蒜鳞片薄壁细胞衰败过程中类外连丝的形成及其共质传输能力的调节（简报）

在植物生长发育过程中,由于局部组织（细胞）的衰退或脱落．存活细胞与衰亡（或脱落）细胞分界壁上的胞间连丝衍变为类外连丝结构。这已先后在小麦胚胎发育、幼胚分化、蒜鳞茎休眠进程中以及玉米根冠组织中得到了论证。前文已曾报道．在玉米根冠细胞生长脱落进程中,脱落细胞与相邻细胞间胞间连丝有被拉伸、断裂形成类外连丝的结构变化．并经药理学试验表明。肌动蛋白和肌球蛋白共同参与了类外连丝通透性的调节。     

植物细胞的外连丝与类外连丝的结构与功能

外连丝作为特化的通道结构存在于植物的表皮细胞外侧壁中,而在植物局部组织衰败过程中衰亡细胞与存活细胞分界壁上有类似外连丝的半胞间连丝存在,可称之为类外连丝。本对外连丝和类外连丝的结构、功能方面的研究结果与近年进展予以综述,并讨论了植物细胞胞壁上类外连丝的出现在共质运输和细胞内含物再分配中的可能意义。     

蒜鳞片休眠进程中胞间联络的变化及类外连丝结构与功能的研究

利用电子显微镜术,对蒜休眠进程中鳞片薄壁细胞间胞间联络的特征进行了实验观察,发现不同时期胞间联络具有随细胞间生理关系密切程度而呈现相应结构变化的特点。并观察到萌芽期鳞片中衰败细胞与存活细胞之间有类外连丝型胞间连丝的存在;以激光共聚焦荧光显微镜结合荧光标记物示踪检测,发现不透膜荧光物质分子量为457Da 的萤黄(Lucifer yellow,LYCH),可以共质体运输方式进入存活细胞内,论证了类外连丝这一胞间连丝特定修饰态的存在,并可在一段时间内继续保持生理活性,起到进行物质共质运输的功能。     

离体蒜苔贮存中薄壁细胞超微结构的变化

离体蒜苔贮存中薄壁细胞逐渐衰老,原生质表现出有序的降解和胞间转移。由细胞内膜产生的自体吞噬泡将细胞器消化。降解的原生质组分通过共质体和质外体两种途径转移,并最终运输至顶端作为珠蒜生长的营养。     

蒜鳞片休眠进程中胞间联络的变化及类外连丝结构与功能的研究

利用电子显微镜术,对蒜休眠进程中鳞片薄壁细胞间胞间联络的特征进行了实验观察,发现不同时期胞间联络具有随细胞间生理关系密切程度而呈现相应结构变化的特点。并观察到萌芽期鳞片中衰败细胞与存活细胞之间有类外连丝型胞间连丝的存在;以激光共聚焦荧光显微镜结合荧光标记物示踪检测,发现不透膜荧光物质分子量为457Da的萤黄(Lucifer yellow,LYCH),可以共质体运输方式进入存活细胞内,论证了类外连丝这一胞间连丝特定修饰态的存在,并可在一段时间内继续保持生理活性,起到进行物质共质运输的功能。     

高等植物根边缘细胞的发育调控及其生物学功能

植物根边缘细胞是从根冠表皮游离出来并聚集在根尖周围的一群特殊细胞 ,以前曾称为根冠脱落细胞。最近的证据表明 ,绝大多数物种边缘细胞具有生物学活性 ,其发育是受内外信号调控。边缘细胞一旦从根表皮游离后 ,其代谢活性大大上升、基因表达明显不同于根冠细胞。最近 ,与边缘细胞发育早期和晚期相关的两个基因PsUGT1和RCPME1分别被克隆和鉴定。边缘细胞能特异性地合成、分泌一系列的化学物质 ,包括花色素苷、抗生素、特异性酶类及其他化学物质能抑制或促进根际周围的细菌、真菌、病毒、线虫等的生长以及中和根际周围一些有毒化学物质如铝毒。因此 ,边缘细胞在植物生长发育过程中起着多种生物学功能     

高等植物根边缘细胞的发育调控及其生物学功能

植物根边缘细胞是从根冠表皮游离出来并聚集在根尖周围的一群特殊细胞,以前曾称为根冠脱落细胞.最近的证据表明,绝大多数物种边缘细胞具有生物学活性,其发育是受内外信号调控.边缘细胞一旦从根表皮游离后,其代谢活性大大上升、基因表达明显不同于根冠细胞.最近,与边缘细胞发育早期和晚期相关的两个基因PsUGT1和RCPME1分别被克隆和鉴定.边缘细胞能特异性地合成、分泌一系列的化学物质,包括花色素苷、抗生素、特异性酶类及其他化学物质能抑制或促进根际周围的细菌、真菌、病毒、线虫等的生长以及中和根际周围一些有毒化学物质如铝毒.因此,边缘细胞在植物生长发育过程中起着多种生物学功能.     

