In plants, light quality plays significant roles in photomorphogenesis and photosynthesis. Efficient in vitro plant propagation techniques involve tailoring of various environmental cues and culture media according to the plant species. Plant tissue culture consists of several applications in scientific research, agriculture, biotechnology, and commercial industrial purposes. Utilization of light to enhance the quality of the in vitro raised plants have been evidenced by numerous researchers in plant tissue culture. The advent of light‐emitting diode‐ (LED‐) based artificial lighting systems in plant tissue culture for micropropagation has enhanced callus induction, shoot and root organogenesis, and acclimatization of in vitro propagated plants. Plants tend to perceive the light spectra present in the photosynthetically active region (PAR) ranging from 400 to 700 nm; this includes blue and red light wavelengths. Although the influence of spectral quality is being investigated in diverse plant species, particularly, its importance in in vitro propagated horticultural crops is gaining notable interest among researchers. In recent days, the application of LEDs provides better amenability according to the plant species of interest for efficient plant regeneration. Considering the growing necessity and emerging applications of LED supplemental lights for propagation of plants in in vitro, the present review summarizes the outcomes of various research studies dealing with LEDs in plant tissue culture. Moreover, the present endeavor has provided a comprehensive overview on the effects of LEDs in the morphogenesis of plants cultured in vitro.

Lower quality and longer production periods of grafted seedlings, especially grafted plug seedlings of fruit vegetables, may result from insufficient amounts of light, particularly in rainy seasons and winter. Supplemental artificial lighting may be a feasible solution to such problems. This study was conducted to evaluate light intensity’s influence on the quality of grafted tomato seedlings, ‘Super Sunload’ and ‘Super Dotaerang’ were grafted onto the ‘B-Blocking’ rootstock. To improve their quality, grafted seedlings were moved to a glasshouse and grown for 10 days. The glasshouse had a combination of natural lighting from the sun and supplemental lighting from LEDs (W₁R₂B₂) for 16 h/day. Light intensity of natural lighting was 490 μmol·m⁻²·s⁻¹ photosynthetic photon flux density (PPFD) and that of supplemental lighting was 50, 100, or 150 μmol·m⁻²·s⁻¹ PPFD. The culture environment had 30/25 °C day/night temperatures, 70% ± 5% relative humidity (RH), and a natural photoperiod of 14 h as well. Compared with quality of seedlings in supplemental lighting of 50 μmol·m⁻²·s⁻¹ PPFD, that of seedlings in supplement lighting of 100 or 150 μmol·m⁻²·s⁻¹ PPFD improved significantly. With increasing light intensity, diameter, fresh weight, and dry weight, which were used to measure shoot growth, greatly improved. Leaf area, leaf thickness, and root biomass were also greater. However, for quality of seedlings, no significant differences were discovered between supplement lighting of 100 μmol·m⁻²·s⁻¹ PPFD and supplement lighting of 150 μmol·m⁻²·s⁻¹ PPFD. Expressions of PsaA and PsbA (two photosynthetic genes) as well as the corresponding proteins increased significantly in supplement lightning of 100 and 150 μmol·m⁻²·s⁻¹ PPFD, especially in 100 μmol·m⁻²·s⁻¹ PPFD. Overall, considering quality and expressions of two photosynthetic genes and proteins, supplemental light of 100 μmol·m⁻²·s⁻¹ PPFD (W₁R₂B₁) would be the best choice to cultivate grafted tomato seedlings.

Browning is prevalent in tissue cultures of Paeonia lactiflora Pall. (herbaceous peony), and severely affects and restricts the growth and differentiation of the explants. In this study, dipping excised explants in a sodium chloride (NaCl) solution as a pretreatment, adding polyvinyl pyrrolidone (PVP) to the culture medium, storing planted explants at 4 °C for 24 h, and transferring planted explants to a new medium after 24 h were considered as browning-suppression methods in tissue cultures of herbaceous peony ‘Festival Maxima’. The treated petal explants were cultured in a culture room with a 16-hour photoperiod, 25 °C temperature, and 80% relative humidity in darkness for 4 to 8 weeks. The results demonstrated that dipping excised explants in a 0.5 g·L⁻¹ NaCl solution, adding 0.5 g·L⁻¹ PVP to the medium, storing planted explants at 4 °C for 24 h, and transferring planted explants to the same fresh medium after 24 h could effectively inhibit browning. Adding PVP to the medium led to the greatest browning suppression percentage of 95%. Storing planted explants at 4 °C for 24 h reduced the effectiveness of other treatments in suppressing browning. After 8 weeks, dipping excised explants in a NaCl solution resulted in the highest callus induction percentage of 75%, while storing explants at 4 °C for 24 h suppressed callus formation. It was observed in all treatments that decreases in browning was accompanied with higher levels of phenols and lower activities of phenylalanine ammonia-lyase (PAL) and polyphenoloxidase (PPO). Overall, the results suggest that dipping in a NaCl solution was effective in alleviating the browning issues of herbaceous peony tissue cultures, and had positive synergistic effects with PVP on browning suppression and callus induction.

