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Anther Culture of Pepper: Morphological Charactersitics of Fruits of
Androgenetic Pepper Lines (Capsicum Annuum L.)
Keywords:
Anther culture, embryo induction, fruit parameters, botanic maturation.
ABSTRACT:
The presented study describes the effectiveness of induced androgenesis in
in vitro pepper anther culture. The aim of this study was the establishment of
effective technology for induction of embryogenesis in pepper anther culture;
development of the embryos into plantlets; successful adaptation and acclimatization
of plantlets from sterile to greenhouse conditions, and the breeding process of
obtained androgenetic pepper lines in the plastic tunnel conditions. From 19 pepper
genotypes under investigation, 12 possessed potential for embryo formation in
anther culture. After the acclimatization and adaptation of plantlets, seed material
from four pepper genotypes were collected: Piran, Kurtovska kapija SR, Zlaten medal
SR and Féherözön. From the collected seed material, breeding processes of
androgenetic pepper lines was set up in plastic tunnel (from April-October
2007-2010). The pepper genotypes and androgenetic lines as their products differ
among themselves in the length of phonological phases, fruit type and fruit utilization.
Detailed study for characterization of morphological and production parameters of
the fruits was established that indicate to sort out lines with positive characteristics.
136-145 | JRA | 2012 | Vol 1 | No 2
This article is governed by the Creative Commons Attribution License (http://creativecommons.org/
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www.jagri.info
Journal of Research in
Agriculture
An International Scientific
Research Journal
Authors:
Liljana Koleva Gudevaand
Fidanka Trajkova.
Institution:
University Goce
Delcev - Stip, Faculty of
Agriculture, Krste Misirkov
b.b., P.O. Box 201, 2000
Stip, R. of Macedonia.
Corresponding author:
Liljana Koleva Gudeva.
Phone no:
+389 34 550 627.
Email:
liljana.gudeva@ugd.edu.mk
Web Address:
http://www.jagri.info
documents/AG0028.pdf.
Dates:
Received: 10 Sep 2012 Accepted: 02 Oct 2012 Published: 17 Oct 2012
Article Citation:
Liljana Koleva Gudevaand Fidanka Trajkova.
Anther Culture of Pepper: Morphological Charactersitics of Fruits of Androgenetic
Pepper Lines (Capsicum Annuum L.).
Journal of Research in Agriculture (2012) 1(2): 136-145
Original Research
Journal of Research in Agriculture
JournalofResearchinAgriculture An International Scientific Research Journal
INTRODUCTION
Pepper is one of the most important cultures with
a long breeding tradition, but on the other hand, scientists
very often announce decrease of the pepper yield due to
the presence of pathogens and pests. Thus, there is a
need for creation of new, pepper genotypes, resulting
with higher quality and quantity of the yield (Study for
biodiversity in the Republic of Macedonia, 2003). Pepper
anther culture is well developed and used method in
plant biotechnology and plant breeding. The research on
pepper androgenesis was intensive by the end of
twentieth century, and still current: Dolcet-Sanjuan et al.,
(1997); Dumas de Valux et al., (1981); George and
Narayanaswamy (1973); Kim et al., (2008); Kuo et al.,
(1973); Lantos et al., (2009); Mityko et al., (1995);
Mityko and Fari (1997); Özkum and Tipirdamaz (2002) ;
Rodeva et al., (2004, 2006); Wang et al., (1973).
Establishing the effective method of anther culture is an
advance in abounding and improving the genetic
resources of pepper, Koleva-Gudeva et al., (2007, 2009).
Using the method of pepper anther culture, fertile
androgenetic plants from the genotypes of Kurtovska
kapija, Zlaten medal, Piran and Féherözön are created,
and also the comparative study was set up for the
characterization of the androgenetic lines of pepper.
MATERIALS AND METHODS
Anther-donor plant material and anther culture
conditions
Nineteen pepper genotypes were used as anther-
donor plants (Table 1). Anther-donor plants were grown
under greenhouse conditions. The flower buds were
harvested when the corolla was of the same length as the
calyx or slightly longer (Figure 1a). The developmental
stage of the microspores was determined in microscopic
slides of acetocarmine squashes. Flower buds were
surface sterilized in 70% ethanol for several seconds,
then in 5% calcium hypochlorite Ca(ClO)2 + 2-3 drops
Tween 20 for 10 minutes, and rinsed three times in
sterile distilled water. After the removal of the filaments,
anthers from three flower buds were placed in Petri dish
(6 cm), with the concave face down, touching the
culture medium. The method of Dumas de Valux et al.,
(1981) was used for induction of embryogenesis.
137 Journal of Research in Agriculture (2012) 1(2): 136-145
Gudeva and Trajkova, 2012
Table 1. Embryo induction from anthers of different pepper genotypes
Pepper genotype
Total nr. of
anthers
Embryogenic
anthers (%)
Embryos
per 100 anthers
Embryogenic
response
Féherözön 1502 17.39 a 32.60 bc Excellent
Tura 300 17.05 a 17.05 ab Good
Pritavit F1 330 9.23 abc 9.39 abc Fair
California wonder 151 6.67 abc 5.67 c Fair
Zlaten medal SR 1031 6.12 abc 8.97 bc Fair
Majori 330 5.83 abc 6.73 c Fair
Piran 823 5.03 abc 34.05 ab Poor
Zlaten medal ŠT 723 4.29 bc 18.57 bc Poor
Tomato shaped sweet 360 4.17 bc 4.54 c Poor
Kurtovska kapija BG 620 2.90 bc 50.55 a Poor
Kurtovska kapija SR 875 2.73 bc 10.20 bc Poor
Slatko luta 140 2.43 bc 3.33 c Poor
Feferona 79 0.00 c 0.00 c No
Vezena luta 83 0.00 c 0.00 c No
Sivrija 104 0.00 c 0.00 c No
Rotund 109 0.00 c 0.00 c No
Kurtovska kapija TU 236 0.00 c 0.00 c No
Kurtovska kapija MK 122 0.00 c 0.00 c No
Bonbona 270 0.00 c 0.00 c No
Mean within a column followed by the same letters are not significantly different at p < 0.05
according to Duncan’s multiple range test.
The anthers were cultivated on CP medium
+ 0.01 mg L-1
KIN + 0.01 mg L-1
2.4-D with incubation
of eight days in darkness at 35±2ºC, the following four
days the anthers were transferred to clime chamber at
25±2ºC with photoperiod of 12h light/12h dark.
Afterwards, the anthers were subcultured on R1 medium
+ 0.01 mg L-1
KIN and placed in clime chamber at
25±2ºC with photoperiodic 12h light/12h dark. Young
shoots emerging from the anthers were transferred onto
hormone free V3 media for rooting. Plantlets were
planted on sterile mixture of perlite : peat : sand (1:1:1)
and acclimatized in clime chamber, and afterwards
placed in greenhouse under cover in order to prevent
crosspollination (Figure 1 b, c, d).
Field conditions
Different androgenetic pepper lines from the
genotypes Kurtovska kapija SR, Zlaten medal SR, Piran
and Féherözön, obtained by the regeneration of embryos,
using the method of anther culture, were fertile and
produce seed material. Seeds collected from the fertile
androgenetic plants were used for their characterization
in the plastic tunnels in 2007. The collected seeds from
the peppers cultivated in 2007, 2008 and 2009 were used
for characterization in the experimental year 2008, 2009
and 2010, respectively. The same genotypes Kurtovska
kapija SR, Zlaten medal SR, Piran and Féherözön were
used as control plants (KKk, ZMk, Pk, Fk).
During the four year of the field investigation
(from April – October, 2007-2010), a total number of
36 pepper lines from four pepper genotypes Kurtovska
kapija SR, Zlaten medal SR, Piran and Féherözön (KK,
ZM, P, F) were subject of study. Experiments were
performed at the fields of Faculty of Agriculture, Goce
Delcev University in Strumica in plastic tunnel (Figure 2,
Walter clime diagrams). In blossom stage, plants were
covered with agrill to prevent the foreign pollination
between different genotypes (Figure 1e).
