Soil nutrient distribution and imbalance were studied in the root zone of 0~80 cm layer and far from the trunk 0-200 cm in Weibei highland orchard, while the replant diseases of potted apple plants were analyzed. Results indicated that soil nutrients advanced along with increasing of the tree root base distance in level distribution;In vertical direction,other soil nutrients dropped along with deepening of the soil layer except for available Ca and Mg. Available P, Ca, Mg, Zn, Mn were deficit in orchard soils and N/P, K/P, Ca/P, Ca/Mg, Ca/Mn, Ca/Zn were imbalance in the root zone. The average of replant plant height, shoot length and rough, leaf area and root-activity were reduced 44.93%,34.46%,23.88%,49.48% and 11.40% separately, which represented replant disease evidently, and which aggravated follow comply with deepening of the layer and lighten as far from the tree trunk in orchard. To sum up, deficiency of Zn and imbalance of Ca/Zn were one of main factors to cause replant diseases; The replant diseases were lighter relatively in the zone of 0~40 cm layer and far from the trunk 100-200 cm, where Soil nutrients were concentrated, which will provide some reference to solve replant diseases in old orchard.
‘Selva’ strawberries (Fragaria×ananassa) were used to study the effects of the mechanism of anthocyanins and flavonols. 12 anthocyanins and 7 flavonols were detected in 'Selva' fruits. The results showed that no anthocyanins were accumulated while abundant flavonols were synthesized in young fruits 15 to 25 days after full bloom. Thereafter, the anthocyanins increased continuously with the fruit development. On the contrary, the content of flavonols in fruits was decreased. Shading reduced fruit anthocyanins and flavonols by 70%~90%, particularly cyanins and quercitrins by 90%. These results may imply that the accumulation of anthocyanins and flavonols were restrained by shading in strawberry, and the light effects on cyanidin and quercetin were greater than on pelargonidin and kaempferol. Two major biosynthates were found in the pathway of accumulating anthocyanins, they were dihydroquercetin at the stage of young fruit and pelargonidin at the stage of mature fruit.
28 accessions of trifoliate orange (Poncirus trifoliata Raf.), hybrids and seven accessions of its relatives, were analyzed for genetic diversity and phylogenetic relationship using nuclear and chloroplast SSR markers. Average PIC (Polymorphism Information Content) value of 0.51 and average expected heterozygosity of 0.52 were given according to nuclear SSR results. 22 common trifoliate orange accessions could be divided into four groups with a genetic distance of 0.16. It indicates a rich genetic diversity of China trifoliate orange germplasm. cpSSR revealed no difference among common trifoliate orange accessions which indicates a relatively conservative chloroplast genome. Four cpSSR loci were found different between Fumin(P. polyandra S. Q. Ding et al.)and common trifoliate orange. Fumin trifoliate orange is genetically distant from common trifoliate orange, from its hybrids as well as relatives. It therefore could be regarded as a true species. The combined application of nuclear and chloroplast SSR could serve a more accurate way to identify trifoliate orange hybrids.
Malate, ubiquitously existing in plant, plays a crucial role in various metabolic pathways, including respiration, nitrogen fixation, phosphorus acquisition, and aluminum tolerance. Malate dehydrogenase(MDH) catalyzes the interconversion of oxaloacetate and malate. Previous results suggested that overexpressing MDH gene transgenic plants elevated tolerance to aluminum toxicity. Citrus junos, one of main rootstocks of citrus fruits, is widely used in the Southern of China. As most of soils are acid in the south, to investigate the mechanism of tolerance to aluminum in citrus plants, a clone referred CjMDH (Genbank Accession No. ABI75147) was isolated from the cDNA library of root from Citrus junos cv.Ziyang. CjMDH has an open reading frame (ORF) of 1 269 bp encoding a putative protein with 412 amino acid residues, which shows high identity to other MDHs in plants. The deduced protein contains a NAD binding site and eight malate binding sites. Chloroplast transit pepite is found in N-terminal of CjMDH through iPSORT software. BlastP analysis result reveals over 80% identity and 85% similarity with Arabidopsis thaliana, Nicotiana tabacum, Glycine max, Medicago sativa. Amino acids comparison between CjMDH and other plants MDH reveals highly identity in NAD and malate binding site. Southern blot suggested that CjMDH is a single copy gene in Citrus junos genome. Northern blot and Real time RT-PCR data indicated that CjMDH expressed strongly in root and leaf, especially highest in root than leaf and stem. Subsequently, the CjMDH was constructed into over-expression vector driven by constitutive CaMV35S promoter. The construction was introduced into tobacco mediated by Agrobacterium tumerfaciens, the overexpression transgenic tobacco lines were obtained through Northern blot. Transgenic lines increased Al-tolerance in hydroponic culture, providing evidence that MDH is a potential Al-tolerance gene for plant in acid soils.
