果树自交不亲和性的遗传与生理机制及其研究

在简要介绍植物（包括果树）自交不亲和性与生理控制机制的基础上，着重对梨、苹果、杏等果树自交不亲和性的研究进行了综述，内容包括花柱内花粉管生长特点、花柱S糖蛋白的特性与作用机理以及果树自交不亲和的分子生物学研究，并提出了该领域有待研究的问题。     

茉莉酸对苹果气孔运动及抗旱性的影响

50、75、100、150 mg／L JA处理苹果叶片表皮，使开放气孔的气孔开度分别减小27．4％、37．5％、56．9％和63．8％，使关闭后的气孔在光下开放时气孔开度分别减小15％、18％、28．8％、52．5％、61．3％；处理植株后干旱胁迫，叶片相对电导率分别降低15％、18％、31％、58％，脯氨酸含量分别提高0．09％、0．40％、0．42％、0．54 ng／gFW，可溶性糖含量分别提高1．89％、2．53％、3．80％、5．06％。25 mg／L JA处理与对照均无显著差别。JA的作用表现出明显的浓度效应。     

苹果梨花芽孕育期生长锥细胞超微结构的观察

利用透射电镜对苹果梨花芽孕育期芽内生长锥细胞进行了观察，结果显示，在花芽孕育形成的过程中，生长锥细胞的超微结构发生了一系列变化：蛋白体和脂类小滴逐渐增加；核外膜向外延伸到胞质中与内质网相连，其上分布的核糖体增多；线粒体和内质网数目丰富且分布均匀；核糖体大量游散在胞质中；质体呈浅裂，中央缢缩；微管分布于靠近质膜处等。以上超微结构的变化表现出细胞旺盛分裂和分化的特点，反映了花芽孕育过程中的细胞学特征。     

PF455S插秧机及其侧离合器手柄的探讨和改善

PF455S插秧机的行走底盘与国产独轮驱动插秧机相比,水田机动性能和通过性较好,但也存在手柄安装夹紧不当等问题。介绍PF455S动力插秧机的系统组成、设计原理与主要参数,对发现的侧离器手柄问题进行改进,达到了设计目的。     

水位检测远程传输系统

本系统以STC89C51单片机为控制核心,HC-SR04超声波模块进行测距,GSM模块进行远程传输[1],LCD12864和矩阵键盘进行数据显示和更改等操作。据实验,该系统测量结果准确、灵敏度高、使用可靠、性价比高,具有很好的实用价值。     

基于RFID技术的电动车充电系统

本文设计了基于RFID技术的一种刷卡式的充电服务终端硬件装置,实现刷卡自动计费。本程序以AT89S52单片机为主控制器,用MFRC500射频识别芯片进行识别,并与射频卡进行通信。     

单片机技术在自动给料系统中的应用

文章设计了基于单片机控制的送料机自动送料机控制系统,论述了单片机AT89C51在实现其生产过程控制的自动给料系统的设计方法。     

Anthelmintic Actions of the Cyclic Depsipeptide PF1022A and its Electrophysiological Effects on Muscle Cells of Ascaris suum

The cyclic depsipeptide PF1022A, given orally to mice, showed very good anthelmintic activity against Heligmosomoides polygyrus and Heterakis spumosa at 50 mg kg⁻¹. In vitro, PF1022A was very active against Trichinella spiralis and had good activity against Nippostrongylus brasiliensis at 1 μg ml⁻¹. An 18-membered enniatin analogue, JES 1798, showed good activity only against N. brasiliensis at 10 μg ml⁻¹. The optical antipode of PF1022A had poor activity even at 100 μg ml⁻¹. The effects of PF1022A on the membrane potential and input conductance of somatic muscle of Ascaris suum were examined using a two-microelectrode current-clamp technique. PF1022A did not antagonize the effects of the selective nicotinic agonist levamisole. PF1022A and an analogue, JES 1798, but not the PF1022A antipode, produced a small time-dependent increase in input conductance associated with no potential change. The increase in input conductance did not occur in the Cl⁻-free bathing solution, suggesting that the increase in input conductance was mediated by Cl⁻ ions. The addition of high concentrations of Ca²⁺ to the preparation after the addition of PF1022A did not lead to production of Ca²⁺-activated Cl⁻ channels, suggesting that its mode of action was not that of a Ca²⁺ ionophore. The mechanism by which the cyclic depsipeptide might increase the Cl⁻ conductance is discussed.     

