Dark Response of Seedlings Evaluated by Chlorophyll Concentration in Maize Natural Population ()
1. Introduction
As the most important pigment in the world, chlorophyll (Chl) plays a central role in photosynthesis and is responsible for absorbing sunlight and converting it into chemical energy [1] . Maintaining a higher Chl content for a longer period in the reproductive stage is essential for increasing crop production [2] [3] . However, excess Chl in its free state produces reactive oxygen species and results in cell death [4] ; therefore, plant cells must degrade these species through self-metabolism. Green plants contain two major Chl components, chlorophyll a (Chla) and chlorophyll b (Chlb), both with the same absorption spectra [5] [6] . Chla and Chlb function as photoreceptors in photosynthesis. Chla is a unique pigment that exists in all oxygenic photosynthetic organisms [7] . Chlb functions in the light-harvesting Chla/b protein complexes (LHCs) that harvest and transfer light energy to both photosystems [8] .
The Chl content is an important experimental parameter in agronomy and plant biology research [9] . The Chl content is used as an effective index to assess photosynthetic efficiency in breeding programs [10] . This parameter is fundamental to understanding the response of a plant to the adverse environment in which it resides. Because it is a quantitative trait, it is difficult to select for Chl content in breeding programs [11] . The amount of Chl varies depending on many edaphic and climatic factors, such as salt stress [12] -[14] , light [15] -[19] , water stress [20] -[25] , air pollution [26] , fertilization [27] , the vegetation period [28] , plant species and leaf position [29] . Therefore, the tolerance of plants for stresses such as cold and drought [30] -[33] or low temperature [34] [35] can be determined by the Chl concentration.
Maize (Zea mays L.) is the world’s most widely grown crop. It is also an important source of biofuel, animal feed and raw material in industry [36] . In addition, maize is an important model organism for cytogenetic, genetic, genomic, and functional genomic studies based on complete whole genome sequencing [37] . Increasing the grain yield and biomass per acre is one of the most important goals of maize production [38] . Nowadays, adverse weather and environmental diversity threaten maize yield, which has resulted in a research hotpot on the maize response to adverse environmental conditions. In this present study, a natural population with 139 inbred maize lines was used to investigate the variation in the Chl content before and after dark treatment and to evaluate the response of different inbred lines to dark treatment.
2. Materials and Methods
2.1. Experimental Conditions and Treatments
The inbred maize lines were provided by the National Maize Improvement Centre of China [39] . Two seed replicates were germinated in petri dishes for 4 days and transplanted to enriched soil (light nutritional soil: vermiculite = 1:1) under the following growth conditions: light/dark: 10/14 hours; temperature: 25˚C; white light: 400 μmol∙m−2∙s−1. When the second leaf had emerged completely, one replicate was placed under light and the other was placed in the dark for four days. All the phenotypic data were collected after four days of dark treatment.
2.2. Phenotypic Determination and Analysis
When two leaves had fully unfolding, two types of methods were used for Chl determination before and after 4 days of dark treatment. The first method was the use of the SPAD-502 chlorophyll meter (Minolta Camera Co., Osaka, Japan) and the second was the chemical method in which Chl from the green part of three plants was extracted using 80% acetone and measured using spectrophotometer at wavelengths of 645 nm and 663 nm [40] . All data were analyzed by using SPSS v.19 software and the Microsoft Excel program, including basic statistics description, mono factor analysis of variance and Pearsoncorrelation. The relative contents of chlorophyll a, b and total chlorophyll (Tchl = Chla + Chlb) and Chla/b (Chla/Chlb) were calculated using the following equations [40] .
(1)
(2)
(3)
(4)
where A645 = absorbance at 645 nm; A663 = absorbance at 663 nm; V = solvent volume, W = fresh weight of the extracted tissue, N = dilution factor.
3. Results
3.1. Phenotypic Analysis
In general, there was wide variation in the SPAD value and the Chl concentration measured in the light and dark. The average SPAD values were 38.02 and 29.83 under light and dark conditions, respectively, and the variation was double that measured in the natural population. The largest values were 48.35 from ZaC546 and 42.12 from Shen137, and the smallest SPAD values were 26.33 from NMJT and 18.32 from HSBN under light and dark conditions, respectively. This suggested that a smaller variation of 22.03 was observed in the light compared with a greater variation of 23.80 in the dark (Table 1).
