Under the field conditions in winter, diurnal variations and light response of photosynthesis in leaves of three cultivated species and their wild species of Ziziphus mauritiana Lam. were investigated by using the Li-6400 portable photosynthesis system. The results indicated that the diurnal variation of net photosynthetic rate (Pn) exhibited dual-peak curves because of midday depression. Pn, transpiration rate (Tr) and water use efficiency (WUE) of Dacuimi cultivar were significantly higher than those of Misi and Wuqian cultivars. The lightly increase in Ci and the decrease in stomatal limitation (Ls) accompanied a reduction of Pn at noon indicated that the depression of photosynthetic rate was mainly due to the non-stomatal limitations. The light compensation point (LCP) and saturation point (LSP) were 21.2~51.6 (mol·m-2·s-1 and 800~1800 (mol·m-2·s-1 ,respectively, in these cultivars, and the apparent quantum yield(AQY) were 0.032~0.057. Thus, it is suggested that the tested four Ziziphus mauritiana Lam. were heliophilous plants. Because of higher LSP in Dacuimi and wild species, these plants showed heliophilous abilities. However, the LSP and LCP of Wuqian were lower than the others, which might reveal a helioskiophyte feature. Therefore, it was suggested that appropriate cultivars and managing methods should be chosen by different photosynthetic traits such as Pn, WUE and Tr in the production of Ziziphus mauritiana Lam.
A conserved fragment of ACC oxidase cDNA, and its corresponding 5'- and 3'-end sequences were successfully obtained from sand pear (Pyrus pyrifolia Nakai 'Zaosheng Xinshui' ) by RT-PCR and RACE. They were spliced into a 1 225 bp full length cDNA which designated as Pyp-ACO. Its open reading frame is 945 nucleotides in length, and its upstream and downstream are 63 bp of 5'-UTR and 217 bp of 3'-UTR. The sequence was deposited in GenBank database, accession number EF451060. The nucleic acid of Pyp-ACO shares 98.3% and 98.1% sequence identity with those of P. communis L. and Malus×domestica Borkh.. The deduced amino acid sequence of Pyp-ACO was 314 residues and contains twelve conserved residues belonging to non-heme iron (II) dependent family of oxygenases/oxidases and three residues essential for emzyme activation. A binary antisense expression vector with Pyp-ACO coding region was constructed by inserting the target fragment in reverse orientation in pYPX145. The expression of the gene is controlled by a double 35S promoter. The vector was successfully introduced into Agrobacterium tumefaciens strain LBA4404 for further transformation to develop transgenic pear for fruit with longer shelf life.
Present study was conducted based on the previous research of Apple scar skin viroid (ASSVd) for apple and pear, used material of apricot was those that showed positive signal of blot hybridization detection. Full-length special fragment of ASSVd for apricot was amplicated using RT-PCR protocol, then was recycled, cloned and sequenced. It was demonstrated that the full-length genome of ASSVd of apricot is 330 nt long (GenBank numbered with EU031477 to EU031486). The exist of ASSVd in apricots was reconfirmed by the results of In situ RT - PCR , and ASSVd mainly located in nucleolus of mesophyll cell. The fact of infecting capability of apricot enlarged the host ranges of ASSVd.
The sequence encoding three nuclear localizing signals (NLSs) at the C-terminal of pthA, was amplified by PCR from the plasmid of Xanthomonas axonopodis pv. citri. and cloned into PET32a(+) vector. The recombinant plasmid named PthA-NLS was identified by restriction digestiion and sequence analysis. The sequence of the cloned NLSs had 99.9% of similarity with that of pthA in GenBank. The recombinant fusion protein was expressed in E.coli BL21 (DE3) and analyzed by 12% SDS-PAGE. A 48 kD of recombinant fusion protein was purified with Ni2+-NTA resin. The antiserum was obtained by immunizing Balb/c mouse with the purified recombinant protein and then identified by Western Blotting and ELISA analysis. The result demonstrated that the antiserum could specifically bind to the recombinant protein and the PthA from X. axonopodis pv. citri., as well as to partially inhibit the disease development. The successful cloning, expression and the preparation of PthA-NLS specific mouse antiserum offered the ways for better understanding the pathogenesis of pthA and the development of a rapid method for molecular detection of citrus canker.
