Development,differentiation,and material distribution of secondary phloem in Pinus massoniana

Phloem is the woody tissue for the storage and long-distance transport of organic matter in vascular bundles.To reveal the process of secondary phloem development and differentiation in Pinus massoniana,the structure of the secondary phloem and the distribution of cell inclusions were observed by histochemical staining,spontaneous fluorescence of phenolic substances and cell segregation.Based on tissue development and differentiation characteristics of P.massoniana secondary phloem,the secondary phloem development was divided into seven stages:the functional phloem stage;the sieve cell lignification stage;the phloem ray bending stage;the parenchyma cell dedifferentiation and division stage;the dedifferentiated parenchyma cell population formation stage;the periderm alteration stage,and the rhytidome stage.An analysis of cell morphology and inclusion distribution characteristics showed that the sieve cells were deformed during lignification,the quantities of parenchyma and resin ducts increased with development and the crystal content in cells,as well as the levels of sugars and lipids in phloem parenchyma cells,increased with development.The results indicate that the P.massoniana phloem first lost longitudinal transport function and then increased its secretory,storage and mechanical functions.Ultimately,the parenchyma differentiated into the cortex and periderm,and the tissue outside the new periderm lignified to form the rhytidome,which fully developed into the protective tissue of the stem.

Evidence of the predominance of passive symplastic phloem loading and sugar transport with leaf ageing in Camellia oleifera

Phloem loading and transport of sugar from leaves to sink tissues such as fruits are crucial for yield formation.Camellia oleifera is an evergreen horticultural crop with high value;however,its low production limits the development of the C.oleifera industry.In this study,using a combination of ultrastructural observation,fluorescence loss in photobleaching(FLIP)and inhibitor treatment,we revealed that C.oleifera leaves mainly adopt a symplastic loading route from mesophyll cells to the surrounding vascular bundle cells in minor veins.HPLC assays showed that sucrose is the main sugar transported and only a small amount of raffinose or stachyose was detected in petioles,supporting a passive symplastic loading route in C.oleifera leaves.Compared to leaves grown this year(LT),the carbohydrate synthesis capacity in leaves grown last year(LL)was decreased while LL retained more soluble sugar,suggesting a decrease in transport capacity with leaf ageing.TEM and tissue staining showed that a reduction in plasmodesmata density leads to a decline in the degree of cellular coupling and is responsible for the weakening transport capacity in older leaves.RNA-seq revealed several differentially expressed genes(DEGs)including CoPDCB1-1,CoSUT1 and CoSWEET12,which are likely involved in the regulation of phloem loading and sugar transport.An expression correlation network is constructed between PD-callose binding protein genes,sugar transporter genes and senescence-associated genes.Collectively,this study provides the evidence of the passive symplastic phloem loading pathway in C.oleifera leaves and constructs the correlation between sugar transport and leaf ageing.

Effects of Weak Light on the Ultrastructural Variations of Phloem Tissues in Source Leaves of Three-Year-Old Nectarine Trees(Prunus persica L.var. nectarina Ait.)

Leaves from three_year_old solar greenhouse nectarine trees ( Prunus persica L. var. nectarina Ait. “Zao Hong Yan”) were used as materials in this study. It was the first time that the ultrastructural characteristics of phloem tissues of source leaves were observed and compared in normal and weak light intensities using the transmission electron microscopy. Results showed that the average diameters of companion cells (CC) and sieve elements (SE) of all kinds of veins were bigger in normal than that in weak light intensity, indicating that light could influence the cell development and growth. Dense cytoplasm with abundant mitochondria, endoplasmic reticulums, multivesicular bodies, vesicles and plastids were observed in normal light intensity. On the contrary, CC with small vacuolar structures and few mitochondrias, endoplasmic reticulums were shown in weak light. Misalignment of grana thylakoid margins of nectarine leaves also was seen in weak light. The sieve pores of SEs were obstructed in weak light. Chloroplasts with numerous starch grains and few mitochondrias were noticed in the mesophyll cell (MES) surrounding the bundle sheath in weak light. The storage of starch grains appeared to result from an unbalance between photosynthate production and export of photosynthates. This observation provided a strong support to the point that most leaves export the most of assimilates in the light time. Plasmodesmal densities between SE/CC, CC/PP (phloem parenchyma cell), PP/PP and PP/BSC (bundle_sheath cell) decreased in weak light. Plasmodesmata were observed between CC/SE (NS) (nacreous_walled sieve element), PP/BSC in branch veins in normal light intensity, but not in weak light. Thus apoplasmic pathway may be the main mode of transport of assimilates in weak light, however symplasmic pathway may be the main mode of transport of assimilates in normal light intensity. These results demonstrated that the solar greenhouse nectarine trees could be adapted to the weak light via the ultrastructure variation of phloem tissues of the source leaves.

