路易斯碱催化的烯胺不对称还原研究

手性胺不仅是许多天然产物和手性药物的重要结构单元，而且也是非常有用的拆分试剂、手性配体和手性催化剂。亚胺和烯胺的不对称催化还原是制备手性胺的最直接有效的方式之一，手性有机小分子催化的亚胺不对称还原已取得了很大的进展，但到目前为止，有机小分子催化的烯胺不对称还原极少见文献报道。 本研究以廉价的三氯氢硅为氢源、DMF 等路易斯碱为催化剂实现了烯胺的高效还原。通过反应条件的优化，各种烯胺底物在0.1 eq. DMF 催化下、12 个小时内可以获得非常高的收率（>93%）。 在本课题组前期研究的基础上，我们筛选并设计了一系列以手性哌啶酸和叔丁基亚磺酰胺为母体的有机小分子路易斯碱催化剂，它们能催化三氯氢硅对(Z)-N-苄氧羰基-1-苯基丙烯胺的不对称还原，获得很高的收率和中等的对映选择性，并且具有很好的底物普适性。另外，通过机理方面的研究，我们推测在反应过程中一分子烯胺先捕获一个质子而转变为亚胺正离子，然后受到路易斯碱活化的三氯氢硅中的富电氢原子进攻该亚胺正离子得到还原产物。 另外，本文列出了在此课题进展中所发现的一些新反应，并且试图去阐释这些反应的作用机理。 Catalytic enantioselective reduction of imines and enamines represents one of the most straightforward and efficient methods for the preparation of chiral amines, which are not only important building blocks of many natrural products and chiral drugs, but also can serve as useful resolution reagents, chiral ligands and chiral catalysts. By now, asymmetric reduction of enamines catalyzed by organocatalysts has scarcely been reported, although organocatalyzed enantioselective reduction of imines has already gained great progress. In this study, we report the DMF-catalyzed reduction of enamines with high yields using HSiCl3 as the reducing agent. Under the optimized reaction conditions, various enamines can be reduced in the presence of 0.1 eq. DMF with high yields (>93%) in 12 hours. We screened a set of Lewis base organocatalysts derived from chiral pipecolinic acid and tert-butanesulfinamide for the reduction of (Z)-N-Cbz-1- phenylpropenamine, including newly designed ones and some of those previously developed in our lab. However, only moderate stereoselectivities, albeit high yields were obtained. As for the mechanism, we speculate that the enamine firstly engages a proton to form an iminium species, which is then attacked by the nucleophlic hydrogen of HSiCl3 activated by Leiws base. During the above studies, we have also discovered some new reactions, for which feasible mechanisms were proposed.

