试述高等学校《植物学》单子叶植物部分教学内容的改革

高等学校《植物学》课程单子叶植物部分的主要教学内容包括：１）单子叶植物的主要特征;２）单子叶植物与双子叶植物特征的比较;３）单子叶植物的主要类群等。此外还庆集中讲授或强凋下列６个方面的主要内容;１）单子叶植物的习性及生境;２）单子叶植物的大类群和数目;３）单子叶植物的传统类群或“历史名称”;４０单子叶植物传粉受精以及演化趋势;５）单子叶植物的沼生型胚肥及全面胎座;６）单子叶植物生物学研究的新进展。     

运城盐湖十种耐盐植物体内无机及有机溶质含量的比较研究

运城盐湖的 1 0种耐盐植物体内的有机及无机溶质含量差异较大。总无机溶质含量在各种植物间的变化幅度小于总有机溶质 ,其中双子叶植物 (除二色补血草外 )地上部 K+ 含量及 K/Na比均低于单子叶植物 ,而双子叶植物地上部的Na+ 含量明显高于单子叶植物。双子叶植物 (除二色补血草外 )的 Na/Cl>1 ,而单子叶植物的 Na/Cl≈ 1。二色补血草的二价离子 Ca2 +和 Mg2 +含量较高。单子叶植物的可溶性糖及游离氨基酸含量高于双子叶植物 (除枸杞外 ) ,碱莞、盐角草、盐地碱蓬、碱地肤、二色补血草的脯氨酸含量均较低 ( <7μmol/g FW) ,且脯氨酸占游离氨基酸的比例高于其它植物。另外还计算了各种溶质占 COP的百分比 ,并讨论了它们在植物渗透调节过程中的作用。     

单子叶植物和双子叶植物的叶发育方式

叶侧生于茎上并与茎共同构成植物的枝条;叶是植物进行光合作用的主要器官,是植物体最富有特征的结构部分之一。单子叶植物和双子叶植物是被子植物的两大类群,人们观察它们的叶,发现其外部形态和内部构造都存在着很大的不同。这种差异,又是与这两类植物的叶发育方式相关联的。     

花同源异型MADS-box基因在被子植物中的功能保守性和多样性

MADS-box基因家族成员作为转录调控因子在被子植物花发育调控中发挥关键作用。本文以模式植物拟南芥（Arabidopsis thaliana）和水稻（Oryza sativa）为例,综述了近10年来对被子植物（又称有花植物）两大主要类群——核心真双子叶植物和单子叶植物花同源异型MADS-box基因的研究成果,分析MADS-box基因在被子植物中的功能保守性和多样性,同时探讨双子叶植物花发育的ABCDE模型在多大程度上适用于单子叶植物。     

南昌市不同植物类群叶片氮磷浓度及其化学计量比

对南昌大学前湖校区89种主要植物叶片的N、P浓度及其化学计量比进行了研究,结果表明:乔灌、常绿、针叶、种子、裸子和单子叶植物类群的N浓度分别低于相对应的草本、落叶、阔叶、蕨类、被子和双子叶植物类群,而C3和C4植物差异不显著;乔灌、常绿和裸子植物类群的P浓度含量分别低于相对应的草本、落叶和被子植物类群,而针叶和阔叶、蕨类和种子、单子叶和双子叶、C3和C4植物类群间差异不显著;乔木、阔叶、被子和双子叶植物类群叶片N/P分别高于相对应的灌草、针叶、裸子和单子叶植物类群,而常绿和落叶、蕨类和种子、C3和C4植物类群之间差异不显著.可见,不同类型植物对N和P的吸收利用存在差异,且对不同养分供应采取不同的适应对策.结合研究区土壤养分现状,建议优先选择常绿、针叶、裸子和单子叶植物类群作为城市园林植物.     

高原鼢鼠对高寒草甸植被特征及生产力的影响

本研究结果表明,高原鼢鼠栖息10年的斑块,植物群落的物种数减少,植物物种多样性指数下降,地上、地下总生物量显降低,单子叶和可利用双子叶植物生物量极显减少,但不可利用双子叶植物生物量显增加。高原鼢鼠去除5年后,斑块内植物群落的单子叶植物物种数增加,而双子叶植物下降,植物群落物种多样性指数下降,地上、地下总生物量显增加,单子叶和可利用双子叶植物生物量增加极显,不可利用双子叶植物生物量显降低。高原鼢鼠栖息10年的斑块,净初级生产量较未栖息地区减少68.98%。高原鼢鼠去除5年后,净初级生产量增加,但仅达到未栖息地区的58.69%。     

青海高原植物生理生态学研究：Ⅱ.高寒草甸植物的光合作用

青海高原高寒草甸植物柔软紫苑和糙毛鹅冠草,在同一海拔高度（３２００ｍ）,由于种的不同,净光合速率和表观光合量子效率（ＡＱＹ＝１／ＡＱＲ）也不同。双子叶植物柔软紫苑较单子叶植物糙毛鹅冠草高一些。同一垂穗披碱草,而在不同海拔高度（２３００ｍ和３２００ｍ）,由于海拔和气压不同,Ｐｎ和ＡＱＹ也不同。在高海拔地区（３２００ｍ）,长期生长的垂穗披碱草的Ｐｎ和ＡＱＹ较低海拔地区（２３００ｍ）同一植物的低,在青海     