Development and Ultrastructure of the Phloem Ganglion in Bamboo Node

The development, cytological characters and ultrastructure of phloem ganglion in the nodal region of Phyllostachys edulis (Carr.) H. de Lehaie, a most economically important bamboo, were investigated and the possible physiological function of this special structure was proposed. The phloem ganglion derived directly from procambium is situated at the sites where the vascular bundle forks and is present in pairs. The phloem ganglion is spindle_like in appearance and usually consists of 4 to 6 layers. Two kinds of cells in the ganglion could be distinguished. In the middle, there are two layers of filiform cells with pointed ends so that there are no normal sieve plates. Nevertheless, there are many pits on the lateral wall of the filiform cells. The other type of cells located at both ends of the spindle which possess an intermediate form between the filiform cell and the normal sieve tube. The walls of these cells towards the filiform cells are strongly convex forming a special sieve plate. Ultrastructure study showed that cells in the ganglion are connected by enriched plasmodesma. During early differentiation, the paramural body and the ingrowth of cell wall could be observed. It indicates that the cells of phloem ganglion have the character of transfer cells. The organelles in the mature cells are mainly plastids with abundant accumulation of proteins of crystalline structure. The above_mentioned results suggest that the physiological function of the phloem ganglion is closely related with substance transport.

Anatomical and FTIR analyses of phloem and xylem of Tetracentron sinense

The fast growth of Tetracentron sinense is a potential valuable timber resource, but whether its anatomy and chemical components are suitable for timber is unknown. We used light microscopy and SEM to examine the anatomical structure and FITR to measure the chemical components of the phloem and xylem of this tree. Radial variations in growth ring width and tracheid dimensions were also evaluated. The sieve tube, phloem parenchyma cell and sclereids clusters were the main cells in phloem, and the tracheid was the fundamental cell in xylem. An unusual tracheid type, fiber-tracheids or vessel-liked elements was visible. Wood rays nonstoried, uniseriate and multiseriate, including heterogeneous II, occasionally I, and usually 3-6 cells wide. The mean growth-ring width was 2.53 +/- 0.46 mm, and the percentage of late wood was over 60%. For radial variation, growth-ring width increased at an early growth stage, and reached the largest increment during years 11-15, then decreased. The maximum growth-ring width was 5.313 mm. During late growth (60-85 years), trees also maintained a high radial growth increment. Radial variation in the percentage of late wood was uniform, about 50-70%, throughout the growth years. Growth patterns in the length and width of early and late wood were similar as the trees aged. From the FTIR results, the chemical components differed significantly between xylem and phloem, hemicellulose in particular was higher in the xylem than in the phloem, where it was apparently absent. All of these suggest that the composition of phloem in T. sinense is very similar to that of hardwood, and it has higher growth ratio and uniform wood properties.

