In vitro Shoot Cut: A High Frequency Multiplication and Rooting Method in the Bamboo Dendrocalamus hamiltonii
Rajneesh K. Agnihotri
Shyamal K. Nandi
A rapid and high frequency reproducible in vitro regeneration protocol of a multipurpose bamboo species Dendrocalamus hamiltonii Nees et Arn. Ex Munro has been developed through single node cutting taken from the lateral branches of a 20 year old field grown elite bush. Axillary buds on the nodal explants sprouted within a fortnight of culture on Murashige and Skoog (MS) medium without any Plant Growth Substance (PGS). After 3-4 weeks of incubation, the sprouted buds were excised from the mother stumps and placed on MS medium supplemented with different concentrations of 6-benzylaminopurine (BAP; 2.0-12.0 μM) and 1.0 μM α-naphthaleneacetic acid (NAA). Enhanced proliferation was induced on the propagules (small clusters with 3-5 multiple shoots and rhizomatous part) on medium supplemented with 8.0 μM BAP and 1.0 μM NAA; subsequent removal of the shoots (about 1.5 cm) from the rhizomatous portion (shoot cut) and placing them on the same media combination influenced multiplication capacity. A multiplication of 20 folds was achieved on MS medium supplemented with 8.0 μM BAP and 1.0 μM NAA at the end of the 2nd subculture. Enhanced root formation (>90%) occurred when the propagules following shoot cut were placed on to MS medium supplemented with 100 μM indole-3-butyric acid (IBA) for 10 days and then transferred to IBA-free medium. This is the first report from this species where 20-fold multiplication was obtained and subsequent enhanced rooting (>90%). The hardened plants, established in the field, exhibited normal growth even after 2 years.
Bamboo is the most diverse group of plants in the Poaceae family and the most
primitive sub-family. They are distinguished by having woody culms and complex
branching, a complex and generally robust rhizome system and infrequent flowering.
It has a cosmopolitan distribution, reaching elevations as high as 4000 m in
the Himalayas and parts of China (Anonymous, 1978). There
is high demand of bamboo for commercial purposes; however, productivity of bamboo
forest in India is far below compared to China and can be attributed to over
exploitation, lack of scientific management, recurrent fire, poor natural regeneration
and damage by cattle (INBAR, 1991). Cultivation of bamboo
in India is still at infancy stage. Almost 99% of annual bamboo production in
the country comes from the natural stands in the forests and only 1% is derived
from plantations. Nevertheless, increased productivity can be achieved following
selection of the right species, elite clones, genotype match with site characteristics
and proper management practices (Gielis et al., 2001).
In Indian Central Himalaya and particularly in Uttarakhand, bamboo forests are
very much limited and only few stands can be seen here and there; these are
also man-made (human plantations). In view of the importance, the need for bamboo
cultivation has been realized.
Dendrocalamus hamiltonii Nees et Arn. Ex Munro, a multipurpose, fast
growing bamboo species with strong culms is commonly used in the Western Himalayan
Region for its leaves as good quality cattle fodder particularly during winter
months holds considerable promise in Central Himalaya also as a green fodder
(Negi et al., 1980). Moreover, its use in paper
production, house building, making furniture, agricultural implements, mat boards,
baskets, handicrafts and numerous traditional uses is well known. Thus, this
bamboo has a great potential for hilly regions of the Indian Central Himalaya.
Use of tissue culture for plant multiplication and subsequent field plantation
has also been reported for this species (Chambers et al.,
1991; Godbole et al., 2002; Sood
et al., 2002). Although, multiple shoot formation occurs routinely,
rooting has been inconsistent with up to only 30% rooting only (Sood
et al., 2002), which limits large scale plant production.
Use of the cytokinin 6-benzylaminopurine (BAP), either alone or in combination
with kinetin (cytokinin) or the auxin α-naphthaleneacetic acid (NAA) in
basal medium has resulted in higher rate of shoot multiplication in several
species of bamboo (Arya et al., 1999; Bag
et al., 2000; Bag, 2001; Sood
et al., 2002; Arshad et al., 2005;
Kapoor and Rao, 2006; Ramanayake
et al., 2006; Jimenez et al., 2006).