Estimation of morphological and production
characteristic of fruits
Ten pepper fruits in the stage of botanical
Journal of Research in Agriculture (2012) 1(2): 136-145 138
Gudeva and Trajkova, 2012
a b c
d e f
Figure 1. a) Morphological characteristics of pepper anther buds when microspores
are in uninucleate phase; b, c) Development of the embryos into plantlets on
V3 medium; d Fully developed plants on acclimatization in climate chamber;
e) breeding of androgenic pepper lines in plastic tunnel conditions; f) Caryotype of
root tip meristem cells of dihaploid plant obtained via androgenesis 2n=24 (x 1250).
maturation were taken as sampled from each pepper line,
and the controls, for analyze of fruit: length, width, total
weight, fruit weight without handle and seeds, pericarp
thickness, number of fruit locules, weight of dry seed per
fruit, number of seeds per fruit, and dry matter according
to Ipgri, Avrdc and Catie (1995).
Estimation of number of chromosomes
The number of chromosomes was counted in root
tip meristems. The tissue was prepared according to
Tjio and Levan (1950) cytological technique, as well as
standard “squash” method. The plant material after
germination in Petri dishes was pretreated with
8-hydrohyquinoline 0,002 M for 12-24 hours, fixed in
aceto- alcohol (1:3), hydrolysed with HCl 1N at 60o
C for
9 minutes and stained with 1-1,5% Gomori’s
hematoxylin by Konstantinov et al., (1985), Figure 1f.
Data analysis
All data on percentage of embryogenic anthers
and number of embryos per 100 anthers were subjected
to analysis of variance (ANOVA), and the mean values
were evaluated at the p < 0.05 level of significance using
Duncan’s Multiple Range Test. Data statistical analyses,
concerning morphological and production characteristics
of fruits, are done with the software SPSS.10, One-way
ANOVA and Duncan posthoc test, with the level of
significance 0.05% are carried out.
RESULTS AND DISCUSSION
Not all genotypes under investigation were able
to produce embryos (Table 1). After the induction period
on CP medium for 12 days the anthers were subcultured
on R1 medium, where since the beginning the embryos
showed totipotency, progression in development, growth
and shoot formation (Figure 1b). The shoots continued
the development on V3 medium where in absence of
plant growth regulators young plants were formed
(Figure 1c). The rooting was performed on V3 medium
and well rooted shoots were transferred on sterile
139 Journal of Research in Agriculture (2012) 1(2): 136-145
Gudeva and Trajkova, 2012
Walter climte diagram - Strumica, 2008
0
25
50
IV V VI VII VIII IX X
Months
Temperature(oС)
0
20
40
60
80
100
Precipitation(mm)
temperature
precipitation
Walter climte diagram - Strumica, 2009
0
30
60
IV V VI VII VIII IX X
Months
Temperature(oС)
0
20
40
60
80
100
120
Precipitation(mm)
temperature
precipitation
Walter climte diagram - Strumica, 2010
0
50
100
IV V VI VII VIII IX X
Months
Temperature(oС)
0
100
200
Precipitation(mm)
temperature
precipitation
Figure 2. Walter climate diagram for pepper vegetation period in Strumica: a) 2007; b) 2008; c) 2009;
d) 2010.
Walter climte diagram - Strumica, 2007
0
35
70
IV V VI VII VIII IX X
Months
Temperature(oС)
0
20
40
60
80
100
120
140
Precipitation(mm)
temperature
precipitation
a b
c d
Precipitation(mm)
Precipitation(mm)
Precipitation(mm)Precipitation(mm)
Temperature(°C)Temperature(°C)
Temperature(°C)Temperature(°C)
Months
Months
Months
Months
mixture of sand : perlite : peat in the ratio of 1:1:1. In
this stage the plants were ready for adaptation and
acclimatization (Figure 1d). Seed material from four
androgenetic pepper genotypes was collected: Kurtovska
kapija SR, Zlaten medal SR, Piran and Féherözön, and
were used for breeding process and for investigation of
morphological characteristics of fruits in plastic tunnel
conditions 2007 – 2010 (Table 2, 3, 4 and 5).
Climate conditions (Figure 2) in the vegetation
period, IV - X month, were favorable for the cultivation
of pepper fruits. Figure 2 b shows that 2008 was a
drought year, but with proper irrigation it did not
reflected unfavorably in the cultivation of the studied
genotypes of pepper.
The results from the characterization of the
androgenetic lines of pepper during 2007 are shown in
Table 2. The results showed that line KK3 has significant
differences from the control variety Kurtovska kapija for
the fruit weight and the fruit weight without handle and
seeds. Lines P3 and P4 showed significant differences
compared to the control variety Piran for fruit length,
total fruit weight, fruit weight without handle, seeds and
pericarp thickness. Results for the lines ZM1 and ZM2
compared with the control variety Zlaten medal, showed
that line ZM1 does not differ from the control, but the
line ZM2 has lower values for the majority of the
analyzed characteristics. One of the characteristics for
the androgenetic lines obtained from the variety
Féherözön is that line F8 did not give fertile fruits as
compared to the other lines from the variety Féherözön.
Results from the second experimental year
(2008) are shown in the Table 3. The highest value of
the fruit width, total fruit weight, fruit weight without
handle and seeds, weight of dry seeds and number of
seeds per fruit show the line KK1/1 which significantly
differ from the results for the other lines and the control.
Androgenetic lines obtained from the variety Zlaten
medal have significant differences in the value of the
weight of dry seeds per fruit, where the seeds from the
fruits of line ZM1/3 has the highest value of 1.18 g.
Androgenetic line F6/8 has the highest value for the dry
Gudeva and Trajkova, 2012
Journal of Research in Agriculture (2012) 1(2): 136-145 140
KKk 11.50a 4.78a 60.01b 53.73b 0.35a 2.50a 0.49a 66.50a 10.48a
КК1 11.54a 4.77a 67.73ab 60.30ab 0.35a 2.50a 0.39a 54.25a 10.12a
КК3 12.65a 5.12a 86.94a 76.81a 0.38a 2.25a 0.66a 65.75a 9.55a
Pk 12.77b 4.41a 60.23a 52.16a 0.34a 2.20a 0.78a 103.40a 9.96a
Р3 10.97b 3.55b 48.22a 38.66b 0.22b 2.50a 0.52a 71.90a 8.62a
Р4 16.99a 3.65b 57.40a 47.71ab 0.24b 2.60a 0.98a 103.50a 8.48a
ZMk 12.93a 4.35a 62.26a 52.40a 0.35a 2.20b 0.66a 82.80a 9.96a
ZM1 13.44a 4.30a 62.04a 53.68a 0.32a 2.20b 0.32b 67.80ab 9.62a
ZM2 10.74b 3.18b 31.22b 28.66b 0.26b 3.20a 0.21b 27.00b 8.48b
Fk 7.79b 5.60ab 66.16c 51.84b 0.46ab 4.00a 0.20a 161.80a 5.120b
F5 6.46c 6.35a 84.39b 76.77a 0.50a 3.18bc 0.31a 59.80c 9.491a
F6 9.97a 5.99a 94.24a 85.22a 0.39bc 2.70c 0.47a 91.10b 9.200a
F8 4.76d 4.91b 35.916d 33.80c 0.35c 3.70ab / / 9.480a
Table 2. Morphological and production characteristics of fruits in different pepper genotypes in botanical
maturation grown in plastic tunnel in 2007
Mean within a column followed by the same letters are not significantly different at p < 0.05 according to
Duncan’s multiple range test.
Genotypecode
Fruitlength(cm)
Fruitwidth(cm)
Totalfruitweightg)
Fruitweightwithout
handleandseeds(g)
Pericarp
thickness(cm)
Numberoffruit
locules
Wightofdryseeds/
fruit(g)
Numberofseeds/
fruit
Drymatter(%)
matter (7.30%) as compared to the other Féherözön lines
and the control variety Féherözön.
Results from the third experimental year (2009)
are given in Table 4. Characterization of the
androgenetic lines from the variety Kurtovska kapija and
the control show significant differences only for weight
of dry seeds per fruit. The total fruit weight of the control
Piran and the weight of the fruit without seeds and
handle are the lowest values, as compared to the same
parameters of the other androgenetic lines. Regarding
results of fruit characteristics of the control and the
androgenetic lines of the variety Zlaten medal, there are
significant difference for and pericarp thickness.
