Chiral metal–organic frameworks (MOFs) have aroused great attention in the chiral separation field based on their excellent characteristics, including abundant topological structures, large surface area, adjustable pore/channel sizes, multiple active sites, and good chemical stability. However, the irregular morphology and nonuniformity of the synthesized MOF particles cause low column efficiency and high column backpressure for MOF-packed columns, which significantly affects their separation performance. Herein, we prepared a homochiral d-his-ZIF-8@SiO2 composite by growing of d-his-ZIF-8 on the carboxylic-functionalized SiO2 microspheres via a simple one-pot synthesis approach. The d-his-ZIF-8@SiO2 core–shell microspheres with uniform particles and narrow size distribution were applied as the chiral stationary phase (CSP) for enantioseparations in HPLC. Various racemates were separated on the d-his-ZIF-8@SiO2-packed columns with n-hexane/isopropanol as the mobile phase. Eighteen racemates including alcohol, phenol, amine, ketone, and organic acid were well resolved on the homochiral d-his-ZIF-8@SiO2 CSP. The d-his-ZIF-8@SiO2 core–shell microspheres’ CSP possesses an excellent chiral resolution ability toward various racemic compounds with good reproducibility and stability. Hence, the fabrication of chiral MOF@SiO2 core–shell microspheres is an effective strategy to improve the application of homochiral MOFs as CSPs in the field of chromatography.

Rosa rugosa is an important shrub with economic, ecological, and pharmaceutical value. A high-quality chromosome-scale genome for R. rugosa sequences was assembled using PacBio and Hi-C technologies. The final assembly genome sequences size was about 407.1 Mb, the contig N50 size was 2.85 Mb, and the scaffold N50 size was 56.6 Mb. More than 98% of the assembled genome sequences were anchored to 7 pseudochromosomes (402.9 Mb). The genome contained 37,512 protein-coding genes, with 37,016 genes (98.68%) that were functionally annotated, and 206.67 Mb (50.76%) of the assembled sequences are repetitive sequences. Phylogenetic analyses indicated that R. rugosa diverged from Rosa chinensis approximately 6.6 million years ago, and no lineage-specific whole-genome duplication (WGD) event occurred after divergence from R. chinensis. Chromosome synteny analysis demonstrated highly conserved synteny between R. rugosa and R. chinensis, between R. rugosa and Prunus persica as well. Comparative genome and transcriptome analysis revealed genes related to color, scent, and environment adaptation. The chromosome-level reference genome provides important genomic resources for molecular-assisted breeding and horticultural comparative genomics research.

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Rosa rugosa is a famous Chinese traditional flower with high ornamental value and well environmental adapt ability. The cultivation of new colorful germplasms to improve monotonous flower color could promote its landscape application. However, the mechanism of flower color formation in R. rugosa remains unclear. In this study, combined analyses of the chemical and transcriptome were performed in the R. rugosa germplasms with representative flower colors. Among the identified anthocyanins, cyanidin 3,5-O-diglucoside (Cy3G5G) and peonidin 3,5-O-diglucoside (Pn3G5G) were the two dominant anthocyanins in the petals of R. rugosa. The sum content of Cy3G5G and Pn3G5G was responsible for the petal color intensity, such as pink or purple, light- or dark- red. The ratio of Cy3G5G to Pn3G5G was contributed to the petal color hue, that is, red or pink/purple. Maintaining both high relative and high absolute content of Cy3G5G may be the precondition for forming red-colored petals in R. rugosa. Cyanidin biosynthesis shunt was the dominant pathway for anthocyanin accumulation in R. rugosa, which may be the key reason for the presence of monotonous petal color in R. rugosa, mainly pink/purple. In the upstream pathway of cyanidin biosynthesis, 35 differentially expressed structural genes encoding 12 enzymes co-expressed to regulate the sum contents of Cy3G5G and Pn3G5G, and then determined the color intensity of petals. RrAOMT, involved in the downstream pathway of cyanidin biosynthesis, regulated the ratio of Cy3G5G to Pn3G5G via methylation and then determined the color hue of petals. It was worth mentioning that significantly higher delphinidin-3,5-O-diglucoside content and RrF3’5’H expression were detected from deep purple-red-flowered 8-16 germplasm with somewhat unique and visible blue hue. Three candidate key transcription factors identified by correlation analysis, RrMYB108, RrC1, and RrMYB114, might play critical roles in the control of petal color by regulating the expression of both RrAOMT and other multiple structural genes. These results provided novel insights into anthocyanin accumulation and flower coloration mechanism in R. rugosa, and the candidate key genes involved in anthocyanin biosynthesis could be valuable resources for the breeding of ornamental plants in future.

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