The influences of silicon (Si) on the signaling systems of phosphoinositides and calmodulin (CaM) in flowering Chinese cabbage (Brassica Campestris L. ssp. Chinensis var. utilis Tsen et Lee ) was studied using the inoculation of anthracnose (Colletotrichum higginsianum) at different Si levels. Results indicated that Si played a manifest regulating role on the formation of phosphatidylinositol (PI) and phosphatidylinositol-4-monophosphate (PIP). After the infection by anthracnose, there were clearly different fluctuations of PI contents between different cultivars . At the suitable Si level, infection induced high PI content. Due to the infection, PI content increased manifestly in the susceptible cultivar at medium Si level and in the resistant cultivar at low and medium Si levels, but showed unstable trend in other treatments. The accumulation of PIP was inhibited at the early infection stage and turned to be promoted at the late infection stage in the susceptible cultivar, but the accumulation pattern of PIP was completely reverse in the resistant cultivar. At suitable Si level, the infection by anthracnose manifestly increased PIP contents in both susceptible and resistant cultivars, especially in the late infection stage with stronger induction. This is probably related to the degradation of PI in large amount and the transfer of disease-resisting signals at the late infection stage. Si also affected the CaM contents, with the extents relating to the infection by anthracnose. Low Si level clearly promoted the inducing effect of anthracnose on CaM in the susceptible cultivar, while medium Si level showed strong promoting effect on the
收稿日期:2008-01-02 ;修回日期:2008-
With cotyledonary petiole and hypocotyl explants, the shoot regeneration frequencies of three turnip (Brassica rapa L. ssp. rapifera) cultivars were examined. To achieve a high-frequency regeneration system, the hormone combination of thidiazuron (TDZ) and naphthaleneacetic acid (NAA) was compared with combination of benzyladenine (BA) and NAA on shoot regeneration. The results show that cotyledonary petioles were the best explant and that Murashige and Skoog (MS) medium containing 7.0 mg·L-1TDZ and 1.0 mg·L-1 NAA was suitable recipe for getting high-frequency shoot regeneration. Based the recipe, the effects of AgNO3 concentration, seedling age, pre-culture time of 2,4-dichlorophenoxyacetic acid (2,4-D) were investigated to optimize the shoot regeneration system. The results suggseted that petiolate cotyledon with seedling age of 5 d cultured in MS medium containing TDZ 7.0 mg·L-1 + NAA 1.0 mg·L-1 + AgNO3 5.0 mg·L-1 followed by pre-culture with 2,4-D 1.0 mg·L-1 for 2d can be induced with highest-frequency regeneration. The highest shoot formation rate was about 90%. The rooting percentage of shoots was 100% on MS supplemented with 0.1 mg·L-1 indole-3-butyric acid (IBA). The 95% rooted shoots survived in a greenhouse.
The aim of this study is to obtain transgenic pepper plants resistant to TMV and CMV that could be used in breeding new pepper variety with virus-resistant traits. The primers were designed based on the sequences of PAP in Phytolacca Americana to amplify non-virulent defective PAP gene , PacPAP1 from genomic DNA of leaves in Phytolacca acinosa. The expression vectors was constructed and the PacPAP1 was transferred into pepper (Capsicum annuum L.) by flamingo bill mediated-Agrobacterium. In the transgenic plants , the molecular test were done and resistance assay was performed at 25d following artificial inoculation with TMV or CMV. The results showed that the size of the isolated non-virulent defective PacPAP is 714bp, bearing 99.7% identity with PamPAP from Phytolacca american. The accession numbers of the gene in GenBank is AY603353. The transgenic pepper plants were obtained with PacPAP. The non-transgenic pepper plants were susceptible to virus, no symptoms were observed in the positive transgenic plants. This suggests that transgenic pepper plant resistant to TMV and CMV can be obtained by transferring PacPAP1.
This paper reported the discovery process and identification method for the first intersectional hybrid between sect. Moutan and sect. Paeonia in China, which was named after 'He Xie'. According to observation and comparison on morphology of sect. Moutan, sect. Paeonia and 'He Xie', the morphology of 'He Xie' had the features similar to both herbaceous peony and tree peony, but more similar to herbaceous peony; Using SRAP (Sequence-related amplified polymorphism) molecular marker technique, the results revealed that the amplified fragments respectively unique to sect. Moutan and sect. Paeonia showed additivity in 'He Xie', which proved that it was could be the hybrid of the both section. 'He Xie' was proposed to be perennial herb by intersectional hybridization between the two sections identified from the aspects of morphology and molecular biology.
45S rDNA was mapped on the chromosomes of Lilium. longiflorum, L. leichtlinii, L. auratum and L. pardalinum of the genus Lilium using fluorescence in situ hybridization in this paper. The result showed that 45S rDNA were localized near the centromere region in these four species, but the number of the 45S rDNA sites, which chromosomes having the 45S rDNA signal, and the intensity of the 45S rDNA signal somewhat varied in the four species. Three pairs of chromosomes have the 45S rDNA signal in L. longiflorum and L. pardalinum, while four pairs of chromosomes have the 45S rDNA signal in L. leichtlinii and L. auratum. Nevertheless, the two pairs of metacentric chromosomes of L. auratum have the 45S rDNA signal, one pair of metacentric chromosomes of L. leichtlinii have the 45S rDNA signal, but no 45S rDNA signal is on any metacentric chromosome of L. longiflorum and L. pardalinum. Considering the four species belonging to different sections in Lilium, the result supplies some molecular evidence for supporting the Lilium classification.