珠蒜苞鳞衰退组织中原生质撤离的两条途径的电子显微镜观察

高等植物衰退组织内的半解体原生质,可通过胞间运动转移出去提供给正在兴旺生长的组织。娄成后等曾在大蒜鳞片等材料中应用光学显微镜观察到衰退组织的原生质撤离甚至入侵导管的现象。我们用电子显微镜对上述现象作了进一步观察,观察到原生质撤离的胞间运动以及半解体的原生质进入细胞间隙和导管。     

胞间连丝：共质体运输的动态通道

胞间连丝作为一种细胞质结构将相邻的细胞连系起来而形成植物的共质体。胞间连丝通过调控许多离子和分子的共质体运输而广泛地参与植物的生命活动。胞间连丝的主要构成部分是细胞质膜、连丝小管、以及位于二之间的环层细胞质。这三都很容易在电子显微镜下观察到。细胞骨架的成分（肌动蛋白和肌球蛋白）起到稳定胞间连丝的作用。同时,钙结合蛋白可能具有调节间连丝功能的作用。在胞间连丝里,环层细胞质为大多数溶质提供共质体运输的通道,而有些 共质体运输则可能是通过连丝小管的内腔、连丝小管的壳层、甚或是细胞质膜来实现的。共质体可以细分为数个区块,它们各自允许不同大小的分子（从低于1000到高于10000道尔顿）通过。从发生上看,胞间连丝可以是初生的,也可以是次生的。前是伴随着新细胞壁的形成则产生的,而后则是在已有的细胞壁上产生的。胞间连丝的动态性质还表现在它们的频率是处于变化之中,这是由于组织或植物整体的发育和生理状态决定的。虽然共质体运输的基本形式是扩散,但胞间连丝对于某些离子和分子却是选择性的。在病毒感染细胞时,病毒的移动蛋白作用于胞间连丝的受体蛋白,结果,胞间连丝被显地扩张（其机理尚不清楚）。于是,病毒的移动蛋白连同与之结合在一起的病毒基因组进入毗邻的健康细胞。一些植物源性的蛋白质也能够通过胞间连丝来运输;推测其方式类似于病毒的移动蛋白。有些植物蛋白质本身就是信号分子,它们调节分化和其他活动。与此相反,还有一些植物蛋白质的共质体运输并不是通过特异的方式来实现的。     

植物组织电阻及其应用

植物组织可分为质外体和共质体,其中,质外体由细胞壁、细胞间隙和导管组成,共质体由胞间连丝把相邻的原生质贯穿在一起而成。对于一鲜嫩植物组织来说,可将组织中质外体部分和共质体部分分别看作一连续整体,在两者之间有近似绝缘层的高电阻膜存在。此细胞膜的比电阻一般可达10~3—10~4Ω·cm,和5nm厚的油层相近。因此,可以近似地将共质体和质外体看作是电学上相并联的两条支路。其中,共质体电阻由膜电阻、胞内电阻和胞问电阻相互串联而成。由于胞内离子强度较     

Root Growth Inhibitors from Root Cap and Root Meristem of Zea mays L.

A micro-assay based on the growth inhibition of root segmentsof the seminal roots of Zea mays has been used to investigatethe root-growth-inhibiting substances in root caps and meristemsrespectively of the roots of Zea mays. This micro-assay is sensitiveto 50 pg of IAA or less. Paper chromatography of the acid fractionof methanolic extracts shows the presence of one main inhibitorin root caps and a different main inhibitor in root meristems.Neither is IAA, whose presence in meristems is sometimes indicatedby small inhibitions (or stimulations) at the characteristicRf of IAA. A Commelina leaf-epidermis assay shows the presenceof one stomata-closing ABA-like substance in root caps and onein meristems, one corresponding in Rf to the main root-growthinhibitor from the root cap. The implications of these findingsfor the geotropic responses of roots is briefly discussed.     

