Histone Deacetylases gene MdHDA19（MDP0000132078）was cloned from‘Gala’apple. Its ORF was 1 494 bp，which encoded 497 amino acids. The molecular mass of this protein was 55.73 kD，and pI was 4.98. The phylogenetic tree indicated that the HDA19 had sequence conservation among different species. MdHDA19 exhibited the highest sequence similarity with Theobroma cacao TcHDA19 （87.05%）. The MdHDA19 gene was expressed in all the tissues of apple，especially in root and flower. The MdHDA19 interacted with MdSAT18. The NaCl stress induces the expression level of MdHDA19. MdHDA19 might involve NaCl stress response. The resulted showed that MdHDA19 gene was induced in low temperature（4 ℃）and high temperature（40 ℃）. In addition，the MdHDA19 recombinant protein was obtained. The results established the foundation for the further functions research of MdHDA19 protein.

It is one of the key practices for the high efficiency mode of apple production to properly select and combine scion and rootstocks. Flower formation and plant shaping of apple sapling are the important indexes to evaluate their performances，which was closely related to the root distributions with these combinations. With three year young trees from 8 kinds of typical scion-rootstock combinations as its subjects，this study investigated root distributions with the different scion-rootstock combinations by sectoral digging and trenching. The results showed that：the root architecture of young trees from 8 kinds of typical scion-rootstock combinations were classified into five types，M dwarfing rootstock combinations，SH dwarfing rootstock combinations，vigorous rootstock combinations，M dwarfing interstock combina- tions and SH dwarfing interstock combinations. It showed that the roots of the apple saplings with three years distributed horizontally and vertically within the limits of 0–60 cm，and the further away from their trunks and the deeper into soil，the less dense they distributed. With the different scion-rootstock combinations，the longest roots were roots with diameters of < 2 mm，followed by roots with diameters of 2–5 mm，and the shortest roots were those with diameters of more than 10 mm. There were more thick roots and less fibrous roots with the arborescent seedling root stocks than with the dwarfing clone rootstocks. Among the dwarfing rootstocks，fibrous roots dominated with the M rootstocks and less with the SH and Qingzhen rootstocks. Of the trees，stem diameters and crown diameters，but significantly positively correlated with the branch number，short-shoot proportion and flower bud number. Evaluations of the scion-rootstock combinations in terms of flower formation and plant shaping indicated that in irrigation-available regions of the Weibei Highlands，the trees from the M rootstock and interstock were able to set fruits early and easy to shape；the trees from the SH rootstock were easy to shape and poorly performed in early fruit set；and the trees from the arborescent combinations performed most poorly in early fruit set，which was closely related to the root distributions with these scion-rootstock combinations.

Direct tissue blot immunoassay（DTBIA）was developed to detect Citrus yellow vein clearing virus（CYVCV）by exploring the optimal dilution of rabbit-anti-CYVCV polyclonal antibody （first antibody）and Alkaline phosphatase（Ap）conjugated goat-anti-rabbit IgG（secondary antibody）. The DTBIA was the most effective when the first antibody and secondary antibody diluted in 8 000 and 2 000 separately. Using the method，only CYVCV infected samples showed positive among detected samples associated with different citrus diseases；CYVCV could be effectively detected in 90 days after the tissue blotting membranes kept at 4 ℃. The consistency between DTBIA and one-step RT-PCR was 97.92% in CYVCV detection of citrus varieties. The results showed that the DTBIA method is rapid，simple，stable，specific and reliable，and can be applied for rapid detection of CYVCV in the field，which providing the important practical significance for control of the transmission of citrus yellow vein clearing virus and spreading of the disease widely.

Transgenic orchid(Phalaenopsis CV．White Hikaru)plants were regenerated by inoculating a
needle wounded protocorm．1ike body (PLB)with Agrobacterium tumefaciens strain LBA4404 harboring
pCAMBIA 1300-SmGFP that carries green fluorescent protein gene( )and hygromycin phosphotransferase
gene( f)．The expression and presence of the transgenes， and f were assessed by detection of green
fluorescent protein under microscope and Southern analysis，respectively．

The effect of DNA methylation inhibitor ( 5-azacytidine, 5-azaC) to chrysanthemum (Dendranthem a ×grandiflorum ) has been studied by the method of in vitro treatment. The results indicated that 500μmol·L - 1 of 5-azaC caused death, above 100μmol·L - 1 of 5-azaC inhibited the materials’development. The multiple buds differentiation of chrysanthemum was inhibited by every concentration of 5-azaC and the inhibiting effect of 5-azaC has time and dose additive effect. 5-azaC treatment at low concentration induced
the flowering early, this effect were stability and could be inherited through asexual multiplication. The results of MSAP (methylation sensitive amplified polymorphism technique) indicated that, the genomic of treated materials DNA methylation decreased distinctly. Part of the sites kept demethylation status in the successive transfer culture when 5-azaC removed.