Overexpression of rice F-box phloem protein gene OsPP12-A13 confers salinity tolerance in Arabidopsis

Salinity is a serious challenge for agriculture production by limiting the arable land.Rice is a major staple food crop but very sensitive to salt stress.In this study,we used Arabidopsis for the functional characterization of a rice F-box gene LOC_Os04g48270(OsPP12-A13)under salinity stress.OsPP12-A13 is a nuclear-localized protein that is strongly upregulated under salinity stress in rice and showed the highest expression in the stem,followed by roots and leaves.Two types of transgenic lines for OsPP12-A13 were generated,including constitutive tissue over-expression using the CaMV35S promoter and phloem specific over-expression using the pSUC2 promoter.Both types of transgenic plants showed salinity tolerance at the seedling stage through higher germination percentage and longer root length,as compared to control plants under salt stress in MS medium.Both the transgenic plants also exhibited salt tolerance at the reproductive stage through higher survival rate,plant dry biomass,and seed yield per plant as compared to control plants.Determination of Na+concentration in leaves,stem and roots of salt-stressed transgenic plants showed that Na^(+) concentration was less in leaf and stem as compared to roots.The opposite was observed in wild type stressed plants,suggesting that OsPP12-A13 may be involved in Na+transport from root to leaf.Transgenic plants also displayed less ROS levels and higher activities of peroxidase and glutathione S-transferase along with upregulation of their corresponding genes as compared to control plants which further indicated a role of OsPP12-A13 in maintaining ROS homeostasis under salt stress.Further,the non-significant difference between the transgenic lines obtained from the two vectors highlighted that OsPP12-A13 principally works in the phloem.Taken together,this study showed that OsPP12-A13 improves salt tolerance in rice,possibly by affecting Na^(+) transport and ROS homeostasis.

Free amino acid (FAA) analysis of phloem sap in hybrid rice Shanyou 63 and its parents

Hyhrid rice has greatly contributed to rice production inChina. But concurrently a dramatic upsurge of rice plant-hopper occurred, particularly for the whitebacked plant-hopper (WBPH), Sogatella furcifera. It has become animportant economic insect pest of hybrid rice, although ithad only been a minor herbivore of rice before nation-wideexploitation of hybrid rice.

Leafhopper salivary carboxylesterase suppresses JA-Ile synthesis to facilitate initial arbovirus transmission in rice phloem

Plant jasmonoyl-L-isoleucine(JA-Ile)is a major defense signal against insect feeding,but whether or how insect salivary effectors suppress JA-Ile synthesis and thus facilitate viral transmission in the plant phloem remains elusive.Insect carboxylesterases(CarEs)are the third major family of detoxification enzymes.Here,we identify a new leafhopper CarE,CarE10,that is specifically expressed in salivary glands and is secreted into the rice phloem as a saliva component.Leafhopper CarE10 directly binds to rice jasmonate resistant 1(JAR1)and promotes its degradation by the proteasome system.Moreover,the direct association of CarE10 with JAR1 clearly impairs JAR1 enzyme activity for conversion of JA to JA-Ile in an in vitro JAIle synthesis system.A devastating rice reovirus activates and promotes the co-secretion of virions and CarE10 via virus-induced vesicles into the saliva-storing salivary cavities of the leafhopper vector and ultimately into the rice phloem to establish initial infection.Furthermore,a virus-mediated increase in CarE10 secretion or overexpression of CarE10 in transgenic rice plants causes reduced levels of JAR1 and thus suppresses JA-Ile synthesis,promoting host attractiveness to insect vectors and facilitating initial viral transmission.Our findings provide insight into how the insect salivary protein CarE10 suppresses host JA-Ile synthesis to promote initial virus transmission in the rice phloem.