Identification of Rosellinia species as producers of cyclodepsipeptide PF1022 A and resurrection of the genus Dematophora as inferred from polythetic taxonomy

Rosellinia (Xylariaceae) is a large, cosmopolitan genus comprising over 130 species that have been defined based mainly on the morphology of their sexual morphs. The genus comprises both lignicolous and saprotrophic species that are frequently isolated as endophytes from healthy host plants, and important plant pathogens. In order to evaluate the utility of molecular phylogeny and secondary metabolite profiling to achieve a better basis for their classification, a set of strains was selected for a multi-locus phylogeny inferred from a combination of the sequences of the internal transcribed spacer region (ITS), the large subunit (LSU) of the nuclear rDNA, beta-tubulin (TUB2) and the second largest subunit of the RNA polymerase II (RPB2). Concurrently, various strains were surveyed for production of secondary metabolites. Metabolite profiling relied on methods with high performance liquid chromatography with diode array and mass spectrometric detection (HPLC-DAD/MS) as well as preparative isolation of the major components after re-fermentation followed by structure elucidation using nuclear magnetic resonance (NMR) spectroscopy and high resolution mass spectrometry (HR-MS). Two new and nine known isopimarane diterpenoids were identified during our mycochemical studies of two selected Dematophora strains and the metabolites were tested for biological activity. In addition, the nematicidal cyclodepsipeptide PF1022 A was purified and identified from a culture of Rosellinia corticium, which is the first time that this endophyte-derived drug precursor has been identified unambiguously from an ascospore-derived isolate of a Rosellinia species. While the results of this first HPLC profiling were largely inconclusive regarding the utility of secondary metabolites as genus-specific chemotaxonomic markers, the phylogeny clearly showed that species featuring a dematophora-like asexual morph were included in a well-defined clade, for which the genus Dematophora is resurrected. Dematophora now comprises all previously known important plant pathogens in the genus such as D. arcuata, D. bunodes, D. necatrix and D. pepo, while Rosellinia s. str. comprises those species that are known to have a geniculosporium-like or nodulisporium-like asexual morph, or where the asexual morph remains unknown. The extensive morphological studies of L.E. Petrini served as a basis to transfer several further species from Rosellinia to Dematophora, based on the morphology of their asexual morphs. However, most species of Rosellinia and allies still need to be recollected in fresh state, cultured, and studied for their morphology and their phylogenetic affinities before the infrageneric relationships can be clarified.     

一个潜在催化莱鲍迪D苷合成的新型糖基转移酶

尿苷二磷酸糖基转移酶(uridine diphosphate glycosyltransferases,UGTs)催化糖基转移反应,与植物次生代谢密切相关。本研究根据甜叶菊(Stevia rebaudiana)转录组数据库,克隆到一个催化莱鲍迪D苷(rebaudioside D,RD)合成的新型糖基转移酶候选基因,对其开展生物信息学分析。结果表明,该基因开放阅读框长1380 bp,编码459个氨基酸,等电点(pI)预测为5.54,理论分子量约49.66 kD,系统发育分析表明该基因与向日葵中的UGT89A2同源,故将其命名为SrUGT89A2。构建pET28a-SrUGT89A2原核表达载体,并在大肠杆菌(BL21(DE3))中诱导表达得到重组蛋白,HPLC检测表明粗酶液能催化甜叶菊提取液形成一个新的色谱峰,该峰保留时间与莱鲍迪D苷一致。经进一步纯化UGT89A2蛋白,添加不同甜菊糖苷标准品为催化底物,但未鉴定出该蛋白催化的具体糖苷。该潜在催化甜菊糖RD苷合成的新型糖基转移酶基因SrUGT89A2的发现,为RD苷的生物合成和甜菊糖苷的生物途径研究提供新的理论依据。