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STUDIES ON THE USE AND EFFECT OF ALTERNATIVE
MATRICES AND CARBON SOURCE IN PLANT IN
VITRO SYSTEM
Submitted by
Roll- PG/VUOGP57/BIT-IVS No- 037
Registration No- 02188 of 2020-2021
Introduction
Commercial application of tissue culture technology is restricted due to high production
costs (Babbar and Jain, 2006).
The micropropagation method allows for large-scale production of uniform seedlings,
especially in a short time.
 Low-cost tissue culture is beneficial not only for the farmers but also for routine large-
scale commercial multiplication.
Pineapple (Ananas comosus L Merr.) –
 Third most crucial tropical fruit in the world.
 Vital supply of vitamins and protein digestive enzyme.
 Consumed fresh or processed into canned fruit, juice, or jam.
Vanilla (Vanilla planifolia Andrews) -
 Most healthful spicy orchid in the tropic regions.
 Highly regarded for its dried fragrant beans.
 One of the second most expensive spices.
Aims and Objectives:
To establish an efficient reproducible protocol for the in vitro induction of Pineapple
and Vanilla plants using shoot tips and nodal segments in MS media supplemented
with different combinations and concentrations of plant growth regulators.
To optimize the standard tissue cultural condition for the maximum proliferation of
in vitro Pineapple and Vanilla plants in different types of alternative matrices instead
of Agar and normally available commercial sugar as a carbon source.
To find out the standard condition for large scale production of tissue culture
generated plantlets using the said alternatives.
Materials and Methods:
Materials:
 Aseptic culture of Ananas comosus and Vanilla planifolia procured from OIST tissue culture
laboratory facility as the explants under the present study.
 Use commercially available sugar instead of tissue culture grade sucrose.
 Use agar and three low cost alternative matrices (coir, bagasse, and luffa sponge).
 Agar and luffa sponge - pineapple micropropagation.
 Coir and bagasse – vanilla micropropagation.
Media: MS basal media (with different nutrient combinations). MS [Murashige and Skoog, 1962]
basal media with different combinations and concentrations of growth regulators were used. The
nutrient media used in the present study was the conventional Murashige and Skoog media.
Methods:
 Aseptic cultures of pineapple and vanilla were collected from the OIST plant tissue
culture laboratory.
 Then the MS basal media with different concentrations and combinations was prepared
with the help of conventional MS media procedure protocol.
 The low cost alternative matrices were collected from local shops and then made ready to
use in micropropagation.
 After that the inoculation was done in proper condition at the tissue culture laboratory.
 After about 45 days of inoculation, the responses were observed and enlisted in copy.
Different concentrations and combinations:
P
A
1
BA- 0.5mg/l
Kin- 0.1mg/l
IAA- 0.2mg/l
P
A
2
BA- 1.0mg/l
Kin- 0.2mg/l
IAA- 0.4mg/l
P
A
3
BA- 1.5mg/l
Kin- 0.3mg/l
IAA- 0.6mg/l
P
A
4
BA- 2.0mg/l
Kin- 0.4mg/l
IAA- 0.8mg/l
S
U
C
R
O
S
E
LS- Tissue culture grade sucrose or Lab Sugar
CS- Commercially available sucrose or Common Sugar
Results and Discussion
PA1CS and PA4CS media was shown poor response (25%).
PA2CS and PA3LS media was shown better response (87%).
Figure 1: Inoculation of explants of Pineapple
(Ananas comosus L Merr.). Figure 2: Inoculation of explants of
Pineapple (Ananas comosus L Merr.).
All the alternative matrices showed good results except PA2LS media, with the help of
low cost alternative matrix bagasse showed very established positive results (100).
Figure 3: Inoculation of
explants in cost-effective
gelling media (Coir and
Bagasse) of Vanilla (Vanilla
planifolia Andrews).
Figure 5: Inoculation of explants in alternative
low cost matrix (Coir and Bagasse) of Vanilla
(Vanilla planifolia Andrews).
Figure 4: Establishment and proliferation of
explants in alternative low cost matrix (Luffa
Sponge) of Pineapple (Ananas comosus L Merr.).
45
40 40
42
54
49
0
30
0
10
20
30
40
50
60
LS CS LS CS LS CS LS CS
PA1 PA2 PA3 PA4
RESPONSE
PERCENTAGE
(%)
MS media with low-cost alternative matrix (Coir)
62
25
37
87 87
75 75
25
0
10
20
30
40
50
60
70
80
90
100
LS CS LS CS LS CS LS CS
PA1 PA2 PA3 PA4
RESPONSE
PERCENTAGE
(%) MS media with conventional gelling agent (Agar)
Figure 6: Graphical representation of several
responses (%) of in vitro culture of Ananas
comosus in different media supplements
(PA1LS - PA4CS).
