外源NO对NaCl胁迫下辣椒幼苗氧化损伤的保护效应

以辣椒品种陇椒2号为试验材料,研究了外源NO供体硝普钠(SNP)对辣椒幼苗氧化损伤的影响.结果显示,在100 mmol/L NaCl胁迫下,辣椒叶片的MDA含量、质膜相对透性和脯氨酸含量均增加,保护酶SOD、CAT活性降低,而POD活性只在胁迫18 d时降低.0.1 mmol/L SNP处理可减缓NaCl胁迫下辣椒幼苗叶片MDA含量的上升,降低叶片质膜相对透性,并诱导SOD、POD和CAT活性增加,提高脯氨酸含量,表明外源NO可以通过提高盐胁迫下辣椒幼苗叶片组织的抗氧化能力来缓解氧化损伤.而SNP相似物NaNO2和K3Fe(CN)6处理对盐胁迫引起的氧化损伤并没有起到明显的缓解作用,进一步证实了NO对辣椒幼苗耐盐性具有专一性的调节作用.     

外源GSH对盐胁迫下番茄幼苗生长及抗逆生理指标的影响

采用营养液栽培法,研究外源谷胱甘肽(GSH)对NaCl胁迫下番茄幼苗生长、根系活力、电解质渗透率和丙二醛(MDA)、脯氨酸(Pro)、可溶性糖含量以及超氧化物歧化酶(SOD)、过氧化物酶(POD)、过氧化氢酶(CAT)活性的影响,为利用外源物质减轻盐胁迫伤害提供理论依据。结果显示:(1)NaCl胁迫显著抑制了番茄幼苗的生长、根系活力和SOD、POD、CAT活性,提高了电解质渗透率及MDA、Pro、可溶性糖含量;(2)外源喷施GSH能够诱导NaCl胁迫下番茄幼苗叶片抗氧化酶SOD、POD、CAT活性上调,电解质渗透率及MDA含量下降,Pro和可溶性糖含量恢复至对照水平;(3)外源喷施还原型谷胱甘肽抑制剂(BSO)使NaCl胁迫下番茄幼苗的根系活力以及抗氧化酶SOD、POD、CAT活性下降,脯氨酸含量提高;(4)喷施GSH可诱导BSO和NaCl共处理番茄植株的根系活力、SOD、POD、CAT活性提高,MDA和Pro含量降低。研究表明,外源GSH可通过提高促进盐胁迫下番茄幼苗植株渗透调节能力及清除活性氧的酶促系统的防御能力、降低细胞膜脂过氧化程度、保护膜结构的完整性,从而有效缓解NaCl胁迫对番茄幼苗生长的抑制,提高其耐盐性。     

外源5-氨基乙酰丙酸对NaCl胁迫下黑果枸杞幼苗生理及生长的影响

5-氨基乙酰丙酸(ALA)是植物血红素、叶绿素等四吡咯化合物的关键生物合成前体,对植物适应非生物胁迫至关重要。为验证外源ALA对黑果枸杞幼苗生理生长的影响,该研究用300 mmol·L^-1 NaCl和不同浓度(0、5、10、15、20、25 mg·L^-1)的ALA共同处理黑果枸杞幼苗,并测定其相关的生理指标和生长指标,综合评价各处理幼苗的耐盐性。结果表明：(1)NaCl胁迫使黑果枸杞幼苗总生物量和叶片总叶绿素、类胡萝卜素、可溶性糖含量以及过氧化物酶(POD)活性较CK分别显著降低了33.39%、19.06%、24.38%、39.57%和47.91%(P<0.05),使黑果枸杞幼苗脯氨酸和丙二醛的含量较CK分别显著增加了165.74%和49.16%。(2)当外源ALA和NaCl同时处理时,黑果枸杞幼苗叶片类胡萝卜素和丙二醛含量、POD和过氧化氢酶(CAT)活性以及株高、总生物量均恢复至对照水平,叶片总叶绿素和脯氨酸含量以及SOD活性较CK显著增加。(3)黑果枸杞幼苗叶片叶绿素和脯氨酸含量以及抗氧化酶活性、生物量等指标随ALA浓度增加均呈先...     