The method to construct Chinese Cabbage core germplasm based on four types of sampling proportion methods in group, six overall sampling scales and two sampling methods were studied in light of 1 651 accessions of Chinese cabbage germplasm and their data of 43 morphological characters in the national medium-term genebank of vegetable germplasm resources. The main results were as follows: The best proper sampling proportion within group was based on index of genetic diversity which enabled the sampled number or proportion from different groups tend to balance, and better maintained the variability of original collection .The index of genetic diversity of the core germplasm established according to the method of genetic diversity index proportion reached maximum and the ratio of phenotypic retained reached 98% when the overall sampling scale increased to 15%. Although the proportion of phenotypes retained nearly 100% and phenotypic variability changed little, the genetic diversity index of the core germplasm decreased accordingly when the overall sampling scale increased to over 20%. So 15% of the overall sampling sizes were more appropriate. In certain sampling proportion method and sampling scale, I, RPR and CV of the core germplasm constructed by cluster sampling was much higher than that by random sampling. Based on the optimized sampling scheme, the Chinese cabbage core gernplasm of 248 accessions of Chinese cabbage gernplasm were established.
Podosphaera xanthii (DC.)VP Gelyuta race 2F caused melon (Cucumis melo L.) powdery mildew was the prevailing race in Beijing. The segregation of resistance had been evaluated in F2S6 population of the cross between the resistant Japanese cantaloupe(Cucumis melo L. ssp. melo.convar. cantalupa (Pang.) Greb.)line K7-1 and the susceptible Xinjiang Hami melon(Cucumis melo L. ssp. melo. convar. ameri (Pang.) Greb.)line K7-2. The resistance to P. xanthii race 2F in K7-1 was controlled by one single dominant Pm-2F gene. SSR technique had been used for the identification of markers linked to powdery mildew resistance. Two specific fragments CMBR120-172 and CMBR8-98 were closely linked to Pm-2F gene at a distance of 1 cM and 3 cM, respectively. The efficiency of CMBR120-172 was about 87.5% in 120 melon germplasms. The markers identified in this experminent were closest to Pm-2F gene to date, and the research, therefore, can be used in melon molecular breeding.
Gynogenic embryos originating from unpollinated ovary culture were cultured on differentiation medium to induce homozygous autotetraploid cucumber. In total, thirty-three plantlets were regenerated, and seven were observed as autotetraploid (2n=4x=28) after chromosome counts. These autotetraploid plants were identified as homozygote after simple sequence repeat (SSR) analysis. Genetic stability of the progenies from self-crossing of these autotetraploid was studied, no ploidy variation occurred among these progenies after morphology and chromosome observation. Comparative studies were carried out between autotetraploid plants from ovary culture and autotetraploid plants from colchicines treatment, using parameters i-e, stainability of pollen grains, viability of pollen grains and number of seeds per fruit. Higher pollen fertility and number of seeds per fruit were found in the gynogenic induced autotetraploid plants. These results indicate that it is a method to induce autotetraploid through unpollinated ovary culture, and the obtaining of homozygous autotetraploid with higher fertility will be quite useful in cucumber breeding programs.
