The experiment was carried out in 2013 at the fruit garden of the Chinese Academy of Agricultural Sciences in Liaoning,which was equipped with a core grape technology demonstration garden.‘Italy’grape cultivars were grafted on Beta as test materials. And their row spacing was 0.7 m,line spacing was 2 m. The lean dragon trunk matches the V shape leaf curtain,and used the integrated management of water and fertilizer,other management was the same as the routine. Since the beginning of August 1st to the defoliation day before dark for half an hour to fill 24:00,use red light and blue light to deal with the grape cultivars,with no-fill-light grapes as contrast,studying morphological characteristics,chlorophyll content,net photosynthetic rate,Fv/Fm value,soluble proteins content and chloroplast ultrastructure of grape leaves in aging process,to provide theoretical basis for the research and development of leaf anti-aging technology. The research result showed that compared with the control group,red light treatment increased the chlorophyll content,net photosynthetic rate,Fv/Fm value and soluble proteins content of leaf,the chloroplast grana were arranged in order,the disintegration of chloroplast ultrastructure was obviously slowed down,leaf senescence was delayed significantly. Blue light treatment significantly reduced the leaf chlorophyll content,net photosynthetic rate,soluble proteins content and Fv/Fm value,the ultrastructure of chloroplasts was destroyed,and the aging process of grapes was accelerated. But in the later stage of leaf senescence,the chlorophyll content of leaf,the net photosynthetic rate,soluble proteins content and Fv/Fm value of the blue light treatment was higher than that of the control. Moreover,the grana lamellae of leaf chloroplasts are arranged in order,leaf senescence was delayed in some degree. The content of soluble proteins in leaf of blue light treatment was significantly higher than that of red light treatment and control group. Summing up the above,the red light as supplement light had the best effect,the leaf senescence process was delayed effectively,and the physiological function of leaves was prolonged.
Potassium transporters play important roles in the transmembrane transport of potassium ions. In this study,it was found that CsKT1 had the characteristics of Shaker potassium channel,and displayed the highest homologous to AKT1 in Shaker family members of Arabidopsis thaliana. The experiments showed that the K+-uptake deficient yeast containing CsKT1 can grow under the conditions with K+ concentration of 10,1 and 0.1 mmol · L-1. qRT-PCR assays showed that the expression of CsKT1 in root was higher than that in shoot,and the transcription level was not changed after 24 h low potassium treatment(0.1 mmol · L-1)in Citrus sinensis plants. CsKT1 exhibited plasma membrane localization specifically. The yeast two hybrid experiments showed that the C-terminal cytosolic region of CsKT1 protein not only interacted with AtCIPK23,but also interacted with CsCIPK7 protein,which displayed the highest homology with AtCIPK23. CsCIPK7 could also interact with AtCBL1. There were 8 members in citrus CBL family,in which CsCBL1 displayed the highest similarity with AtCBL1/AtCBL9. These results suggested that CsKT1 function as an AKT1-like potassium transporter.
Citrus greening or Huanglongbing(HLB)is one of the most destructive diseases of citrus and causes significant economic losses worldwide. HLB can cause phloem necrosis and blockage in citrus,resulting in poor transport of photosynthetic assimilates and large accumulation of starch. In this study,0.1 g · tree-1 and 0.2 g · tree -1 oxytetracycline(OTC)were injected into the 4 year old Valencia (Citrus sinensis)infected with HLB. The qPCR detection showed that the abundance of Las(Candidatus Liberibacter asiaticus)in leaves was reduced effectively in 90 d. There was no difference of the OTC treatment effect between 0.1 g · tree-1 and 0.2 g · tree-1 OTC. I2/KI coloration and LM observation showed that the content of starch in the treated group of 0.2 g · tree-1 decreased from 18.58 μg · mm-2 to 5.24 μg · mm-2 after injection. But 0.1 g · tree-1 treatment had no significant effect on reducing starch content. The results of high performance liquid chromatography(HPLC)showed that OTC gradually degraded in the plant over time. Expression analysis showed that AGPase,GPT2,β-amylase and GBSS expressed in leaves decreased after 0.2 g · tree-1 OTC injection. Among them,AGPase has the highest decreased expression. This is consistent with the results of starch content in leaves 30 and 90 days after OTC injection.