The Effect of Coumarin on Root Growth and Root Histology

The effect of coumarin on the root growth was studied on roots from intact plants, isolated roots and isolated elongating zones. All material was cultivated aseptically. A new method was developed for sterile culture of intact plants in flowing nutrient medium. The effects on cell division and cell elongation were studied separately. An effect on both these processes can be established at all concentrations that affect the root growth. The concentration-growth curve has an “all-or-none” appearance. Coumarin inhibits the transverse divisions in all cell layers; the perivascular layers seem to be more sensitive. Also the mitotic activity that is involved in the initiation of laterals is inhibited. The longitudinal divisions within the stele are enhanced. Coumarin decreases the cell length in all cell layers, most likely with greater relative sensitivity in the perivascular layers. Studies on the time course of cell elongation in both attached corn roots and isolated elongating zones reveal that the decrease in cell length is caused exclusively by a decrease in the maximal rate of elongation, whereas the duration of the elongation is unchanged. With each decrease of the cell length, the cell diameter is increased. The two changes are intimately connected within the greater part of the active region of concentration. Studies on the time course of the radial expansion in isolated elongating zones show a strict connection in time between cell elongation and radial expansion. The radial expansion leads to unchanged or increased cell volume at most concentrations and for most cell types. Coumarin causes an inhibition of the longitudinally directed processes and a stimulation of the radially directed ones. This is interpreted as indicating that the formative system is disengaged or reorientated, i.e., the polarity of the cells is changed. Through experiments partly with isolated elongating zones and partly by disruption of the linear phase by means of mannitol, the inhibitory effect of coumarin could be localized to the first non-linear phase of the elongation. The results were compared with earlier findings in the literature. The microtubuli are proposed as a conceivable main Component in the formative system common to both cell division and cell elongation. These are assumed to be affected by changes in the SH/SS balance produced by coumarin.     

Dependence of Root Cell Growth and Division on Root Diameter

Primary roots of 98 species from different families of monocotyledonous and dicotyledonous plants and adventitious roots obtained from bulbs and rhizomes of 24 monocot species were studied. Root growth rate, root diameter, length of the meristem and elongation zones, number of meristematic cells in a file of cortical cells, and length of fully elongated cells were evaluated in each species after the onset of steady growth. The mitotic cycle duration and relative cell elongation rate were calculated. In all species, the meristem length was approximately equal to two root diameters. When comparing different species, the rate of root growth increased with a larger root diameter. This was due to an increase in the number of meristematic cells in a row and, to a lesser degree, to a greater length of fully elongated cells. The duration of the mitotic cycle and the relative cell elongation rate did not correlate with the root diameter. It is suggested that the meristem size depends on the level of nutrient inflow from upper tissues, and is thereby controlled during further growth.     

Shoot and Root Growth of Lettuce Seedlings Following Root Pruning

Hydroponically-grown lettuce seedlings with 13 to 18 primarylateral roots were root pruned in one of four ways; the rootapices were removed from the main root only (1) or from allthe root membranes (2), or half the total root system was removedwith the remaining apices left intact (3) or removed (4). Duringthe following 8 d the rate of lateral root production on prunedplants increased, decreased, and then increased again relativeto the unpruned control. Conversely, the rate of increase intotal root length decreased, then increased, and if all theroot apices were removed, declined again, prior to increasingon day 8. These changes in the rates of lateral root productionand growth resulted in similar, but less pronounced, patternsof change in the total root length and the total number of lateralroots with time. The changes in total lateral root productionwere related to differences in the rates of primary, secondaryand tertiary root emergence. The shoot d. wt of the most severely root pruned seedlings (treatment4) fell below that of the control 4 d after pruning and remainedlower than the control on day 14, whereas the root d. wt hadrecovered to the control level by day 6. The root: shoot d.wt ratio, which was reduced by root pruning, rose above thatof the control on days 6 and 8. Lactuca sativa L., lettuce, root pruning, root growth, lateral root, nutrient solution     

Root Growth, Secondary Root Formation and Root Gravitropism in Carotenoid-deficient Seedlings of Zea mays L.

The effect of ABA on root growth, secondary-root formation androot gravitropism in seedlings of Zea mays was investigatedby using Fluridone-treated seedlings and a viviparous mutant,both of which lack carotenoids and ABA. Primary roots of seedlingsgrown in the presence of Fluridone grew significantly slowerthan those of control (i.e. untreated) roots. Elongation ofFluridone-treated roots was inhibited significantly by the exogenousapplication of 1 mM ABA. Exogenous application of 1 µMand 1 nM ABA had either no effect or only a slight stimulatoryeffect on root elongation, depending on the method of application.The absence of ABA in Fluridone-treated plants was not an importantfactor in secondary-root formation in seedlings less than 9–10d old. However, ABA may suppress secondary-root formation inolder seedlings, since 11-d-old control seedlings had significantlyfewer secondary roots than Fluridone-treated seedlings. Rootsof Fluridone-treated and control seedlings were graviresponsive.Similar data were obtained for vp-9 mutants of Z. mays, whichare phenotypically identical to Fluridone-treated seedlings.These results indicate that ABA is necessary for neither secondary-rootformation nor for positive gravitropism by primary roots. Zea mays, gravitropism, carotenoid-deficient, Fluridone, root growth, vp-9 mutant     