拟南芥HHP2基因对韧皮部蔗糖装载的调控功能

【目的】探究膜蛋白HHP2在韧皮部蔗糖装载中的作用与机制,为作物增产增效提供理论依据。【方法】利用多种生物信息学分析方法,对HHP2及其同源蛋白序列以及HHP2基因的转录表达谱进行分析,以预测其功能并发掘其他同源蛋白。使用荧光共聚焦显微镜对HHP2蛋白和蔗糖转运蛋白SUC2进行共定位分析,利用荧光共振能量转移试验检测HHP2与SUC2蛋白的互作,通过七叶树苷摄取试验检测HHP2对SUC2蛋白的直接影响。通过实时荧光定量PCR和Western-Blot试验,分析和比较hhp2突变体SUC2基因的转录水平和蛋白水平;利用离子色谱方法分析和比较hhp2突变体的韧皮部蔗糖输出效率;采用AlphaFold和Autodock软件,对HHP2蛋白结构及HHP2和蔗糖分子之间的潜在对接能力进行分析。【结果】HHP2同源蛋白共有5个保守模体和1个保守结构域。HHP2基因在拟南芥叶和茎等蔗糖输出器官中低表达,在根、花和种子等蔗糖需求器官中高表达。在本氏烟草远轴面表皮细胞中瞬时表达HHP2,发现其与SUC2蛋白共定位。HHP2与SUC2蛋白存在互作,且HHP2能抑制SUC2的蔗糖转运活性。HHP2缺失突变分析表明,HHP2是SUC2的负调控因子,HHP2缺失突变导致SUC2转录水平提高至6倍左右,蛋白水平提高至1.3倍左右,hhp2缺失突变体的蔗糖转运效率提高至2倍左右。分子对接分析表明,HHP2可能通过与蔗糖结合发挥其调控功能。【结论】HHP2是SUC2的负调控因子,参与调控植物体内蔗糖的转运与分配,可能是分子育种的潜在靶标。

园艺植物韧皮部卸载研究进展

植物韧皮部卸载包括一系列复杂的过程,韧皮部卸载在园艺植物(果树、蔬菜、观赏植物)同化物的运输和分配中具有重要作用。本研究概述了韧皮部卸载的主要途径,并重点综述了韧皮部卸载在园艺植物生长发育方面的主要研究成果,内容包括:①韧皮部运输的主要糖分物质;②韧皮部卸载方式;③韧皮部卸载研究方法;④园艺植物韧皮部卸载研究。随着研究的深入和新技术的出现,园艺植物韧皮部卸载过程中涉及的关键酶与蔗糖转运蛋白等需得到更深入地阐释,进一步助力解析植物韧皮部卸载参与园艺植物生长发育的分子调控机制,并有望为更多的植物韧皮部卸载研究提供新的思路。

Ultrastructure of compatible and incompatible interactions in phloem sieve elements during the stylet penetration by cotton aphids in melon

Resistance of the melon line TGR-1551 to the aphid Aphis gossypii is based on preventing aphids from ingesting phloem sap. In electrical penetration graphs （EPGs）, this resistance has been characterized with A. gossypii showing unusually long phloem salivation periods （waveform El） mostly followed by pathway activities （waveform C） or if followed by phloem ingestion （waveform E2）, ingestion was not sustained for more than 10 min. Stylectomy with aphids on susceptible and resistant plants was performed during EPG recording while the stylet tips were phloem inserted. This was followed by dissection of the penetrated leaf section, plant tissue fixation, resin embedding, and ultrathin sectioning for transmission electron microscopic observation in order to study the resistance mechanism in the TGR. The most obvious aspect appeared to be the coagulation of phloem proteins inside the stylet canals and the punctured sieve elements. Stylets of 5 aphids per genotype were amputated during sieve element （SE） salivation （El） and SE ingestion （E2）. Cross-sections of stylet bundles in susceptible melon plants showed that the contents of the stylet canals were totally clear and also, no coagulated phloem proteins occurred in their punctured sieve elements. In contrast, electron-dense coagulations were found in both locations in the resistant plants. Due to calcium binding, aphid saliva has been hypothesized to play an essential role in preventing/suppressing such coagulations that cause occlusion of sieves plate and in the food canal of the aphid＇s stylets. Doubts about this role of E 1 salivation are discussed on the basis of our results.