高原鼢鼠挖掘对植物生物量的效应及其反应格局

高原鼢鼠取食洞道处,在植物根系受损条件下,主要测定各类植物生物量变动的格局。原生植被样区,取食洞道回填土壤后,单子叶植物地上生物量显增加,双子叶植物地上生物量及地下总生物量显降低。植物地上总生物量与取食洞道的厚度密切相关。土厚厚度＜5cm的取食洞道,植物地上及地下生物量显下降,土层厚度＞10cm,植物地上及地下生物量无显变化。高原鼢鼠长期栖息植被退化的斑块地,在取食洞道区域,单子叶及双子叶植物地上生物量和地下总生物量均显降低。结果验证了本提出的地下啮齿动物对双子叶直根类植物的存活具有负效应,对单子叶须根类植物则产生正效应的假设。     

农杆菌转化单子叶植物的可能性及问题

本文评述从农杆菌转化单子叶植物的可能性以及农杆菌转化单子叶植物后外源基因表达活性的影响因素,试图对提高农杆菌转化单子叶植物的可能性的途径进行探讨。     

影响苏云金芽孢杆菌基因在转基因植物中表达的因素

苏云金芽孢杆菌（Bacillus thuringiensis,Bt）杀虫晶体蛋白基因是植物抗虫基因工程中应用最广泛的基因资源。影响Bt基因在转基因植物中表达的因素繁多,阐明这些因素的效应对于获得Bt基因在受体植物中的稳定高效表达具有重要意义。现对Bt基因表达的主要影响因子,如Bt基因表达单元、植物发育、外部环境条件、受体植物遗传背景、整合位点及Bt基因沉默现象等进行了综述。     

Absence in monocotyledonous plants of the diffusible plant factors inducing T-DNA circularization and vir gene expression in Agrobacterium

Summary T-DNA circularization is one of the molecular events specifically induced in agrobacterial cells upon their infection of dicotyledonous plant cells. We developed a seedling co-cultivation procedure to determine whether or not monocotyledonous plants have the ability to induce T-DNA circularization and vir gene expression. Co-cultivation of Agrobacterium tumefaciens with seedlings of dicotyledonous plants showed that the circularization event takes place efficiently. The exudates and extracts of the seedlings also effectively induced T-DNA circularization and vir gene expression, indicating that dicotyledonous seedlings contain diffusible factors capable of inducing these molecular events. In contrast, neither T-DNA circularization nor vir gene expression was detectable when Agrobacterium was incubated with seedlings of monocotyledonous plants. Supplementing with acetosyringone, a known inducer of vir gene expression and T-DNA circularization, resulted in the induction of circularization during co-cultivation with monocotyledonous seedlings. These results indicate that the seedlings of monocotyledonous plants have no detectable amounts of diffusible inducers, unlike dicotyledonous seedlings. Therefore, it is unlikely that the vir genes are expressed in Agrobacterium inoculated in monocotyledonous plants. This may be one of the blocks in tumorigenesis of monocotyledonous plants by Agrobacterium.     

Mechanisms of crown gall formation: T-DNA transfer fromAgrobacterium tumefaciens to plant cells

Agrobacterium tumefaciens harbouring the Ti plasmid incites crown gall tumor on dicotyledonous species. Upon infection of these plants, T-DNA in the Ti plasmid is transferred by unknown mechanisms to plant cells to be integrated into nuclear DNA. WhenAgrobacterium is incubated with protoplasts or seedlings of dicotyledonous plants, circulation of T-DNA and expression ofvir (virulence) genes on the Ti plasmid are induced. The circularization event is efficiently induced by mesophyll protoplasts of tobacco which are highly competent for transformation by the T-DNA, and is also induced by diffusible phenolic compounds excreted from the protoplasts. The circularization and formation of crown gall both require the expression of thevirD locus, one of the induciblevir genes. These results suggest that the circularization of T-DNA reflects one of steps of the T-DNA transfer during formation of crown gall. In contrast to dicotyledonous plants, monocotyledonous plants are thought to be unresponsive to infection byAgrobacterium. We showed that monocotyledonous plants do not excrete diffusible inducers for the expression ofvir genes, while they contain a novel type of a signal substance(s). This inducer is not detected in the exudates of seedlings of monocotyledonous plants, but is found in the extracts from the seedlings, and also those from the seeds, bran and germ of wheat and oats. This finding suggests that T-DNA processing, and possibly its transfer, should take place whenAgrobacterium invades seedlings and seeds of monocotyledonous plants. Recipient of the Botanical Society Award for Young Scientists, 1987.     

Metabolic factors capable of inducing Agrobacterium vir gene expression are present in rice (Oryza sativa L.)

