The DNA polymorphism of thirty-five hawthorn accessions (Crataegus pinnatifida Bge.) was analyzed using randomly amplified polymorphic DNA (RAPD) and inter-simple sequence repeat (ISSR) markers in the present study. Twelve RAPD primers generated a total of 110 clear and reproducible bands, of which 89 were polymorphic, with an average of 7.4 polymorphic fragments per primer. Thirteen ISSR primers generated a total of 110 clear and reproducible bands, of which 94 were polymorphic, with an average of 7.2 polymorphic fragments per primer. The dendrogram based on RAPD and ISSR data were constructed separately by using UPGMA analysis. The distance coefficient of the analyzed materials ranged from 0 to 0.62 and 0 to 0.64 for RAPD and ISSR markers, respectively. Our results indicated that the C. pinnatifida species has high level of genetic diversity.
Inter-simple sequence repeat (ISSR) was used to determine the genomic DNA variations and relationships in Torreya grandis Fort.. Seventeen individuals including 9 cultivars and 8 elite clones were used in ISSR analysis. Of the 50 ISSR primers subjected to screening, 12 produced reproducible, polymorphic and disc- repant fragments. Using these primers, 104 DNA bands were amplified, of which 84.6% were polymorphic. The average number of DNA bands amplified by each primer was 11. DNA profiles based on ISSRs have revealed potential diagnostic for various individual accessions. A dendrogram generated using the Unweighted Pair Group Method with Arithmetic Average based on Nei's distance showed that the Torreya grandis cultivars were clustered into two groups. The first group include Dayuanfei, Mifei, Xuanwenfei, Liaoyafei, Zhimafei and Luoshuangfei, the second group include Xiangyafei, Xiaoyuanfei, Qiefei and the clone varieties of Torreya grandis 'Merrillii'.
Using degenerate oligoncleotide primers corresponding to conserved domains of the Ty1-copia retrantranspon reverse transcriptase, a fragment of 260 bp was amplified by PCR from Cucumis hystrix and C.sativus. The amplicons were cloned into pGEM-T Easy vector after purification, positive clones selected and identified by colony PCR, then sequenced and analyzed. 21 different sequences of reverse transcriptase from Cucumis hystrix and C. sativus-"Beijingjietou" were obtained, and five families were distinguished after cluster and alignment analyses of their nucleotide sequences. These sequences showed high heterogeneity mainly characterized by deletion mutation. The length of the nucleotide sequences varied from 255bp-272bp, and homology ranged from 27.0% to 98.1%. When translated into amino acids, four sequences presented stop codon mutation, and six sequences presented frameshift mutation. The amino cluster and alignment analyses of these sequences with other reverse transcriptase sequences from other accessions showed that they may have the same origin.
Pollen morphology of 17 original Malus species and 25 ornamental crabapple cultivars were observed using environment scanning electron microscope. The results indicated that the apple pollen belonged to the N3P4C5 type, bilateral symmetry, prolate sphericity or ultra prolate sphericity, with three germinal furrows extending almost to the full length of the grain. The exine surface had a striate pattern and some small pores. From the UPGMA cluster analysis, the 42 taxa could be classified into four groups. The first group contained M. florentina, M. sylvestri, M. 'Robinson' and other 7 cultivars. The second group included M. baccata and other 8 species and 3 crabapple cultivars, like M. 'Hopa'. The third group consisted of M. sieversii and 3 more species and cultivar M. 'Dolgo'. The last group comprised of M. coronaria, M. platycarpa M. 'Kelsey' and 13 more crabapple cultivars. Twenty-five ornamental crabapple cultivars originated from a very complicated genetic complex, which could be stated as cross-hybrids from species from North America, Europe, and Asia.
The effects of 1-MCP and DPA treatments on polyphenols, antioxidant activity of epicuticular wax of apple were studied. Total phenolic compounds and flavonoids in all the samples increased first and then decreased during the cold storage. 1μL·L-1 1-MCP and 2g·L-1 DPA treatments increased total phenolic compounds, flavoniods content, and DPPH·and ABTS+ radical scavenging activity in wax. Antioxidant activity was remarked positive correlated with polyphenols.
The effects of fruit bagging on fruit quality and antioxidant capacity were studied in white flesh loquat fruit (Eriobotrya japonica Lindl cv. 'baiyu') with four different types of bags (one-layer white paper bag, one-layer yellow paper bag, two-layer yellow paper bag and two-layer grey-out-dark-in paper bag). The results showed that bagging promoted the luster of loquat fruits. Compared with control, the treatment of one-layer white paper bag increased the content of total soluble solids and total sugars, while the treatment of other three types of bags decreased the content of total soluble solids, and increased the titratable acids in mature fruit of 'Baiyu'. The contents of total phenolic and flavone and antioxidant capacity in bagging fruit were lower than those in control. The lowest occurred in the fruit bagged with two-layer grey-out-dark-in paper bag. The decrease of total antioxidant capacity in bagging fruit was attributed to the decrease of the content of total phenolic and flavone in bagging fruit. According to above results, the one-layer white paper bag was the most suitable for bagging of 'Baiyu' loquat fruit.
The composition and content of glucosinolates (GSs) in sprouts, leaves and edible roots of radish (Raphanus sativus L.) were analyzed by HPLC-MS. A total of eight GSs were identified in different tissues of radish, including five aliphatic GSs (4-methylsulfinyl-3-butenyl GS, 2-hydroxy-3-butenyl GS, ethyl GS, 4-methylthio-3-butenyl GS and 6-heptenyl GS) and three indole GSs (1-methoxyindol-3-ylmethyl GS, indol-3-ylmethyl GS, 4-hrdroxyindol-3-ylmethyl GS). Remarkable differences in glucosinolate profiles in sprouts, leaves and edible roots of radish were observed. The contents of total GSs in the sprouts and edible roots were higher than in the leaves. The major GS in edible roots and sprouts was 4-methylthio-3-butenyl GS, accounting for 75.5% and 71.5% of the total GSs, respectively. Indol-3-ylmethyl GS was the major GS in radish leaves, accounting for 57.1% of the total leaf GSs.
Double stranded RNA (dsRNA) were extracted from leaf tissues of radish (Raphanus sativus-root cv. Yidianhong) grown in Hangzhou China. Complementary DNAs corresponding to the dsRNA segments were obtained by using a modified single primer amplification technique (SPAT), and followed by cloning and sequencing. The results revealed that a new dsRNA sequence, different from all the previously reported sequences RasR1-RasR5, was obtained. And the newly detected RasR 6 (EU285027) was found to be 1778 bp in length. It predicted that the positive strand of RasR 6 potentially encoded a protein of about 55.1 kDa, containing 502 amino acids. Five members of Partitiviridae, all of which encoded putative viral CPs, were found to have some identity with RasR 6. Multiple alignments showed that RasR 6 were highly conserved at the 5(UTR regions with RasR 1 and RasR 2 previously reported from the same radish varities, but had no similarity with RasR 3-RasR 5. Thus, it could be presumed that both RasR 6, RasR 1 and RasR 2 should belong to Raphanus sativus virus 1(RasV 1), and RasR 6 encods CP together with RasR 2, or is a satellite dsRNA of this virus.
Solanum peruvianum is wild species related to S. lycopersicum, and possesses potential value for genetic improvement of tomato. In order to effectively utilize S.peruvianum and provide available information for tomato genetic improvement, we reviewed origin, taxonomy, biology character, and molecular biology of S.peruvianum, as well as progress in overcoming distant hybridization barriers between S.lycopersicum and S.peruvianum. The strategies of using S. peruvianum for tomato improvement were discussed in this paper.