Recycling of Solanum Sucrose Transporters Expressed in Yeast, Tobacco, and in Mature Phloem Sieve Elements

The plant sucrose transporter SUT1 （from Solanum tuberosum, S. lycopersicum, or Zea mays） exhibits redoxdependent dimerization and targeting if heterologously expressed in S. cerevisiae （Krtigel et al., 2008）. It was also shown that SUT1 is present in motile vesicles when expressed in tobacco cells and that its targeting to the plasma membrane is reversible. StSUT1 is internalized in the presence of brefeldin A （BFA） in yeast, plant cells, and in mature sieve elements as confirmed by immunolocalization. These results were confirmed here and the dynamics of intracellular SUT1 localization were further elucidated. Inhibitor studies revealed that vesicle movement of SUT1 is actin-dependent. BFA-mediated effects might indicate that anterograde vesicle movement is possible even in mature sieve elements, and could involve components of the cytoskeleton that were previously thought to be absent in SEs. Our results are in contradiction to this old dogma of plant physiology and the potential of mature sieve elements should therefore be re-evaluated. In addition, SUT1 internalization was found to be dependent on the plasma membrane lipid composition. SUT1 belongs to the detergent-resistant membrane （DRM） fraction in planta and is targeted to membrane raft-like microdomains when expressed in yeast （Kr（igel et al,, 2008）, Here, SUT1-GFP expression in different yeast mutants, which were unable to perform en- docytosis and/or raft formation, revealed a strong link between SUT1 raft localization, the sterol composition and mem- brane potential of the yeast plasma membrane, and the capacity of the SUT1 protein to be internalized by endocytosis. The results provide new insight into the regulation of sucrose transport and the mechanism of endocytosis in plant cells.

Plant lncRNAs are enriched in and move systemically through the phloem in response to phosphate deficiency

In response to phosphate(Pi) deficiency, it has been shown that micro-RNAs(miRNAs) and mRNAs are transported through the phloem for delivery to sink tissues. Growing evidence also indicates that long noncoding RNAs(lncRNAs) are critical regulators of Pi homeostasis in plants. However, whether lncRNAs are present in and move through the phloem, in response to Pi deficiency, remains to be established. Here, using cucumber as a model plant, we show that lncRNAs are enriched in the phloem translocation stream and respond,systemically, to an imposed Pi-stress. A well-known lncRNA, IPS1, the target mimic(TM) of miRNA399,accumulates to a high level in the phloem, but is not responsive to early Pi deficiency. An additional 24 miRNA TMs were also detected in the phloem translocation stream; among them miRNA171 TMs and miR166 TMs were induced in response to an imposed Pi stress.Grafting studies identified 22 lncRNAs which move systemically into developing leaves and root tips. A CU-rich PTB motif was further identified in these mobile lncRNAs. Our findings revealed that lncRNAs respond to Pi deficiency, non-cell-autonomously, and may act as systemic signaling agents to coordinate early Pi deficiency signaling, at the whole-plant level.

Phloem-Mobile AuxlIAA Transcripts Target to the Root Tip and Modify Root Architecture

In plants, the phloem is the component of the vascular system that delivers nutrients and transmits signals from mature leaves to developing sink tissues. Recent studies have identified proteins, mRNA, and small RNA within the phloem sap of several plant species. It is now of considerable interest to elucidate the biological functions of these potential long-distance signal agents, to further our understanding of how plants coordinate their developmental programs at the whole-plant level. In this study, we developed a strategy for the functional analysis of phloem-mobile mRNA by focusing on IAA transcripts, whose mobility has previously been reported in melon （Cucumis melo cv. Hale＇s Best Jumbo）. Indoleacetic acid （IAA） proteins are key transcriptional regulators of auxin signaling, and are involved in a broad range of developmental processes including root development. We used a combination of vasculature-enriched sampling and hetero-grafting techniques to identify IAA18 and IAA28 as phloemmobile transcripts in the model plant Arabidopsis thaliana. Micro-grafting experiments were used to confirm that these IAA transcripts, which are generated in vascular tissues of mature leaves, are then transported into the root system where they negatively regulate lateral root formation. Based on these findings, we present a model in which auxin distribution, in combination with phloem-mobile Aux/IAA transcripts, can determine the sites of auxin action.

