磷有效性对大豆菌根侵染的调控及其与根构型、磷效率的关系

以30个不同根构型的大豆基因型为材料,通过盆栽试验,研究了生长介质磷有效性对大豆接种摩西球囊霉属丛枝菌根真菌的影响及其与根构型、磷效率的关系.结果表明：生长介质磷有效性显著地影响大豆菌根真菌的接种效果.低磷条件下接种菌根真菌效果明显,菌根侵染率较高,菌根对大豆磷吸收的贡献率较大;高磷条件下接种菌根真菌效果不显著,菌根侵染率较低,菌根对大豆磷吸收的贡献率较低.磷有效性和大豆根构型对菌根真菌接种的影响具有交互作用.低磷条件下,中间型和深根型大豆的菌根侵染率最高,浅根型最小.高磷条件下,根构型与菌根侵染率间的关系不明显.根构型和菌根侵染状况对大豆磷效率的贡献存在互利互补关系,磷效率高的大豆基因型一般具有较好的根构型或较高的菌根侵染率.     

脂环酸芽孢杆菌A1的分离鉴定及其对中低品位磷矿的溶磷研究

微生物溶磷技术为充分利用我国丰富但难选的中低品位磷矿开辟了一条新的途径。旨在筛选出针对中低品位磷矿的高效溶磷菌,从湖北宜昌磷矿的酸性矿坑水中分离出一株兼性嗜酸异养菌A1。经菌株形态特征、生理生化指标和16S r DNA序列分析,鉴定属于Alicyclobacillus aeris。分析A1菌在4种不同培养基的生长及浸磷情况,结果显示,菌株A1在YSG培养基中生长及溶解中低品位磷矿的情况最佳,其中磷的浸出率高达77.22%,与无菌对照的化学浸出相比约提高了62%。根据原始磷矿和A1菌在YSG培养基中溶解的磷矿矿渣的物相分析及相应浸矿液的高效液相色谱检测,结果表明,A1菌发酵有机碳源代谢产生以草酸和柠檬酸为主的混合有机酸,磷矿石中的氟磷灰石、碳氟磷灰石经过这些有机酸的溶解,析出可溶性磷酸盐并同时生成石膏。     

内蒙古露天煤矿区回填土壤具生态适应能力丛枝菌根真菌的筛选

在盆栽试验条件下,应用灭菌的露天煤矿区回填土壤为培养基质,研究8个丛枝菌根真菌菌种(株)对沙打旺生长及根系侵染的影响.结果表明,分离自江西和新疆的Glomus mosseae的2个菌株在露天煤矿区回填土壤上能够显著提高沙打旺的生物量,并能有效改善植株的磷、氮营养;其侵染率均在50%以上,且根外繁殖体数显著高于其他接种处理.说明此两个菌株在该土壤上具有良好的生态适应能力,有助于露天煤矿区植被重建和生态恢复等研究工作的进一步开展.     

不同浓度和形态磷处理下内生真菌感染对高羊茅的影响

以感染内生真菌(endophyte-infected,EI)和不感染内生真菌(endophyte-free,EF)的高羊茅(Festuca arundinacea Schreb.)为材料,在温室沙培条件下研究内生真菌对高羊茅适应缺磷及利用不同形态磷肥的影响。结果表明,1)缺磷条件下,高羊茅EI和EF植株生长差异不显著;正常供磷条件下,高羊茅EI植株拥有更多分蘖数和绿叶数。说明正常供磷条件下内生真菌改善了宿主高羊茅的生长。2)与水溶性磷相比,高羊茅根有机酸和酸性磷酸酶(acid phosphatase,APase)活性在难溶性磷条件下显著增加,而根总酚含量无显著变化。在水溶性磷条件下,高羊茅EI植株根总酚含量显著高于EF植株,此时EI植株比EF植株拥有更多分蘖数和绿叶数,说明在水溶性磷条件下内生真菌对宿主地上部生长具有一定贡献。在难溶性磷条件下,虽然高羊茅EI植株根总酚含量仍然高于EF植株,但同时EI植株根有机酸含量显著低于EF植株,因此内生真菌感染只是增大了宿主植物的根冠比,而对分蘖数和绿叶数等无显著影响,说明内生真菌对宿主利用难溶性磷贡献不大。可见,内生真菌对宿主植物的生长在水溶性磷条件下更有利。     

聚磷菌的诱变选育及其生长特性

方法:采用氮离子注入技术对巢湖底泥中筛选出的一株细菌进行辐照诱变处理,选育出2株高效聚磷菌,并对这两株菌的生长特性进行了研究,根据生理生化及生长试验,并参照《伯杰氏细菌手册》进行菌种分类鉴定,这两株菌被鉴定为假单胞菌属细菌(Pseudomonas sp),并研究了菌量、温度、pH、氧、碳源对两株假单胞菌(Pseudomonas sp)的生长特性及聚磷代谢的影响。结果:试验表明,诱变后的聚磷率明显高于试验出发菌,为出发菌的1.43~3.89倍。两株菌的最适生长温度为30℃,最适pH和菌量分别为6、8和OD=0.6、0.4。最适菌量在厌氧条件下出现放磷现象,好氧条件下过量摄磷现象,经过先厌氧条件的培养其去磷率明显高于直接好氧培养条件下的去磷率,以乙酸钠为碳源时其聚磷率高于乳糖、甲醇、乙醇为碳源时的摄磷量。     

