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R2R3-MYB transcription factors (TFs) form one of the most important TF families involved in regulating various physiological functions in plants. The heartwood of Dalbergia odorifera is a kind of high-grade mahogany and valuable herbal medicine with wide application. However, the role of R2R3-MYB genes in the growth and development of D. odorifera, especially their relevance to heartwood formation, has not been revealed. A total of 126 R2R3-MYBs were screened from the D. odorifera genome and named DodMYB1-126 based on their location on 10 chromosomes. The collinearity results showed that purification selection was the main driving force for the evolution of the R2R3-MYB TFs family, and whole genome/fragment replication event was the main form for expanding the R2R3-MYB family, generating a divergence of gene structure and function. Comparative phylogenetic analysis classified the R2R3-MYB TFs into 33 subfamilies. S3-7,10,12-13,21 and N4-7 were extensively involved in the metabolic process; S9,13,16-19,24-25 and N1-3,8 were associated with the growth and development of D. odorifera. Based on the differential transcriptional expression levels of R2R3-MYBs in different tissues, DodMYB32, DodMYB55, and DodMYB89 were tentatively screened for involvement in the regulatory process of heartwood. Further studies have shown that the DodMYB89, localized in the nucleus, has transcriptional activation activity and is involved in regulating the biosynthesis of the secondary metabolites of heartwood by activating the promoters of the structural genes DodI2'H and DodCOMT. This study aimed to comprehensively analyze the functions of the R2R3-MYB TFs and screen for candidate genes that might be involved in heartwood formation of D. odorifera. [ABSTRACT FROM AUTHOR]

The purpose of this study was to characterize and quantify the chemical constituents of heartwood and sapwood of Dalbergia oliveri extract in order to investigate the chemical components that determine the formation of heartwood's color. In this work, the types of pigments in heartwood and sapwood extract were analyzed using UV-Visible (UV) Spectrophotometer, and the main pigment components of heartwood and sapwood extract were identified and quantified using ultra-high performance liquid chromatography-mass spectrometry (UHPLC-MS). The results showed that the difference in content of the main components between heartwood and sapwood of Dalbergia oliveri was slight, and the lignin structure between heartwood and sapwood is basically identical; flavonoid pigments were found to be the primary chromophoric components of heartwood and sapwood extract. However, a total of 21 flavonoids were identified in heartwood and sapwood, of which the unique substances to heartwood were vitexin, isorhamnetin, and pelargonidin, and the content of isoliquiritigenin, formononetin, and biochanin A were 253, 37, and 583 times higher in the heartwood than in the sapwood, respectively, which could be the main pigment components affecting the significant color difference between heartwood and sapwood of Dalbergia oliveri. These results will provide a foundation for revealing the underlying mechanism of color difference between heartwood and sapwood and provide a theoretical basis for wood coloring. [ABSTRACT FROM AUTHOR]

To analyze the chemical composition and evaluate the potential commercial value of Dalbergia odorifera leaves, the chemical component and content of the essential oils (EOs), fatty acids (FAs), polyphenols and flavonoids in the leaves of D. odorifera were studied. The composition of the EOs obtained by simultaneous distillation extraction (SDE) (at the yield of 0.092%) and hydro-distillation (HD) (at the yield of 0.050%) from D. odorifera leaves was analyzed by gas chromatography-mass spectrometry (GC-MS). Seventy-six compounds were identified and the major compounds were phytol (22.5–24.3%), 4-vinylguaiacol (8.7–12.7%), dihydroedulan II (7.4–11.2%), γ-elemene (5.1–6.2%), cedrol (2.8–6.1%), coumaran (0.9–3.1%) and hexahydrofarnesyl acetone (2.5–2.7%). The FA yield extracted by ultrasound was 1.145% (w/w), and the most abundant FA components were palmitic acid (C16:0), oleic acid (C18:1) and linoleic acid (C18:2) in leaves. The results of the 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2′-azino-bis (3-ethylbenzothiazoli-ne-6-sulfonic acid (ABTS+) radical scavenging experiments demonstrated that the EOs and FAs possess strong antioxidant activity. The ethanol extract of the leaves had a high polyphenol content [16.00 mg gallic acid equivalent (GAE) g−1 dry weight (DW)] and flavonoid content [8.92 mg rutin equivalent (RE) g−1 DW]. This research has determined qualitatively and quantitatively the isoflavonoids (biochanin A, isoliquiritigenin, tectorigenin and genistein) by ultra-performance liquid chromatography-electrospray ionization-tandem mass spectrometry (UPLC-ESI-MS/MS). The phytochemical analysis (EOs, FAs and flavonoids) of the extract showed that the D. odorifera leaf is a rich source of high bioactive compounds and might have the potential to be recommended for further cosmetics, food and pharmaceutical applications. [ABSTRACT FROM AUTHOR]

