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New ForestsInternational Journal on the Biology,Biotechnology, and Management ofAfforestation and Reforestation ISSN 0169-4286 New ForestsDOI 10.1007/s11056-014-9435-7
Light intensity affects the growth andflavonol biosynthesis of Ginkgo (Ginkgobiloba L.)
You Xu, Guibin Wang, Fuliang Cao,Cancan Zhu, Guangyu Wang & YousryA. El-Kassaby
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Light intensity affects the growth and flavonolbiosynthesis of Ginkgo (Ginkgo biloba L.)
You Xu • Guibin Wang • Fuliang Cao • Cancan Zhu • Guangyu Wang •
Yousry A. El-Kassaby
Received: 30 September 2013 / Accepted: 20 May 2014� Springer Science+Business Media Dordrecht 2014
Abstract Response of growth and secondary metabolites to light intensity are useful
measurements to determine suitable silviculture treatments for the cultivation of medicinal
plants. Here, we analyzed the growth, flavonols (total flavonol, quercetin, kaempferol, and
isorhamnetin) content, flavonols yield per plant, and expression of flavonoid biosynthesis-
related genes in 2-year Ginkgo (Ginkgo biloba L.) seedlings at four different light inten-
sities (100, 76, 40, and 25 % of full sunlight) in a greenhouse setting. Across all light
intensities, the 76 % sunlight treatment produced the highest growth of total biomass, root,
stem, and leaf, indicating negative effects of either fulllight or heavy shading on Ginkgo
seedling development. Both flavonols (total flavonol, quercetin, kaempferol, and isorh-
amnetin) content and expression of flavonoid biosynthesis-related genes [PAL (Phenyl-
alanine ammonia-lyase), CHS (Chalcone synthase), F3H (Flavanone 3-hydroxylase), and
FLS (Flavonol synthase)] in leaves were highest under 100 % sunlight, suggesting that full
sunlight promotes the expression of flavonoid biosynthesis-related genes and increases
flavonoid biosynthesis. The highest and lowest flavonol contents were found in leaves and
stems, respectively. The 76 % sunlight treatment produced the highest flavonols yield
while the 100 % sunlight produced the highest flavonoids content in leaves, indicating that
flavonol production per unit land area depends not only flavonol content but also biomass.
Overall, in order to achieve the highest flavonols yield per area in Ginkgo leaf-harvesting
plantations, it is important to manipulate light conditions of field.
You Xu and Guibin Wang contributed equally to this work.
Y. Xu � G. Wang � F. CaoCollege of Forest Resources and Environment, Nanjing Forestry University, Nanjing 210037,People’s Republic of China
C. ZhuInstitute of Botany, Jiangsu Province and Chinese Academy of Sciences, Nanjing 210014,People’s Republic of China
G. Wang � Y. A. El-Kassaby (&)Faculty of Forestry, University of British Columbia, Vancouver, BC V6T 1Z4, Canadae-mail: [email protected]
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Keywords Ginkgo biloba � Light intensity � Biomass production � Secondary
metabolites � Gene expression
Introduction
Plants, including trees, are potential sources of natural bioactive compounds such as
secondary metabolites with commercial importance as pharmaceutical compounds.
Flavonoids are important secondary plant metabolites with wide distribution in many plant
parts (flowers, fruits, seeds, and leaves). Flavonoids are a large group of phenolic plant
constituents and their bioavailability varies greatly among different subgroups and com-
pounds (Erlund 2004). Flavonoids have many biological functions, such as protection
against ultraviolet radiation and phytopathogens (Wang et al. 2009), visual signal that
attracts pollinators (Koes et al. 1994), and controlling fall colour in many plants (Field
et al. 2001). Flavonoids have antioxidant functions in higher plants that are challenged with
a range of environmental (Agati et al. 2012) and wounding stresses (Chalker-Scott 1999).
They have proven benefits to human health such as vasodilatory, anti-inflammatory,
-allergenic, -bacterial, -viral, -carcinogenic, and immune-stimulating, as well as being
inhibitors of some oxidases, such as glutathione reductase, lipoxygenase, cyclooxygenase,
xanthine oxidase, and phospholipase A2 (Jaakola and Hohtola 2010; Rice-Evans et al.
1996; Zhang et al. 2010).
