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The proliferation and differentiation of rhizomes are crucial for the propagation of Cymbidium species. We systematically assessed the effects of different concentrations of 20 amino acids on the proliferation and differentiation of C. goeringii rhizomes. Rhizome proliferation rates were significantly higher in media with 2.0 mmol·L−1 cysteine, 0.5 mmol·L−1 arginine, 0.2 mmol·L−1 asparagine, 1.0 mmol·L−1 proline, and 0.5 mmol·L−1 lysine compared with those in the control. Additionally, 1.0 mmol·L−1 tyrosine, 0.5 mmol·L−1 asparagine, and 0.2 mmol·L−1 aspartate were beneficial for rhizome differentiation. Furthermore, two combinations of amino acids, 0.5 mmol·L−1 arginine + 1.0 mmol·L−1 proline and 0.5 mmol·L−1 arginine + 2.0 mmol·L−1 cysteine, resulted in proliferation rates of 3.05 and 3.01, respectively, after 60 days. The highest differentiation rate (5.39 after 60 days) was observed in media with 0.5 mmol·L−1 asparagine + 0.2 mmol·L−1 aspartate. This study demonstrated that certain combinations of amino acids can effectively promote the proliferation and differentiation of rhizomes during the rapid propagation of C. goeringii.
Melatonin plays an important role in plant resistance to stress. The role of melatonin in the propagation of plant tissue, such as rhizome proliferation, differentiation, and seedling rooting in Cymbidium species, remains unknown. In this study, we selected C. goeringii and C. faberi as experimental materials and attempted to understand the effect of melatonin on this process. We found that 1.0 μM melatonin was beneficial for rhizome proliferation of C. goeringii, with a proliferation rate of 5.52. In terms of C. faberi, the highest proliferation rate of 8.29 was observed in the medium with 0.5 μM melatonin. In proliferation, the cut rhizome of C. goeringii is more likely to cause browning phenomenon than that of C. faberi. The addition of melatonin can significantly inhibit the browning phenomenon and improve the survival rate of C. goeringii rhizome. The highest number of shoot buds per explant (3.11 after 60 days) was observed in the medium with 1.0 μM melatonin. The number of shoot buds per explant (3.28 after 60 days) was significantly higher for C. faberi in the medium with 5.0 μM melatonin than that for the control. Furthermore, culture medium incorporated with 1.0 μM of melatonin had the best comprehensive effect of seedling height and root number and length of C. goeringii. By contrast, 0.5 μM melatonin significantly promoted root elongation of C. faberi, reaching 1.77 cm, whereas it was 0.28 cm in the control. We demonstrated that melatonin in specific concentrations effectively promote rhizome proliferation, differentiation, and seedlings rooting in the rapid propagation of C. goeringii and C. faberi.
Cymbidium faberi, a member of the Cymbidium genus known for its fragrant blooms and graceful foliage, has recently become endangered in the wild due to reproductive challenges. This study aimed to establish systematically a tissue culture system for Cymbidium faberi Rolfe (wild species) by evaluating the effects of various plant growth regulators its propagation stages, including rhizome proliferation, differentiation, shoot strengthening, and rooting. The results showed that 0.5 mg·L−1 thidiazuron significantly promoted rhizome proliferation, achieving a proliferation coefficient of 6.08 after 60 days of culture. For adventitious bud induction, 1.92 mg·L−1 brassinolide was most effective, inducing 6.43 buds per rhizome with an average bud height of 5.25 mm after 90 days of culture. The optimal strategy for shoot growth was using 3.0 mg·L−1 1-naphthaleneacetic acid, resulting in an average shoot height of 6.47 cm after 60 days. The highest rooting rate of 87.5% was achieved with 0.5 mg·L−1 zeatin, producing an average of 3.5 roots per shoot with an average root length of 3.06 cm. This study successfully developed a propagation system for C. faberi and highlighted the significant role of BL in promoting rhizome differentiation. In conclusion, this study provides a robust propagation method to support the conservation and industrial development of C. faberi.