In order to provide inducible promoter for chrysanthemum [Dendronthema ×grandiflora (Ramat.) Kitam.] transgenic breeding, referring to the strategy of 5′RACE, four promoter sequences of betaine aldehyde dehydrogenase (BADH) gene from Dendranthema lavandulifolium (Fisch. ex Trautv.) Makino were cloned by anchored PCR walking, which were named DBP11, DBP12, DBP21 and DBP22 (GenBank accession No. DQ497620~DQ497623). The four sequences are 1 230 bp, 1 249 bp, 1 273 bp and 574 bp long respectively. The homology of the corresponding regions between every two sequences is above 89%. DBP12 and DBP21 are the promoters of DlBADH1 and DlBADH2 (GenBank accession No. DQ011151 and DQ011152), DBP11and DBP22 are the promoters of other members in BADH gene family from Dendranthema lavandulifolium. Many cis-acting elements related to water stress and ABA inducement were found in all the sequences. New expression vectors were constructed by replacing the 35S-CaMV promoter with the above promoter sequences to drive the reporter gene GUSplus of the expression vector pCAMBIA1305.2. The new vectors were transferred into Agrobacterium to infect leaf disks of Dendranthema lavandulifolium. The result of transient expression indicated that all the sequences had the function to drive reporter gene.
In the winter of 2007, a new virus disease on tomato broke out in Jiangsu and caused great losses to local tomato production. The infected tomato showed severely stunted, upward curling and prominent yellowing along margins and interveinal regions. Based on its symptoms and the occurrence of Bemisia tabaci in the fields, Whitefly-transmitted geminivirus (WTG) was suspected to be the pathogen, and WTG was identified in all the 20 samples. The nucleotide sequence identities between these isolates were extremely high (over 98.9%), which means no complex infection was found. The result of BLAST revealed they shared high sequence identities (over 99%) with a member of Begomovirus: Tomato yellow leaf curl virus (TYLCV).
This studies were carried out to investigate dynamic changes in ultraweak luminescence (UWL) intensity, respiration rate, contents of ATP, soluble sugar and soluble protein of chrysanthemum leaves during floral differentiation. The results showed that the UWL intensity increased 119.3%, respiration rate increased 102.4%, contents of ATP, soluble sugar and soluble protein increased 148.6%, 95.5%, 18.3% respectively at initial stage of floral bud differentiation (II) compared with those of vegetative stage of apical bud (I), and then UWL intensity, respiration rate and contents of ATP reduced slowly respectively at stage of involucre primordial differentiation (III), stage of floret primordial differentiation (IV) and stage of crown form (V). Contents of soluble sugar decreased mostly at stage IV and stage V, and the levels neared to those of controls. Contents of soluble protein maintained higher levels at stage II, stage III, and stage IV, decreased mostly at stage V, but it still increased 14.0% compared with those of controls. But all of UWL intensity, respiration rate, and contents of ATP, soluble sugar and soluble protein maintained stable status in all stages of controls of non-short day treatments. This suggested that the UWL has close relation to respiration and energy metabolism of leaves during differentiation of chrysanthemum.
In order to study the reduce of dependence on peat and cost in the soilless culture of flowers, the effects of experimenting different mixing substrates, taking sawdust, corn stalk and wheat-straw as the primary growing media of Euphorbia pulcherrima were investigated. The results indicated that the physical and chemical characteristics of the two treatments V(corn stalk):V(sawdust):V(perlite)2:1:1, and V(wheat-straw):V(sawdust):V(perlite)1:2:1 satisfied the general requirements of growing media. Not only the roots of Euphorbia pulcherrima in those treatments were robust, the comprehensive performance of growth and development were also significantly better than that in control. Thus, the treatments can be good substitutes as soilless growing media of Euphorbia pulcherrima.
Lily mottle virus(LMoV)was detected in Narcissus pseudonarcissus using one set of specific primer by reverse transcription-polymerase chain reaction (RT-PCR). A 553bp DNA fragment was amplified from the sample of ‘Pink-charm’ using primers L1 (5'-TGGGCACCTTGTGAATTAC-3') and L2 (5'- TGCTGTATGCCTCTCCGTGC-3'). The primer was designed according to the published sequence of the coat protein of LMoV in the GenBank. Nucleotide sequence of the fragment(GenBank Accession No. EU167936)showed more than 98% identity with other isolates(GenBank Accession Nos.:AJ748256;AJ564636;AB053256;AF531458;AJ564637;AJ748257). Remarkably high Similarity in the nucleotide has been observed despite of their different origins. Besides, amino acid sequence of the amplified virus fragments(GenBank Accession No. ABW16938)is overlapped by the amino acid sequence of LMoV Coat protein(GenBank Accession No .NP-945145).