Flavonoid biosynthesis and accumulation in plants are affected by many-factors, such as
light, water, temperature, soil type, microbial interactions, altitude, nutritional status,
pathogenesis, wounding, defoliation, plant growth regulators, and various developmental
processes (Downey et al. 2006; Azuma et al. 2012; Lafuente et al. 2011; Jaakola and
Hohtola 2010; Schmidt et al. 2010; Cohen et al. 2012; Ballizany et al. 2012; Castellarin
et al. 2007). Goto-Yamamoto et al. (2010) reported that high temperature moderately
reduced proanthocyanidin and quercetin concentrations while various temperature and
water regimes had different influences on each group of flavonoids in grape berry skins.
Light is an important environmental factor that drives photosynthesis and regulates
plant growth and development, and it also has been shown to exert an important effect on
flavonoid biosynthesis (Awad et al. 2001). High and low light intensity had significantly
positive and negative effects on flavonoid accumulation in grape bunches, respectively
(Cortell and Kennedy 2006; Fujita et al. 2006; Matus et al. 2009). Visible light primarily
induces biosynthesis of proanthocyanidins and affects their composition, whereas UV light
specifically induces biosynthesis of flavonols (Koyama et al. 2012). Jaakola and Hohtola
(2010) found that photoperiod influences the biosynthesis of many secondary metabolites
in a number of plant species. Accumulation of flavonoids in Brassica napus was sup-
pressed by increasing the amount of far-red light in the spectrum, and addition of UVB
(290–320 nm) to the spectrum altered the flavonoid composition by causing significant
changes in the quantities of individual flavonoids (Gerhardt et al. 2008).
Ginkgo (Ginkgo biloba L.), a deciduous gymnosperm species, is native to China. It is
the only remaining species of the once large order Ginkgoales, with geological records
indicating its presence on earth for 150–200 million years (He et al. 2009). Ginkgo leaves
have been cultivated for their medicinal properties for several thousand years (Ward et al.
2002), and also as an ingredient in functional foods in China. Extracts from Ginkgo leaves
are useful for a broad range of pharmacological activities, and have been used to cure
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various common geriatric complaints (Clostre, 1999; Ward et al. 2002). The main bio-
active constituents are flavonoid glycosides and terpene trilactones which are considered
responsible for the pharmacological activities of its standardized leaf extract (Singh et al.
2008; van Beek 2002). Owing to Ginkgo’s multiple beneficial effects on human health, a
substantial production of leaves is required for Ginkgo tea production, for medical use and
for functional food. However, most studies on Ginkgo were focused on extract activities,
whereas less attention was paid to its silvics.
It is of biological and commercial importance to understand the environmental factors
affecting flavonoids biosynthesis as this knowledge is essential to the development and
production of high-flavonoid yielding plantations. Several studies have been conducted to
investigate the effects of light, temperature, and drought on flavonol content in Ginkgo
leaves (Xie and Wang 2006; Leng et al. 2001) and genomic studies have been conducted to
understand their biosynthesis through the cloning and study of several flavonoid biosyn-
thesis genes [e.g., CHS (Pang et al. 2005); PAL (Xu et al. 2008a); ANS (Xu et al. 2008b)].
Understanding the effects of light intensity on leaf yield and flavonoid content is a proper
step towards the development of silvicultural measurement in leaf-harvesting Ginkgo
plantations, so higher flavonoid yield could be attained. Additionally, increasing knowl-
edge about secondary metabolism theory, especially the relation between light intensity
and flavonoid biosynthesis would be beneficial for the commercial utilization of this
resource.
This study was conducted to investigate the inter-relationship of light intensity on
growth and flavonol accumulation in Ginkgo. Furthermore, it has not yet been clarified
how the genes of flavonoid biosynthesis pathway respond to different light intensity (Wang
et al. 2012). The main objectives were to assess the effect of light intensity on growth,
flavonol content (total flavonol, quercetin, kaempferol, and isorhamnetin), and the
expression of flavonoid biosynthesis-related genes. Information generated from this study
is expected to be of great value for providing optimal growing (cropping for leaf har-
vesting) conditions for the commercial production high flavonol yielding Ginkgo
plantations.
Materials and methods
Plant materials and experimental procedures
Wind-pollinated seed of Ginkgo (Ginkgo biloba L. ‘Ddajinzhui’) were harvested in early
October 2009 and were treated with stratification method for dormancy breaking (seed
mixed with wet sand (1:3) and stored at 4 �C for 90 days). After stratification (early
January 2010), seed were field sown for seedling production. After 1-year in the field
(January 2011), seedlings of uniform size were selected and planted in pots (12 9 15 cm
(diameter x height)) containing medium composed of loam, yellow sand, and peat (2:1:1).