Although, the auxin indole-3-butyric acid (IBA) has been generally effective
in in vitro rooting (Bag et al., 2000;
Bag, 2001; Sood et al., 2002;
Arshad et al., 2005; Ramanayake
et al., 2008), the phenolic compound coumarin (Saxena,
1990; Ramanayake and Yakandawala, 1997; Mishra
et al., 2007; Ramanayake et al., 2008)
and glucose (Yashodha et al., 2007) have also
been successful in bamboo.
In the present study, an efficient and high frequency in vitro multiplication protocol for D. hamiltonii, using nodal explants taken from a 20 year old field grown elite mother bush to enhance multiplication following shoot cut method has been described.
MATERIALS AND METHODS
Single node cutting, taken from one year old lower and lateral branches of
a 20 year old vegetatively propagated plant (mother bush) of D. hamiltonii
growing at the Institute nursery at Kosi, District Almora (79°3810"E
and 29°2815"N; 1150 m altitude) were collected during May 2004 and
used for developing in vitro cultures. The cutting (about 3.0 cm in length)
was soaked in distilled water containing Labolene (Liquid detergent; 0.2% v/v;
Qualigens, India) for about 2-3 min, washed with distilled and sterilized water
3-4 times, disinfected with 0.2% mercuric chloride (w/v, BDH, India; 5 min)
and again rinsed with distilled and sterilized water (x4). Subsequently both
the ends were trimmed and segments cultured on Murashige and
Skoogs (1962) medium (20 mL) with out any Plant Growth Substances
(PGSs) by placing them vertically in test tubes (15x1.5 cm). The pH of the medium
was adjusted to 5.8 and gelled with 0.2% phytagel (w/v, Sigma) before autoclaving
(1.05 kg cm-2, 121°C, 20 min). All the cultures were maintained
at 25±1°C in a culture room with 14/10 h day/night cycle. All laboratory
experiments and hardening of in vitro raised plants were carried out
at the Institute and its nursery located at Kosi-Katarmal, District Almora (1200
After 3-4 weeks of incubation the axillary buds sprouted from the nodal explants; these buds (2.0-2.5 cm long) were excised from the mother stumps and cultured on MS medium supplemented with different concentrations of BAP (2.0-12.0 μM) and 1.0 μM NAA. The buds produced small clusters of 3-5 multiple shoots (2.5-3.0 cm) with a rhizomatous portion, hereafter called propagules. The shoots were individually cut about 1.5 cm above the base and discarded, while the propagules, now referred to as shoot cut was separated and further cultured for multiplication. For rooting these propagules (with shoot cut) were separated again and placed in 1/2 MS media containing IBA at different concentrations (10.0-200.00 μM) for 7 days followed by placing in medium without IBA for 2 weeks. The plantlets were removed from the flasks, thoroughly washed with water, transferred to plastic cups (6x6x7 cm) containing 250 g of autoclaved soil and placed under greenhouse conditions (25°C air temperature, relative humidity 65%; 18/6 h day/night cycle) for 15 days. Following another 15 days, they were shifted to polythene bags (16x10 cm) containing equal proportion of soil and farm yard manure (1:1) and transferred to a polyhouse/nethouse for hardening. Following one month of hardening, the plants were planted in the field and their growth performance was monitored.