Results from the fourth experimental year (2010)
are given in Table 5. The fruits of line KK3/1 were the
longest and with the highest value for fruit weight
without seeds and handle as compared to the fruits from
the other Kurtovska kapija androgenetic lines and the
control. The Piran androgenetic lines and the control
significantly differ in the fruit length and the pericarp
thickness. The analysis of fruit parameters for
Féherözön control and androgenetic lines showed that
there is significant difference for the fruit width, total
fruit weight, fruit weight without handle and seeds,
pericarp thickness, number of fruit locules, weight of dry
seeds per fruit and number of seeds per fruit.
Slightest differences in the fruit morphology of
androgenetic lines and the mother line are present at
variety Zlaten medal SR during the three year
investigation period, while the biggest differences are
noticed at lines of Féherözön in the first experimental
year and lines of Kurtovska kapija in the second
experimental year. Although Féherözön genotype
showed the highest degree of formation of embryos
141 Journal of Research in Agriculture (2012) 1(2): 136-145
Gudeva and Trajkova, 2012
KKk 13.55b 6.50b 89.70c 72.53c 0.38c 2.00c 1.49b 258.80ab 7.30a
КК1/1 14.49ab 7.63a 167.30a 142.90a 0.42bc 2.20c 2.19a 297.60a 7.70a
КК1/8 15.15a 6.59b 138.31b 117.60b 0.42abc 2.40bc 1.45b 198.60b 7.30a
КК3/2 13.87b 6.22b 129.30b 107.80b 0.46ab 3.00a 1.67ab 215.40b 7.20a
КК3/4 14.33ab 6.43b 135.60b 114.95b 0.50a 2.80ab 1.86ab 222.60ab 7.40a
Pк 15.90b 3.58c 46.70c 38.60c 0.28b 3.00a 0.30c 80.80b 8.8ab
Р3/3 17.74ab 4.77a 70.00ab 55.73ab 0.42a 2.00b 1.57a 186.80a 7.20b
Р3/8 17.70ab 4.58a 74.70a 59.95a 0.24b 2.60ab 1.09b 158.40a 7.80ab
Р4/1 18.25ab 3.81bc 58.00bc 48.42b 0.31b 2.40ab 0.53c 61.80b 9.10a
Р4/7 20.67a 4.39ab 79.80a 62.83a 0.26b 2.80ab 1.78a 200.40a 8.10ab
ZMk 13.47a 4.99a 88.00a 70.30a 0.39a 2.20a 0.80b 131.80a 6.60a
ZM1/2 14.61a 4.98a 80.99a 66.92a 0.41a 2.40a 0.79b 164.00a 7.20a
ZM1/3 13.30a 5.34a 94.50a 73.53a 0.48a 2.80a 1.18a 190.60a 7.50a
Fk 8.12b 7.18ab 123.50a 98.23a 0.40b 3.80a 1.35a 222.40a 6.40b
F5/2 6.89bc 7.24ab 111.00a 87.85a 0.43ab 3.00b 1.55a 239.80a 5.40d
F5/9 6.59c 7.74a 129.10a 122.50a 0.46ab 3.40ab 1.41a 214.80a 5.60cd
F6/3 10.20a 6.82b 126.20a 104.60a 0.49a 3.20ab 0.71a 114.00a 6.20bc
F6/8 10.55a 6.77b 134.90a 109.90a 0.50a 3.60ab 1.01a 197.20a 7.30a
Table 3. Morphological and production characteristics of fruits in different pepper genotypes in botanical
maturation grown in plastic tunnel in 2008
Mean within a column followed by the same letters are not significantly different at p < 0.05 according to
Duncan’s multiple range test.
Genotypecode
Fruitlength(cm)
Fruitwidth(cm)
Totalfruitweightg)
Fruitweightwithout
handleandseeds(g)
Pericarp
thickness(cm)
Numberoffruit
locules
Wightofdryseeds/
fruit(g)
Numberofseeds/
fruit
Drymatter(%)
(32.60 numbers of embryos per 100 anthers, Table 1),
the domestic varieties Kurtovska kapija SR, Zlaten
medal SR and Piran showed priority in the selection
process.
There are several factors affecting androgenesis
in many species, such as genotypes (Mityko et al., 1995;
Rodeva et al., 2004), growth of donor plants,
pre-treatments of anthers (Özkum and Tripirdamaz,
2002; Koleva-Gudeva, 2003; Ashok Kumar et al., 2003),
composition of medium (Irikova and Rodeva, 2004;
Koleva-Gudeva and Spasenoski, 2007; Dolcet-Sanjuan
et al., 1997) and the source of plant material. The
mechanism of cold and heat-shock treatment for
induction of somatic embryogenesis has been explored
and discussed by many authors (Dolcet-Sanjuan et al.,
1997; Dumas de Valux et al., 1981). The studies on
somatic embryogenesis of pepper (C. annuum L.) are in
the domain of androgensis: George and Narayanaswamy
(1973), Dumas de Valux et al. (1981), Mityko et al.,
(1995), Dolcet-Sanjuan et al., (1997) and Rodeva et al.,
(2004). According to the literature, the heat thermal
stress (+35o
C) has greater effect than the cold one (+7o
C)
in the process of stimulation of macrospore division of
pepper (Kim et al., 2008). These findings are in
agreement with the results obtained in the present study.
From all pepper genotypes under investigation,
12 possessed potential for formation of embryos. The hot
genotypes Feferona, Vezena luta, Sivrija and Bonbona
and the sweet genotypes Rotund, Kurtovska kapija TU
and Kurtovska kapija MK did not show androgenetic
potential, i.e. in anther culture did not form embryos
shoots (Table 1). The experiment showed that the
effectiveness of androgenesis process depends on pepper
genotype and the conditions for anther culture
Journal of Research in Agriculture (2012) 1(2): 136-145 142
Gudeva and Trajkova, 2012
Table 4. Morphological and production characteristics of fruits in different pepper genotypes in botanical
maturation grown in plastic tunnel in 2009
KKk 13.62a 5.31a 84.78a 71.17a 0.37b 2.00a 0.25b 55.80b 8.50a
КК1/8/1 13.27a 5.71a 77.54a 91.60a 0.402ab 2.00a 0.76a 128.75a 6.00c
КК3/4/5 12.61a 5.56a 95.50a 78.96a 0.44ab 2.40a 0.29b 57.33b 6.50c
КК3/4/3 12.84a 5.29a 83.71a 71.06a 0.44ab 2.20a 0.09b 28.00b 7.50b
Pk 15.08a 3.07a 34.85b 29.31b 0.24b 2.40ab 0.18b 40.0b 6.60a
P3/3/1 15.66a 3.41a 54.04a 43.28a 0.23b 2.00b 0.97b 40.0b 6.00ab
Р3/3/3 14.41a 3.62a 49.90a 41.08a 0.34a 2.40ab 0.52b 66.80ab 6.10a
Р4/7/3 15.51a 3.47a 51.45a 40.75a 0.26b 2.80a 0.41b 119.40ab 6.50a
Р4/7/1 16.29a 3.84a 55.39a 41.62a 0.25b 2.00b 1.12a 138.60a 4.80b
ZMk 14.77a 5.35a 100.61a 73.13a 0.48a 2.60a 0.56a 96.80a 6.10b
ZM1/2/4 15.49a 5.18a 90.46a 75.69a 0.51a 2.60a 0.65a 159.80a 8.10a
ZM1/2/5 13.37a 5.35a 94.30a 92.05a 0.39b 2.60a 0.82a 164.80a 7.60a
Fk 9.67a 7.57a 140.43a 103.32a 0.51a 3.08ab 0.59a 100.20a 5.00a
F6/3/1 10.55a 6.59a 113.82a 90.83ab 0.40b 3.40bc 0.40a 73.60a 5.20a
F6/3/5 10.51a 7.12a 126.27a 97.03ab 0.50a 3.40bc 0.34a 56.60a 5.30a
F5/2/2 7.50b 7.67a 123.10a 92.99ab 0.498a 3.00c 0.85a 143.60a 5.50a
F5/2/3 5.91c 7.30a 109.39a 79.45b 0.514a 4.00a 0.76a 118.80a 5.00a
Mean within a column followed by the same letters are not significantly different at p < 0.05 according to
Duncan’s multiple range test.