The basic nutrients of medium were organic matter 50 g kg-1, soluble nitrogen
121.6 mg kg-1, available phosphorous (P2O5) 27 mg kg-1, available potassium (K2O)
11.7 mg kg-1, and 6.7 pH. Two seedlings of similar size were planted in each pot (mean
height = 33 cm and basal diameter = 6.75 mm) for experimental use.
During 2011 growing season, the experiment was carried out in Nanjing Forestry
University, China (March, 2011) and pots were transferred to greenhouse. After 1 month
(April, 2011) shading treatments were conducted. The experimental design was a ran-
domized block design with three replications. Treatments consisted of four shading
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intensities [four light intensity regimens: 100 % of solar radiation without shading net
(L1), 76 % of solar radiation covered with one layer of shading net (L2), 40 % of solar
radiation covered with two layers of shading net (L3), and 25 % of solar radiation covered
with three layers of shading net (L4)]. Shading nets were placed at 2 m above the potted
plants. The average light intensity passing through in each shading treatment was about
1,300, 990, 510, and 300 lmol m-2 s-1 of photosynthetically active radiation (PAR)
during noon time (May 2011) for L1–L4, respectively. The monthly sunshine durations
from April to October were 169.6, 194.4, 162.8, 196.7, 201.6, 164.0 and 164.2 h,
respectively. For each block-replication combination (3 9 4 = 12), 30 pots with 60
seedlings were used. During the experiment, the monthly average temperatures from April
to October were 17.6, 23.1, 26.8, 30.1, 29.6, 25.3, and 19.6 �C in the greenhouse,
respectively, while the outdoor temperature was 2 �C higher. Minor temperature differ-
ences were observed among the four light treatments as they were located within the same
greenhouse. We used the weight method to control soil moisture, and the whole pots
(including soil and plants) would be assessed every 2 days, and any moisture loss through
evaporation was adjusted by adding tap water, so soil moisture of all treatments was the
same. No fertilizer was added during experimental period, so the soil mix and nutrients for
all treatments were identical.
Growth and biomass assessment
Growth and biomass assessments of the seedlings were conducted before the start (April,
2011) and at the end of treatments (October, 2011). Before the start of treatments, the
height and basal diameter of each seedling within each treatment were measured, and the
mean basal diameter and height were calculated. According to mean basal diameter and
height, six seedlings were selected and harvested. After harvesting, each sampled seedling
was washed and leaf, stem, and root components were separated, weighed, and dried at
70 �C. At the end of experiment, the mean basal diameter and height of all seedlings for
each replication were measured, and mean basal diameter and height of each replication
were calculated. According to the mean basal diameter and height, four sample seedlings
were selected and harvested for each replication. After harvesting, each sampled seedling
was also washed and leaf, stem, and root components were separated, weighed, and dried
at 70 �C. The total dry biomass of each seedling was calculated as the sum of the three
parts (leaves, stem, and root) dry weights. All dried samples were ground to fine powder
and stored at room temperature prior to analysis of flavonol contents. Growth of total
biomass (root, stem, and leaves) (GB) = total dry biomass at the end of experiment—total
dry biomass before treatment. The same was calculated for growth of leaves (GL), stem
(GS), and root (GR).
Analysis of flavonol content
The flavonol content of roots, stems, and leaves were determined using high performance
chromatography (HPLC) (Chinese Pharmacopoeia Commission 2010). A 1.0 g of the
powdered sample was refluxed with 50 mL petroleum ether for 2 h in Soxhlet extractors,
then evaporated to dryness to obtain residue with a rotary evaporator. The residue was
refluxed again with 50 mL methanol for 4 h at 80 �C. After the extract was evaporated to
dryness, the residue was refluxed with 25 mL mixture of methanol and HCl (4:1) at 100 �C
for 30 min. The extract was cooled and filtered by a 0.45 lm organic phase filter. The
filtrate was removed to 50 mL volumetric flask, diluted with methanol to volume for HPLC
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analysis. Identification and quantification of flavonols was performed injecting 10 lL in
HPLC system (Waters 2695, USA) equipped with a C18 reversed phase column
(200 mm 9 4.6 mm, 5 lm). The isocratic elution was mixture of methanol and 0.4 %
phosphoric acid solution (50:50 v/v). The flow rate was 1.0 mL min-1, and the run time
was 18 min. Detection was performed at a wavelength of 360 nm. Quantitative calcula-
tions of quercetin, kaempferol, and isorhamnetin were carried out according to calibration
curves of standards. Total flavonol content = (quercetin ? kaempferol ? isorhamnetin
contents) 9 2.51 (Chinese Pharmacopoeia Commission 2010). Flavonol yield per
plant = flavonol content 9 leaf biomass per plant.