Commercial strawberries are mainly propagated using daughter plants produced on aerial runners because asexual propagation is faster than seed propagation, and daughter plants retain the characteristics of the mother plant. This study was conducted to investigate the effective factors for runner induction, as well as the molecular mechanisms behind the runner induction. An orthogonal test with 4 factors (photoperiod, temperature, gibberellin, and 6-benzyladenine), each with 3 levels was performed. Proteins were also extracted from the crowns with or without runners and separated by two-dimensional electrophoresis. The results of the orthogonal test showed that a long-day (LD) environment was the most influential factor for the runner formation, and 50 mg·L⁻¹ of 6-BA significantly increased the number of runners. A proteomic analysis revealed that 32 proteins were differentially expressed (2-fold, p < 0.05) in the strawberry crowns with and without runners. A total of 16 spots were up-regulated in the crowns with runners induced by LD treatment. Identified proteins were classified into seven groups according to their biological roles. The most prominent groups were carbohydrate metabolism and photosynthesis, which indicated that the carbohydrate content may increase during runner formation. A further analysis demonstrated that the soluble sugar content was positively correlated with the number of runners. Thus, it is suggested that the photoperiod and 6-BA break the dormancy of the axillary buds and produce runners by increasing the soluble sugar content in strawberry.

Insufficient exposure to light in the winter may result in a longer production periods and lower quality of seedlings in greenhouses for plug growers. Supplementary artificial lighting to plug seedlings may be one solution to this problem. The objective of this study was to assess the effects of the duration of the supplementary light on the growth and development of two watermelon cultivars, ‘Speed’ and ‘Sambok Honey’ grafted onto ‘RS-Dongjanggun’ bottle gourd rootstocks (Lagenaria siceraria Stanld). Seedlings were grown for 10 days in a glasshouse with an average daily natural light intensity of 340 μmol·m⁻²·s⁻¹ photosynthetic photon flux density (PPFD) and daily supplementary lighting of 8, 12 or 16 h from mixed LEDs (W₁R₂B₁, chip ratio of white:red:blue = 1:2:1) at a light intensity of 100 μmol·m⁻²·s⁻¹ PPFD, a group without supplementary light was set as the control (CK). The culture environment in a glasshouse had 25/15 °C day/night temperatures, an 85 ± 5% relative humidity, and a natural photoperiod of 8 h. The results showed that all the growth and development parameters of seedlings grown with supplementary light were significantly greater than those without supplementary light (CK). The 12 and 16 h supplementary light resulted in greater growth and development parameters than the 8 h supplementary light did. The same trend was also found with the indexes that reflect the quality of the seedlings, such as the dry weight ratio of the shoot and root, total biomass, dry weight to height ratio of scions, and specific leaf weight. The 12 h and 16 h light supplements resulted in greater Dickson’s quality indexes compared to the 8 h supplementary light, and the 12 h supplementary light showed the greatest use efficiency of the supplementary light. 16 h of daily supplementary light significantly increased the H₂O₂ content and the antioxidant enzyme activities in seedlings compared to the other treatments. This indicated that 16 h of supplementary light led to certain stresses in watermelon seedlings. In conclusion, considering the energy consumption, 12 h of supplementary light was the most efficient in improving the quality of the two cultivars of grafted watermelon plug seedlings.

Plants are exposed to numerous biotic and abiotic stresses, and light is one of the most important factors that influences the plant morphology. This study was carried out to examine how the lighting direction affected the plant morphology by investigating the growth parameters, epidermal cell elongation, stomatal properties, and physiological changes. Seedlings of two head lettuce (Lactuca sativa L.) cultivars, Caesar Green and Polla, were subjected to a 12 h photoperiod with a 300 μmol·m⁻²·s⁻¹ photosynthetic photon flux density (PPFD) provided by light emitting diodes (LEDs) from three directions: the top, side, and bottom, relative to the plants. Compared with the top and side lighting, the bottom lighting increased the leaf angle and canopy by stimulating the epidermal cell elongation in leaf midrib, reduced the leaf number and root biomass, and induced large stomata with a low density, which is associated with reduced stomatal conductance and carbohydrate contents. However, the proline content and quantum yield exhibited no significant differences with the different lighting directions in both cultivars, which implies that the plants were under normal physiological conditions. In a conclusion, the lighting direction had a profound effect on the morphological characteristics of lettuce, where the plants adapted to the changing lighting environments.