Genotypecode
Fruitlength(cm)
Fruitwidth(cm)
Totalfruitweightg)
Fruitweightwithout
handleandseeds(g)
Pericarp
thickness(cm)
Numberoffruit
locules
Wightofdryseeds/
fruit(g)
Numberofseeds/
fruit
Drymatter(%)
maintenance. The embryogenesis resulted in embryo
formation that developed into plantlets which were
acclimatized in climate chamber and greenhouse
conditions. Mityko and Fari (1997) concluded that
bell-shape varieties have the highest androgenic ability,
while the rest showed very low or no androgenic activity,
which is consistent with our results, where the bellshape
varieties Féherözön and California Wonder showed a
higher potential for embryogenesis compared to the hot
and the sweet ones. The anthers of Féherözön variety
showed low callus formation, but the androgenic ability
was the highest on the same medium. In general, once
the callus was initiated, the induction of somatic embryos
did not occur, which is similar with the results reported
by Binzel et al., (1996). After successful acclimatization
of the regenerated plant, seed material from four pepper
genotypes was collected: Kurtovska kapija SR, Zlaten
medal SR, Piran and Féherözön, and were used for
characterization and breeding process in plastic tunnel
conditions 2007 - 2010. The characterization of different
androgenic lines compared to the mother genotype
showed that there is great variability in some pepper
yield-related characteristics from certain lines
(Thul et al., 2009). The lines that showed such potential
can be used as starting material for future pepper
breeding (Portis et al., 2004; Rodeva et al., 2007).
CONCLUSION
From 19 pepper genotypes under investigation,
12 possessed potential for embryo formation. The hot
genotypes Feferona, Vezena luta, Sivrija and Bonbona
and the sweet genotypes Rotund, Kurtovska kapija TU
and Kurtovska kapija MK did not show androgenetic
potential. According to the classification of Mityko and
143 Journal of Research in Agriculture (2012) 1(2): 136-145
Gudeva and Trajkova, 2012
KKk 11.694ab 4.74a 63.99b 51.73b 0.45b 2.22a 0.43a 69.00a 7.80b
КК1/2 10.294c 5.37a 53.72b 43.22b 0.46b 2.23a 0.28a 45.20a 7.00c
КК3/1 12.691a 5.43a 91.92a 75.72a 0.54a 2.40a 0.45a 38.80a 8.70a
КК4/2 11.074bc 5.21a 61.01b 54.15b 0.48ab 2.41a 0.65a 103.80a 7.80b
Pk 14.763b 3.68a 59.62a 50.33a 0.52a 3.00a 0.17b 27.33b 7.60a
P1/3 17.80a 3.48a 59.89a 48.56a 0.41b 2.40a 0.62ab 69.60ab 7.60a
Р2/3 15.01b 3.17a 49.77a 40.41a 0.36b 2.61a 0.29b 31.60b 7.60a
Р4/3 17.75a 3.34a 56.29a 44.71a 0.36b 2.40a 0.84a 96.80a 8.00a
Fk 7.93b 6.94b 109.91b 80.38bc 0.51c 3.83a 0.94c 144.00c 7.20ab
F1/2 11.40a 7.73ab 119.64b 95.84b 0.57bc 3.00bc 0.94c 231.00b 6.30cd
F2/5 10.40a 5.79c 81.48c 64.17c 0.53c 2.60c 0.56c 97.40c 6.80bc
F3/3 8.47b 8.39a 154.74a 119.80a 0.89a 3.40ab 1.42b 325.20a 7.90a
F4/5 7.72b 7.02b 109.53b 78.80bc 0.64b 3.20ab 0.59c 86.00c 5.90d
ZMk 15.81a 5.45a 96.98a 90.22a 0.44a 2.60a 0.84a 117.80a 5.80b
ZM2/2 14.01a 3.88b 58.58b 46.63b 0.35b 2.67a 0.64b 124.30a 6.20a
Table 5. Morphological and production characteristics of fruits in different pepper genotypes in botanical
maturation grown in plastic tunnel in 2010
Mean separation in columns by Duncan’s multiple range test. In each column, values followed by the same
letter do not differ significantly at P<0.05 for all genotypes except ZMk and ZM2/2.
Genotypecode
Fruitlength(cm)
Fruitwidth(cm)
Totalfruitweightg)
Fruitweightwith-
outhandleandseeds
(g)
Pericarp
thickness(cm)
Numberoffruit
locules
Wightofdryseeds/
fruit(g)
Numberofseeds/
fruit
Drymatter(%)
Fari (1997) for identification of androgenetic potential,
based on percentage of anthers that give embryos, in our
research twelve genotypes showed ability for embryo
formation: 1 genotype with excellent androgenetic
potential: Féherözön; 1 genotype with good androgenetic
potential: Tura; 4 genotypes with fair androgenetic
potential: Pritavit F1, Californian wonder, Zlaten medal
SR and Majori; 6 genotypes with poor androgenetic
potential: Piran, Zlaten medal ŠT, Tomato shaped sweet,
Kurtovska kapija BG, Kurtovska kapija SR and Slatko
luta; 7 genotypes do not possess androgenetic potential:
Feferona, Vezena Luta, Sivrija, Rotund, Kurtovska
kapija TU, Kurtovska kapija MK and Bonbona.
Collected material will lead to creation of new and
improved pepper genotypes, created for specific
agroecological conditions. Generally, the further process
of selection from all 19 pepper genotypes should be done
towards the improvement of domestic genotypes
Kurtovska kapija SR, Zlaten medal SR and Piran.
REFERENCES
Binzel ML, Sankhla N, Joshi S, Sankhla D. 1996.
Induction of direct somatic embryogenesis and plant
regeneration in pepper (Capsicum annuum L.). Plant Cell
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carbon dioxide enrichment. J Amer Soc Hort Sci 122(4):
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Dumas de Valux R, Chambonnet D, Pochard E. 1981.
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Anthers: high rate plant production from different
genotypes by +35ºC treatments. Agronomie
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George L and Narayanaswamy S. 1973. Haploid
capsicum through experimental androgenesis.
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Ipgri, Avrdc and Catie. 1995. Descriptors for Capsicum
(Capsicum spp.). International Plant Genetic Resources
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Kim M, Jang LC, Kim EJ, Park M, Yoon M. 2008.
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trough isolated microspore culture. Plant Cell Report
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Koleva-Gudeva L, Spasenoski M, Trajkova F. 2007.
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effects of incubation treatments and different media.
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Koleva-Gudeva L, Trajkova F, Dimeska G,
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Konstantinov GH, Belcheva RG, Goranov AK. 1985.
Rykovodstvo za prakticheski zanaytiy po genetika. Sofia.
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HC. 1973. Investigation of the anther culture in vitro of
Nicotiana and Capsicum annuum L. Acta Bot. Sin.
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Lantos C, Juhasz GS, Somogyi KO, Vagi P, Mihaly
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isolated microspore culture (Capsicum annuum L.) via
co-culture with ovary tissue culture of pepper or maze.
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Mityko J, Andrasfalvy G, Csillery G, Fari M. 1995.
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hybrids of pepper. Plant Breeding 114:78-80.
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Gudeva and Trajkova, 2012
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doubled haploid plant production in pepper via anther
and microspore culture. Acta Hort., 447:281-287.
Özkum D, Tipirdamaz R. 2002. The effects of cold
treatment and charcoal on the in vitro androgenesis of
pepper (Capiscum annuum L.). Turk. J. Bot.,
26:131-139.
Rodeva V, Irikova T, Todorova J. 2004. Anther culture
of pepper (Capsicum annuum L.): Comparative study of
effects of the genotype. Biotech and Bitechnol Eq.
18(3):34-38.
Rodeva V, Grozeva S, Todorova V. 2006. In vitro
answer of Bulgarian pepper Capiscum annuum L.
genotypes. Genetica (Serbia) 38(2):129-136.
Rodeva V, Koleva-Gudeva L, Grozdeva S, Trajkova
F. 2007. Obtaining of haploids in anther culture of
pepper Capsicum annuum L. and their including in the
breeding process. Yearbook 7, Goce Delcev University,
Stip, Faculty of Agriculture, 7-17.