Effects of Acetylcholine, Cytochalasin B and Amiprophosmethyl on Phloem Transport in Radish （Raphanus sativas）

We investigated the role of the ＂sieve tube-companion cell complex＂ lining the tube periphery, particularly the microfilament and microtubule, in assisting the pushing of phloem sap flow. We made a simple phloem transport system with a living radish plant, in which the conducting channel was exposed for local treatment with chemicals that are effective in modulating protoplasmic movement （acetylcholine, （ACh） a neurotransmitter in animals and insects; cytochalasin B, （CB） a specific inhibitor of many cellular responses that are mediated by microfilament systems and amiprophos-methyl, （APM） a specific inhibitor of many cellular responses that are mediated by microtubule systems）. Their effects on phloem transport were estimated by two experimental devices： （i） a comparison of changes in the amount of assimilates in terms of carbohydrates and ^14C-labeled photosynthetic production that is left in the leaf blade of treated plants; and （ii） distribution patterns of ^14C-labeled leaf assimilates in the phloem transport system. The results indicate that CB and APM markedly inhibited the transfer of photosynthetic product from leaf to root via the leaf vein, while ACh enhanced the transfer of photosynthetic product in low concentrations （5.0×10^-4 mol/L） but inhibited it in higher concentrations （2.0×10^-3 mol/L） from leaf to root via the leaf vein. Autoradiograph imaging clearly reveals that ACh treatment is more effective than the control, and both CB and APM treatments effectively inhibit the passage of radioactive assimilates. All of the results support the postulation that the peripheral protoplasm in the sieve tube serves not only as a passive semi-permeable membrane, but is also directly involved in phloem transport.

GTR-Mediated Radial Import Directs Accumulation of Defensive Glucosinolates to Sulfur-Rich Cells in the Phloem Cap of Arabidopsis Inflorescence Stem

In the phloem cap region o i Arabidopsis plants,sulfur-rich cells(S-cells)accumulate>100 mM glucosinolates(GLS),but are biosynthetically inactive.The source and route of S-cell-bound GLS remain elusive.In this study,using single-cell sampling and scanning electron microscopy with energy-dispersive X-ray analysis we show that two GLS importers,NPF2.10/GTR1 and NPF2.11/GTR2,are critical for GLS accumulation in S-cells,although they are not localized in the S-cells.Comparison of GLS levels in S-cells in multiple combinations of homo-and heterografts o lg t r l gtr2,biosynthetic null mutant and wild-type plants indicate that S-cells accumulate GLS via symplasmic connections either directly from neighboring biosynthetic cells or indirectly to non-neighboring cells expressing GTR1/2.Distinct sources and transport routes exist for different types of GLS,and vary depending on the position of S-cells in the inflorescence stem.Based on these findings,we propose a model illustrating the GLS transport routes either directly from biosynthetic cells or via GTR-mediated import from apoplastic space radially into a symplasmic domain,wherein the S-cells are the ultimate sink.Similarly,we observed accumulation of the cyanogenic glucoside defensive compounds in high-turgor cells in the phloem cap of Lotus japonicus,suggesting that storage of defensive compounds in high-turgor cells may be a general mechanism for chemical protection of the phloem cap.

Ultracytochemical localization of Ca^(2+) during the phloem ganglion development in Phyllostachys edulis

Ultracytochemical localization of Ca^(2+)was in-vestigated using the potassium pyroantimonate precipitation method during the development of phloem ganglion.The result showed that Ca^(2+)was mainly localized in the cell wall and intercellular spaces in the initiating phase.With the de-velopment of the phloem ganglion,the distribution of Ca^(2+)transferred to the vacuole,and the Ca^(2+)deposits in the cell wall and intercellular space decreased.At the later stage of the developmental phase,Ca^(2+)was distributed in the tono-plast and vacuole phagocytosis,and the vacuole became the main calcium storage in this phase.At the early stage of maturation of the phloem ganglion,most of the phloem ganglion cells’vacuoles cracked,and the cytoplastic Ca^(2+)content increased in large number.In the mature phloem ganglion,not only were there a few Ca^(2+)localized in the cytoplast of mature cells,but also in the differentiating cells in the vacuoles.Ca^(2+)was distributed in the tonoplast and vacuole contents;initiating cells almost had no Ca^(2+).In general,Ca^(2+)concentration in mature phloem ganglion cells was at a low level.The results indicated that the changes in Ca^(2+)distribution evoked the phloem ganglion generation,and Ca^(2+)regulated the physiological function of the phloem ganglion.