SD was calculated following the method of Snedecor and Cochran
RESULTS AND DISCUSSION
The sprouted axillary buds on the nodal explants (Fig. 1A)
were excised and transferred on MS medium containing different concentrations
of BAP (2.0-12.0 μM) and 1.0 μM NAA. Subsequently within the next
3-4 weeks, differentiation was observed and multiple shoots were formed. Out
of the various concentrations of BAP used, the medium supplemented with 8.0
μM BAP and 1.0 μM NAA resulted in profuse shoot formation with increased
rhizomatous portion. Shoot portions were removed and the propagules were separated
and multiplied on media containing different concentrations of BAP (2.0-12.0
μM) and 1.0 μM NAA (Fig. 1B, Table
1). The medium containing 8.0 μM BAP and 1.0 μM NAA further enhanced
multiplication, for example, starting with 1 explant, more than 20 propagules
could be obtained; the average shoot length and leaf size were also highest
when compared to other treatments of BAP (Table 1). This is
the first report from these species where adopting this method higher number
of propagules and multiple shoots were obtained by the end of the 2nd subculture
(Table 1, Fig. 1C). Data on multiplication
of propagules and shoots (Table 2) indicates that by following
in vitro shoot cut method there was a 5-fold increase when compared to
control (without shoot cut); moreover, length of shoots was also found to nearly
double following shoot cut.
||Various stages during the development of in vitro propagation
protocol of D. hamiltonii. (A) establishment of explant in MS medium
without PGSs; bar = 1 cm, (B) a representative photo depicting culture of
propagules following in vitro shoot cut method on MS medium supplemented
with 8.0 μM BAP and 1.0 μM NAA; bar = 1.5 cm, (C) profuse shoot
multiplication after in vitro shoot cut on medium containing BAP
and NAA as in Fig. B, during 2nd subculture; bar = 1.5 cm, (D) and (E) profuse
rooting in propagules after shoot cut and following culture on MS medium
containing 100 μM IBA and subsequently placing in IBA-free medium;
bar = 1.5 cm and (F) transfer of in vitro raised plants to soil and
hardening in a polyhouse; bar = 8 cm
||Effect of BAP and in vitro shoot cut on multiplication
of propagules and shoots of D. hamiltonii
|A propagule consisted of 3 shoots, each treatment consisted
of 5 propagules cultured per flask and conducted in triplicate,
data were recorded after 3 weeks, all results were obtained using propagules
during 2nd subculture, aall concentrations of BAP in the medium
contained 1.0 μM NAA, bMean±SD
||Effect of shoot cut on multiplication of propagules and shoots
of D. hamiltonii
|A propagule consisted of 3 shoots, aeach set represents
treatment given to various batches using 3 propagules per flask and conducted
in triplicate, data were recorded after 3 weeks during 2nd subculture,
Compared to an earlier study (Bag, 2001) wherein a combination
of 5.0 μM BAP and 2.0 μM NAA supplemented to MS medium was used for
multiplication, this study resulted in generation of 20% higher number of multiple
shoots (Table 1, Fig. 1C). Studies using
bunches, each containing 3-5 shoots, for shoot proliferation in bamboo have
been reported earlier, e.g., Thamnocalamus spathiflorus (Bag
et al., 2000) and D. hamiltonii (Bag, 2001;
Sood et al., 2002).
The roles of the cytokinin, particularly BAP in in vitro bud break and
shoot multiplication is well known. Although, BAP has been used to induce bud
break in nodal explants of Bambusa wamin (Arshad
et al., 2005) and Guadua angustifolia (Jimenez
et al., 2006), it was not required in this study as reported earlier
by Bag (2001) and Sood et al.
(2002). Like in several plant species, BAP alone has been very effective
for shoot multiplication in bamboos Dendrocalamus asper (Arya
et al., 1999), Bambusa bambos (Kapoor
and Rao, 2006), B. vulgaris (Ramanayake
et al., 2006) and G. angustifolia (Jimenez
et al., 2006). However, in this investigation, BAP in combination
with NAA was found to be effective; similar results were reported for this species
earlier (Bag, 2001) and in the temperate bamboo T.
spathiflorus (Bag et al., 2000). BAP in conjunction
with kinetin was also demonstrated effective in B. wamin (Arshad
et al., 2005). It must be mentioned that BAP and its metabolites
have been identified as naturally occurring cytokinins in plant tissues (Nandi
et al., 1989a, b).
