Changes of respiratory rate and glycolytic end products in brown lignified roots of sweet cherry, Meizao/Dongbei Shanyingtao(Prunus serrulata G.Don) and Meizao/Mahaleb(P. mahaleb L.), were studied under waterlogging conditions. The results indicated that root respiratory rate of two kinds of rootstocks, Dongbei Shanyingtao and Mahaleb, decreased gradually, and dropped to 73.86%and 80.71%, respectively, after treatment for 120 h. Content of acetaldehyde and ethanol increased obviously. The acetaldehyde content of Mahaleb was higher than that of Dongbei Shanyingtao, while the ethanol content was lower. The pyruvate content of Dongbei Shanyingtao increased initially and then decreased, but that of Mahaleb didn't change much. The content of lactate and succinate in roots of the two kinds of rootstocks increased at first and then decreased, and Dongbei Shanyingtao peaked earlier and higher than Mahaleb. The malate content of Dongbei Shanyingtao more than Mahaleb. The alanine content increased and Mahaleb was higher than that of Dongbei Shanyingtao. Content of aspatate and glutamate decreased obviously and that of Meizao/Mahaleb decreased more. The proline content increased at first and then decreased, and Mahaleb reached the maximum later and proline content was much higher that of Dongbei Shanyingtao. These results suggested that the response of the two kinds of sweet cherry rootstocks to waterlogging was different. Since its respiratory rate decreased more rapidly, and intracellular alkalization ability was lower, Dongbei Shanyingtao is more sentitive to waterlogging than Mahaleb.
PCR were applied for point mutagenesis of MxIRT1 gene. Two pairs of primers were designed according to the Opening Read Frame (ORF) and sequence for mutation of MxIRT1. Two fragments overlapping at the target mutated base were amplified by PCR. The fragments were amplified after dilution with the primers designed with the two ends of ORF, and the two mutated fragments were stringed together. The annealing temperature and extension time were optimized for successful amplification. The mutated MxIRT1 were ligated into pEASY-T2. Sequencing result showed that we mutated MxIRT1 successfully. DNA recollection and purification were not necessary for this experiment. We establish an efficient, simple gene mutagenesis system.
Virus-induced gene silencing (VIGS) is a recently developed technique for gene function studies in plants. In this study, the gusA transgenic tomato plant which constitutively expressed gusA gene was used as material. The gusA gene was silenced by VIGS for the preliminary tissue specificity analysis of VIGS in tomato. The results showed that gusA could be silenced in leafs, flowers, fruits, branches, stems and the points between branch and stem of tomato by virus-induced gene silencing. So VIGS as a powerful tool for the study of gene function could induce target gene systematic silencing in tomato.
Studies on the cell ultrastructure and calcium distribution during tomato pedicel abscission by using scanning electron microscopy and antimoniate precipitate calcium electromicroscopic cytochemical methods. Those enabled us to document that the abscission was initialed in cortex and cellule around vascular bundle in which appearance two inconsecutive cell interspaces, later the cell interspaces of vascular bundle forming consecutive separation parts gradually. As the abscission procession, separation parts were extended to middle of abscission plate, then vascular bundle ruptured, and the marrow tissue and outer epidermis separated latest .Ca2+ location analysis showed that before abscission calcium iron mainly concentrated within vascular and vacuole, cell wall and cell membrane of cortex and marrow. After abscission there was mass calcium deposition in vascular bundle, when marrow separated, calcium grain mainly in degraded cell wall and intercellular space, little detected in cytoplasm. In abscission there were great difference of calcium location and contents between cortex, vascular and marrow which would be mainly caused for different separation procession of the abscission zone tissue.
Based on the observation of species in Chirita and Chiritopsis which were collected from Guangxi Karst hills and areas in the neighborhood, we had analysed and evaluated according to their ornamental characterstics. Twenty nine species and three varieties were screened out from 60 species and 4 varieties in two genuses because of their higher ornamental promising and value.
The interspecific cross was attempted between different species/cultivars of different ploidy in Dendranthema genus. The compatible index were calculated in different interspecific crosses. In addition, pollen adhesion, pollen germination, pollen tube growth, fertilization and ovary development were observed under fluoroscope. The results showed that seed-set was easily obtained from interspecific cross between the species of same ploidy or those between the tetraploid and hexaploid. However, few seed-set was obtained from the interpecifc cross between diploid and tetrapoliod or hexaploid species, i.e., incompatibility was observed. The incompatibility of interspecific cross was characterized by low pollen adhesion, low pollen germination rate, abnormal pollen tube hampered extension on the stigma, calloses deposit on the stigma and collapsed ovary.