磷水平对接种丛枝菌根真菌甜玉米苗期生长的影响

研究了不同外源磷水平条件下,接种丛枝菌根真菌根内球囊霉(Glomus intraradices)对寄主植物甜玉米菌根侵染率、地上部和地下部鲜重、氮磷含量、精氨酸含量影响。结果表明:丛枝菌根真菌能够很好的侵染于玉米植株根系。且不同磷水平条件下,菌根侵染率差异较显著。在低磷水平下,菌根侵染率较高。孢子数量随着磷水平提高而增加。菌丝室根外菌丝鲜重在P40时最高。菌根化的甜玉米生物量及氮磷含量显著高于对照组。此外,低磷水平促使甜玉米地上部和地下部鲜重显著提高。甜玉米地上部总氮和地下部总氮含量分别在P40、P80和P20、P40时最高。地上部总磷和地下部总磷含量分别在P80和P160时最高。菌根精氨酸含量在低磷(P20)时最高。研究表明接种丛枝菌根真菌可促进甜玉米幼苗生长并与外源磷水平有关。     

磷有效性对大豆菌根侵染的调控及其与根构型、磷效率的关系

以30个不同根构型的大豆基因型为材料,通过盆栽试验,研究了生长介质磷有效性对大豆接种摩西球囊霉属丛枝菌根真菌的影响及其与根构型、磷效率的关系.结果表明：生长介质磷有效性显著地影响大豆菌根真菌的接种效果.低磷条件下接种菌根真菌效果明显,菌根侵染率较高,菌根对大豆磷吸收的贡献率较大;高磷条件下接种菌根真菌效果不显著,菌根侵染率较低,菌根对大豆磷吸收的贡献率较低.磷有效性和大豆根构型对菌根真菌接种的影响具有交互作用.低磷条件下,中间型和深根型大豆的菌根侵染率最高,浅根型最小.高磷条件下,根构型与菌根侵染率间的关系不明显.根构型和菌根侵染状况对大豆磷效率的贡献存在互利互补关系,磷效率高的大豆基因型一般具有较好的根构型或较高的菌根侵染率.     

磷对外生菌根真菌松乳菇和双色蜡蘑草酸、氢离子和磷酸酶分泌的影响

在液体培养基中设置无磷、低磷、中磷和高磷四种磷浓度,离体培养松乳菇Lactarius deliciosus的3个株系Ld-01、Ld-02、Ld-03和双色蜡蘑Laccaria bicolor S238N,分别测定外生菌根真菌的生长量、草酸、氢离子和酸性磷酸酶分泌速率。结果表明,在中磷的条件下,外生菌根真菌的生长最好,无磷、低磷或高磷对它们的生长产生抑制作用,抑制程度因菌种(株)不同而异。草酸、氢离子和酸性磷酸酶的分泌速率顺序为:无磷(0gNaH2PO4/L)>低磷(0.229gNaH2PO4/L)>中磷(1.147gNaH2PO4/L)>高磷(5.735gNaH2PO4/L),表现出明显的种(株)间差异,看来外源磷的供应状况可能有调节外生菌根真菌活化土壤无机磷和有机磷的作用。在缺磷和低磷条件下,外生菌根真菌具有较强的活化作用,在足磷的条件下活化作用减小,由此有效地利用土壤中的磷。     

三唑磷降解菌株GS-1的分离鉴定及其降解特性的研究

从有机磷农药污水处理池污泥中分离到一株能高效降解三唑磷的菌株GS-1, 通过生理生化实验和16S rDNA序列同源性分析, 将该菌株鉴定为Diaphorobacter sp.。菌株GS-1能以三唑磷为唯一碳源生长, 能在12 h内降解100 mg/L的三唑磷至检测不出的水平。菌株GS-1降解三唑磷的过程中会产生中间代谢产物苯唑醇(1-苯基-3-羟基-1,2,4-三唑), 36 h后苯唑醇被完全转化。菌株GS-1降解三唑磷的最适pH值为8.0, 最适温度为30°C, 且对杀螟硫磷、辛硫磷、毒死蜱和甲基对硫磷     

铁尾矿区油松根际溶磷泛菌D2的筛选鉴定及溶磷特性

从河北省迁安市马兰庄镇铁尾矿植被恢复区油松根际分离出2株溶磷细菌,经过平板初筛和摇瓶复筛得到1株溶磷能力较强的菌株D2.通过菌落形态、生理生化特性及16S rDNA序列分析,确定此菌株D2属于泛菌属.利用液体发酵试验测定不同碳源、氮源对菌株D2溶磷能力的影响,通过高效液相色谱测定D2在不同氮源条件下产生有机酸的种类和浓度.结果表明:菌株D2对磷酸三钙有较强的溶磷能力,培养液有效磷含量最高为392.13 mg·L^-1,菌株D2的溶磷能力在碳源为葡萄糖、氮源为硫酸铵时效果最好;高效液相色谱测定发现,不同氮源条件下,D2分泌有机酸的种类和浓度存在差异,以硫酸铵、氯化铵、硝酸钾、硝酸钠、硝酸铵为氮源,均产生草酸、甲酸、乙酸和柠檬酸,以硫酸铵、氯化铵、硝酸铵为氮源还产生苹果酸.相关性分析表明,乙酸含量与有效磷含量间呈显著正相关(r=0.886,P<0.05),表明溶磷泛菌D2分泌的乙酸对无机磷的溶解有明显的促进作用,这也很可能是该菌株的重要溶磷机制之一.     

