serving as a food source and growth substrate for bacteria.     

Blue foxes’ motivation to gain access to solid floors and the effect of the floor material on their behaviour

Farmed blue foxes are willing to work to gain access to a sand floor from a wire mesh floor. It is not clear whether the foxes work for the sand floor because of its solidity or because it enables them to perform certain behaviours, e.g. exploration and digging. Here, we measured blue foxes’ motivation to gain access from a wire mesh floor to a floor with 15–30 cm deep sand, a floor with 3–4 cm deep sand, a solid concrete floor, and another wire mesh floor. In addition, we analysed the foxes’ behaviour on these floor materials. Seven male blue foxes were trained and tested in self-constructed operant apparatuses. In an apparatus, the fox could move a bottomless test cage from a wire mesh floor to a neighbouring, alternative floor material for a 4-min visit by pressing a lever in the test cage for a fixed number of times (Fixed Ratio, FR). The foxes worked for each floor material for 12 days. In each daily test session, the foxes were exposed to work on one of the four workloads (FR 6, 12, 24, 48), for 3 h. The behaviour of the foxes was analysed during the 4-min visits on each floor material. The results showed that there was no difference between the floor materials, either in the demand elasticity of the fragment of the demand curve (ranging from −0.46 to −0.33), or in the intensity of the demand. However, the foxes’ behaviour varied between the floor materials. More digging, play, rooting (exploration with the muzzle), and vole jumping were observed on the floor materials with sand, than on the concrete floor and the wire mesh floor. Both the presence and the depth of the sand layer stimulated these behaviours. It is concluded that juvenile blue foxes do not value solid floor materials more than a wire mesh floor. However, the sand floor stimulates more digging, play, vole jumping, and exploration than the concrete floor or wire mesh floor. Furthermore, the depth of sand may be an important factor in eliciting these behaviours. Access to a floor material with sand may improve the welfare of farmed blue foxes by providing the possibility to perform species-specific behaviours.     

Reduction of Prussian Blue by the two iron-reducing microorganisms Geobacter metallireducens and Shewanella alga

Cyanide or cyanide-metal complexes are frequent contaminants of soil or aquifers at industrial sites, which can be released from such sites by outgassing or transport with the groundwater. They form very stable complexes with iron, which may occur in the subsurface as an insoluble blue mineral, the so-called Prussian Blue (Fe(4)[Fe(CN)(6)](3)). In this study, we show that the insoluble and colloidal Fe(III)-cyanide complex Prussian Blue can be reduced and utilized as electron acceptor by the dissimilatory iron-reducing bacteria Geobacter metallireducens and Shewanella alga strain BrY. The microbial reduction of the dark blue pigment Prussian Blue leads to the formation of a completely colourless solid mineral, presumably Prussian White (Fe(2)[Fe(CN)(6)]), which could be reoxidized through exposure to air, regaining the dark blue colour. In addition, the microorganisms were able to grow with Prussian Blue, using it as the sole electron acceptor. Geobacter metallireducens could also reduce Prussian Blue coatings on sand, which was sampled from a contaminated site.     

不同覆盖方式对底泥内源营养盐释放的控制效果

通过底泥内源营养盐释放控制室内模拟试验,考察了塑料包被、斜发沸石、方解石、石英砂和硝酸钙5种覆盖材料对底泥氮磷释放效率的影响,系统分析了各自优劣程度,为实际环境中不同污染背景水体选择适宜的控制技术提供科学依据.结果表明: 不同覆盖材料对底泥总磷释放的控制效果依次为:塑料包被>硝酸钙>斜发沸石>方解石>石英砂;不同覆盖材料对底泥总氮释放的控制效果依次为:斜发沸石>塑料包被>方解石>石英砂>硝酸钙;不同覆盖材料对底泥硝态氮释放的控制效果依次为:塑料包被>斜发沸石>方解石>石英砂>硝酸钙;不同覆盖材料对底泥铵态氮释放的控制效果依次为:硝酸钙>石英砂>斜发沸石>方解石>塑料包被;温度和底泥内源营养盐释放有对应关系,水样中总磷、总氮和硝态氮浓度会随着温度上升而增加,而铵态氮浓度呈下降趋势.     