小麦抗禾谷孢囊线虫（ Heterodera avenae）相关基因的研究

禾谷孢囊线虫严重影响禾谷类作物的产量，在小麦中由禾谷孢囊线虫引起的产量损失可达30-100%。尤其在澳大利亚、欧洲、印度和中东危害严重，目前禾谷孢囊线虫已成为危害我国作物的主要病源。控制禾谷孢囊线虫的方法主要有：作物轮作、杀线虫剂、寄主抗性等等，其中基因工程方法培育抗线虫小麦品种被认为是最经济有效的方法。分离抗禾谷类孢囊线虫基因对揭示抗性基因结构与功能及其表达调控具有重要意义。 尽管小麦是重要的粮食作物，在小麦中已发现的抗禾谷孢囊线虫的基因很少，而比其近缘属如节节麦、易变山羊草、偏凸山羊草中含有丰富的抗源。目前已鉴定出禾谷孢囊线虫抗性位点Cre，并发现了9个禾谷孢囊线虫抗性基因(Cre1,2, 3, 4, 5, 6, 7, 8, and R) ，其中只有Cre1和Cre8直接从普通小麦中获得。从节节麦中获得的Cre3基因能最有效的控制线虫数量，其次是Cre1和Cre8。这些基因的克隆对于了解禾谷孢囊线虫抗性机制及进一步的育种应用都是非常关键的。然而，目前为止仅有Cre3基因通过图位克隆的方法从节节麦中被分离得到。该基因已被克隆得到的多数线虫抗性基因一样均属于核苷酸结合位点区（NBS）－亮氨酸重复序列区（LRR）基因家族。目前，已有很多抗性基因被分离，这些已知的NBS-LRR类抗性基因的保守序列为应用PCR的方法克隆新的抗性基因提供了可能。 因此本课题的目的是采用保守区同源克隆、3′RACE 和5′RACE 等方法从抗禾谷孢囊线虫小麦-易变山羊草小片段易位系E10 中克隆小麦抗禾谷孢囊线虫基因全序列，进而通过半定量PCR 和荧光定量PCR 研究该基因的表达模式。同时通过mRNA 差别显示技术和任意引物PCR（RAP-PCR）技术分离克隆植物禾谷孢囊线虫抗性基因及其相关基因，为阐明植物抗病性分子机制以及改良作物抗病性和作物育种提供基础，为通过分子标记辅助育种和基因工程方法实现高效、定向转移抗病基因到优良小麦品种奠定了重要的理论和物质基础。主要研究结果： 1． 本实验根据此前从抗禾谷孢囊线虫材料E-10 扩增得到的与来自节节麦的抗禾谷孢囊线虫Cre3 基因及其他的NBS-LRR 类抗性基因的NBS 和LRR 保守区序列设计了两对特异性引物，从E10 中扩增到532bp 和1175bp 的两个目标条带，它们有一个32bp 的共同序列，连接构成总长为1675bp 的NBS-LRR 编码区（命名为RCCN）。根据RCCN设计引物，利用NBS-LRR区序列设计引物，通过5′RACE 和3′RACE 技术采用3′-Full RACE Core Set(TaKaRa)和5'-Full RACE Kit (TaKaRa)试剂盒，反转录后通过嵌套引物GSP1 和GSP2 分别进行两轮基因特异性扩增，分别将NBS_LRR 区向5′端和3′端延伸了1173bp 和449bp，并包含了起始密码子和终止密码子。根据拼接的得到的序列重新设计引物扩增进行全基因扩增的结果与上面获得的一致。拼接后得到全长2775 bp 的基因序列（记作CreZ, GenBank 号：EU327996）。CreZ 基因包括完整的开放阅读框，全长2775 bp，编码924个氨基酸。序列分析表明它与已知的禾谷孢囊线虫抗性基因Cre3的一致性很高，并且它与已经报到的NBS-LRR 类疾病抗性基因有着相同的保守结构域。推测CreZ基因可能是一个新的NBS-LRR 类禾谷孢囊线虫抗性基因，该基因的获得为通过基因工程途径培育抗禾谷孢囊线虫小麦新品种奠定了基础，并为抗禾谷孢囊线虫基因的调控表达研究提供了参考。 2． 通过半定量PCR和SYBR Green荧光定量PCR技术对CreZ基因的相对表达模式进行了研究。以α-tubulin 2作为参照，采用半定量PCR 分析CreZ 基因在不同接种时期1d, 5d, 10, 15d 的E-10的根和叶的的表达情况。在内参扩增一致的条件下，CreZ 在E-10的根部随着侵染时间的增加表达量有明显的增加，在没有侵染的E-10的根部其表达量没有明显变化，而在叶中没有检测表达，说明该基因只在抗性材料的根部表达。SYBR Green定量PCR分析接种前后E10根部基因CreZ基因的表达水平为检测CreZ基因的表达建立了一套灵敏、可靠的SYBRGreen I 荧光定量PCR 检测方法。接种禾谷孢囊线虫后E10根内CreZ基因的相对表达水平显著高于接种前。随接种时间的延长持续增加，最终CreZ基因的相对表达量达到未接种的对照植株的10.95倍。小麦禾谷孢囊线虫抗性基因CreZ的表达量与胁迫呈正相关，表明其与小麦的的禾谷孢囊线虫抗性密切相关，推测CreZ基因可能是一个新的禾谷孢囊线虫候选抗性基因。 3． 针对小麦基因组庞大、重复序列较多，禾谷孢囊线虫抗性基因及其相关基因的片断难以有效克隆的问题，通过mRNA 差别显示技术及RAP-PCR 技术分离克隆植物禾谷孢囊线虫抗性及其相关基因。试验最终得到154 条差异表达条带，将回收得到的差异条带的二次PCR 扩增产物经纯化后点到带正电的尼龙膜上，进行反向Northern 杂交筛选，最终筛选得到102 个阳性差异点。将其中81 个进行测序，并将序列提交到Genbank 中的dbEST 数据库，分别获得登录号(FE192210 -FE192265，FE193048- FE193074 )。序列比对分析发现，其中26 个序列与已知功能的基因序列同源；有28 条EST 序列在已有核酸数据库中未找到同源已知基因和EST，属新的ESTs 序列；另外27 个EST 序列与已知核酸数据库中的ESTs 具有一定相似性，但功能未知。其所得ESTs 序列补充了Genbank ESTs 数据库，为今后进一步开展抗禾谷类孢囊线虫基因研究工作打下了基础。结合本试验功能基因的相关信息，对小麦接种禾谷孢囊线虫后产生的抗性机制进行了探讨。接种禾谷孢囊线虫后植物在mRNA 水平上的应答是相当复杂的，同时植物的抗病机制是一个复杂的过程，涉及到多个代谢途径的相互作用。 The cereal cyst nematode (CCN), Heterodera avenae Woll, causes severe yieldreductions in cereal crops. The losses caused by CCN can be up to 30-100% in somewheat fields. At present, cereal cyst nematode has become the major disease sourcein China and it also damaged heavily in Australia, Europe, India and Middle East.The damage caused by CCN can be mitigated through several methods, includingcrop rotation, nematicide application, cultural practice, host resistance, and others.Of these methods, incorporating resistance genes into wheat cultivars and breedingresistant lines is considered to be the most cost-effective control measure forreducing nematode populations. Although wheat is an economically important crop around the world, far fewergenes resistant to CCN were found in wheat than were detected in its relatives, suchas Aegilops taucchi, Aegilops variabilis and Aegilops ventricosa. Cloning these genesis essential for understanding the mechanism of this resistance and for furtherapplication in breeding. Because of the huge genome and high repeat sequencescontent, the efficient methods to clone genes from cereal crops, are still lacking. A resistance locus, Cre, has been identified and 9 genes resistant to CCN (designatedCre1, 2, 3, 4, 5, 6, 7, 8, and R) have been described, in which Cre1 and Cre8 werederived directly from common wheat. The Cre3 locus, which