The red-callus induced from the leaves of‘Zihong 3’apple in F1 population of Malus sieversii f. niedzwetzkyana crossed with‘Fuji’was used as materials. A cold signal relative gene(MDP0000662999)was obtained from apple genome by BLAST searches of the Arabidopsis AtICE1 protein sequence,designated MdICE1. Sequence analysis indicated that the open reading frame(ORF)length of MdICE1 was 1 626 bp,which encoded 541 amino acids. Phylogenetic analysis revealed that MdICE1 was homologous with AtICE1 which was involved in the cold signaling. The aligned protein sequences also revealed that MdICE1 contains the bHLH motif. Furthermore,low temperatures are conducive to anthocyanin biosynthesis in callus. The transcript levels of MdICE1 and anthocyanin biosynthesis related genes(MdMYB10 and MdbHLH3)were significantly higher in callus incubated at 8 ℃ than those at 24 ℃. The yeast two hybrid experiments showed that the MdICE1 could interact with MdMYB10. The subcellular localization assays revealed that MdICE1 was located in the nucleus. In addition,the recombinant protein of MdICE1 was obtained by the prokaryotic expression technique,which laid a foundation for MdICE1 functional identification associated with anthocyanin metabolism.
The full length of cDNA sequences of two ELF4 homolog genes were cloned from Dimocarpus longan‘Red Seed’,named DlELF4-1 and DlELF4-2. The functions of these two genes were analyzed by bioinformatics analysis and real-time quantitative PCR. To further study the function of the DlELF4 genes,DlELF4-1 and DlELF4-2 were overexpressed in Arabidopsis thaliana. Sequence analysis and cluster analysis showed that DlELF4-2 was similar to AtELF4-L1,while DlELF4-1 and AtELF4 showed higher similarity. Overexpression of two DlELF4 genes separately in Arabidopsis thaliana resulted in delaying flowering and adventitious roots phenotypes,suggesting that DlELF4 genes may be repressors of flowering and promoting auxin synthesis. However,expression patterns of DlELF4-1 and DlELF4-2 genes were different during bud differentiation of longan,indicating that the two genes may have different functions in longan.
In order to evaluate antioxidant capacity of peach fruit using phenolic compounds content,fruits of 12 red,7 white and 4 yellow flesh peach cultivars were used to analyze the difference of individual and total phenol content. Comparing with white and yellow flesh peach cultivars,most of the red ones had higher epicatechin and total phenol content. Eight phenol content indices were generalized into 4 independent comprehensive indices through principal component analysis after correlation analysis between different indices. Comprehensive evaluation value(D)was calculated based on both subordinate function value and weight. After comprehensive ranking on flesh antioxidant capacity of different cultivars,we found that the red flesh cultivar‘Beijing Yixianhong’had the highest D value,meanwhile,red flesh types sorting in the front and most of white and yellow types followed behind,which was in accordance with the result of cluster analysis. These results suggested that peach fruit antioxidant capacity was closely related with flesh color. Peach fruit antioxidant capacity could be evaluated synthetically using both individual and total phenol content by principal component analysis,subordinate function method and cluster analysis method. The order of the contribution of phenol to the antioxidant capacity of peach fruit was neochlorogenic acid,total phenol,epicatechin,ferulic acid,chlorogenic acid,rutin,catechin and quercetin.
Expressed sequence tags(EST)- simple sequence repeats(SSR)and sequence related amplified polymorphism(SRAP)markers were applied to assess the genetic diversity and genetic relationship of 10 Toona sinensis populations collected from nine provinces in China. A total of 167 polymorphic loci were detected by 33 SRAP primers with 5.06 polymorphic loci per primer,and 221 polymorphic loci were observed by 45 EST-SSR primers with 4.9 alleles per primer. The results of observed number of alleles(EST-SSR,Na = 2.3506),expected heterozygosity(EST-SSR,He = 0.4632)and the Shannon’s information index(SRAP,I = 0.6140;EST-SSR,I = 0.6752)demonstrated that relatively higher level of genetic diversity possessed in these populations of T. sinensis. The genetic differentiation coefficients data(SRAP,Gst = 0.3124;EST-SSR,Fst = 0.2462)also revealed relatively higher level of genetic polymorphisms among these T. sinensis resources. Cluster analysis divided 10 populations into 3 groups,one group consisted of Hengshui,Tai’an and Taihe populations,another group consisted of Chengdu,Kunming,Wuhan and Ruyang populations,Dezhou and Quanzhou populations were belonging to the third group. The results of Nanjing population were different in two kind of markers. Genetic relationship among these T. sinensis populations have no significant correlation with their geographical distribution.
Through the combination of tissue culture and radiation mutation,radiation breeding of Boston fern(Nephrolepis exaltata‘Bostoniensis Murano’)was investigated by using green globular bodies(GGB)as materials radiated by various dose of 60Co-γ rays. The results showed that the LD50 of GGB was about 128 Gy. With increasing dose of 60Co-γ rays,the multiplication and differentiation of Boston fern GGB were depressed. Morphology damage of Boston fern GGB radiated by 60Co-γ rays included darken color,increased density and the depression of multiplication and differentiation,and cellular damage included reduction of embryonic cell and initiation of cellular micronucleus. At 50–200 Gy,with increasing dose of 60Co-γ rays,the height of Boston fern plants differentiated from GGB became dwarf,and leaf mutation rate increased. Moreover,leaf mutant Neg1 was obtained at 150 Gy.
According to the different bases of Actin gene sequences between Phytophthora capsici Leonian,P. infestans and other eight common soil pathogenic pathogens,we designed and screened out a specific primer pair YM2F/YM2R to establish a real-time fluorescent quantitative PCR detection assay of P. capsici,and using this assay to monitor P. capsici in soil samples prepared by artificial simulation and collecting form attacked yields. The results showed that the assay had a good liner relationship and a high sensitivity of 1 × 10-1 pg ? μL-1 DNA,which is 100 times more than normal PCR. P. capsici could be detected rapidly,specifically and quantitatively in infected soil without isolation or cultivation by the RT-PCR assay. The detection result of soil samples collected form attacked field indicated that the incidence and epidemiology of disease were proportional to the density of pathogenic bacteria within a certain range,which can provide scientific basis for the epidemic and early prevention of the disease.
‘Chunlei’is a mid-late ripening and big-fruit sweet cherry cultivar bred by crossing‘Hongdeng’and‘Van’. Tree vigor is high and branch ability is middle. The fruits are big,purpish red,kidney-shape,with sunken fruit top and short fruit stem. The fruit weighs 8.5 g on average. The soluble solids,total sugar,titrtable acid and vitamin C content is 16.5%,10.11%,0.74% and 0.089 mg ? g-1,respectively. The flesh is purpish red and crisp-hard with pleasant sweet and little sour taste. S-genotype is S3S9,self-unfruitful. It has very little malformed fruit,highly resistance to flowering high-temperature and hot humid summer weather,with very early fruiting and high yield(18 000 kg ? hm-2). Fruit ripening period is 25–30 May in Zhengzhou,and fruit development period is 55–60 days.
‘Luaijiao’is a new bamboo cultivar derived from Dendrocalamopsis oldhami(Munro)Keng f. The cultivar has a short culm,small diameter at breast height,short internode and low branch. The bamboo shooting period is from late May to late October. The bamboo shoot handle is skew and small,large taper. The texture of bamboo shoots is delicate and crisp,having a high nutritional value.