Pyridoxal 5-phosphate, Phenyl Phosphate and Acetyl Phosphate, as Inhibitors of Photophosphorylation Competitive with Phosphate

Pyridoxal 5-phosphate, phenyl phosphate and acetyl phosphate,as well as rß-naphthyl monophosphate, inhibited photophosphorylationof spinach chloroplasts competitively with P_i and noncompetitivelywith ADP. The apparent dissociation constant of the inhibitor-enzymecomplex (K_i) values of pyridoxal 5-phosphate, phenyl phosphateand acetyl phosphate for the P_i site were 1.1, 3.8 and 2.4 _mM,respectively. These organic phosphates inhibited Ca²⁺-ATPaseof the isolated coupling factor 1 (CF₁) (EC 3.6.1.3 [EC] ) noncompetitivelywith ATP. AMP, creatine phosphate, fructose 1,6-bisphosphate,glucose 6-phosphate, 3-phosphoglyceric acid, ribose 5-phosphateand PP_i did not significantly inhibit photophosphorylation.Like rß-naphthyl monophosphate, pyridoxal 5-phosphateand phenyl phosphate inhibited photophosphorylation and thecoupled electron transport, but were almost without effect onthe basal electron transport. On the other hand, acetyl phosphateconsiderably inhibited photophosphorylation, but had almostno effect on the coupled electron transport rate and the basalrate. The results suggest that these organic phosphates inhibitphotophosphorylation by binding at the P_i site on the activecenter of CF₁ and that their binding inhibits the ATPase activityof isolated CF₁. These four organic phosphates which inhibited photophosphorylationcompetitively with Pi could not substitute for ADP or ATP ininhibiting ferricyanide photoreduction by decreasing H⁺-permeabilitythrough CF₁ and in protecting the ATPase of isolated CF₁ againstcold-anion inactivation. ¹ This work was supported in part by Grants-in-Aid for ScientificResearch from the Ministry of Education, Science and Culture,Japan to H.S. (Received May 25, 1981; Accepted September 28, 1981)     

Phosphate Transport and Apoplastic Phosphate Homeostasis in Barley Leaves

Levels of apoplastic inorganic phosphate (P_i) in leaves andP_i-transport activities of mesophyll cells were measured insitu in control and P_i-deficient plants. When detached leaveswere fed a solution that contained 10 mM P_i, the apoplasticP_i levels, as measured by an infiltration method, remained almostconstant. When the leaves were immersed in pure water, the apoplasticP_i level gradually decreased. With 50 mM P_i in the feeding solution,the level increased dramatically. The apoplastic P_i levels inP_i-deficient leaves were somewhat, but not very much lower thanthose in controls. When the immersion medium was changed topure water 60 mm after feeding with 10 mM P_i, the apoplasticP_i levels started to decrease and then returned to the initiallevel. It is suggested that intracellular P_i may be transportedback to the apoplast to maintain the apoplastic P_i levels ata constant value. Changes in cytoplasmic pH were measured during feeding of P_ito the leaves by use of the pH-sensitive fluorescent dye, pyranineafter Yin et al. (l990a, b). On feeding of P_i the cytoplasmicpH decreased in P_i-deficient plants as a result of co-transportof P_i and protons in situ. After removal of P_i from the immersionmedium, the cytoplasmic pH returned to the original value. ³ Present address: Institute für Biochemische Pflanzenpathologie,GSF-München, D-8042 Neuherberg, Germany.     

Phosphate Deficiency in Maize. IV. Changes in Amounts of Sucrose Phosphate Synthase during the Course of Phosphate Deprivation

With low-P treatment of maize, the level of sucrose phosphatesynthase (SPS) protein decreased to 15% of the control, whilethe "V_max" activity stayed relatively high (100–80% ofthe control) and the substrate limiting activity increased about2 fold in the leaves. These results suggest that leaf phosphatestatus has dual effects on the amount of SPS protein and theactivation state of SPS. (Received January 20, 1992; Accepted April 14, 1993)     

Phosphate rock bioleaching

Summary Microbiological acid solutions produced byThiobacillus ferrooxidans andThiobacillus thiooxidans on pyritiferous concentrate were used to solubilize phosphate rock with a high grade in P₂O₅. Five different mixtures of pyritiferous concentrate and phosphate rock, in different proportions, were used in adequate liquid culture media. Phosphate solubilization ranged from 12% to 100% when 9K nutrients medium was used and from 12% to 89% when medium contained only 3.0g/l ammonium sulphate.