Twenty-six fruit characters were collected and determined from 50 local pear germplasm resources in Fujian Province. Distribution frequency,coefficient of variation,and Shannon-Weaver index were analyzed. Q cluster,R cluster and principal component analysis were used to evaluate the germplasm resources and characters. The results showed that the diversity of local pear fruit description characters was abundant. Conspicuous fruit dot,many fruit russeting,rough skin,crisp flesh,sour-sweet flavor,absent astringency,small fruit core and maturity in September had more proportion than other corresponding descriptors,accounting for 92%,52%,54%,50%,50%,70%,54% and 80%,respectively. The average variation coefficient of content of vitamin C and titratable acid,ratio of SS and TA,and ratio of TSS and TA was 67.60%,48.26%,42.22% and 41.14%,respectively,which was higher than that of other numerical characters. The fruit peel color and shape was found to have the richest diversity among 13 description characters,with 1.660 and 1.605 of Shannon-Weaver index. And the indexes of 13 numerical characters range from 1.698 to 2.074,which was higher than that of 13 description characters with 0.324 to 1.660 of Shannon-Weaver index,indicating that the numerical characters had richer diversity than description characters. Q cluster analysis showed that all the tested germplasm resources were divided into five groups at the Euclidean distance of 14.71,and there were differences of fruit characters among difference groups without regional trend. R cluster analysis showed that 26 characters closely related were significantly clustered into five groups at coefficient of 1.236. Twenty-six characters were mainly composed of 10 independent principal components with the cumulative contribution rate of 86.545%,which showed dispersion of contribution rate and multi-directional variation of local pear fruit characters. Positively increasing the first principal component factor will be favorable for improving the fruit interior quality,while positively increasing the second and fourth principal component factor will be favorable for improving the fruit exterior quality,and negatively increasing the third principal component factor will be beneficial to increase fruit size.
Through the comparative analysis of phylogenetic relationships,basic physical and chemical properties,conservative motifs,the promoter cis-elements of CpERFs and combining with papaya RNA-seq data,which conclude different treatments [ethylene and ethylene inhibitor 1-methyl propylene(1-MCP)treatments] and different ripening stages in pulp,this research selected 22 CpERFs members for expression analysis. Through RNA-seq 18 members of ERF family were found,which suggests that these genes may play important role in response to fruit ripening in papaya.
The three-year-old seedlings of Vaccinium uligiuosum L. were selected as testing materials. The seedlings were exposed to the control(23 ℃,daylength 14 h),low-temperature and short day(4 ℃,daylength 10 h) and low-temperature and long day(4 ℃,daylength 14 h)under controlled environment chamber for 21 d respectively. The changes in the protein expression of shoot tissues after treatment were recorded. iTRAQ-based quantitative proteomics techniques were used in this study. The results showed that of 5 972 proteins and 600 differential expression proteins identified by a mass spectrometric analysis,140 proteins were significantly up-regulated and 114 were significantly down-regulated in low temperature and short-day vs control;255 proteins were significantly up-regulated and 122 were significantly down-regulated in low temperature and long-day vs control;39 proteins were significantly up-regulated and 187 were significantly down-regulated in low temperature and short-day vs low temperature and long-day. They included proteins were mainly involved in(1)RNA metabolism;(2)protein posttranslational modification;(3)carbohydrate metabolic;(4)energy production and conversion;(5)lipid metabolism;(6)secondary metabolites biosynthesis;(7)antioxidant and stress defense;(8)photosynthesis;(9)inorganic ion transport and metabolism. The differential expression proteins related to freezing tolerance were mainly induced by low temperature. In addition,expression of a few proteins is affected by both low temperature and photoperiod,and low temperature and short photoperiod are more favorable to freezing resistance acquisition. Cold acclimation increased significantly abundance of protein involved in RNA metabolism,protein posttranslational modification,antioxidant and defense responses,secondary metabolites biosynthesis,and lipid metabolism,revealed these metabolic pathways and related proteins may play an important role in freezing resistance mechanism in Vaccinium uligiuosum L.
We used tomato(Solanumly copersicum L.)‘Micro-Tom’as the test material,after 30 days of seed germination. The seedlings were transferred to the artificial climate chamber and exposed to the following light conditions:red/blue combined light(1︰1),red/blue combined light(3︰1),red/blue combined light(5︰1),red/blue combined light(7︰1),and white light as the control. Fruits were harvested at the mature green,breaker,and ripe stages,then we determined the fruit volatile compounds content and proteomic. The results showed that in breaker and ripe stages of tomato fruits,hexanal,trans-2-hexenal,β-ionone,geranylacetone,6-methyl-5- hepten-2-one,2-phenylethanolx,callus lignan,which have positive effects on tomato flavor were the highest in the red/blue combined light(3︰1)treatment. The content of methyl salicylate,which has a negative effect on tomato flavor was low,and no methyl salicylate was detected at the ripe stage. To further elucidate the effects of light quality on volatile compounds content of tomato fruit,total protein was extracted from the control and red/blue combined light(3︰1). A subsequent proteomic analysis revealed that twelve proteins related to volatile compounds were differentially abundant between the control and red/blue combined light(3︰1)during ripening. Among the twelve differentially abundant proteins related to volatile compounds,eight were up-regulated and four were down-regulated. The differential abundances of the twelve proteins were validated by determining the expression levels of the corresponding genes by qRT-PCR. The expression levels of eleven of the genes were consistent with the abundances of the corresponding proteins. There was a lack of consistency in the gene expression levels and protein abundances for phenylpyruvate tautomerase(MIF).