Effect of Root Moisture Content and Diameter on Root Tensile Properties

The stabilization of slopes by vegetation has been a topical issue for many years. Root mechanical characteristics significantly influence soil reinforcement; therefore it is necessary to research into the indicators of root tensile properties. In this study, we explored the influence of root moisture content on tensile resistance and strength with different root diameters and for different tree species. Betula platyphylla, Quercus mongolica, Pinus tabulaeformis, and Larix gmelinii, the most popular tree species used for slope stabilization in the rocky mountainous areas of northern China, were used in this study. A tensile test was conducted after root samples were grouped by diameter and moisture content. The results showedthat:1) root moisture content had a significant influence on tensile properties; 2) slightly loss of root moisture content could enhance tensile strength, but too much loss of water resulted in weaker capacity for root elongation, and consequently reduced tensile strength; 3) root diameter had a strong positive correlation with tensile resistance; and4) the roots of Betula platyphylla had the best tensile properties when both diameter and moisture content being controlled. These findings improve our understanding of root tensile properties with root size and moisture, and could be useful for slope stabilization using vegetation.     

Effect of Root Position on Measured Root Position on Measured Root Membrane Potentials

Root membrane potentials were measured by interposing a plantroot between two KCI solutions of different concentrations.The potentials measured across the two calomel electrodes werefound to depend on the position of the root. The potentialswere found to be lower when the root tip rather than the rootbase was in contact with the more concentrated solution. Thisindicates that the two parts of the root do not have the samein transport properties. Using an approximate theoretical treatmentthe observed potentials could be accounted for.     

根瘤形成过程中豆科植物根毛和根外层传递细胞的诱发

对7种豆科植物接种根瘤菌后根部的形态和内部结构进行了研究.结果表明:根瘤菌可诱发根瘤形成部位根段的根毛增生、形变和根外层传递细胞的发育.根外层传递细胞发生在根毛伸长形变时期,一直可持续到根瘤形成,传递细胞壁内突发育过程是先由根表皮细胞外切向壁一侧细胞质膜向细胞质内陷形成囊状壁傍体,次生细胞壁物质在初生壁上沉积并逐渐充满囊状体,最终形成传递细胞典型的壁内突结构.根瘤形成过程中根外层传递细胞的诱发与培养方式(水培、固培)没有直接关系.在不接菌的对照苗的根段内未发现壁内突结构,研究证明豆科植物根外层传递细胞的形成是由根瘤菌诱导所致.     

Root Density and Water Potential Gradients near the Plant Root

The models of Gardner (1960) and Cowan (1965) for water transferto the plant root are used to estimate the differences in waterpotential between the root and the bulk soil for a wide rangeof root densities and water extraction rates at a series ofmatric potentials for a Yolo light clay. For root densities and extraction rates reported both in theliterature and in this paper there is good evidence to suggestthat the large potential gradients originally predicted by Gardnerand Cowan are restricted to situations involving very low rootdensities and high extraction rates in relatively dry soil.     

Root Caps and Rhizosphere

In this paper we discuss recent work on the physiological, molecular, and mechanical mechanisms that underlie the capacity of root caps to modulate the properties of the rhizosphere and thereby foster plant growth and development. The root cap initially defines the rhizosphere by its direction of growth, which in turn occurs in response to gradients in soil conditions and gravity. The ability of the root cap to modulate its environment is largely a result of the release of exudates and border cells, and so provides a potential method to engineer the rhizosphere. Factors affecting the release of border cells from the outer surface of the root cap, and function of these cells and their exudates in the rhizosphere, are considered in detail. Release of border cells into the rhizosphere depends on soil matric potential and mechanical impedance, in addition to a host of other environmental conditions. There is good evidence of unidentified feedback signals between border cells and the root cap meristem, and some potential mechanisms are discussed. Root border cells play a significant mechanical role in decreasing frictional resistance to root penetration, and a conceptual model for this function is discussed. Root and border cell exudates influence specific interactions between plant hosts and soil organisms, including pathogenic fungi. The area of exudates and border cell function in soil is an exciting and developing one that awaits the production of appropriate mutant and transgenic lines for further study in the soil environment.