was derived from Ae.tauschii, has the greatest impact on reducing the number of female cysts, followed byCre1 and Cre8. Cloning these genes is essential for understanding the mechanism ofthis resistance and for further application in breeding. However, to this point, only Cre3, a NBS-LRR disease resistance gene, has been obtained through mappingcloning in Ae. tauschii. The majority of nematode resistance genes cloned so far belong to a super familywhich contains highly conserved nucleotide-binding sites (NBS) and leucine-richrepeat (LRR) domains. To date, many NBS-LRR resistance genes have been isolated.The conserved sequences of these recognized NBS-LRR resistance genes provide thepossibility to isolate novel resistance genes using a PCR-based strategy. The aim of the present study was to clone the resistance gene of CCN fromWheat/Aegilops variabilis small fragment chromosome translocation line E10 whichis resistant to CCN and investigate the espression profiles of this gene withsemi-quantitative PCR and real-time PCR. Another purpose of this study is cloningthe relational resistance gene for CCN by mRNA differential display PCR andRAP-PCR. These works will offer a foundation for disease defence of crop andbreeding and directional transferring resistance gene into wheat with geneengineering. Primary results as following: 1．According to the conversed motif of NBS and LRR region of cereal cystnematode resistance gene Cre3 from wild wheat (Triticum tauschlii) and the knownNBS-LRR group resistance genes, we designed two pairs of specific primers for NBSand LRR region respectively. One band of approximately 530bp was amplified usingthe specific primers for conversed NBS region and one band of approximately 1175bpwas amplified with the specific primers for conversed LRR region. After sequencing,we found that these two sequences included 32bp common nucleotide having 1675bpin total, which was registered as RCCN in the Genbank. Based on the conservedregions of known resistance genes, a NBS-LRR type CCN resistance gene analog wasisolated from the CCN resistant line E-10 of the wheat near isogenic lines (NILs), by5′RACE and 3′ RACE.designated as CreZ (GenBank accession number: EU327996) .It contained a comlete ORF of 2775 bp and encoded 924 amino acids. Sequencecomparison indicated that it shared 92% nucleotide and 87% amino acid identitieswith those of the known CCN-resistance gene Cre3 and it had the same characteristic of the conserved motifs as other established NBS-LRR disease resistance genes. 2． Usingα-tubulin 2 as exoteric reference, semi-quantitative PCR and real-timePCR analysis were conducted. The expression profiling of CreZ indicated that it wasspecifically expressed in the roots of resistant plants and its relative expression levelincreased sharply when the plants were inoculated with cereal cyst nematodes. therelative expression level of the 15days-infected E10 is the 10.95 times as that ofuninfected E10,ultimately. It was inferred that the CreZ gene be a novel potentialresistance gene to CCN. 3．We cloned the relational resistance gene for CCN by mRNA differentialdisplay PCR and arbitrarily primed PCR fingerprinting of RNA from wheat whichpossess huge and high repeat sequence content genomes. Total 154 differentialexpression bands were separated and second amplified by PCR. The products werenylon membrane. The 102 positive clones were filtrated by reverse northern dot blotand 81 of those were sent to sequence. The EST sequences were submitted toGenbank (Genbank accession: FE192210 - FE192265, FE193048 - FE193074). Thesequences alignment analysis indicated 26 of them were identical with known genes;28 were not found identical sequence in nucleic acid database; another 27 ests wereidentical with some known ests, but their functions were not clear. These ESTsenriched Genbank ESTs database and offered foundation for further research ofresistance gene of CCN.