Flower color is one of the most important ornamental characters. This study is the first report on the polymorphism of flower color of the ornamental sunflower. The floral color was measured according to the Royal Horticultural Society Colour Chart (RHSCC) and by a NF333 spectrophotometer. And UV-Visible spectra of flower pigments were performed. The results indicated that the floral color of the ornamental sunflower includes the red group and the yellow group. The results also showed that there are 9 anthocyanins of all 36 ornamental sunflower genotypes. Only one anthocyanin was detected in all 36 experimental materials. The results of the multilevel mass spectrum showed that the anthocyandin of the sunflower was cyanidin. The cyanidin was combined to glucose, rhamnose and/or arabinose to form glucosides. But we did not detect the cyanin in the pure yellow sunflower. This supposes that the cyanin was the matter of the red group of the ornamental sunflower.
A protocol for plant regeneration from protoplast of Musa AAB Silk cv. Guoshanxiang via somatic embryogenesis was developed. Viable protoplasts were isolated from embryogenic cell suspension (ECS) in a enzyme mixture of 3.5% cellulose R-10, 1% macerozyme R-10, 0.15% pectinase Y-23 and 0.41 mol/L manntitol, the yield was 3.1×107 protoplasts per mL packed cell volume (PCV) ECS. Liquid and feeder layer culture systems with medium 'A' and medium 'B' were used respectively for protoplast culture. In liquid culture system, medium 'B' was more efficient for inducing cell division and colony formation which was about 3-fold and 10-folod respectively, compared to that with medium 'A'. However, all protoplast-derived cell colonies obtained from liquid culture system could not develop further. In feeder layer culture system, there was no significant difference between medium 'A' and medium 'B' on cell division and colony formation of the cultured protoplasts. Protoplast-derived cell colonies from feeder layer culture system were then transferred onto embryo induction medium for somatic embryogenesis. Forty-five days after the cell colonies were transferred on embryo induction medium, 1550 mature embryos were obtained from 105 protoplasts. After another 30 d of culture, 7.8% of mature embryos germinated. Normal plantlets were obtained from MS basal medium supplemented with 0.1% activated charcoal and the plantlets were transferred into pots and grew well.
The characteristic of ethylene production and gene expression of ethylene receptors were studied in pre-cooled broccoli which were stored under 20 ℃. The results showed that during 0-6 h of storage, the ethylene production increased in the cross section of stem (0-2 mm), while decreased markedly in florets. Changes in the activity of ACC synthase were in agreement with those of the ethylene production rate. ACC content increased from 0 h to 6 h and decreased from 6 h to 12 h in all tested tissues. The florets had the lowest level of ACC content. The MACC level in florets was relatively high and remained stable during the experimental period. The lowest level of MACC appeared in the basal portion of florets. Though it was significantly higher in florets than that in the stem tissues, the activity of ACC oxidase increased from 0 h to 12 h in all tested tissues,which was inconsistent with the ethylene production. Northern blot analysis showed that mRNA levels of BO-ACS1 and BO-ACO2 in stem tissues were higher than that in florets at 0 h; mRNA levels at 12 h were lower than that at 0 h. In florets, the mRNA level of BO-ACS1 didn't increase at 12 h, however mRNA level of BO-ACO2 increased significantly. The transcripts of BO-ETR1, BO-ERS, and BO-ETR2 in the first layer of the cross section of stem and the BO-ERS in the florets were higher at 12 h than that at 0 h. The mRNA of BO-ETR2 could be only detected in the stem tissues.
The valley in the middle and lower reaches of the Yarlung Zangbo River , and the basins in Nujiang River, Lancangjiang River and Jinshajiang River on the north of the Hengduan Mountains in Changdu are the main fruit production areas in Tibet . Based on analyzing the current situation of fruit industry, the background of market, climate resources and fruit tree germplasm resources of main fruit production areas in Tibet, the paper provides thoughts on the development of characteristic fruit industry of Tibet , the market aim of which is mainly serving for tourism in Tibet, and suggestion of developing fruit industry. It also marks out the blueprint for sustainable development of the fruit industry.
'Heishuai Yuanqie' is an excellent eggplant hybrid. It has a series of good characteristics: stronger growth, higher setting-fruit ability, excellent merchandise quality and edible quality, higher tolerant to heat temperature, middling and later maturity, Its fruit is ball, purple-dark and full of shine. Its pulp is whiteness, It is delicious. Its seeds is small and few in fruit. It is suitable for Plastic Tunnel and outdoor cultivation in the north of China.