For the Chla, Chlb, and Tchl concentrations, there was two-fold difference between the light and dark for the average values; however, a small difference was observed in Chla/b under light and dark conditions. The average Chla concentration was 0.57 mg/g (range = 1.03 mg/g) in the light, compared with 0.22 mg/g (range = 0.54 mg/g) in the dark. The variation of Chlain the population was more than ten-fold, and ranged from 0.18 - 1.21 mg/g and 0.04 - 0.58 mg/g under light and dark conditions, respectively. The highest concentration was measured in Mo17 and the lowest in K14 in the light, compared with the highest concentration in TY-2 and the lowest in Zheng-35 in the dark. The Chlb concentrations ranged from 0.26 mg/g (238) to 0.96 mg/g (Qi319) in the light, i.e., almost a four-fold variation, compared with the range from 0.06 mg/g (Dan598) to 0.58 mg/g (TY-2) in the dark, i.e., almost a ten-fold variation. The average Chlb concentrations determined in the light and dark were 0.52 mg/g and 0.26 mg/g, respectively. The Tchl concentration in the light ranged from 0.55 - 2.05 mg/g, with a high variation of 1.51 mg/g and an average value of 1.09 mg/g, compared with the range of 0.12 - 1.16 mg/g, a variation of 1.05 mg/g and an average of 0.49 mg/g measured under dark conditions. The Chla/b range was 0.44 - 1.49 and the average was 1.07 under light conditions, compared with the range of 0.09 - 1.21 and the average of 0.84 under dark conditions. When we measured the Chla and Chlb percent in Tchl under light and dark conditions, only a small difference was found between the average values. A two-fold variation in the Chla percent in Tchl (range of 30.95 - 59.92) was observed in the light, and a seven-fold variation was measured in the dark (range of 8.26 - 54.79). With respect to the Chlb percent in Tchl, there was a two-fold variation under the light and dark conditions, where ranges of 40.08 - 69.05 and 45.21 - 91.74, respectively, were measured (Table 1). Under light conditions, a higher Chla percent was observed compared with a lower value under dark conditions. This indicates that the seedlings required the condition of a distribution in the Chla and Chlb concentrations to adapt to changes in the environment.
3.2. Correlation Coefficients between the SPAD Readings and the Chl Concentration
To explore the relationship between the SPAD readings and the Chl concentration, Pearson correlation coefficients were calculated for the different treatments as shown in Table 2. For the SPAD readings, there was a highly significant relationship, with a value of 0.561, between the light and dark. However, no significant correlation was detected between the SPAD readings and the Chl concentration for the light or dark treatment. Furthermore, there was no significant correlation between the light and dark treatment for a particular Chl component, including Chla/b. Chla under light conditions was highly significantly positively correlated with Chlb (0.845), Tchl (0.973), and Chla/b (0.608), similar to the dark conditions. In addition, a highly significant positive relationship was also found between Chlb and Tchl, i.e., 0.944 and 0.949 under light and dark conditions, respectively. Chla/b had a highly significant positive correlation with Chla (0.608) but not with Chlb or Tchl under light conditions, and similar associations were observed in the dark. There was no significant difference in the chlorophyll components between the different treatments (Table 2).
3.3. Difference in Chl Concentration under Light and Dark Conditions
The relative difference in the Chl content between the light and dark treatments was also analyzed for this population, as shown in Table S1. It was found that the Top 10 least difference for Tchl was less than 35%, and the inbreds were Chuan48-2, 4F1, 303WX, 9642, and LY042. However, the difference between the Chla and Chlb contents was less than 40%. Therefore, we considered that these inbreds could be insensitive to dark treatment. On the other hand, it was determined that the inbreds Dan598, Zheng29, Zheng35, DH29, and R08 obtained the Top highest difference percent of more than 70% for Tchl and Chla, and a difference percent of more than 60% for Chlb. Compared with Chlb, Tchl and Chla showed a more rapid degradation under dark treatment, which suggested that these inbreds might be highly sensitive to dark treatment.
