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1.
BMC Plant Biol ; 21(1): 414, 2021 Sep 09.
Article in English | MEDLINE | ID: mdl-34503445

ABSTRACT

BACKGROUND: Adventitious root formation is considered a major developmental step during the propagation of difficult to root plants, especially in horticultural crops. Recently, adventitious roots induced through plant tissue culture methods have also been used for production of phytochemicals such as flavonoids, anthocyanins and anthraquinones. It is rather well understood which horticultural species will easily form adventitious roots, but the factors affecting this process at molecular level or regulating the induction process in in vitro conditions are far less known. The present study was conducted to identify transcripts involved in in vitro induction and formation of adventitious roots using Arnebia euchroma leaves at different time points (intact leaf (control), 3 h, 12 h, 24 h, 3 d, 7 d, 10 d and 15 d). A. euchroma is an endangered medicinal Himalayan herb whose root contains red naphthoquinone pigments. These phytoconstituents are widely used as an herbal ingredient in Asian traditional medicine as well as natural colouring agent in food and cosmetics. RESULTS: A total of 137.93 to 293.76 million raw reads were generated and assembled to 54,587 transcripts with average length of 1512.27 bps and N50 of 2193 bps, respectively. In addition, 50,107 differentially expressed genes were identified and found to be involved in plant hormone signal transduction, cell wall modification and wound induced mitogen activated protein kinase signalling. The data exhibited dominance of auxin responsive (AUXIN RESPONSE FACTOR8, IAA13, GRETCHEN HAGEN3.1) and sucrose translocation (BETA-31 FRUCTOFURANOSIDASE and MONOSACCHARIDE-SENSING protein1) genes during induction phase. In the initiation phase, the expression of LATERAL ORGAN BOUNDARIES DOMAIN16, EXPANSIN-B15, ENDOGLUCANASE25 and LEUCINE-rich repeat EXTENSION-like proteins was increased. During the expression phase, the same transcripts, with exception of LATERAL ORGAN BOUNDARIES DOMAIN16 were identified. Overall, the transcriptomic analysis revealed a similar patterns of genes, however, their expression level varied in subsequent phases of in vitro adventitious root formation in A. euchroma. CONCLUSION: The results presented here will be helpful in understanding key regulators of in vitro adventitious root development in Arnebia species, which may be deployed in the future for phytochemical production at a commercial scale.


Subject(s)
Boraginaceae/genetics , Plant Leaves , Plant Proteins/genetics , Plant Roots/growth & development , Plant Roots/genetics , Boraginaceae/growth & development , Gene Expression Profiling , Gene Expression Regulation, Plant , Indoles/pharmacology , Molecular Sequence Annotation , Plant Leaves/drug effects , Plant Leaves/genetics , Plants, Medicinal/genetics , Plants, Medicinal/growth & development , Sequence Analysis, RNA , Tissue Culture Techniques/methods
2.
Appl Biochem Biotechnol ; 173(1): 248-58, 2014 May.
Article in English | MEDLINE | ID: mdl-24643453

ABSTRACT

Cell suspension cultures of Arnebia euchroma were established from the friable callus on liquid Murashige and Skoog medium supplemented with 6-benzylaminopurine (10.0 µM) and indole-3-butyric acid (5.0 µM). Salicylic acid was used to study its effect on the enzymes which participate in shikonin biosynthesis with respect to metabolite (shikonin) content in the cell suspension culture of A. euchroma. In our study, phenylalanine ammonia lyase and PHB geranyltransferase were selected from the entire biosynthetic pathway. Results showed that phenylalanine ammonia lyase is responsible for growth and PHB geranyltransferase for metabolite production. Salicylic acid exhibited an inverse relationship with the metabolite content (shikonin); salicylic acid (100 µM) completely inhibited shikonin biosynthesis. The results presented in the current study can be successfully employed for the metabolic engineering of its biosynthetic pathway for the enhancement of shikonin, which will not only help in meeting its industrial demand but also lead to the conservation of species in its natural habitat.