Tjio JH, Levan A. 1950. The use of oxuquinoline in
chromosomes analysis. Anal. Extac. Exp. Aula Dei,
2(1):21-64
Thul ST, Lal RK, Shasany AK, Darokar MP, Gupta
AK, Gupta MM, Verma RK, Khanuja SPS 2009.
Estimation of phenotypic divergence in a collection of
Capsicum species for yield-related traits. Euphytica
168:189-196.
Portis E, Acquadro A, Comino C, Sergio L. 2004.
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landrace population of pepper (Capsicum annuum L.),
grown in North-West Italy. Genetic Resources and Crop
Evolution 51:581-590.
Wang JJ, Sun CS, Wang CC, Chein NF. 1973. The
induction of pollen plantlets Capsicum annuum from
anther culture. Sci. Sinica 16(1):147-151.
Journal of Research in Agriculture (2012) 1(2): 136-145 145
Gudeva and Trajkova, 2012
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Pepper Anther Culture Study Yields New Fruit Lines

  • 1. Anther Culture of Pepper: Morphological Charactersitics of Fruits of Androgenetic Pepper Lines (Capsicum Annuum L.) Keywords: Anther culture, embryo induction, fruit parameters, botanic maturation. ABSTRACT: The presented study describes the effectiveness of induced androgenesis in in vitro pepper anther culture. The aim of this study was the establishment of effective technology for induction of embryogenesis in pepper anther culture; development of the embryos into plantlets; successful adaptation and acclimatization of plantlets from sterile to greenhouse conditions, and the breeding process of obtained androgenetic pepper lines in the plastic tunnel conditions. From 19 pepper genotypes under investigation, 12 possessed potential for embryo formation in anther culture. After the acclimatization and adaptation of plantlets, seed material from four pepper genotypes were collected: Piran, Kurtovska kapija SR, Zlaten medal SR and Féherözön. From the collected seed material, breeding processes of androgenetic pepper lines was set up in plastic tunnel (from April-October 2007-2010). The pepper genotypes and androgenetic lines as their products differ among themselves in the length of phonological phases, fruit type and fruit utilization. Detailed study for characterization of morphological and production parameters of the fruits was established that indicate to sort out lines with positive characteristics. 136-145 | JRA | 2012 | Vol 1 | No 2 This article is governed by the Creative Commons Attribution License (http://creativecommons.org/ licenses/by/2.0), which gives permission for unrestricted use, non-commercial, distribution and reproduction in all medium, provided the original work is properly cited. www.jagri.info Journal of Research in Agriculture An International Scientific Research Journal Authors: Liljana Koleva Gudevaand Fidanka Trajkova. Institution: University Goce Delcev - Stip, Faculty of Agriculture, Krste Misirkov b.b., P.O. Box 201, 2000 Stip, R. of Macedonia. Corresponding author: Liljana Koleva Gudeva. Phone no: +389 34 550 627. Email: liljana.gudeva@ugd.edu.mk Web Address: http://www.jagri.info documents/AG0028.pdf. Dates: Received: 10 Sep 2012 Accepted: 02 Oct 2012 Published: 17 Oct 2012 Article Citation: Liljana Koleva Gudevaand Fidanka Trajkova. Anther Culture of Pepper: Morphological Charactersitics of Fruits of Androgenetic Pepper Lines (Capsicum Annuum L.). Journal of Research in Agriculture (2012) 1(2): 136-145 Original Research Journal of Research in Agriculture JournalofResearchinAgriculture An International Scientific Research Journal
  • 2. INTRODUCTION Pepper is one of the most important cultures with a long breeding tradition, but on the other hand, scientists very often announce decrease of the pepper yield due to the presence of pathogens and pests. Thus, there is a need for creation of new, pepper genotypes, resulting with higher quality and quantity of the yield (Study for biodiversity in the Republic of Macedonia, 2003). Pepper anther culture is well developed and used method in plant biotechnology and plant breeding. The research on pepper androgenesis was intensive by the end of twentieth century, and still current: Dolcet-Sanjuan et al., (1997); Dumas de Valux et al., (1981); George and Narayanaswamy (1973); Kim et al., (2008); Kuo et al., (1973); Lantos et al., (2009); Mityko et al., (1995); Mityko and Fari (1997); Özkum and Tipirdamaz (2002) ; Rodeva et al., (2004, 2006); Wang et al., (1973). Establishing the effective method of anther culture is an advance in abounding and improving the genetic resources of pepper, Koleva-Gudeva et al., (2007, 2009). Using the method of pepper anther culture, fertile androgenetic plants from the genotypes of Kurtovska kapija, Zlaten medal, Piran and Féherözön are created, and also the comparative study was set up for the characterization of the androgenetic lines of pepper. MATERIALS AND METHODS Anther-donor plant material and anther culture conditions Nineteen pepper genotypes were used as anther- donor plants (Table 1). Anther-donor plants were grown under greenhouse conditions. The flower buds were harvested when the corolla was of the same length as the calyx or slightly longer (Figure 1a). The developmental stage of the microspores was determined in microscopic slides of acetocarmine squashes. Flower buds were surface sterilized in 70% ethanol for several seconds, then in 5% calcium hypochlorite Ca(ClO)2 + 2-3 drops Tween 20 for 10 minutes, and rinsed three times in sterile distilled water. After the removal of the filaments, anthers from three flower buds were placed in Petri dish (6 cm), with the concave face down, touching the culture medium. The method of Dumas de Valux et al., (1981) was used for induction of embryogenesis. 137 Journal of Research in Agriculture (2012) 1(2): 136-145 Gudeva and Trajkova, 2012 Table 1. Embryo induction from anthers of different pepper genotypes Pepper genotype Total nr. of anthers Embryogenic anthers (%) Embryos per 100 anthers Embryogenic response Féherözön 1502 17.39 a 32.60 bc Excellent Tura 300 17.05 a 17.05 ab Good Pritavit F1 330 9.23 abc 9.39 abc Fair California wonder 151 6.67 abc 5.67 c Fair Zlaten medal SR 1031 6.12 abc 8.97 bc Fair Majori 330 5.83 abc 6.73 c Fair Piran 823 5.03 abc 34.05 ab Poor Zlaten medal ŠT 723 4.29 bc 18.57 bc Poor Tomato shaped sweet 360 4.17 bc 4.54 c Poor Kurtovska kapija BG 620 2.90 bc 50.55 a Poor Kurtovska kapija SR 875 2.73 bc 10.20 bc Poor Slatko luta 140 2.43 bc 3.33 c Poor Feferona 79 0.00 c 0.00 c No Vezena luta 83 0.00 c 0.00 c No Sivrija 104 0.00 c 0.00 c No Rotund 109 0.00 c 0.00 c No Kurtovska kapija TU 236 0.00 c 0.00 c No Kurtovska kapija MK 122 0.00 c 0.00 c No Bonbona 270 0.00 c 0.00 c No Mean within a column followed by the same letters are not significantly different at p < 0.05 according to Duncan’s multiple range test.