Figure 7: Graphical representation of several
responses (%) of in vitro culture of Vanilla
planifolia in different media supplements
(PA1LS - PA4CS) and with the alternative
matrix Coir.
45
0
100
45 46
38
51
0
0
20
40
60
80
100
120
LS CS LS CS LS CS LS CS
PA1 PA2 PA3 PA4
RESPONSE
PERCENTAGE
(%) MS media with low-cost alternative matrix (Bagasse)
48 47 47 48
29
0
38
35
0
10
20
30
40
50
60
LS CS LS CS LS CS LS CS
PA1 PA2 PA3 PA4
RESPONSE
PERCENTAGE
(%)
MS media with low-cost alternative matrix (Luffa Sponge)
Figure 8: Graphical representation of
several responses (%) of in vitro culture of
Vanilla planifolia in different media
supplements (PA1LS - PA4CS) and with
the alternative matrix Bagasse.
Figure 9: Graphical representation of
several responses (%) of in vitro culture of
Ananas comosus in different media
supplements (PA1LS - PA4CS) and with
the alternative matrix Luffa Sponge.
Discussion:
During the establishment and proliferation stage, maximum responses were observed in liquid
media using bagasse as an alternative cost-effective matrix, followed by coir and luffa sponge.
 Cost reduction was maximum in coir matrix followed by bagasse and luffa sponge concerning
conventional agar media.
Liquid media has many advantages over solid media such as efficient nutrient uptake, lower
cost, and dilution of excreted material (Smith and Spoomer, 1995; Aitcken-Christie et al. 1995).
When the liquid media is supported by solid, biodegradable, fibrous matrices, the nutrients can
diffuse easily through it and vitrification can be prevented (Gangopadhyay et al., 2002). Among
the three alternatives, cost-effective gelling agents tested, minimum greening was observed in
media with luffa sponge.
This cost reduction was attributed to the replacement of tissue culture grade sucrose (3%) with
table sugar (3%) which reduced the cost of carbon source by almost 97%.
The carbon source such as tissue culture grade sucrose that is often used in the
micropropagation of plants in the laboratory contributes about 34% of the production cost
(Demo et al., 2008).
Sucrose has been reported as a source of both carbon and energy (Bridgen, 1994).
There is reported success in reducing the 90% cost of tissue culture banana plants by replacing
sucrose. In the plant propagation medium Kaur et al., (2005) substituted sucrose with table
sugar which reduced the cost of the medium considerably by 96.8% similar to the present
study and Prakash et al., (2002) reported the reduction in the cost of the medium by 78 to 87%
using common sugar.
Conclusions:
• PA2CS (BA- 1.0mg/l, Kin- 0.2mg/l, IAA- 0.4mg/l and Commercial Sucrose- 30gm/l) and
PA3LS (BA- 1.5mg/l, Kin- 0.3mg/l, IAA- 0.6mg/l and tissue culture grade sucrose- 30gm/l)
are the best media so far tested for optimum micropropagation of pineapple in in vitro
system with the convention gelling matrix, agar.
• In the case of using alternative matrices with the same combinations and concentrations used
in the agar matrix, bagasse (PA2LS) showed a better comparative result than the coir and
luffa sponge.
• I hope, this investigation will provide an emphasis on the technical knowhow of tissue
culture methods of pineapple and vanilla plants especially the use of commercially available
sucrose over tissue culture grade sucrose and also the using of alternative low-cost
biodegradable matrices such as coir, bagasse, luffa sponge, etc. over conventional gelling
matrix agar for the researchers and industrialists in future.
References:
1. Babbar, S. B., and Jain, N. (1998). `Isubgol' as an alternative gelling agent in plant tissue culture media. Plant cell reports, 17(4), 318–322.
2. Be L.V. and Debergh P.C. 2005. Potential low-cost micropropagation of pineapple (Ananas comosus). South African Journal of Botany 72(2006):191-194.
3. Bhojwani S.S., and Razdan M.K., 2005. Plant tissue culture: Theory and practice, a revised Edition, Reed Elsevier India Pvt. Ltd.
4. Bridgen M. P., 1994. A review of plant embryo culture. Hort. Sci. 29: 1243-1245.
5. Chauhan U., Singh A.K., Godani D., Handa S., Gupta P.S., Patel S. and Joshi P. 2018. Some natural extracts from plants as low cost alternatives for synthetic PGRs in
rose micropropagation. Journal of Applied Horticulture, 20(2): 103-111.