Expression analysis of flavonoid biosynthesis-related genes
Green leaf samples were harvested to determine relative gene expression of enzymes
related with flavonoid biosynthesis (October, 2011). Samples were immediately frozen in
liquid nitrogen and kept at -80 �C until use. Total RNA was isolated from Ginkgo leaves
(three samples for each treatment) following the method of Pang et al. (2005) and cDNAs
were synthesized using a cDNA synthesis kit (Clontech, USA) following the manufac-
turers’ manuals. The expression level of the flavonoid biosynthesis-related genes (PAL
(Phenylalanine ammonia-lyase), CHS (Chalcone synthase), F3H (Flavanone 3-hydroxy-
lase), and FLS (Flavonol synthase)) was determined along with a fragment of glycer-
aldehyde-3-phosphate dehydrogenase (GADPH) coding glyceraldehyde-3-phosphate
dehydrogenase as a reference by quantitative real-time PCR (qRT-PCR) using an ABI
PRISM 7500 Sequence Detection System (Applied Biosystems, Foster City, CA, USA)
and a SYBR Green PCR Master Mix (Applied Biosystems, Foster City, CA, USA) fol-
lowing the manufacturers’ manuals (Xu et al. 2008a) (see Table 1 for primer information
for amplification of the analyzed genes).
Statistical analysis
Data are reported as the mean ± standard deviation (SD), and all tests were performed
using the SigmaPlot 11.0 statistical software program (Systat Software Inc., Chicago, IL,
USA). After a Levene test for homogeneity of variances, one-way analysis of variance
(ANOVA) was conducted to compare the effect of shading treatments on growth, flavonol
content, flavonoid accumulation per plant, and relative gene expression. Duncan’s multi-
ple-range test was performed for each variable.
Results
Variation in biomass production
Shading had a significant effect (p \ 0.05) on total biomass (GB) of Ginkgo seedlings. The
GB per seedling varied among treatments with the following order L2 [ L3 [ L1 [ L4
(Fig. 1). Generally, this trend persisted across the growth of leaves (GL), stem (GS), and
root (GR) (Fig. 1). The GB of L2 exceeded that of L1, L3, and L4 by 28.0, 16.8, and
46.8 %, respectively. Across the four treatments, biomass allocation for root, stem, and
leaves parts yielding 38.5, 25.0 and 36.5 %, respectively. The highest ratio of leaf to GB
was observed in treatments L2 (39.3 %), whereas the greatest ratios of root and stem were
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achieved in treatment L1 (41.6 %) and L4 (30.1 %), respectively. GL per seedling in
treatments L2 was higher than that of L1, L3, and L4 by 55.7, 21.9, and 125.1 %,
respectively.
Variation in flavonol content
Mean flavonol content significantly differed (p \ 0.05) among the different parts of
Ginkgo seedlings (Table 2). Total flavonol content, across the four treatments, was highest
in leaves while stem had the lowest total flavonol content. Leaves’ total flavonol content
was 3.00 and 2.89 times that of stem and root, this trend was consistent across the different
flavonol compounds (Table 2).
Total leaves flavonol content significantly varied (p \ 0.05) across the four light
intensities with L1 and L3 representing the highest and lowest contents, respectively
(Table 3). It is interesting to note that no significant differences were observed between L2,
L3, and L4 (Table 3).
Variation in relative expression of flavonoid biosynthesis related genes
Effect of light intensity on relative gene expression of PAL, CHS, F3H, and FLS in Ginkgo
leaves was significant (p \ 0.05) and varied among treatments (Fig. 2). Generally, the
relative expression of the studied four genes (PAL, CHS, F3H, and FLS) showed
decreasing tendency with light intensity reduction (Fig. 2). Across the four light intensity
treatments, the relative expression of the studied genes was consistently highest under L1
and lowest under L4 (note, there was no significant difference among L2, L3, and L4 for
F3H and FLS) (Fig. 2). Pearson’s Product-Moment correlations (r) between total flavonol
content and the relative expression of PAL, CHS, F3H, and FLS were 0.905, 0.842, 0.883,
and 0.910, respectively, indicating that their expression levels are notably correlated with
total flavonol content in Ginkgo leaves.