碳离子全身辐照对小鼠血清及肝脏中超氧化物歧化酶活性、丙二醛含量和脑组织中还原性谷胱甘肽浓度的影响

用12C6+离子束对小鼠进行吸收剂量分别为0.05、0.1、0.3、0.5、0.75、1、1.5、2Gy的一次性全身照射,5d后测定血清及肝脏中超氧化物歧化酶(Superoxide dismutase,SOD)活性和丙二醛(Maleicdialdehyde,MDA)含量,以及脑组织中还原性谷胱甘肽(Glutathione,GSH)的浓度。结果显示,吸收剂量小于0.75Gy小鼠的血清及肝脏中SOD活性高于对照组,大于0.75Gy则低于对照组;吸收剂量小于0.3Gy小鼠的血清及肝脏中MDA含量小于对照组,大于0.3Gy则大于对照组;吸收剂量小于0.5Gy小鼠的脑组织GSH浓度大于对照组,大于0.5Gy则小于对照组。低剂量的重离子全身辐照对小鼠的抗氧化系统有一定的激活作用,随着照射剂量的增大,抗氧化酶活性明显降低,脂质过氧化水平增高。

Analysis of the xuv photoabsorption spectrum of Au2+, Au3+, and Au4+

The photoabsorption processes of Au2+, Au3+, and Au4+ have been investigated experimentally and theoretically in the 70-127 eV region. Using the dual laser-produced plasma technique, the 4f and 5p photoabsorption spectrum has been recorded at 50 ns time delay and was found to be dominated by a great number of lines from 4f-5d, 6d and 5p-5d, 6s transitions, which have been identified by comparison with the aid of Hartree-Fock with configuration interaction calculations. The characteristic feature of the spectrum is that satellite lines from excited configurations containing one or two 6s electrons are more important than resonance lines, and with increasing ionization, satellite contributions from states with one 6s spectator electron gradually become more important than those with two 6s spectator electrons. Based on the assumption of a normalized Boltzmann distribution among the excited states and a steady-state collisional-radiative model, we succeeded in reproducing a spectrum which is in good agreement with experiment.

Research on EUV spectra of highly ionized titanium

The spectrum of highly ionized titanium was studied by means of the beam-foil technique. Titanium ions were provided by the HI-13 tandem accelerator at China Institute of Atomic Energy. The experimental results are compared with those of laser-produced plasmas. Numerous lines attributed to Ti XVI to XVIII ransitions have been identified, and three of them were newly measured, which were attributed to 2s2p(24)P(3/2)-2p(32)D(3/2), 2s2p(21)S(0)-2sp(31)P(1) and 4p(1)P(0)-5d(1)P(1) transitions.