NaCl胁迫对星苹果叶片生理特性的影响

为研究星苹果Chrysophyllum cainito的耐盐能力及其在NaCl胁迫下的生理特性变化,以0、0.2%、0.4%、0.6%NaCl溶液分别对盆栽幼苗进行胁迫处理,测定叶片的叶绿素、渗透调节物质、丙二醛含量及抗氧化物酶活性。结果表明,在NaCl胁迫下,星苹果叶片的叶绿素合成受到明显抑制;超氧化物歧化酶(SOD)和过氧化物酶(POD)的活性随NaCl浓度增加而呈现先降后升现象;过氧化氢酶(CAT)活性则是先升后降,在0.2%NaCl处理时达最高;可溶性蛋白含量与处理浓度呈负相关;脯氨酸、可溶性糖含量和对照相比有显著增加,两者在胁迫过程中起着重要的渗透调节作用。     

腐植酸浸种对盐碱胁迫下小麦幼苗抗氧化系统的影响

对龙麦26和克旱16两种不同基因型春小麦品种进行腐植酸浸种处理,研究了腐植酸对盐(NaCl)、碱(Na CO3)两种胁迫下小麦幼苗抗氧化系统的影响.结果表明:盐碱胁迫下小麦幼苗叶片脯氨酸含量增加,膜透性增强,地上部鲜质量降低;盐胁迫下,过氧化氢酶(CAT)活性升高,过氧化物酶(POD)活性降低,超氧化物歧化酶(SOD)活性先升后降,而碱胁迫下CAT和POD活性均升高,SOD活性降低;碱胁迫处理的小麦幼苗叶片抗氧化酶系统活性高于同浓度的盐胁迫处理;腐植酸浸种提高了小麦叶片谷胱甘肽含量,提高了SOD和CAT活性,有效缓解了盐碱胁迫对幼苗生长的影响.不同基因型小麦品种在抵御盐碱胁迫的能力和机制上存在一定差异,且与盐离子组成、浓度间存在一定互作,并受浸种方式调控.     

外源褪黑素对盐胁迫下紫花苜蓿幼苗抗氧化能力以及光合作用效率的影响

紫花苜蓿为多年生豆科优良牧草,土壤盐碱化是其产量的重要限制因素。该研究以‘中苜1号’紫花苜蓿为材料,在盐胁迫浓度和褪黑素浓度筛选试验基础上,设置盐(150 mmol/L NaCl)和褪黑素(30、50、80μmol/L)单独及复合处理,采用水培根灌褪黑素的方法,探究外源褪黑素对盐胁迫下紫花苜蓿幼苗生长特性、膜透性、渗透调节、抗氧化物酶以及光合作用指标的影响。结果表明:(1)紫花苜蓿幼苗生长受到盐胁迫的显著抑制,而在单独褪黑素处理下无显著变化;各浓度褪黑素处理均可有效缓解盐胁迫对紫花苜蓿生长造成的伤害,并以150 mmol/L NaCl+80μmol/L褪黑素处理(NaCl+MT2)效果最佳,其幼苗根长、根鲜重和根干重分别比盐胁迫处理显著增加了34.52%、41.93%和19.61%。(2)盐胁迫显著增加了紫花苜蓿幼苗细胞膜系统的透性和膜脂过氧化程度,NaCl+MT2处理幼苗叶片的相对电导率和MDA含量分别比盐胁迫处理显著降低了27.18%和30.24%,同时使幼苗叶片的相对含水量显著提高,脯氨酸含量却显著降低,表明外源褪黑素有效缓解了盐胁迫下细胞失水危害和细胞膜损伤的程度。(3)NaCl+MT2处理幼苗叶片的POD和SOD活性分别比盐胁迫处理显著提高31.45%和41.41%,其CAT活性却无显著变化,表明外源褪黑素可显著增强紫花苜蓿幼苗叶片POD、SOD活性,提高其活性氧的清除能力,减轻盐胁迫诱导的过氧化伤害。(4)盐胁迫显著抑制了紫花苜蓿幼苗光合作用效率,而NaCl+MT2处理幼苗叶片的净光合速率、气孔导度和蒸腾速率较盐胁迫处理分别显著增加了30.27%、45.1%、42.15%。研究发现,盐胁迫致使紫花苜蓿幼苗叶片的活性氧积累显著增加,抗氧化物酶活性显著降低,显著降低了其光合作用效率,外源褪黑素通过提高紫花苜蓿的抗氧化能力和光合作用效率来促进幼苗生长,从而增强了紫花苜蓿的耐盐性。     