Variation in flavonol yield per plant
Leaves’ flavonol content was estimated for each light intensity treatment on individual
seedling level (Fig. 3). Total flavonol yield ranged from 61.1 to 146.5 mg/plant, whereas
Table 1 Primers used for the quantification of gene expression levels by qRT-PCR
Gene name Sequence (50 ? 30) Tm (�C)
PAL Up-50GCGCTGCGGACTCAATCT30 58
Down-50GCCCATCCATTGATTCATAGGA30 51
CHS Up-50CAGCGAATACGGCAACATGT30 60
Down-50CGCATTTCGTCGAGGATGA30 58
F3H Up-50GGCCCAAAGTGGCGTACA30 58
Down-50TCCGGCCAGTGAGATTATGG30 62
FLS Up-50AGCCACGCACACTGTAATGG30 62
Down-50GGCGGCTTTCTGCAACATAT30 60
GAPDH Up-50GGTGCCAAAAAGGTGGTCAT30 60
Down-50CAACAACGAACATGGGAGCAT30 49.6
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the yields of quercetin, kaempferol, and isorhamnetin ranged from 7.9 to 18.8, 11.4 to 25.1,
and 5.8 to 13.4 mg/plant, respectively. ANOVA indicated that the effect of shading on
total flavonol yield as well each compound individually per plant was significant
(p \ 0.05). Similar to the trend detected for growth (above), the greatest total flavonol
yield was detected under L2 (Fig. 3).
Component
GL GR GS GB
Dry
bio
mas
s (g
)
0
5
10
15
20
25
30
L1L2L3L4
c
a
b
d
abb
ca
bb
b
a
b
c
d
Fig. 1 Variation in biomass production of Ginkgo seedlings growing under four different shadingtreatments (L1–L4 represent no shading and shading with one-, two-, and three-layer nets, respectively)(mean ± SD). Bars within a component group with different letters indicate treatments’ significantdifferences (p \ 0.05). GL leaves growth, GR root growth, GS shoot growth, and GB biomass growth
Table 2 Mean flavonol content (mg g-1) in root, stem and leaves of ginkgo seedlings (means across lighttreatments ± SD). Means within a column with different letters are statistically significantly different(p \ 0.05)
Component Total flavonol Quercetin Kaempferol Isorhamnetin
Root 4.92 ± 0.56b 0.48 ± 0.03b 0.47 ± 0.03b 1.01 ± 0.01b
Stem 4.74 ± 0.39c 0.45 ± 0.03b 0.44 ± 0.03c 1.00 ± 0.01b
Leaf 14.23 ± 1.26a 1.87 ± 0.45a 2.51 ± 0.43a 1.29 ± 0.08a
Table 3 Mean flavonol content (mg g-1) in Ginko leaves under four light treatments (L1–L4)(mean ± SD). Means within a column with different letters are statistically significantly different (p \ 0.05)
Treatment Total flavonol Quercetin Kaempferol Isorhamnetin
L1 16.67 ± 1.46a 2.39 ± 0.30a 2.90 ± 0.35a 1.35 ± 0.05a
L2 14.03 ± 1.38b 1.83 ± 0.36b 2.45 ± 0.51ab 1.31 ± 0.07ab
L3 12.42 ± 1.29b 1.52 ± 0.29b 2.20 ± 0.22b 1.23 ± 0.09b
L4 13.81 ± 1.12b 1.73 ± 0.39b 2.49 ± 0.35ab 1.28 ± 0.05ab
Quercetin, kaempferol and isorhamnetin content were determined by HPLC, and total flavonol con-tent = (quercetin content ? kaempferol content ? isorhamnetin content) 9 2.51
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Discussion
Horticultural production has primarily focused on increasing productivity through
improvement of water and fertilizers management (Stefanelli et al. 2010). However, light
intensity is an important environmental factor influencing tree growth and light compen-
sation and saturation points have been reported to be different for various tree species
PAL CHS F3H FLS
Rel
ativ
e ge
ne e
xpre
ssio
n
0
1
2
3
4
5
6
7
L1L2L3L4
a b c ca
b b c
a
bb
b
a
bb
b
Fig. 2 Variation in relative gene expression (PAL, CHS, F3H, and FLS) in Ginko leaves growing underfour different shading treatments (L1–L4 represent no shading and shading with one-, two-, and three-layernets, respectively) (mean ± SD). Bars within a group with different letters indicate treatments’ significantdifferences (p \ 0.05)
Total flavonol Quercetin Kaempferol Isorhamnetin
Flav
onol
yie
ld (
mg/
plan
t)
0
20
40
60
80
100
120
140
160
180
L1L2L3L4
a
bb
c
aa bc
ab b
c a bb c
Fig. 3 Variation in total flavonol, quercetin, kaempferol, and isorhamnetin yield in Ginkgo leaves growingunder four different shading treatments (L1–L4 represent no shading and shading with one-, two-, and three-layer nets, respectively) (mean ± SD). Flavonol yield per plant = flavonol content 9 leaves biomass perplant. Bars within a group with different letters indicate significant differences (P)
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(Zhang et al. 2007). The present study demonstrated that shading had significant effects on