The presence ofRNA molecules in plant phloem sieve elements which can do long-distance transport is an important discovery in plant kingdom. And it has been discovered that there are three kinds of RNA molecules in phloem sap including exogenous viroids or virus RNA，plant endogenous mRNA and small non-protein-coding RNA（snRNA）. Long-distance transport of RNAs in phloem sap can function as signal molecules in mediating plant growth and development. In this paper，the methods of how to collect phloem sap，the RNA molecules in plant phloem sap and the signaling pathways as well as the mechanisms by which how they are transported are discussed and summarized.

The effects of cadmium (Cd)（5、15、30 mg·L^-1）on chlorophyll levels and photosynthesis of cauliflower (Brassica oleracea L. var. botrytis) were studied under different concentrations of Cd using hydroponics system. Meanwhile, the differential centrifugation techniques and sequential extraction methods were used to determine the subcellular distribution and chemical form of Cd in leaves. Cd contents in different parts of plant were also measured after harvest. The results showed that, after different contents of Cd were supplied for two weeks, except intercellular CO₂ concentration(Ci), the levels of chlorophyll a and b, net photosynthesis rate(Pn), stomatal conductance(Gs) and transpiration rate(Tr) all decreased significantly compared with the control. For the leaves, Cd was mainly distributed in the fractions of cytoplasm(70.19%－74.40%) and cell wall (22.56%－27.12%), and less distributed in the fractions of mitochondrion and chloroplast(0.90%－2.49%). The sequential extraction results of Cd in leaves indicated that NaCl extractable Cd was predominated (33%—39%), and the distribution of six Cd forms in leaves was as following: F _NaCl > F_H2O> F_HAC> F_Alcohol> F_HCL> FResidue. Most of Cd absorbed by plant was accumulated in roots, little of them was transported to the aboveground portions. The order of Cd accumulation in different plant parts was: roots>stems, leaves>flowers.

In this study, the extraction efficacity of solvent type and precision of determining-methods for anthocyanins in fruits were compared. Five solvents, acetone:water:formic acid (A), acetonitrile:acetic acid (B), ethanol:water:acetic acid (C), methanol:water:acetic acid (D), and methanol:HCl (E) were used to extract anthocyanins in strawberry and blueberry fruits and the anthocyanin content in the extracts was determined with colorimetry and HPLC. The results showed that extraction efficiency varied among the solvents with different organic-solvent and acid-type. In strawberries, the extraction efficiency of anthocyanin with D was best, followed by E, C, and A. However, B was the worst to extract the anthocyanin, with its value being less than 1/3 that obtained using the extract containing D. A similar tendency was found in blueberries. The anthocyanin contents determined by colorimetry with extracts containing D, E, and C in both fruits were respectively lower than that shown by HPLC. But, the value was obtained by colorimetry with extracts containing B was 2-fold to that by HPLC. In blueberries, obvious differences were not found in the results obtained using the extract containing A employing both methods, although in strawberries the anthocyanin content determined using the spectrophotometric method was higher by about 50% than with those obtained using HPLC. These results suggest that the HPLC method should be utilized to determine the anthocyanin content and that the colorimetry could be used to compare samples from the same kind of fruit, especially, using a low boiling-point alcohol as a solvent.

This article has summarized Rhododendron germplasm resourses and research progress on breeding objectives of Rhododendron around the world，involved in colour，florescence，fragrance，resistance. In the end，the development of breeding techniques，especially cross and genetic engineering，is reviewed. Crossbreeding is still the key method for Rhododendron breeding and molecular biology will be highlighted in the future.

Marker-assisted selection significantly facilitates breeding of new resistant grape varieties，which is widely used in recent years. In addition，with identification and isolation of more and more resistant genes from grape，genetic modification for disease resistance has obtained some preliminary achievements. Progress and achievements of molecular breeding for grape disease resistance have been reviewed. Meanwhile，the problems present was also analyzed and discussed.

The anthocyanins biosynthetic pathway and its influence factors，related regulation genes were summarized in this paper.

At present，10 complete genome sequences are available for fruit trees such as grape，
papaya，apple，banana，pear and sweet orange. In this review，we first surveyed the historical development
of genomic sequence of fruit trees. Then we investigated the evolution history of fruit trees，and
summarized the progress of fruit trees post-genomic research. Challenges in genomics for fruit trees are
raised and the future of post-genomics research interests in fruit trees was discussed in the end.

The concept and classification of the colored-leaf plants and the research progress on the leaf color emergingmechanisms were presented in the paper. We also summarized the environmental effects on leaf color and the progress of the photosynthetic characteristics in colored2leaf p lants. At last, some constructive suggestions about further research emphasis of the colored-leaf plants were discussed.

Terpenoids are important secondary metabolites in plants，which have important physiological and ecological functions as well as economic values. The terpene synthases including monoterpene synthases，sesquiterpene synthases and diterpene synthases，are critical enzymes for the formation of terpenoids. The metabolism of terpenes is characterized with tissure-specificity，which is regulated by developments and by biotic and abiotic factors as well. In addition，the components and contents of terpenoids in transgenic plants can be altered，to some extent，by using genetic engineering. This review mainly summarizes the recent research progress in structure，classification and metabolism of terpene synthases. The regulation of terpene metabolism is also discussed.