Pulse (short) treatment of the propagules with IBA for 7 days resulted in maximum
rooting at 100 μM concentration and using this method more than 90% success
could be achieved (Table 3, Fig. 1D). The
number of roots per plant was more than 6 and the length of longest root was
about 5.0 cm (results not shown). In an previous study using IBA (2.1 or 4.2
μM) or NAA (2.7 or 5.4 μM) up to 30% rooting was observed (Sood
et al., 2002). Well-rooted plantlets (Fig. 1E)
following proper hardening (Fig. 1F) formed profuse root
system with a survival rate of over 85% (Table 3) under polyhouse/nethouse
conditions. The performance of the plants transferred in the field was satisfactory
and exhibited normal growth even after 2 years. A two-step rooting procedure
using IBA treatment followed by transfer to auxin-free media had been reported
by Bag et al. (2000).
The auxin IBA is being widely used as an effective PGS for root induction in
various plant species. In several species of bamboo, medium supplemented with
IBA alone was used for successful rooting; B. wamin (Arshad
et al., 2005), B. vulgaris (Ramanayake
et al., 2006) and Dendrocalamus hookeri (Ramanayake
et al., 2008) are some examples. In this investigation, a short treatment
with IBA alone was sufficient enough to induce rooting as reported earlier in
this species (Bag, 2001) and in T. spathiflorus
(Bag et al., 2000). Phenolic compounds, which
act as auxin protectors, have also been reported to promote rooting. While,
in Bambusa tulda use of coumarin alone resulted in maximum rooting response
of 98% (Mishra et al., 2007), in Dendrocalaamus
giganteus IBA together with coumarin was necessary (Ramanayake
et al., 2008).
||Effect of different concentrations of IBA on rooting of propagules
following in vitro shoot cut
|-: Not applicable. A propagule consisted of 3 shoots, each
treatment consisted of 10 propagules per flask and in replicates of 10,
data were recorded following 7 days treatment in IBA and then placing
in medium without IBA, acalculated on per flask basis
In Bambusa nutans, addition of glucose along with IBA supported 85%
rooting (Yashodha et al., 2007). These results
indicate a close interaction amongst various PGSs and/or with different compounds
to evoke a physiological response.
Nodal segments taken from mature bushes (Ramanayake and
Yakandawala, 1997; Bag, 2001; Sood
et al., 2002; Arshad et al., 2005;
Ramanayake et al., 2006; Jimenez
et al., 2006) were also used in this study; this approach ensures
propagation of true-to-type plants. The shoot cut method used in this study
has enhanced in vitro multiplication by 5 fold (when compared to control)
followed by high rooting efficiency (>90%). In an earlier report only up
to 30% rooting was demonstrated in this species (Sood et
al., 2002). Hardening and field performance of micropropagated plants
are crucial aspects that need utmost attention. Substantial numbers of micropropagated
plants do not survive after transfer from controlled in vitro conditions
to ex vitro environment of the greenhouse and later in the open field.
Present results demonstrated more than 70% plant survival in the field even
after two years of plantation and are comparable with a previous investigation
(Sood et al., 2002).
This study clearly demonstrates high frequency multiplication and enhanced
rooting method for in vitro propagation of D. hamiltonii. These
features are necessary for increased production of true-to-type plants for large-scale
multiplication of this species. Tissue culture method allows the production
of a large number of plantlets identical to the mother plant, is less labour
intensive and cheaper once the protocols has been standardized and hence offers
distinct advantages over conventional methods of multiplication of different
species of elite bamboo clones (Saxena and Dhawan, 1999;
Godbole et al., 2002; Sood
et al., 2002; Das and Pal, 2005; Jimenez
et al., 2006; Ramanayake et al., 2006,
2008; Yashodha et al., 2007).
Therefore, this study will not only help in large scale multiplication of this
useful multipurpose bamboo species for restoration of degraded land but also
result in economic benefits of the inhabitants of Indian Central Himalaya.
Dr. L.M.S. Palni and N. Bag are thanked for valuable suggestions during this study. Director, GBPIHED, Kosi-Katarmal, Almora is thanked for providing necessary facilities. The financial help received from Institute funds and from DBT (No. BT/PR/487/Agr/16/398/2004), Govt. of India, New Delhi is duly acknowledged.
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