Impact of Field Release of Genetically Modified Pseudomonas fluorescens on Indigenous Microbial Populations of Wheat

In a field release experiment, an isolate of Pseudomonas fluorescens, which was chromosomally modified with two reporter gene cassettes (lacZY and Kan(supr)-xylE), was applied to spring wheat as a seed coating and subsequently as a foliar spray. The wild-type strain was isolated from the phylloplane of sugar beet but was found to be a common colonizer of both the rizosphere and phylloplane of wheat as well. The impact on the indigenous microbial populations resulting from release of this genetically modified microorganism (GMM) was compared with the impact of the unmodified, wild-type strain and a nontreated control until 1 month after harvest of the crop. The release of the P. fluorescens GMM and the unmodified, wild-type strain resulted in significant but transient perturbations of some of the culturable components of the indigenous microbial communities that inhabited the rhizosphere and phylloplane of wheat, but no significant perturbations of the indigenous culturable microbial populations in nonrhizosphere soil were found. Fast-growing organisms that did not produce resting structures (for example, fluorescent pseudomonads and yeasts) seemed to be most sensitive to perturbation. In terms of hazard and risk to the environment, the observed microbial perturbations that resulted from this GMM release may be considered minor for several reasons. First, the recombinant P. fluorescens strain caused changes that were, in general, not significantly different from those caused by the unmodified wild-type strain; second, perturbations resulting from bacterial inoculations were mainly small; and third, the release of bacteria had no obvious effects on plant growth and plant health.     

High-performance liquid chromatographic determination of pyrophosphate in the presence of a 20,000-fold excess of orthophosphate.

An HPLC method was based on anion-exchange separation of pyrophosphate (diphosphate) and orthophosphate and postcolumn spectrophotometric detection at 140 degrees C with a molybdenum(V)-molybdenum(VI) reagent. The reagent was easy to prepare, stable for at least 6 months at room temperature, and ready for the determination of pyrophosphate and orthophosphate by the so-called heteropoly blue method without use of any reducing agent. A photodiode-array detector for HPLC indicated the spectral characteristics of the heteropoply blue complex that was detectable at 330-800 nm. The HPLC method had a wide dynamic range from 3 x 10(-7) to 5 x 10(-4) M for both pyrophosphate and orthophosphate with a relative standard deviation of measurement of 10 approximately 2%. Pyrophosphate of 5 x 10(-7) and 5 x 10(-6) M, respectively, could be determined in the presence of a 20,000-fold excess of orthophosphate; 0.01 and 0.1 M.     

Effect of fluorochromes on bacterial surface properties and interaction with granular media.

Simple, efficient, and safe tagging methods are desired in short-term microbial transport studies such as in the study of filtration systems for water and wastewater treatment. Suitability of selected fluorochromes as bacterial tagging agents in transport studies was evaluated on the basis of stability of stained cells and the effect of staining on bacterial surface characteristics and interaction with granular media. Surface properties were characterized by zeta potential and microbial adhesion to hydrocarbons. The effect of staining on interactions between bacteria and porous media was evaluated in terms of removal of bacteria in batch adsorption tests using sand coated with aluminum hydroxide to enhance adsorption. The DNA-specific fluorochrome 4',6-diamidino-2-phenylindole (DAPI) had generally negligible effects on bacterial surface properties and interaction with sand, as indicated in batch adsorption tests using pure cultures (Escherichia coli or Acinetobacter sp.) and wastewater bacteria. Cells stained with DAPI were stable for 48 h at 4 or 20 degrees C. Other nucleic acid fluorochromes tested had different but significant effects on bacterial cells and produced less stable fluorescence. Since transport through porous media is modulated by surface properties, it may be concluded based on these results that the choice of fluorochromes is critical in microbial transport studies. DAPI appeared to be a promising tagging agent. Time dependence of fluorescence of stained cells may limit the use of fluorochrome-tagged cells in long-term transport studies.