Bt杀虫晶体蛋白的土壤残留及其对土壤磷酸酶活性的影响

研究表明以不同形式导入土壤中的杀虫晶体蛋白在土壤中的残留特性及其对土壤磷酸酶活性的影响有所不同。以Bt菌体向土壤导入杀虫晶体蛋白的试验表明 :随着培养时间的延长 ,土壤中杀虫晶体蛋白含量逐渐增加 ,到 1 5d时达到一个峰值 ,而后下降 ,在培养 30d时 ,杀虫晶体蛋白含量基本与初始含量相同。以不同Bt棉组织添加土壤的试验表明 :随着培养时间的延长 ,土壤中的杀虫晶体蛋白含量降低 ,在培养初期下降的速度较快 ,随后下降的速度较慢 ,在培养的中后期基本稳定 ,在培养 5 6d时 ,杀虫晶体蛋白含量为初始值的 4 4 7%(ZK)和 5 6 1 %(GK)。不同Bt棉的盆栽试验表明 :在整个生育期内 ,Bt棉花种植后根际土壤中杀虫晶体蛋白含量均明显比非Bt棉高。Bt菌体和Bt棉组织处理的土壤磷酸酶活性均呈现出比对照高的趋势 ,而在Bt棉种植过程中Bt棉根际土壤的磷酸酶活性则呈现出比非Bt棉低的趋势。无论以何种方式向土壤中导入杀虫晶体蛋白 ,土壤磷酸酶活性在不同杀虫晶体蛋白浓度处理间的差异显著。

丁香花粉生命力及贮藏力的研究

针对丁香杂交育种的花期不遇和远距离杂交困难的问题 ,以7种丁香为试材 ,分别进行了新鲜花粉生命力测定比较、不同贮藏条件对花粉生命力的影响以及不同种丁香花粉贮藏力的差异研究。结果表明 :红丁香的花粉生命力最高 ,可达81.5 % ;小叶丁香的花粉贮藏力最强 ,低温冷藏可达60d以上 ;丁香花粉最适的贮藏温度为0～2℃低温条件 ,在此温度下花粉生命力都能延长到15d以上 ;常温下丁香花粉生命力迅速丧失 ,5d后就已全部接近死亡。用花粉生命力和贮藏力高的丁香品种作父本 ,可提高杂交的成功率

短期菲胁迫对大豆幼苗超氧化物歧化酶活性及丙二醛含量的影响

研究了不同浓度 ( 0～ 2 0 0 μg·g-1)菲胁迫和恢复培养后大豆幼苗生长、超氧化物歧化酶 (SOD)活性及丙二醛 (MDA)含量的变化 .结果表明 ,2 0 0 μg·g-1菲处理 5d后大豆幼苗生长受到抑制 ,但幼苗恢复培养后经短暂停滞期后仍可恢复生长 .菲污染对大豆幼苗SOD活性变化的剂量 效应关系的作用形式比较复杂 ,胁迫 2d时为线性关系 ,胁迫 5d和 8d时为抛物线型 .在菲处理前期 ( 2d) ,幼苗SOD活性被 10 0和2 0 0 μg·g-1菲显著诱导 [分别为对照的 1.15倍 (P <0 .0 5 )和 1.2 6倍 (P <0 .0 1) ].菲暴露 8d时 ,SOD活性显著降低 ,2 0 0 μg·g-1菲处理组SOD活性为对照的 88% (P <0 .0 5 ) .菲处理 5d后恢复培养 2d和 4d ,5 0和10 0 μg·g-1菲处理组幼苗SOD活性得到恢复 ,而 2 0 0 μg·g-1菲处理组幼苗SOD活性仍明显高于对照 (P <0 .0 5 ) .试验亦反映出 ,10 0和 2 0 0 μg·g-1菲处理 5d和 8d ,幼苗MDA含量均比对照显著增加 (P <0 .0 5和P <0 .0 1) .可以认为 ,SOD活性可作为大豆幼苗遭受短期菲胁迫的生物标记物 .