盐分和水分胁迫对菊芋幼苗离子吸收及叶片酶活性的影响

采用砂培试验,用不同浓度的NaCl和等渗PEG6000(聚乙二醇6000,渗透势约为-0．44MPa)处理生长20d的菊芋幼苗,3d后分别测定其根、茎、叶中的Na^ 、K^ 、Cl^-含量以及叶片SOD、POD活性。结果表明,在NaCl和PEG胁迫下,根、茎、叶的Na^ 、Cl^-含量不断升高,而K^ 含量保持稳定。其中,茎中Na^ 含量高于根和叶。NaCl胁迫下,根、茎、叶的SX、Na值随胁迫强度的增加而递增,茎中SK、Na值小于根和叶。随着NaCl胁迫强度的增加,菊芋幼苗叶片的SOD和POD活性先上升后下降;PEG处理下,SOD活性分别高于对照和等渗NaCl处理31．1％和27．1％;而POD活性却分别低于对照和等渗NaCl处理26．0％和36．1％。     

水杨酸和硝普钠对NaCl胁迫下番茄幼苗生长及生理特性的影响

以番茄品种‘秦丰保冠’为试材,采用营养液培养法,研究单独和复配施用外源水杨酸(SA)、一氧化氮(NO)供体硝普钠(SNP)对100 mmol·L-1 NaCl胁迫下番茄幼苗生长及生理特性的影响.结果显示:SA、SNP、SA+SNP处理均能显著提高盐胁迫下番茄幼苗叶片保护酶(SOD、POD、CAT)活性、脯氨酸和叶绿素含量、幼苗根系活力,并显著降低叶片电解质渗漏率及丙二醛(MDA)含量,有效减轻盐胁迫对幼苗造成的伤害,促进幼苗的生长发育,其中SA+SNP复配处理效果最好.研究表明,外源SA和SNP处理均能通过提高番茄幼苗保护酶活性和脯氨酸含量来有效缓解盐胁迫伤害,且SA+SNP复配处理在提高番茄幼苗耐盐性方面具有协同增效作用.     

NaCl胁迫对''金光''杏梅幼苗生长及其生理指标的影响

以‘金光’杏梅盆栽幼苗为试验材料,研究了NaCl胁迫对‘金光’杏梅幼苗生长和生理指标的影响.结果表明:NaCl胁迫显著抑制了‘金光’杏梅幼苗的生长,随着NaCl浓度的升高,‘金光’杏梅的株高、叶面积、叶鲜重、叶干重、茎干重、根干重、叶绿素含量和净光合速率均呈下降趋势;叶片细胞膜透性、丙二醛(MDA)、可溶性糖、脯氨酸(Pro)含量以及POD活性显著增加;而SOD活性在低NaCl浓度下上升,在高NaCl浓度下下降.     

NaCl分根胁迫对羊草幼苗生长及其生理生化特性的影响

在自动控制的遮雨棚中,研究了200 mmol·L-1NaCl胁迫对不同分根处理羊草幼苗生物量、活性氧代谢以及渗透调节物质含量的影响.结果表明:单一胁迫根茎(RHS)、单一胁迫根系(ROS)以及同时胁迫根茎和根系(RHSS)3种处理方式下羊草幼苗各器官干重均低于对照,且大体呈现RHSS>ROS>RHS趋势.在RHS和ROS处理下,羊草叶片和根茎SOD、POD、CAT活性及MDA含量均无显著差异;RHSS处理时根系中SOD、CAT活性相比ROS处理显著降低.3种处理下根茎和根系MDA、可溶性糖、脯氨酸含量均显著高于对照,可溶性糖、脯氨酸含量在RHS和ROS处理间存在显著差异.可见,根茎在羊草响应盐胁迫的生理过程中与根系具有类似的功能;盐胁迫下羊草不同器官同一抗氧化酶对活性氧淬灭具有不同的作用,与POD相比不同器官SOD和CAT作用可能更大;根茎可能参与光合同化物——可溶性糖在羊草地上部和地下部的调节运输,且协同根系增强了羊草对盐胁迫的耐性作用.     