Citrus Huanglongbing（HLB），caused by Candidatus liberibacter，is the most devastating disease of citrus for which no cure has been found. Almost all known citrus varieties including those from their closely related genera can be infected by the bacteria. HLB has been a hot topic of citrus researches
since the disease was discovered in America. In this paper，we are trying to summarize generally the recent advances in the researches of HLB pathogen and pathogen-host interactions. Topics on HLB control and breeding for HLB-resistant/tolerant citrus materials were also touched.

Flowering is the transition from vegetative growth to reproductive growth in plants. Flowering-related gene expression is the basis for achieving this transition. Environment factors and the growth conditions of plant cells on the expression of these genes play regulatory roles. Now, it has been
known that photoperiod stimulation signal was received and apperceived by mature leaves of plants and there are produced flowering signal substances in the mature leaves of plants, and that this kinds of flowering signal
substances transports from leaves to the top of stems, and ultimately causes flowering using model plants Arabidopsis, rice and ornamental plants petunia and Antirrhinum. This article reviewed the study progress in the molecular mechanisms of controlling flowering of plants, in order to provide references for further in-depth studies of photoperiodic flowering molecular mechanism of ornamental plants.

MdWRKY gene family，gene classification，chromosome location，sequence alignment and conserved structure domains of MdWRKY proteins were predicted and analyzed with bioinformatics methods，alignment of amino acid sequences and phylogenetic analysis. The amino acid sequences of the WRKY domain of all MdWRKY and possible orthlogs in Arabidopsis were aligned with Clustal W and the phylogenetic analysis tree was constructed using the neighbor-joining method in MEGA 5.0. The results showed that MdWRKY family contained 116 genes，which was further divided into three groups（GroupⅠ，GroupⅡ and Group Ⅲ）. In addition，members in GroupⅡ can be further divided into five sub-groups（from Ⅱa to Ⅱe）. A total of 112 MdWRKY genes were mapped to 17 chromosomes，whereas only 4 MdWRKY genes were not mapped to any particular chromosome. For example，Chr 1 encompasses the largest number of 12 MdWRKY genes，while the lowest number（Chr 14）contained 2 MdWRKY genes. MdWRKY proteins contained from 118 to 965 amino acids and the isoelectric point is from 4.81 to 10.16. Expression analysis showed that the expression levels of most MdWRKY genes were altered during the ripening process and rootstock-scion interactions process.

Glucosinolate is a group of important bioactive compounds found mainly in the cruciferous family. About 120 natural glucosinolates have been isolated, and they are known to have various functions and bioactivities such as anticarcignogen, plant defense, and flavour2forming. The distribution and biochemical property, glucosinolate breakdown products, and their biological effects are reviewed in this paper.

The experiment studied on the Polyphenol oxidase ( PPO) extracted from Pingguoli Pear. Thechange of PPO activity and characteristics showed that the optimal pH of PPO is 4. 6, and optimal temperature is 40 ℃. The inhibition of the inhibitors is in the following order : sodium bisulphate, Vitamin C, citric acid, sodium sulfate. The effect of different zymolyte or different zymolyte concentration on PPO were studied.

To research the energy-saving and high-efficiency lighting parameters suitable for lettuce growth，LEDA and LEDB lighting were used. LEDA lighting was composed of red with peak at 660 nm（R）and blue with peak at 450 nm（B），LEDB lighting was composed of red with peak at 630 nm（R）and blue with peak at 460 nm（B）. Treatments with R/B ratio of 6，8，10 were performed with LEDA and 　　 LEDB respectively. Results showed that photosynthetic rate of lettuce was significantly higher under LED lighting than under fluorescent lamp. There were no significant differences in photosynthetic rate，transpiration rate，stomatal conductance，intercellular CO2 concentration，vitamin C，total sugar and nitrate content of lettuce between LEDA and LEDB. All those indices showed the same change trend with R/B，and they were the best at the R/B ratio of 8（LEDA2，LEDB2）. Compared with fluorescent treatment，photosynthetic rate and vitamin C content increased 38% and 8.3% respectively，while nitrate content decreased 9.2% in LEDA2 treatment，and photosynthetic rate increased 48% and nitrate content decreased 6.5% in LEDB2 treatment. The content of chlorophyll a，b and（a + b）were significant higher under LEDA lighting than under LEDB lighting，and were the highest under LEDA3 and LEDB2 treatments，respectively. In addition，results of power consumption of lighting device showed，compared with LEDA lighting and fluorescent，the power consumption per plant of LEDB lighting decreased 53.3% and 27.2%，respectively. Thus，LED lighting composed of red with peak at 630 nm and blue with peak at 460 nm，while R/B = 8，not only could improve photosynthesis rate and quality，but also is more energy-saving than other treatments. The aim of efficient and energy-saving was achieved from above three aspects.