Ultraviolet-B(UV-B)receptor gene UVR8 was cloned from eggplant(Solanum melongena L.)using homology-based cloning method,named SmUVR8. Sequence alignment shows SmUVR8 is similar to UVR8 in other Solanaceae plant and Arabidopsis thaliana,indicating SmUVR8 may have the function of AtUVR8. To further study the function of the SmUVR8,SmUVR8 was transformated in the Arabidopsis uvr8 mutant. The result showed SmUVR8 restored the phenotype of hypocotyl elongation,the flowering time and anthocyanin accumulation of Arabidopsis uvr8 mutant,which indicated eggplant SmUVR8 gene have the similar function to the Arabidopsis AtUVR8 gene. Real-time fluorescent quantitation and yeast two hybrid result reveals UV-B signal can influence photomorphogenesis of eggplant by the interaction of SmUVR8 and SmCOP1 activating SmHY5 and SmCHS .
In order to excavate the diversity of TuMV resistant genes and make the genetic improvement strategy and measures for the prevention and control in Chinese cabbage,QTL analysis of the dominant locus was conducted in the study,which would be helpful to cultivate the broad-spectrum resistance of Chinese cabbage varieties. The F2 population was constructed from the parents‘89B’(resistant)and‘Qiangshi’(susceptible),which were the highly inbred Chinese cabbage lines. The F2 population individuals were inoculated by TuMV C4 isolate,and the segregation from F2 did not fit the expected segregation for a Mendelian model 3︰1(χ2 = 4.8 > χ0.052 = 3.84),so quantitative trait locus controlled the character,not a single gene. Choosing 40 highly resistant/susceptible individuals from F2 population,respectively,to mix the pools,and the two parents and two pools were re-sequenced. By calculation analysis of △(SNP-index) between parent and pools,two main regions were obtained(A07 chromosome:13.9–14.4 Mb and A08 chromosome:16.4–17.4 Mb). There were 68 genes in the above two regions,and 6 out of 68 were associated with resistance in plants(Bra028499,Bra028500,Bra016311,Bra016312,Bra016313 and Bra016314). In addition,Bra028499 and Bra028500 coded the disease-resistant proteins,and Bra016311,Bra016312,Bra016313 and Bra016314 coded TMV-resistant proteins. Bra028499,Bra028500,Bra016311 and Bra016314 contained the TIR-NBS-LRR domains. About 80% of the resistance genes cloned in plants belonged to the NBS gene families,indicating that these genes may be associated with Chinese cabbage resistance to TuMV.
A floral mutant was obtained during the construction of a mutant library with Petunia hybrida W138 strain,which was mainly characterized by abnormal development of sepals and petals,and named as aps(abnormal petals and sepals). Compared with normal W138 plant(Wt),the most obvious phenotype of aps is its split corolla,usually with three lobes;simultaneously,two of five sepals in aps mutant are petaloid. Scanning electron microscopy(SEM)analysis indicated that the shape of epidermis cells in the petaloid sepals of aps plants was the same as that in petals of Wt plants. The genetic analysis by selfing,crossing,and backcrossing between aps and its normal sister plants or W115 suggested that the trait of aps is controlled by a single recessive gene. qPCR was used to analyze the expression of floral development related genes in four whorls of organs between aps and Wt flowers. The results showed that three B-class genes(FBP1,PMADS1 and PMADS2)and some E-class genes(FBP2,FBP4 and FBP5)was activated in petaloid sepals of aps mutants,however,the expression of all A-class genes including FBP26,FBP29,PEG,AP2A,AP2B and AP2C,as well as the E-class genes FBP9 and FBP23,are down-regulated in this whorl. In aps petals,except for FBP29 that is not expressed in petals,all other A-class genes are up-regulated,as are the B-class genes,FBP1 and PMADS2,and the E-class genes FBP2,FBP5,FBP23 and PMADS12. The expression of C- and D-class genes are not altered in sepals and petals of the mutants,but both C-class genes are downregulated in stamens and styles of aps plants,like the D-class gene FBP7 in ovaries. The characterization of aps mutant provides a good chance for studying the molecular regulation of floral organ development and for exploring the relationship of floral genes in petunia.