Subject(s)
Boraginaceae/metabolism , Geranyltranstransferase/metabolism , Hydroxybenzoates/metabolism , Naphthoquinones/metabolism , Phenylalanine Ammonia-Lyase/metabolism , Plant Proteins/metabolism , Plants, Medicinal/metabolism , Salicylic Acid/metabolism , Biosynthetic Pathways , Boraginaceae/enzymology , Boraginaceae/growth & development , Cell Culture Techniques , Culture Media/metabolism , Naphthoquinones/chemistry , Plants, Medicinal/enzymology , Plants, Medicinal/growth & development
3.
J Exp Bot ; 63(17): 6115-23, 2012 Oct.
Article in English | MEDLINE | ID: mdl-23028018

ABSTRACT

For many plant species, nutrient availability induces important anatomical responses, particularly the production of low-density tissues to the detriment of supporting tissues. Due to the contrasting biomechanical properties of plant tissues, these anatomical responses may induce important modifications in the biomechanical properties of plant organs. The aim of this study was to determine the effects of nutrient enrichment on the anatomical traits of two freshwater plant species and its consequences on plant biomechanical performance. Two plant species were grown under controlled conditions in low versus high nutrient levels. The anatomical and biomechanical traits of the plant stems were measured. Both species produced tissues with lower densities under nutrient-rich conditions, accompanied by modifications in the structure of the aerenchyma for one species. As expected, nutrient enrichment also led to important modifications in the biomechanical properties of the stem for both species. In particular, mechanical resistance (breaking force and strength) and stiffness of stems were significantly reduced under nutrient rich conditions. The production of weaker stem tissues as a result of nutrient enrichment may increase the risk of plants to mechanical failure, thus challenging plant maintenance in mechanically stressful or disturbed habitats.


Subject(s)
Boraginaceae/anatomy & histology , Mentha/anatomy & histology , Plant Stems/anatomy & histology , Boraginaceae/growth & development , Boraginaceae/metabolism , Fertilizers , Fresh Water , Mentha/growth & development , Mentha/metabolism , Nitrogen/analysis , Nitrogen/metabolism , Phosphorus/analysis , Phosphorus/metabolism , Plant Stems/growth & development , Plant Stems/metabolism , Stress, Mechanical
4.
J Biomed Biotechnol ; 2011: 165852, 2011.
Article in English | MEDLINE | ID: mdl-21772789

ABSTRACT

In pursuit of strong shikalkin-producing cell lines, seeds of the Iranian Arnebia euchroma were collected from Dena altitudes in the central Zagross. Chemical analysis showed that the dried root of the plant contained about 8.5% (w/w) shikalkin pigment. The root explants of the young plantlets, obtained from the germinated seeds, were used for establishing callus. Then, parameters effective on proliferation and pigment production of the resulting calli were studied in detail. Accordingly, two modified media called mLS and mM9 were optimized for propagation and pigment production, respectively. Using these media, the biomass of the A. euchroma calli was increased to 600%, and the pigment production reached to a maximum of 16.3 mg per gram of the wet biomass in a period of a subculture (21 days). Parallel to these experiments, the antimicrobial activity of shikalkin pigment was examined on some fungi and gram-positive and gram-negative bacteria. Results indicated that the pigment was almost ineffective on fungi and gram-negative bacteria, but it was meaningfully effective against Micrococcus luteus.


Subject(s)
Anti-Bacterial Agents/pharmacology , Boraginaceae/chemistry , Boraginaceae/growth & development , Plant Extracts/pharmacology , Tissue Culture Techniques/methods , Anti-Bacterial Agents/chemistry , Anti-Bacterial Agents/isolation & purification , Bacteria/drug effects , Fungi/drug effects , Naphthoquinones/chemistry , Naphthoquinones/isolation & purification , Naphthoquinones/pharmacology , Plant Extracts/chemistry , Plant Extracts/isolation & purification , Plant Roots/chemistry , Seeds/chemistry
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