Heartwood has a high economic value because of its natural durability, beautiful color, special aroma, and richness in active ingredients used in traditional Chinese medicine. However, the mechanism of heartwood formation remains unclear. Dalbergia odorifera was selected as the object of research to analyze this variation in the chemical composition of sapwood, transition zone, and heartwood as well as to elucidate the relationship between this variation and the formation of heartwood. The variation of secondary metabolites was analyzed using gas chromatography-mass spectrometry and ultra-high performance liquid chromatography–mass spectrometry, the variation of lignin was analyzed using Fourier transform infrared spectroscopy and ultraviolet visible spectrophotometry, and the variation law of mineral elements was analyzed using atomic absorption spectrophotometry. The results demonstrated that contents of characteristic secondary metabolites in Dalbergia odorifera were mainly distributed in heartwood (84.3–96.8%), increased from the outer to inner layers of the xylem, and sudden changes occurred in the transition zone (the fourth growth ring). The Dalbergia odorifera lignin can be identified as typical "syringyl–guaiacyl (S–G)" lignin, and the color darkened from the outside to the inside. The results demonstrated that there were more benzene rings and conjugated C=O structures in the heartwood. Additionally, the variation of minerals in the xylem was related to elemental types; the average concentrations of Mg, Ca, Fe and Sr were higher in the heartwood than in the sapwood, whereas the concentrations of K and Zn were higher in the sapwood than in the heartwood owing to the reabsorption of elements. The concentrations of Na and Cu were similar in the heartwood and sapwood. The composition and structural characteristics of secondary metabolites, lignin, and mineral elements in the three typical xylem regions (sapwood, transition zone and heartwood) of Dalbergia odorifera changed. The most abrupt change occurred in the narrow xylem transition zone, which is the key location involved in heartwood formation in Dalbergia odorifera. [ABSTRACT FROM AUTHOR]

Activated carbon fiber was prepared from liquefied wood by chemical activation with ZnCl2 (Z-LWACF) at different impregnation ratios, with a particular focus on its adsorption property, kinetic and isotherm. The characterization and properties of Z-LWACFs were investigated by nitrogen adsorption/desorption, X-ray photoelectron spectroscopy (XPS), methylene blue (MB) and iodine adsorption. Two activation process methods were employed to prepare Z-LWACF and contrasted with others fibers. The results showed that the Z-LWACF obtained by one-step ZnCl2 activation present higher yields and specific surface area than others fibers. Besides, the change of MB adsorption value at different impregnation ratios was consistent with pore structure distribution above 1.5 nm pore size, indicating that larger micropores (1.5 to 2 nm) and mesopores played a major role in the MB adsorption by Z-LWACF. The kinetics of MB adsorption process was found to follow the pseudo-second-order kinetic model and the adsorption rate was controlled by chemisorption. It was also found that MB adsroption by Z-LWACF belonged to monolayer adsorption and Z-LWACF was easy to adsorb MB. [ABSTRACT FROM AUTHOR]