  • 3. The anthers were cultivated on CP medium + 0.01 mg L-1 KIN + 0.01 mg L-1 2.4-D with incubation of eight days in darkness at 35±2ºC, the following four days the anthers were transferred to clime chamber at 25±2ºC with photoperiod of 12h light/12h dark. Afterwards, the anthers were subcultured on R1 medium + 0.01 mg L-1 KIN and placed in clime chamber at 25±2ºC with photoperiodic 12h light/12h dark. Young shoots emerging from the anthers were transferred onto hormone free V3 media for rooting. Plantlets were planted on sterile mixture of perlite : peat : sand (1:1:1) and acclimatized in clime chamber, and afterwards placed in greenhouse under cover in order to prevent crosspollination (Figure 1 b, c, d). Field conditions Different androgenetic pepper lines from the genotypes Kurtovska kapija SR, Zlaten medal SR, Piran and Féherözön, obtained by the regeneration of embryos, using the method of anther culture, were fertile and produce seed material. Seeds collected from the fertile androgenetic plants were used for their characterization in the plastic tunnels in 2007. The collected seeds from the peppers cultivated in 2007, 2008 and 2009 were used for characterization in the experimental year 2008, 2009 and 2010, respectively. The same genotypes Kurtovska kapija SR, Zlaten medal SR, Piran and Féherözön were used as control plants (KKk, ZMk, Pk, Fk). During the four year of the field investigation (from April – October, 2007-2010), a total number of 36 pepper lines from four pepper genotypes Kurtovska kapija SR, Zlaten medal SR, Piran and Féherözön (KK, ZM, P, F) were subject of study. Experiments were performed at the fields of Faculty of Agriculture, Goce Delcev University in Strumica in plastic tunnel (Figure 2, Walter clime diagrams). In blossom stage, plants were covered with agrill to prevent the foreign pollination between different genotypes (Figure 1e). Estimation of morphological and production characteristic of fruits Ten pepper fruits in the stage of botanical Journal of Research in Agriculture (2012) 1(2): 136-145 138 Gudeva and Trajkova, 2012 a b c d e f Figure 1. a) Morphological characteristics of pepper anther buds when microspores are in uninucleate phase; b, c) Development of the embryos into plantlets on V3 medium; d Fully developed plants on acclimatization in climate chamber; e) breeding of androgenic pepper lines in plastic tunnel conditions; f) Caryotype of root tip meristem cells of dihaploid plant obtained via androgenesis 2n=24 (x 1250).
  • 4. maturation were taken as sampled from each pepper line, and the controls, for analyze of fruit: length, width, total weight, fruit weight without handle and seeds, pericarp thickness, number of fruit locules, weight of dry seed per fruit, number of seeds per fruit, and dry matter according to Ipgri, Avrdc and Catie (1995). Estimation of number of chromosomes The number of chromosomes was counted in root tip meristems. The tissue was prepared according to Tjio and Levan (1950) cytological technique, as well as standard “squash” method. The plant material after germination in Petri dishes was pretreated with 8-hydrohyquinoline 0,002 M for 12-24 hours, fixed in aceto- alcohol (1:3), hydrolysed with HCl 1N at 60o C for 9 minutes and stained with 1-1,5% Gomori’s hematoxylin by Konstantinov et al., (1985), Figure 1f. Data analysis All data on percentage of embryogenic anthers and number of embryos per 100 anthers were subjected to analysis of variance (ANOVA), and the mean values were evaluated at the p < 0.05 level of significance using Duncan’s Multiple Range Test. Data statistical analyses, concerning morphological and production characteristics of fruits, are done with the software SPSS.10, One-way ANOVA and Duncan posthoc test, with the level of significance 0.05% are carried out. RESULTS AND DISCUSSION Not all genotypes under investigation were able to produce embryos (Table 1). After the induction period on CP medium for 12 days the anthers were subcultured on R1 medium, where since the beginning the embryos showed totipotency, progression in development, growth and shoot formation (Figure 1b). The shoots continued the development on V3 medium where in absence of plant growth regulators young plants were formed (Figure 1c). The rooting was performed on V3 medium and well rooted shoots were transferred on sterile 139 Journal of Research in Agriculture (2012) 1(2): 136-145 Gudeva and Trajkova, 2012 Walter climte diagram - Strumica, 2008 0 25 50 IV V VI VII VIII IX X Months Temperature(oС) 0 20 40 60 80 100 Precipitation(mm) temperature precipitation Walter climte diagram - Strumica, 2009 0 30 60 IV V VI VII VIII IX X Months Temperature(oС) 0 20 40 60 80 100 120 Precipitation(mm) temperature precipitation Walter climte diagram - Strumica, 2010 0 50 100 IV V VI VII VIII IX X Months Temperature(oС) 0 100 200 Precipitation(mm) temperature precipitation Figure 2. Walter climate diagram for pepper vegetation period in Strumica: a) 2007; b) 2008; c) 2009; d) 2010. Walter climte diagram - Strumica, 2007 0 35 70 IV V VI VII VIII IX X Months Temperature(oС) 0 20 40 60 80 100 120 140 Precipitation(mm) temperature precipitation a b c d Precipitation(mm) Precipitation(mm) Precipitation(mm)Precipitation(mm) Temperature(°C)Temperature(°C) Temperature(°C)Temperature(°C) Months Months Months Months
  • 5. mixture of sand : perlite : peat in the ratio of 1:1:1. In this stage the plants were ready for adaptation and acclimatization (Figure 1d). Seed material from four androgenetic pepper genotypes was collected: Kurtovska kapija SR, Zlaten medal SR, Piran and Féherözön, and were used for breeding process and for investigation of morphological characteristics of fruits in plastic tunnel conditions 2007 – 2010 (Table 2, 3, 4 and 5). Climate conditions (Figure 2) in the vegetation period, IV - X month, were favorable for the cultivation of pepper fruits. Figure 2 b shows that 2008 was a drought year, but with proper irrigation it did not reflected unfavorably in the cultivation of the studied genotypes of pepper. The results from the characterization of the androgenetic lines of pepper during 2007 are shown in Table 2. The results showed that line KK3 has significant differences from the control variety Kurtovska kapija for the fruit weight and the fruit weight without handle and seeds. Lines P3 and P4 showed significant differences compared to the control variety Piran for fruit length, total fruit weight, fruit weight without handle, seeds and pericarp thickness. Results for the lines ZM1 and ZM2 compared with the control variety Zlaten medal, showed that line ZM1 does not differ from the control, but the line ZM2 has lower values for the majority of the analyzed characteristics. One of the characteristics for the androgenetic lines obtained from the variety Féherözön is that line F8 did not give fertile fruits as compared to the other lines from the variety Féherözön. Results from the second experimental year (2008) are shown in the Table 3. The highest value of the fruit width, total fruit weight, fruit weight without handle and seeds, weight of dry seeds and number of seeds per fruit show the line KK1/1 which significantly differ from the results for the other lines and the control. Androgenetic lines obtained from the variety Zlaten medal have significant differences in the value of the weight of dry seeds per fruit, where the seeds from the fruits of line ZM1/3 has the highest value of 1.18 g. Androgenetic line F6/8 has the