leaf and total biomass production of Ginkgo seedlings and specifically light intensity
treatment, L2, resulted in the highest growth for all the seedlings’ parts (GB, GS, GR, and
GL), indicating that either low or high light intensity would not yield optimum growth of
Ginkgo. The relatively lower biomass accumulation of L1 (no shading) could be explained
by photoinhibition. The light saturation point of 2-year-old Ginkgo is
1,062.2 lmol m-2 s-1, and the light intensity of L1 treatment is 1,300 lmol m-2 s-1 (Tao
et al. 1999), so light intensity is higher than light saturation. The observed growth response
of Ginkgo seedlings to light intensity was similar to that of many tree species growing
under various light intensities (Poorter 1999; Cai et al. 2009; Deng et al. 2012). The present
study also indicates that Ginkgo seedlings increased their leaf biomass ratio at light
intensity (L2), whereas no shading (L1) or heavy shading (L4) elevated the root and stem
biomass ratios, respectively. Under no shading condition, higher transpiration rate leads to
increased root biomass allocation to favor their growth and respiration, so root water
uptake can satisfy the increased water need of the seedlings’ growth. Our results were in
agreement with that reported for Rauvolfia species, Cyclocarya paliurus, Anoectochilus
formosanus, and freshwater macrophytes (Cai et al. 2009; Deng et al. 2012; Ma et al. 2010;
Cronin and Lodge 2003).
Flavonoid accumulation can be influenced by a number of environmental conditions,
such as temperature (Tarara et al. 2008; Goto-Yamamoto et al. 2010), soil moisture (Yuan
et al. 2012), and light (Deng et al. 2012; Ma et al. 2010). Light intensity is known to affect
not only plant growth and development but also the biosynthesis of both primary and
secondary metabolites (Hemm et al. 2004). Deng et al. (2012) reported that shading had a
significant negative effect on contents of total flavonoid, kaempferol, quercetin, and
isorhamnetin in C. paliurus leaves. It has been reported that sunlight-exposed tea
(Camellia sinensis (L.) O. Kuntze) leaves accumulate higher concentration of proantho-
cyanins and O-glycosylated flavonols as compared to their shaded counterparts (Wang
et al. 2012). Cronin and Lodge (2003) also found leaf phenolics content of two freshwater
macrophytes were 72 % higher in unshaded than in shaded plants. In the present study,
shading treatments significantly affected total flavonol, quercetin, kaempferol, and isorh-
amnetin contents in Ginkgo leaves (Table 2). Overall, shading had a significantly negative
effect on the contents of total flavonol, quercetin, kaempferol and isorhamnetin, suggesting
that high levels of photosynthetically active radiation stimulate the biosynthesis of
flavonoids in Ginkgo seedling, and the result is also correlated with antioxidant functions
of flavonoids (Agati et al. 2009). Our results were consistent with other studies on tea
(Wang et al. 2012), C. paliurus (Deng et al. 2012), and freshwater macrophytes (Cronin
and Lodge 2003), suggesting that controlling light intensity would be an effective tool for
stimulating secondary plant metabolite accumulation, especially for medical trees under
intensive management system (Deng et al. 2012). Flavonoid biosynthesis in Ginkgo leaves
requires coordinated expression of genes encoding enzymes in the core phenylpropanoid
pathway and in branch pathways, such as PAL, CHS, CHI, F3H, and FLS. PAL is a link
between primary and secondary metabolism and high PAL expression is often found in
parallel with high levels of flavonoids (Lillo et al. 2008). The CHS gene, which encodes
the first committed enzyme in flavonoid biosynthesis, has been used extensively as a model
for identifying and studying elements that control the expression of flavonoid biosynthetic
genes. F3H and FLS are key enzymes of flavonol biosynthesis as they convert di-
hydrokaempferol or dihydroquercetin to the corresponding flavonols, kaempferol and
quercetin, respectively. In the present study, shading treatments significantly affected the
relative gene expression of PAL, CHS, F3H, and FLS in Ginkgo leaves. The relative