共基质对10株细菌降解苯并芘的作用研究

从石油污染的污泥中分离驯化出10株细菌(SB01～SB10),利用生物摇床实验对其降解苯并芘(BaP)的效能进行试验,研究了有(或无)共基质(葡萄糖Glu,或菲PHE)对细菌降解BaP的影响,并采用ANOVA和Tukey多重比较进行分析。结果表明(,1)当以BaP为惟一碳源和能源且BaP初始浓度为50mg·L-1时(MS1),SB01的降解率最高,5d可降解31.0%;以Glu为共代谢基质时(MS2),SB09的降解率最高,可达36.9%;以PHE为共代谢基质时(MS3),SB01对BaP的降解率为46.0%。(2)Glu对SB01、SB02、SB03、SB07、SB10降解BaP有抑制作用,对SB01抑制作用最明显,使SB01的降解率降低了13.1%,Glu对SB05,SB08降解率无明显促进或抑制作用。(3)PHE对细菌降解BaP均表现出促进作用,对SB01的促进作用最明显,使其降解率提高15.0%。(4)Glu对SB09的促进作用大于PHE的促进作用,而对SB06,PHE的促进作用大于Glu。

共基质对10株细菌降解芘的作用

从石油污染的污泥中分离出10株细菌(SB01-SB10),研究了有(或无)共基质(葡萄糖Glu,或菲PHE)对细菌降解芘(PYR)的影响.结果表明:当以PYR为唯一碳源和能源时(MS1),SB01的PYR降解率最高,5d可降解30.4%;以Glu为共代谢基质时(MS2),SB09的PYR降解率最高,可达37.7%;以PHE为共代谢基质时(MS3),SB10的PYR降解率为50.2%.Glu抑制SB01、SB03对PYR的降解,对SB01抑制作用最明显,使SB01的PYR降解率降低7.9%;Glu对SB02、SB07、SB08、SB10降解率无明显促进或抑制作用.PHE对细菌降解PYR均有促进作用,对SB10的促进作用最明显,使其降解率提高29.8%.Glu与PHE对SB04和SB09降解PYR的促进作用无显著差异,而对其它各菌株而言,PHE对PYR降解的促进作用大于Glu.

几种不同下垫面地表粗糙度动态变化及其对通量机理模型模拟的影响

在众多地表通量模拟模型和遥感通量反演模型中,空气动力学粗糙度(z0)是一个重要的地表参数．选取代表典型农田的禹城站,代表复杂下垫面的千烟洲站和代表森林下垫面的长白山站3个通量观测站的风速和温度廓线资料,运用最小二乘法拟合迭代,分别计算得到各站点通量塔所在地的零平面位移和空气动力学粗糙度．在此基础上,分别分析不同下垫面的空气动力学粗糙度随作物高度和叶面积指数(LAI)、风向(地形)、风速、摩擦速度等因子的变化．并采用SEBS模型分析地表空气动力学粗糙度动态变化对地表通量计算的影响．结果表明:空气动力学粗糙度随植被特征(如作物高度,叶面积指数等)以及风向、风速和摩擦速度等因子而变化．禹城和长白山站通量塔所在风浪区的空气动力学粗糙度明显随作物生长期植被高度及叶面积指数变化,即先随LAI增加而增加,达到峰值后,随LAI增加而减小;千烟洲叶面积指数变化较小,空气动力学粗糙度随叶面积指数的变化不明显;地形较平坦的禹城和长白山站空气动力学粗糙度随风向变化较小,而地形起伏较大的千烟洲站空气动力学粗糙度随风向变化较大．随着风速的变化,禹城站空气动力学粗糙度没有明显变化,而千烟洲和长白山空气动力学粗糙度表现出随风速增加而减小的趋势．各站空气动力学粗糙度的这种动态变化对模型通量反演有较大影响,通过模型分析, 5月1日～6月3日禹城空气动力学粗糙度日平均值、千烟洲及长白山通量塔空气动力学粗糙度5d平均值与模型所取z0值相比,由于z0的动态变化造成相同时间尺度显热通量H的计算相对误差的绝对值最大可分别达到2．726％,33．802％和18．105％．