棉秆韧皮浆粕的制备与性能测试

通过高温蒸煮和有机酸与乙醇组合溶解方式对棉秆韧皮进行制浆,并以浆粕得率为依据进行工艺优化。用核磁共振、红外光谱和热重分析等技术对制浆前棉秆韧皮和制浆所得浆粕的聚合度、相对分子量、Iα纤维素含量、分子结构和热学性能等指标进行表征。结果表明:棉秆韧皮制浆的最佳工艺为温度100℃、处理时间120 min、过氧化氢质量分数10%、乙醇质量分数60%;经制浆处理,棉秆韧皮中的木质素和半纤维素发生了部分酯化和酰化,使得其中的Iβ纤维素和微纤维结构受到破坏,热学性能下降,Iα纤维素含量增加。

植物中金属纳米粒子的转运与转化机制研究进展

金属纳米粒子(MNPs)的广泛使用对生态环境造成了较大的风险并引起了广泛的关注;虽然已有关于对植物毒害以及植物对其吸收的相关研究,但是MNPs在植物体内转运和转化的机制仍未得到系统的阐明。系统地阐述了MNPs在高等植物木质部、韧皮部中的转运机制,以及其在植物体内的溶解转化和化学转化机制,同时探讨了影响MNPs在植物体内转运转化的影响因素。结果表明:(1)MNPs首先吸附在植物的根部或叶部,再通过质外体或共质体途经向植物内部转移;(2)植物对MNPs的转化机制主要包括溶解转化、化学转化和生物转化(酶降解、蛋白质功能化等);(3)复杂的理化和生物因素(如粒子的种类大小、表面电荷、植物种类等)能够影响植物对MNPs转运及其形态转化。以期为金属纳米粒子污染土壤的生态环境治理和人类健康风险评估提供参考依据。

Inhibition of α-glucosidase activity by N-deoxynojirimycin analogs in several insect phloem sap feeders

Secondary metabolites and synthetic iminosugars that structurally resemble monosaccharides are potent inhibitors of a-glucosidase activity. The enzyme is core in cleaving sucrose in phloem feeding insects and it also plays a crucial role of reducing osmotic stress via the formation of oligosaccharides. Inhibition of hydrolysis by iminosug- ars should result in nutritional deficiencies and/or disruption of normal osmoregulation. Deoxynojirimycin （DNJ） and 2 N-alkylated analogs [N-butyl DNJ （NB-DNJ） and N-nonyl DNJ （NN-DNJ）] were the major iminosugars used throughout the study. The extensive experiments conducted with a-glucosidase of the whitefly Bemisia tabaci indicated the competitive nature of inhibition and that the hydrophilic DNJ is a potent inhibitor in com- parison to the more hydrophobic NB-DNJ and NN-DNJ compounds. The same inhibitory pattern was observed with the psyllid Cacopsylla bidens a-glucosidase. In contrast to the above pattern, enzymes of the aphids, Myzus persicae and Aphis gossypii were more sen- sitive to the hydrophobic iminosugars as compared to DNJ. In vivo experiments in which adult B. tabaci were fed dietary iminosugars, show that the hydrophilic DNJ was far less toxic than the lipophilic NB-DNJ and NN-DNJ. It is proposed that this pattern is attributed to the better accessibility of the hydrophobic NN-DNJ to the a-glucosidase membrane- bound compartment in the midgut. Based on the inhibitory effects of certain polyhydroxy N-alkylated iminosugars, a-glucosidase of phloem feeding hemipterans could serve as an attractive target site for developing novel pest control agents.