highest value for the dry Gudeva and Trajkova, 2012 Journal of Research in Agriculture (2012) 1(2): 136-145 140 KKk 11.50a 4.78a 60.01b 53.73b 0.35a 2.50a 0.49a 66.50a 10.48a КК1 11.54a 4.77a 67.73ab 60.30ab 0.35a 2.50a 0.39a 54.25a 10.12a КК3 12.65a 5.12a 86.94a 76.81a 0.38a 2.25a 0.66a 65.75a 9.55a Pk 12.77b 4.41a 60.23a 52.16a 0.34a 2.20a 0.78a 103.40a 9.96a Р3 10.97b 3.55b 48.22a 38.66b 0.22b 2.50a 0.52a 71.90a 8.62a Р4 16.99a 3.65b 57.40a 47.71ab 0.24b 2.60a 0.98a 103.50a 8.48a ZMk 12.93a 4.35a 62.26a 52.40a 0.35a 2.20b 0.66a 82.80a 9.96a ZM1 13.44a 4.30a 62.04a 53.68a 0.32a 2.20b 0.32b 67.80ab 9.62a ZM2 10.74b 3.18b 31.22b 28.66b 0.26b 3.20a 0.21b 27.00b 8.48b Fk 7.79b 5.60ab 66.16c 51.84b 0.46ab 4.00a 0.20a 161.80a 5.120b F5 6.46c 6.35a 84.39b 76.77a 0.50a 3.18bc 0.31a 59.80c 9.491a F6 9.97a 5.99a 94.24a 85.22a 0.39bc 2.70c 0.47a 91.10b 9.200a F8 4.76d 4.91b 35.916d 33.80c 0.35c 3.70ab / / 9.480a Table 2. Morphological and production characteristics of fruits in different pepper genotypes in botanical maturation grown in plastic tunnel in 2007 Mean within a column followed by the same letters are not significantly different at p < 0.05 according to Duncan’s multiple range test. Genotypecode Fruitlength(cm) Fruitwidth(cm) Totalfruitweightg) Fruitweightwithout handleandseeds(g) Pericarp thickness(cm) Numberoffruit locules Wightofdryseeds/ fruit(g) Numberofseeds/ fruit Drymatter(%)
  • 6. matter (7.30%) as compared to the other Féherözön lines and the control variety Féherözön. Results from the third experimental year (2009) are given in Table 4. Characterization of the androgenetic lines from the variety Kurtovska kapija and the control show significant differences only for weight of dry seeds per fruit. The total fruit weight of the control Piran and the weight of the fruit without seeds and handle are the lowest values, as compared to the same parameters of the other androgenetic lines. Regarding results of fruit characteristics of the control and the androgenetic lines of the variety Zlaten medal, there are significant difference for and pericarp thickness. Results from the fourth experimental year (2010) are given in Table 5. The fruits of line KK3/1 were the longest and with the highest value for fruit weight without seeds and handle as compared to the fruits from the other Kurtovska kapija androgenetic lines and the control. The Piran androgenetic lines and the control significantly differ in the fruit length and the pericarp thickness. The analysis of fruit parameters for Féherözön control and androgenetic lines showed that there is significant difference for the fruit width, total fruit weight, fruit weight without handle and seeds, pericarp thickness, number of fruit locules, weight of dry seeds per fruit and number of seeds per fruit. Slightest differences in the fruit morphology of androgenetic lines and the mother line are present at variety Zlaten medal SR during the three year investigation period, while the biggest differences are noticed at lines of Féherözön in the first experimental year and lines of Kurtovska kapija in the second experimental year. Although Féherözön genotype showed the highest degree of formation of embryos 141 Journal of Research in Agriculture (2012) 1(2): 136-145 Gudeva and Trajkova, 2012 KKk 13.55b 6.50b 89.70c 72.53c 0.38c 2.00c 1.49b 258.80ab 7.30a КК1/1 14.49ab 7.63a 167.30a 142.90a 0.42bc 2.20c 2.19a 297.60a 7.70a КК1/8 15.15a 6.59b 138.31b 117.60b 0.42abc 2.40bc 1.45b 198.60b 7.30a КК3/2 13.87b 6.22b 129.30b 107.80b 0.46ab 3.00a 1.67ab 215.40b 7.20a КК3/4 14.33ab 6.43b 135.60b 114.95b 0.50a 2.80ab 1.86ab 222.60ab 7.40a Pк 15.90b 3.58c 46.70c 38.60c 0.28b 3.00a 0.30c 80.80b 8.8ab Р3/3 17.74ab 4.77a 70.00ab 55.73ab 0.42a 2.00b 1.57a 186.80a 7.20b Р3/8 17.70ab 4.58a 74.70a 59.95a 0.24b 2.60ab 1.09b 158.40a 7.80ab Р4/1 18.25ab 3.81bc 58.00bc 48.42b 0.31b 2.40ab 0.53c 61.80b 9.10a Р4/7 20.67a 4.39ab 79.80a 62.83a 0.26b 2.80ab 1.78a 200.40a 8.10ab ZMk 13.47a 4.99a 88.00a 70.30a 0.39a 2.20a 0.80b 131.80a 6.60a ZM1/2 14.61a 4.98a 80.99a 66.92a 0.41a 2.40a 0.79b 164.00a 7.20a ZM1/3 13.30a 5.34a 94.50a 73.53a 0.48a 2.80a 1.18a 190.60a 7.50a Fk 8.12b 7.18ab 123.50a 98.23a 0.40b 3.80a 1.35a 222.40a 6.40b F5/2 6.89bc 7.24ab 111.00a 87.85a 0.43ab 3.00b 1.55a 239.80a 5.40d F5/9 6.59c 7.74a 129.10a 122.50a 0.46ab 3.40ab 1.41a 214.80a 5.60cd F6/3 10.20a 6.82b 126.20a 104.60a 0.49a 3.20ab 0.71a 114.00a 6.20bc F6/8 10.55a 6.77b 134.90a 109.90a 0.50a 3.60ab 1.01a 197.20a 7.30a Table 3. Morphological and production characteristics of fruits in different pepper genotypes in botanical maturation grown in plastic tunnel in 2008 Mean within a column followed by the same letters are not significantly different at p < 0.05 according to Duncan’s multiple range test. Genotypecode Fruitlength(cm) Fruitwidth(cm) Totalfruitweightg) Fruitweightwithout handleandseeds(g) Pericarp thickness(cm) Numberoffruit locules Wightofdryseeds/ fruit(g) Numberofseeds/ fruit Drymatter(%)
  • 7. (32.60 numbers of embryos per 100 anthers, Table 1), the domestic varieties Kurtovska kapija SR, Zlaten medal SR and Piran showed priority in the selection process. There are several factors affecting androgenesis in many species, such as genotypes (Mityko et al., 1995; Rodeva et al., 2004), growth of donor plants, pre-treatments of anthers (Özkum and Tripirdamaz, 2002; Koleva-Gudeva, 2003; Ashok Kumar et al., 2003), composition of medium (Irikova and Rodeva, 2004; Koleva-Gudeva and Spasenoski, 2007; Dolcet-Sanjuan et al., 1997) and the source of plant material. The mechanism of cold and heat-shock treatment for induction of somatic embryogenesis has been explored and discussed by many authors (Dolcet-Sanjuan et al., 1997; Dumas de Valux et al., 1981). The studies on somatic embryogenesis of pepper (C. annuum L.) are in the domain of androgensis: George and Narayanaswamy (1973), Dumas de Valux et al. (1981), Mityko et al., (1995), Dolcet-Sanjuan et al., (1997) and Rodeva et al., (2004). According to the literature, the heat thermal stress (+35o C) has greater effect than the cold one (+7o C) in the process of stimulation of macrospore division of pepper (Kim et al., 2008). These findings are in agreement with the results obtained in the present study. From all pepper genotypes under investigation, 12 possessed potential for formation of embryos. The hot genotypes Feferona, Vezena luta, Sivrija and Bonbona and the sweet genotypes Rotund, Kurtovska kapija TU and Kurtovska kapija MK did not show androgenetic potential, i.e. in anther culture did not form embryos shoots (Table 1). The experiment showed that the effectiveness of androgenesis process depends on pepper genotype and the conditions for anther culture Journal of Research in Agriculture (2012) 1(2): 136-145 142 Gudeva and Trajkova, 2012 Table 4. Morphological and production characteristics of fruits in different pepper genotypes in botanical maturation grown in plastic tunnel in 2009 KKk 13.62a 5.31a 84.78a 71.17a 0.37b 2.00a 0.25b 55.80b 8.50a КК1/8/1 13.27a 5.71a 77.54a 91.60a 0.402ab 2.00a 0.76a 128.75a 6.00c КК3/4/5 12.61a 5.56a 95.50a 78.96a 0.44ab 2.40a 0.29b 57.33b 6.50c КК3/4/3 12.84a 5.29a 83.71a 71.06a 0.44ab 2.20a 0.09b 28.00b 7.50b Pk 15.08a 3.07a 34.85b 29.31b 0.24b 2.40ab 0.18b 40.0b 6.60a P3/3/1 15.66a 3.41a 54.04a 43.28a 0.23b 2.00b 0.97b 40.0b 6.00ab Р3/3/3 14.41a 3.62a 49.90a 41.08a 0.34a 2.40ab 0.52b 66.80ab 6.10a Р4/7/3 15.51a 3.47a 51.45a 40.75a 0.26b 2.80a 0.41b 119.40ab 6.50a Р4/7/1 16.29a 3.84a 55.39a 41.62a 0.25b 2.00b 1.12a 138.60a 4.80b ZMk 14.77a 5.35a 100.61a 73.13a 0.48a 2.60a 0.56a 96.80a 6.10b ZM1/2/4 15.49a 5.18a 90.46a 75.69a 0.51a 2.60a 0.65a 159.80a 8.10a ZM1/2/5 13.37a 5.35a 94.30a 92.05a 0.39b 2.60a 0.82a 164.80a 7.60a Fk 9.67a 7.57a 140.43a 103.32a 0.51a 3.08ab 0.59a 100.20a 5.00a F6/3/1 10.55a 6.59a 113.82a 90.83ab 0.40b 3.40bc 0.40a 73.60a 5.20a F6/3/5 10.51a 7.12a 126.27a 97.03ab 0.50a 3.40bc 0.34a 56.60a 5.30a F5/2/2 7.50b 7.67a 123.10a 92.99ab 0.498a 3.00c 0.85a 143.60a 5.50a F5/2/3 5.91c 7.30a 109.39a 79.45b 0.514a 4.00a 0.76a 118.80a 5.00a Mean within a column followed by the same letters are not significantly different at p < 0.05 according to Duncan’s multiple range test. Genotypecode Fruitlength(cm) Fruitwidth(cm) Totalfruitweightg) Fruitweightwithout handleandseeds(g) Pericarp thickness(cm) Numberoffruit locules Wightofdryseeds/ fruit(g) Numberofseeds/ fruit Drymatter(%)