科尔沁沙地15种禾本科植物种子萌发特性比较

在实验室条件下,观测了科尔沁沙地乌兰敖都地区禾本科植物当年新采种子的萌发特点。15种植物中,披碱草、糙隐子草、冠芒草、大油芒、芦苇、虎尾草、野古草、狼尾草的发芽率超过80％,水稗草、牛鞭草、虱子草、狗尾草的发芽率不足10％。1～3d开始发芽的植物有大油芒、画眉、芦苇、虎尾草、披碱草、冠芒草、毛马唐、糙隐子草、超过10d基本不发芽的植物包括狗尾草、虱子草、牛鞭草.发芽持续期小于10d的植物包括毛马唐、水稗草、芦苇、画眉草、大油芒;发芽持续期21～30d的植物有披碱草、冠芒草。发芽种子超过总发芽种子的50％需要天数为虎尾草2d,芦苇3d,大油芒4d,披碱草5d,糙隐子草5d,野古草7d,冠芒草7d,狼尾草10d。与英国Sheffield地区相比,乌兰敖都地区一年生禾草发芽率低的所占比重更大,发芽更为缓慢;乌兰敖都地区多年生禾草的发芽率差别很小,但发芽更为缓慢。杂草植物萌发的风险分摊能力相对明显,因此抗干扰能力相对较强。

盘式吸渗仪吸渗率计算方法比较

选用盘径为5 cm和15 cm的盘式吸渗仪,对杨凌土(粘土)和神木砂黄土(砂壤土)两种质地的土壤在0、-3、-6、-9-、12 cm水头5种负压下进行了室内吸渗实验,分析了不同盘径和负压对累积吸渗量的影响;并选用4种吸渗率公式对这两种质地土壤吸渗率进行了计算,以Vandervaere法为参考方法对该4种方法的适用性进行了分析。结果表明,在相同的时间内,两种土壤5 cm盘径下的累积吸渗量均大于15 cm盘径下的累积吸渗量,砂黄土累积吸渗量大于相同负压下土累积吸渗量;在4种吸渗率计算方法中,无论土还是砂黄土,Haverkamp公式所得吸渗率值与参考方法最接近。

慢生大豆根瘤菌(Bradyrhizobiumjaponicum)聚羟丁酸合成酶基因(phbC)的克隆和序列测定

以苜蓿根瘤菌Rm10 2 1的 phaC基因突变体菌株Rm1114 4 (phaC ::Tn5 - 2 33)为受体菌 ,通过功能互补 ,成功地从构建的Bradyrhizobium japonicum USDA110基因文库中 ,筛查到能与Rm1114 4互补 ,使之恢复在以乙酰乙酸为唯一碳源的M9培养基 (M9-AA)平板上 5d形成明显可见菌落 ,以及在MOPS平板上形成粘液型菌落的表型的重组粘粒 pDC2 ;经证实 ,该粘粒带有 phbC基因 .完成了该基因的全序列测定并已在GenBank登记 ,登记号为AY0 775 80 .B .japonicumphbC基因由 180 3碱基对组成 ,GC含量 6 1.8% ,AT含量 38.2 % ;编码 6 0 0个氨基酸 ,Mr=6 6 .95× 10 3 .图 3表 3参 13

芘在土壤中的共代谢降解研究

高分子量多环芳烃 (PAHs)的降解通常以共代谢方式进行 .研究比较了高分子量多环芳烃代表种类芘作为唯一C源和能源的降解过程和有共代谢底物存在下芘的降解过程 ,结果表明 ,2 5d后前者中芘的降解率5 7% ,而后者中芘的降解率为 80 % .且有共代谢底物存在下 ,芘在降解过程中半衰期缩短 ;水杨酸 ,邻苯二甲酸 ,琥珀酸钠能作为共代谢底物提高芘的降解率 ,琥珀酸钠效果最好 .芘和低分子量多环芳烃之间也有共代谢关系 ,菲促进了芘的降解 ,但萘未出现同样的结果 .此外 ,这阐明了共代谢原理和适宜作高分子量多环芳烃共代谢底物的物质 .