Effects of Ca(NO3)2 under different concentrations on rooting and activities of superoxide dismutase (SOD), peroxidase (POD) and catalase (CAT) and ascorbate peroxidase (APX), and malondialdehyde (MDA) content in the leaves of cuttings of Dendrandema grandiflora 'Wangsheng' were studied. The results showed that the root number was the highest in 60 mg·L-1 Ca2+ treated cuttings with significant increase in fresh and dry weights of the cuttings compared to the controls. But root number, fresh and dry mass and rooting rates decreased at 80 mg·L-1 Ca2+. In 60 mg·L-1 Ca2+ treated plants, the activities of SOD, POD, CAT and APX increased and MDA content decreased significantly compared with other plants. These results indicated that Ca2+ treatments at proper dosage might enhance rooting of cuttings by increasing the activities of antioxidant enzymes and decreasing membrane lipid peroxidation during rooting in the cuttings of D. grandiflora.
Effect of N, P and K fertilization on Calenduld officinalis L. growth and suitable fertilizer formula of NPK nutrients ratio for the flower was carried out through pot experiment with "3414" incomplete regression-orthogonal design. Our results showed that the N and P played important role in vegetative and reproductive growth. The effect of K was mainly reflected in late growth stage. There is a obvious positive interactions of N and P. Regarding total flowers, functional leavers, plant height and dry weight as the target, it was showed that the recommended fertilizer amount of N, P2O5 and K2O for pot application were 0.4, 0.2 and 0.3 g·kg-1 (each pot filled with 2 kg substrate) .
Content of mineral elements, sugar and acid components of fruits in 2 intraspecific populations(Gongliu and Xinyuan County in Ily State) of M.sieversii from 88 seedlings were studied, as well as their contents comparison to 3 M.domestica cultivars (Fuji, Golden delicious, Starimson).The results indicated that variation coefficients of mineral elements(Ca, Mg, Fe, Cu, Mn, Zn), sugar components(fructose, glucose, sucrose) and malate in M.sieversii seedlings were more than 23%, which revealed rich genetic diversity. The content of Ca in M.sieversii was 3.1 times of that in M.domestica and the sugar composition in M.sieversii was significantly different to that in M.domestica.
This study analyzed Malus xiaojinensis Cheng et Jiang, apple trees were similar to Malus xiaojinensis Cheng et Jiang differentiated from M. toringoides Hughes, M. toringoides Hughes×M. kansuensis Rehd, M. kansuensis Rehd, M. toringoides Hughes by AFLP to explore the origin of M.xiaojinensis Cheng et Jiang. There were high degree of genetic identity among M.xiaojinensis Cheng et Jiang, apple trees were similar to M. xiaojinensis Cheng et Jiang differentiated from M. toringoides Hughes and M. toringoides Hughes×M. kansuensis Rehd, and their genetic similar coefficient were from 0.977 to 0.986. M. xiaojinensis Cheng et Jiang, meanwhile there were 98.08% bands of M. xiaojinensis Cheng et Jiang were from M. kansuensis Rehd and M. toringoides Hughes. The results showed that M. kansuensis Rehd and M. toringoides Hughes had close relationship. According to the AFLP analysis and previous researchs, we discussed the origin of M. xiaojinensis Cheng et Jiang and proposed that the species may derive from M. toringoides Hughes×M. kansuensis Rehd. Our findings have provided basic research data and important directions for the cultivation and exploitation of the Malus xiaojinensis.
DNA from thirty-eight Cymbidium ensifolium cultivars was examined using polymerase chain reaction (PCR) to determine the efficiency of randomly amplified polymorphic DNA (RAPD) markers in genetic diversity and genetic relationship. A total of 116 RAPD markers, 88.79% of which were polymorphic, were produced from 18 10mer arbitrary primers. Genetic distances among the cultivars were estimated based on the amount of band sharing and ranged from 0.0420~0.5385 with an average of 0.2902. Unweighted pair-group method with arithmetic averaging (UPGMA) of genetic distances estimates grouped 'suxin' cultivars and 'caixin' cultivars together with each other, and 'suxin' cultivars diverged from 'caixin' cultivars, thereby agreeing with known traditional classification information. Four cultivars, 'Minxi Yuchen', 'Yuchen Dagong', 'Yuchen' and 'Yinbian Yuchen' could be distinguished from all the rest based only on the S153-650 fragment, and 'Shiliu Luohan' and 'Yuchen' based only on the S38-1 200 fragment. Cultivar 'Ma′er Siji' could be differentiated from all the rest by lack of the S38-800 fragment.
MADS-box genes play important role in various plant development processes,especially in the development of floral organs.The flowering-related MADS-box gene, named as NTMADS1 (GenBank accession number:EF421828), was cloned from the first strand of N. tazetta var. chinensis cDNA through RT-PCR using primers designed according to the MADS-box gene family conserved region. The fragment was 879 bp long and contained an open reading frame of 693 bp coding a polypeptide of 230 amino acids which had a typical MADS-box domain. Homology analysis showed that the deduced NTMADS1 protein was highly homologous to other MADS-box proteins from different species, especially with Asparagus virgatus to 89%. Phylogenetic tree analysis also indicated that NTMADS1 belongs to AG subfamily.