  • 8. maintenance. The embryogenesis resulted in embryo formation that developed into plantlets which were acclimatized in climate chamber and greenhouse conditions. Mityko and Fari (1997) concluded that bell-shape varieties have the highest androgenic ability, while the rest showed very low or no androgenic activity, which is consistent with our results, where the bellshape varieties Féherözön and California Wonder showed a higher potential for embryogenesis compared to the hot and the sweet ones. The anthers of Féherözön variety showed low callus formation, but the androgenic ability was the highest on the same medium. In general, once the callus was initiated, the induction of somatic embryos did not occur, which is similar with the results reported by Binzel et al., (1996). After successful acclimatization of the regenerated plant, seed material from four pepper genotypes was collected: Kurtovska kapija SR, Zlaten medal SR, Piran and Féherözön, and were used for characterization and breeding process in plastic tunnel conditions 2007 - 2010. The characterization of different androgenic lines compared to the mother genotype showed that there is great variability in some pepper yield-related characteristics from certain lines (Thul et al., 2009). The lines that showed such potential can be used as starting material for future pepper breeding (Portis et al., 2004; Rodeva et al., 2007). CONCLUSION From 19 pepper genotypes under investigation, 12 possessed potential for embryo formation. The hot genotypes Feferona, Vezena luta, Sivrija and Bonbona and the sweet genotypes Rotund, Kurtovska kapija TU and Kurtovska kapija MK did not show androgenetic potential. According to the classification of Mityko and 143 Journal of Research in Agriculture (2012) 1(2): 136-145 Gudeva and Trajkova, 2012 KKk 11.694ab 4.74a 63.99b 51.73b 0.45b 2.22a 0.43a 69.00a 7.80b КК1/2 10.294c 5.37a 53.72b 43.22b 0.46b 2.23a 0.28a 45.20a 7.00c КК3/1 12.691a 5.43a 91.92a 75.72a 0.54a 2.40a 0.45a 38.80a 8.70a КК4/2 11.074bc 5.21a 61.01b 54.15b 0.48ab 2.41a 0.65a 103.80a 7.80b Pk 14.763b 3.68a 59.62a 50.33a 0.52a 3.00a 0.17b 27.33b 7.60a P1/3 17.80a 3.48a 59.89a 48.56a 0.41b 2.40a 0.62ab 69.60ab 7.60a Р2/3 15.01b 3.17a 49.77a 40.41a 0.36b 2.61a 0.29b 31.60b 7.60a Р4/3 17.75a 3.34a 56.29a 44.71a 0.36b 2.40a 0.84a 96.80a 8.00a Fk 7.93b 6.94b 109.91b 80.38bc 0.51c 3.83a 0.94c 144.00c 7.20ab F1/2 11.40a 7.73ab 119.64b 95.84b 0.57bc 3.00bc 0.94c 231.00b 6.30cd F2/5 10.40a 5.79c 81.48c 64.17c 0.53c 2.60c 0.56c 97.40c 6.80bc F3/3 8.47b 8.39a 154.74a 119.80a 0.89a 3.40ab 1.42b 325.20a 7.90a F4/5 7.72b 7.02b 109.53b 78.80bc 0.64b 3.20ab 0.59c 86.00c 5.90d ZMk 15.81a 5.45a 96.98a 90.22a 0.44a 2.60a 0.84a 117.80a 5.80b ZM2/2 14.01a 3.88b 58.58b 46.63b 0.35b 2.67a 0.64b 124.30a 6.20a Table 5. Morphological and production characteristics of fruits in different pepper genotypes in botanical maturation grown in plastic tunnel in 2010 Mean separation in columns by Duncan’s multiple range test. In each column, values followed by the same letter do not differ significantly at P<0.05 for all genotypes except ZMk and ZM2/2. Genotypecode Fruitlength(cm) Fruitwidth(cm) Totalfruitweightg) Fruitweightwith- outhandleandseeds (g) Pericarp thickness(cm) Numberoffruit locules Wightofdryseeds/ fruit(g) Numberofseeds/ fruit Drymatter(%)
  • 9. Fari (1997) for identification of androgenetic potential, based on percentage of anthers that give embryos, in our research twelve genotypes showed ability for embryo formation: 1 genotype with excellent androgenetic potential: Féherözön; 1 genotype with good androgenetic potential: Tura; 4 genotypes with fair androgenetic potential: Pritavit F1, Californian wonder, Zlaten medal SR and Majori; 6 genotypes with poor androgenetic potential: Piran, Zlaten medal ŠT, Tomato shaped sweet, Kurtovska kapija BG, Kurtovska kapija SR and Slatko luta; 7 genotypes do not possess androgenetic potential: Feferona, Vezena Luta, Sivrija, Rotund, Kurtovska kapija TU, Kurtovska kapija MK and Bonbona. Collected material will lead to creation of new and improved pepper genotypes, created for specific agroecological conditions. Generally, the further process of selection from all 19 pepper genotypes should be done towards the improvement of domestic genotypes Kurtovska kapija SR, Zlaten medal SR and Piran. REFERENCES Binzel ML, Sankhla N, Joshi S, Sankhla D. 1996. Induction of direct somatic embryogenesis and plant regeneration in pepper (Capsicum annuum L.). Plant Cell Rep., 15:536-540. Dolcet-Sanjuan R, Claveira E, Huerta A. 1997. Androgenesis in pepper Effects of carbohydrate and carbon dioxide enrichment. J Amer Soc Hort Sci 122(4): 468-475. Dumas de Valux R, Chambonnet D, Pochard E. 1981. In vitro culture of pepper (Capsicum annuum L.) Anthers: high rate plant production from different genotypes by +35ºC treatments. Agronomie 1(10):859-864. George L and Narayanaswamy S. 1973. Haploid capsicum through experimental androgenesis. Protoplasma 78:467-470. Ipgri, Avrdc and Catie. 1995. Descriptors for Capsicum (Capsicum spp.). International Plant Genetic Resources Institute, Rome, Italy. Study for biodiversity in the Republic of Macedonia. 2003. First national report, Ministry of environment and physical planning, Skopje 1-217. Kim M, Jang LC, Kim EJ, Park M, Yoon M. 2008. Embryogenesis and plant regeneration of hot pepper trough isolated microspore culture. Plant Cell Report 27:425-434. Koleva-Gudeva L, Spasenoski M, Trajkova F. 2007. Somatic embryogenesis in pepper anther culture: The effects of incubation treatments and different media. Scientia Horticulturae 111:114-119. Koleva-Gudeva L, Trajkova F, Dimeska G, Spasenoski M. 2009. Androgenesis efficiency in anther culture of pepper (Capsicum annuum L.). Acta Hort. (ISHS). 830:183-190. Konstantinov GH, Belcheva RG, Goranov AK. 1985. Rykovodstvo za prakticheski zanaytiy po genetika. Sofia. Kuo JS, Wang ZZ, Chein NF, Ku SJ, Kung ML, Hsu HC. 1973. Investigation of the anther culture in vitro of Nicotiana and Capsicum annuum L. Acta Bot. Sin. 15:43-47. Lantos C, Juhasz GS, Somogyi KO, Vagi P, Mihaly R, Kristof Z, Somogyi N, Pank J. 2009. Improvment of isolated microspore culture (Capsicum annuum L.) via co-culture with ovary tissue culture of pepper or maze. Plant Cell Tissue Organ Culture 97:285-293. Mityko J, Andrasfalvy G, Csillery G, Fari M. 1995. Anther culture response in different genotypes and F1 hybrids of pepper. Plant Breeding 114:78-80. Journal of Research in Agriculture (2012) 1(2): 136-145 144 Gudeva and Trajkova, 2012
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