Summary The effects of exudates and extracts from suspension cultures or various parts of rice (Oryza sativa L.) plants on induction of vir (virulence) gene expression in Agrobacterium tumefaciens were examined. Only leaf extracts from panicle-differentiating plants to flowering plants were able to strongly induce activation and expression of vir genes. This induction was similar to that observed with 2 M acetosyringone (AS), yet there was no synergy between AS and rice extracts. Responses to vir-inducing metabolites and signal molecules were different among various vir loci. These results demonstrate that one or more inducing factors for vir gene expression are also present in rice, but only in specific parts and developmental stages.     

Light-regulated and cell-specific expression of tomato rbcS-gusA and rice rbcS-gusA fusion genes in transgenic rice.

A previously isolated rice (Oryza sativa) rbcS gene was further characterized. This analysis revealed specific sequences in the 5' regulatory region of the rice rbcS gene that are conserved in rbcS genes of other monocotyledonous species. In transgenic rice plants, we examined the expression of the beta-glucuronidase (gusA) reporter gene directed by the 2.8-kb promoter region of the rice rbcS gene. To examine differences in the regulation of monocotyledonous and dicotyledonous rbcS promoters, the activity of a tomato rbcS promoter was also investigated in transgenic rice plants. Our results indicated that both rice and tomato rbcS promoters confer mesophyll-specific expression of the gusA reporter gene in transgenic rice plants and that this expression is induced by light. However, the expression level of the rice rbcS-gusA gene was higher than that of the tomato rbcS-gusA gene, suggesting the presence of quantitative differences in the activity of these particular monocotyledonous and dicotyledonous rbcS promoters in transgenic rice. Histochemical analysis of rbcS-gusA gene expression showed that the observed light induction was only found in mesophyll cells. Furthermore, it was demonstrated that the light regulation of rice rbcS-gusA gene expression was primarily at the level of mRNA accumulation. We show that the rice rbcS gene promoter should be useful for expression of agronomically important genes for genetic engineering of monocotyledonous species.     

Specific attachment of Agrobacterium tumefaciens to bamboo cells in suspension cultures.

Agrobacterium tumefaciens was tested for its ability to attach to tissue culture cells of bamboo, a monocotyledonous plant. Phase-contrast microscopy and kinetic experiments with radiolabeled bacteria showed that attachment to bamboo cells was indistinguishable from attachment to cells of dicotyledonous plants. Bacterial mutants defective in attachment to dicotyledonous plants showed similar behavior with bamboo, and extensive washing of the bamboo cells had no effect on the number of bacteria which attached.     

Swimming against the tide: chemotaxis in Agrobacterium.

Chemotaxis in bacteria is an excellent model for signal transduction processes. In Agrobacterium tumefaciens, the causative agent of crown gall tumour on wounded plants, it is a vital part of the organism's biology. A chromosomally-determined chemotaxis system causes the bacterium to be attracted into the rhizosphere by chemoattractants in plant exudates. By interfacing with this system, the multifunctional products of two Ti-plasmid encoded genes, virA and virG, allow the sensing of specific wound phenolics such as acetosyringone. This attracts Ti-plasmid harbouring A. tumefaciens to wound sites, where the higher acetosyringone concentrations lead to virA and virG-mediated induction of the vir-genes. The products of the induced genes, act in concert to effect transfer of the T-DNA to the plant cell.     

Identification of rice (Oryza sativa L.) signal factors capable of inducing Agrobacterium vir gene expression

Two kinds of signal factors capable of inducing Agrobaorerium vir gene expression were purified and identified from leaf extracts of panicle-differentiating to flowering stage of rice (Oryza saliva L. cv. IR 72) detected by Agrobacterium vir(?) lacZ. fusion genes. The induction was similar to that observed with 5 μm actosyringone (AS). Based on the comprehensive analysis of the data by UV, IR, NMR, MS, HMQC and HMBC, the structures of these two signal factors are identified as 5, 7, 4'-trihydroxy-3', 5'-dimethoxy-flavone (named tricin) and 5, 4' -dihydroxy-3', 5' -dimethoxy-7- (β-D-glucosyloxy) -flavone, respectively. These results demonstrate that monocotyledonous plants do contain highly efficient vir gene inducing factors of Agrobacterium, and the reason why monocotyledonous plants are difficult to transform by Ayrobacterium is not due to absence of vir gene inducing factors, but due to the signal factors only produced in specific stage and tissue of monocotyledonous plants     

Mutant genes of plant tubulins as selective marker genes for genetic engineering

This review describes different approaches to employment of new marker genes in selection of transformed plant cells, which are based on the use of mutant tubulin genes from natural plant biotypes and, in prospect, induced plant mutants. The results of studies of plant (biotypes, mutants) resistance to herbicides with antimicrotubular mode of action at molecular and cellular levels were summarized. The reports on the transfer and expression of mutant tubulin genes conferring resistance to amiprophosmethyl (phosphorothioamidate herbicide) and trifluralin (dinitroaniline herbicide) from corresponding Nicotiana plumbaginifolia mutants in related and remote plant species by somatic hybridization methods were analyzed. The results of experiments on transformation of monocotyledonous and dicotyledonous plants by mutant α-tubulin gene conferring resistance to dinitroanilines are described to test the possibility of its use as a marker gene and simultaneously obtaining dinitroaniline-resistant plants.