Molecular characterization and expression analyses of an anthocyanin synthase gene from Magnolia sprengeri Pamp.

Anthocyanin synthase (ANS), which catalyzes the conversion of colorless leucoanthocyanins into colored anthocyanins, is a key enzyme in the anthocyanin biosynthetic pathway. It plays important roles in plant development and defense. An ANS gene designated as MsANS was cloned from Magnolia sprengeri using rapid amplification of complementary DNA (cDNA) ends technology. The full-length MsANS is 1171-bp long and contains a 1080-bp open reading frame encoding a 360 amino acid polypeptide. In a sequence alignment analysis, the deduced MsANS protein showed high identity to ANS proteins from other plants: Prunus salicina var. cordata (74 % identity), Ampelopsis grossedentata (74 % identity), Pyrus communis (73 % identity), and Prunus avium (73 % identity). A structural analysis showed that MsANS belongs to 2-oxoglutarate (2OG)- and ferrous iron-dependent oxygenase family because it contains three binding sites for 2OG. Real-time quantitative polymerase chain reaction analyses showed that the transcript level of MsANS was 26-fold higher in red petals than in white petals. The accumulation of anthocyanins in petals of white, pink, and red M. sprengeri flowers was analyzed by HPLC. The main anthocyanin was cyanidin-3-o-glucoside chloride, and the red petals contained the highest concentration of this pigment.

Genome-wide transcriptome analysis of genes involved in flavonoid biosynthesis between red and white strains of Magnolia sprengeri pamp.

BACKGROUND: Magnolia sprengeri Pamp is one of the most highly valuable medicinal and ornamental plants of the Magnolia Family. The natural color of M. sprengeri is variable. The complete genome sequence of M. sprengeri is not available; therefore we sequenced the transcriptome of white and red petals of M. sprengeri using Illumina technology. We focused on the identity of structural and regulatory genes encoding the enzymes involved in the determination of flower color. RESULTS: We sequenced and annotated a reference transcriptome for M. sprengeri, and aimed to capture the transcriptional determinanats of flower color. We sequenced a normalized cDNA library of white and red petals using Illumina technology. The resulting reads were assembled into 77,048 unique sequences, of which 28,243 could be annotated by Gene Ontology (GO) analysis, while 48,805 transcripts lacked GO annotation. The main enzymes involved in the flavonoid biosynthesis, such as phenylalanine ammonia-Lyase, cinnamat-4-Hydroxylase, dihydroflavonol-4-reductase, flavanone 3-hydroxylase, flavonoid-3'-hydroxylase, flavonol synthase, chalcone synthase and anthocyanidin synthase, were identified in the transcriptome. A total of 270 transcription factors were sorted into three families, including MYB, bHLH and WD40 types. Among these transcription factors, eight showed 4-fold or greater changes in transcript abundance in red petals compared with white petals. High-performance liquid chromatography analysis of anthocyanin compositions showed that the main anthocyanin in the petals of M. sprengeri is cyanidin-3-O-glucoside chloride and its content in red petals was 26-fold higher than that in white petals. CONCLUSION: This study presents the first next-generation sequencing effort and transcriptome analysis of a non-model plant from the Family Magnoliaceae. Genes encoding key enzymes were identified and the metabolic pathways involved in biosynthesis and catabolism of M. sprengeri flavonoids were reconstructed. Identification of these genes and pathways adds to the current knowledge of the molecular biology and biochemistry of their production in plant. Such insights into the mechanisms supporting metabolic processes could be used to genetically to enhance flower color among members of the Magnoliaceae.

[Soil respiration characteristics in the clear-cutting site of Quercus aliena var. acuteserrata forest in Xiaolong Mountain in Qinling Mountains].

By using Li-6400 portable photosynthesis system with soil chamber, the soil respiration rates (Rs) of Quercus aliena var. acuteserrata forest land (control site) and their clear-cutting site were measured in Xiaolong Mountain of Qinling Mountains from May 2011 to April 2012 to understand the diurnal and monthly dynamics of soil respiration rate and the influences from soil temperature, soil moisture, soil physical and chemical properties. The results showed that both diurnal and monthly dynamics of soil respiration rate presented a single-peak curve, similar to the variation of soil temperature at the clear-cutting and control sites. During the study period, the maximum monthly mean values of soil respiration rate at the clear-cutting and control sites occurred in July (4.63 and 4.01 micromol x m(-2) x s(-1), respectively) and the minimum values presented in February (0.10 and 0.30 micromol x m(-2) x s(-1), respectively). Soil respiration rate in 4-6 months after clear-cutting was higher than at the control site, and became lower afterwards. 89. 6% -90. 8% of soil respiration rate variation was interpreted by the multiple regression models of soil temperature, soil moisture and their interaction at the clear-cutting site, and 94.7%-95.5% at the control site. The Q10 values computed by exponential equations were 3.47-4.22 and 3.54-3.96 at the clear-cutting and control sites, respectively. The C fluxes at the clear-cutting and control sites were 344.8 and 512.9 g x m(-2) annually, and 24.2 and 40.9 g x m(-2) in winter, respectively.

[Carbon sequestration of young Robinia pseudoacacia plantation in Loess Plateau].

In order to understand the carbon sequestration of ecological forests in Loess Plateau, a comparative study was made on the organic carbon density (OCD) of soil, litter, and plant organs in an 8-year-old Robinia pseudoacacia plantation and nearby barren land. Comparing with the barren land, the young R. pseudoacacia plantation had a decrease (0.26 kg x m(-2)) of soil OCD, but the OCD in its litter, root system, and aboveground organs increased by 121.1%, 202.0%, and 656. 7%, respectively, with a total carbon sequestration increased by 3.3% annually, which illustrated that R. pseudoacacia afforestation on Loess Plateau had an obvious positive effect on carbon sequestration.