Entwicklungsgeschichte und Ultrastruktur von Pollenkitt und Exine bei nahe verwandten entomophilen und anemophilen Angiospermensippen derAlismataceae,Liliaceae, Juncaceae,Cyperaceae, Poaceae undAraceae

Some closely related members of the monocotyledonous familiesAlismataceae, Liliaceae, Juncaceae, Cyperaceae, Poaceae andAraceae with variable modes of pollination (insect- and wind-pollination) were studied in relation to the ultrastructure of pollenkitt and exine (amount, consistency and distribution of pollenkitt on the surface of pollen grains). The character syndromes of pollen cementing in entomophilous, anemophilous and intermediate (ambophilous or amphiphilous) monocotyledons are the same in principal as in dicotyledons. Comparing present with former results one can summarize: 1) The pollenkitt is always produced in the same manner by the anther tapetum in all angiosperm sub-classes. 2) The variable stickiness of entomophilous and anemophilous pollen always depends on the particular distribution and consistency of the pollenkitt, but not its amount on the pollen surface. 3) The mostly dry and powdery pollen of anemophilous plants always contains a variable amount of inactive pollenkitt in its exine cavities. 4) A step-by step change of the pollen cementing syndrome can be observed from entomophily towards anemophily. 5) From the omnipresence of pollenkitt in all wind-pollinated angiosperms studied one can conclude that the ancestors of anemophilous angiosperms probably have been zoophilous (i.e. entomophilous) throughout.

     

Identification and Characterization of the First Equine Parainfluenza Virus 5

正Dear Editor,Parainfluenza virus 5 (PIV5), known as canine parainfluenza virus in the veterinary field, is a negative-sense,nonsegmented, single-stranded RNA virus belonging to the Paramyxoviridae family (Chen 2018). The virus was first reported in primary monkey kidney cells in 1954 (Hsiung1972), then it has been frequently discovered in various     

Pathogenic Characterization and Full Length Genome Sequence of a Reassortant Infectious Bursal Disease Virus Newly Isolated in Pakistan

<正>Dear Editor,Infectious bursal disease (IBD) is one of the most important diseases of the poultry. The IBD virus (IBDV), a nonenveloped virus belonging to the Birnaviridae family with a genome consisting of two segments of double-stranded RNA (segments A and B), targets B lymphocytes of bursa of Fabricious leading to immunosuppression. In Pakistan,poultry farming is the second biggest industry and IBD is the second biggest disease threating the poultry sector.However, there is limited genome information of IBDV     

Mink Circovirus Can Infect Minks,Foxes and Raccoon Dogs

正Dear Editor,Mink circovirus (MiCV), which is clustered in the genus Circovirus of the family Circoviridae, was first described in minks from farms in Dalian, China in 2013 (Lian et al.2014). The complete single-stranded circular genome of the virus is 1,753 nucleotides long and contains two major open reading frames (ORFs), designated ORF1 (Rep gene)and ORF2 (Cap gene)(Lian et al. 2014; Ge et al. 2018).Sequence analysis has shown that MiCV is most closely     

CypA Regulates AIP4-Mediated M1 Ubiquitination of Influenza A Virus

Cyclophilin A (CypA) is a peptidyl-prolyl cis/trans isomerase that interacts with the matrix protein (M1) of influenza A virus (IAV) and restricts virus replication by regulating the ubiquitin–proteasome-mediated degradation of M1. However,the mechanism by which CypA regulates M1 ubiquitination remains unknown. In this study, we reported that E3 ubiquitin ligase AIP4 promoted K48-linked ubiquitination of M1 at K102 and K104, and accelerated ubiquitin–proteasome-mediated degradation of M1. The recombinant IAV with mutant M1 (K102 R/K104 R) could not be rescued, suggesting that the ubiquitination of M1 at K102/K104 was essential for IAV replication. Furthermore, CypA inhibited AIP4-mediated M1 ubiquitination by impairing the interaction between AIP4 and M1. More importantly, both the mutations of M1 (K102 R/K104 R) and CypA inhibited the nuclear export of M1, indicating that CypA regulates the cellular localization of M1 via inhibition of AIP4-mediated M1 ubiquitination at K102 and K104, which results in the reduced replication of IAV.Collectively, our findings reveal a novel ubiquitination-based mechanism by which CypA regulates the replication of IAV.