In particular, there was a miniscule increment in Chla in inbreds 4F1 and 9642, with a small decrease in Tchl and a higher decrease in Chlb. Meanwhile, there was a small increment in Chla in inbred 303WX, which exhibited a 15% decrease in Chla and a 7% decrease in Tchl. This result verified that the mode of transition between Chla and Chlb during the dark treatment differed between individual inbred lines (Table S1).
4. Discussion
A significant relationship between SPAD readings and the Chl concentration was determined by using chemical extraction in a previous report [41] ; however, this relationship was not significant in the current study. It was possible that a different leaf part was used for the chemical extraction. In this study, which was in contrast to previous reports, only the middle section of the first leaf was measured by using the SPAD-502 meter, and all the green parts of the seedling were used for Chl determination. In other studies, however, the same part of the ear leaf was used to evaluate the Chl content.
According to differences in their Chl contents between light and dark, inbred lines were identified as sensitive or insensitive to dark. Inbreds such as Dan598, Zheng29, Zheng35, DH29, and R08 will be likely senescence rapidly under dark conditions, and Chuan48-2, 4F1, 303WX, 9642, and LY042 exhibit a stay-green phenotype with slow senescence in the dark. In addition, there were several inbred lines that exhibited a miniscule increment in one type of Chl but a decrease in another type of Chl and in Tchl. It can be concluded that the mechanism of transition between Chla and Chlb is different in different inbred lines under dark conditions.
Contrary to our expectations, Qi319 was not identified as a stay-green inbred under dark induced-senescence at the seedling stage, although it was classified as a stay-green type at the mature stage according to reference [41] . We infer that the mechanisms in the maize leaf differ under natural and induced senescence. This is consistent with the conclusion from the differential expression analysis using transcription analysis [42] .
5. Conclusion
The amount of Chl in leaves varies and is affected by many factors. In this study, it was observed that the Chl concentration was five-fold higher in the light than in the dark, and inbreds that were sensitive or insensitive to dark treatment were identified according to their different response to dark. During the dark treatment, the transition between Chla and Chlb was different in the different inbreds. Moreover, a difference was observed between natural and induced leaf senescence in maize. Determination of Chl content can be used in many field studies, and its related research should be increased and performed for efficient use of Chl content.
Acknowledgements
We greatly acknowledge Dr. Yan J.B. from Huazhong Agriculture University and Dr. Yang X.H. from China Agriculture University for supplying the inbred maize lines. We also thank for the foundation of Chinese Universities Scientific Fund of Northwest A&F University (Z109021515) and the PhD research startup foundation of Northwest A&F University (Z109021408). We thank LetPub (www.letpub.com) for its linguistic assistance during the preparation of this manuscript.
Author Contributions
Conceived and designed the experiments: Xue, J. Q. and Xu, S. T.; Performed the experiments: Aye, N. C., Shi, Y. Q. and Li, Y. N.; Analyzed the data: Aye, N. C. and Xu, S. T.; Contributed to modify the manuscripts: Li, Y. J., Guo, D. W. and Xue, J. Q.; Wrote the paper: Xu, S. T. and Aye, N. C.,
Competing Interests
The authors have declared that no competing interests exist.
Appendices
Table 1. Descriptive statistics of traits for Chl content in inbred lines population.
Note: SPAD value, Chlorophyll compounds content; Chla, Chlb: chlorophyll a and chlorophyll b content (mg/g); TChl: total chlorophyll (Chla + b) (mg/g); Chla/b: the ratio of chlorophyll a and b content; Chla%, Chlb%: chlorophyll a and b percent in total chlorophyll content; SD = standard deviation, SPAD reading and Chla/b have no unit.
Table 2. Correlation coefficients for SPAD readings and Chl concentration.
Note: SPAD: SPAD readings; Chla: Chlorophyll a; Chlb: Chlorophyll b; TChl: total chlorophyll (Chl a + b); Chla/b: the ratio of chlorophyll a and b; L: light; D: dark; **Significant at the 0.01 probability level.
Supplementary Information
Note: Chla: Chlorophyll a; Chlb: Chlorophyll b; Tchl: Total chlorophyll (Chl a + b).
NOTES
*These authors contributed equally to this work.
#Corresponding author.