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expression of key flavonoid upstream pathway genes PAL and CHS were notably
decreased under shading treatments. F3H and FLS genes, which are involved in the bio-
synthesis of different flavonols, also had notably decreased activity in the shade-treated
leaves. This result suggests that shade treatment was effective in reducing flavonols bio-
synthesis. So, because key enzyme activity is reduced in the flavonol biosynthesis pathway
(phenylpropanoid pathway), flavonol accumulation of Ginkgo leaves decreases under
shading. The relative light intensity related gene expression of Ginkgo leaves was similar
to that reported for other tree species growing under various light intensities (Wang et al.
2012; Azuma et al. 2012).
In leaf-harvest plantations of Ginkgo, we hope to obtain not only higher quality (higher
flavonol content) but also higher yield (higher leaf biomass). In order to achieve this goal,
we can implement specific silvicultural measures in plantations, such as pruning, fertil-
ization, irrigation, and shading, but it should be noted that any measure potentially has a
dual nature. For example, moderate prunning results in higher leaf yield and flavonoid
content, but heavy pruning significantly decreases leaf yield, and light pruning has no
effect on increasing flavonol content (Cao et al. 1999). For C. paliurus, the treatment of full
sunlight (no shading) resulted in the highest flavonol, but yielded the second best leaf
biomass, while the treatment of shading with one layer of netting achieved highest leaf
biomass, but produces the second best flavonol content. Considering flavonol yield per
plant (flavonol content multiplied by leaf biomass), one layer shading treatment is the best
treatment for leaf-harvest plantation (Deng et al. 2012). So, the balance of silvicultural
measures is important in production practice in order to obtain higher flavonol yield. Our
results also highlighted the effect of shading on total flavonol yield per plant in Ginkgo
leaves and identified the role of L2 as the best shading treatment for leaf biomass pro-
duction and the second best for total flavonol content (L1 yielded highest total flavonol
content). These results suggest that L2 condition shows higher effectiveness in maintaining
the balance between biomass production and secondary metabolites content for obtaining
higher yield of health-promoting substances per area in the plantation.
Conclusion
Significant changes in biomass accumulation and allocation were found in Gingko seed-
lings growing under variable light intensities in an experimental settings, and the treatment
of 76 % solar radiation (L2) was the best in achieving the highest dry biomass. Both
flavonol content (including total flavonol, quercetin, kaempferol, and isorhamnetin) and
flavonol yield per plant were significantly affected by light intensity and the highest
flavonol content and flavonol yield were obtained under 100 and 76 % solar radiation (L1
and L2), respectively. These results indicate that 100 % sunlight is conducive to flavonoids
biosynthesis and accumulation in Ginkgo leaves, but flavonoids accumulation per area
depends on biomass production as well. The expression of flavonoid biosynthesis-related
genes (PAL, CHS, F3H, and FLS) and total flavonol content coincided with different light
intensity treatments, which was supported by the notable positive correlations between the
genes’ expression levels and flavonol content.
Acknowledgments This study was supported by a Grant from the research program ‘‘The environmentalinducing mechanisms of flavonoids in the leaves of Ginkgo biloba L.’’ (31070557) provided by the NationalNatural Science Foundation of China, and ‘‘Research and demonstration of oriented cultivation technologyin Ginkgo and neem plantations’’ (2012BAD21B04) provided by Science and Technology Department of
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China, and ‘‘The planting technologies of medical plantation for Ginkgo and camphor trees’’ (20120460102)provided by State Forestry Bureau.
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