6. Daud N., Taha R.M., Noor N.N.M. and Alimon H. 2011. Provision of low cost media options for in vitro culture of Celosia sp. African Journal of Biotechnology,
10(80): 18349-18355.
7. Demo P, Kuria P, Nyenda AB, Kahangi EM (2008). Table sugar as an alternative low-cost medium component for in vitro micro-propagation of potato (Solanum
tuberosum L.). Afr. J. Biotechnol. 7: 2578-2854.
8. Dipak D. Kadam, Amit A. Chhatre, Shivaji A. Lavale and Nalini A. Shinde. 2018. Low-Cost Alternatives for Conventional Tissue Culture Media.
Int.J.Curr.Microbiol.App.Sci. 7(04): 2523-2529.
9. Dutta I., Bhadra J., Ghosh P., Saha B. and Datta S. 2013. An Efficient and Cost Effective Protocol for In vitro Propagation of Pineapple. Journal of Ornamental Plants,
3(4): 229-234.
10. Ganapathi, T.R., Mohan, J.S.S., Suprasanna P., Bapat V.A. and Rao P.S. 1995. Current Science 68(6): 646-650.
11. Gangopadhyay G., Das S., Mitra S.K., Poddar R., Modak B.K., Mukherjee K.K. (2002). Enhanced rate of multiplication and rooting through the use of coir in aseptic
liquid culture media. Plant Cell Tissue Organ Cult. 68: 301-310.
12. Gangopadhyay G., Roy S.K. and Mukherjee K.K. 2009. Plant response to alternative matrices for in vitro root induction. African Journal of Biotechnology
8(13):2923-2928.
13. Gangopadhyay, G., Bandyopadhyay, T., Basu Gangopadhyay, S. and Mukherjee, K.K. 2004. Luffa sponge-a unique matrix for tissue culture of philodendron. Curr
Sci. 86: 315-319.
14. Jain R., and Babbar S. B. (2006). Xanthan gum: an economical substitute for agar in plant tissue culture media. Plant cell reports, 25(2), 81–84.
15. Kadam DD, Chhatre AA, Lavale SA and Shinde NA. Low-cost Alternatives for Conventional Tissue Culture Media. Int. J. Curr. Microbiol. App. Sci. 2018;7(4)
(pp.2523-29).
16. Kaur, R., Gautam, H. and Sharma, D.R. (2005). A LOW COST STRATEGY FOR MICROPROPAGATION OF STRAWBERRY
(FRAGARIA × ANANASSA DUCH.) CV. CHANDLER. Acta Hortic. 696, 129-133.
17. Murashige, T., Skoog, F., 1962. A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiologia Plantarum 15, 473– 497.
18. Prakash S., Hoque M.I. and Brinks T. 2002. Culture media and containers in low-cost options for tissue culture technology in developing countries. Proc. of Tech. in
Food and Agricultural, Austria, Vienna.pp.29-40.
19. Raghu A.V., Martin G., Priya V. and Geetha S.P. 2007. Journal of Plant Sciences 2(6): 592-599.
20. Roy S.K., Gangopadhyay G., Bandyopadhyay T., Modok B.K., Datta S. and Mukherjee K.K. 2006. Enhancement of in vitro microcorm production in Gladiolus using
alternative matrix. African Journal of Biotechnology. 12: 1204 -1209.
21. Saraswathi M.S., Uma S., Kannan G., Selvasumathi M., Mustaffa M.M. and Backiyarani S. 2016. Cost-effective tissue culture media for large-scale propagation of
three commercial banana (Musa spp.) varieties, The Journal of Horticultural Science and Biotechnology, 91:1, 23-29.
22. Smith M.A.L. and Spoomar L.A. 1995. Vessels, gels, liquid media and support systems. P. 371-405. In: Aitken–Christie J, T. Kozai, M.A.L. Smith (eds) Automation
and environmental control in plant tissue culture. Kluwer Academy Publication, Dordreeht.
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Arnim Banerjee OIST

  • 1. STUDIES ON THE USE AND EFFECT OF ALTERNATIVE MATRICES AND CARBON SOURCE IN PLANT IN VITRO SYSTEM Submitted by Roll- PG/VUOGP57/BIT-IVS No- 037 Registration No- 02188 of 2020-2021
  • 2. Introduction Commercial application of tissue culture technology is restricted due to high production costs (Babbar and Jain, 2006). The micropropagation method allows for large-scale production of uniform seedlings, especially in a short time.  Low-cost tissue culture is beneficial not only for the farmers but also for routine large- scale commercial multiplication. Pineapple (Ananas comosus L Merr.) –  Third most crucial tropical fruit in the world.  Vital supply of vitamins and protein digestive enzyme.  Consumed fresh or processed into canned fruit, juice, or jam. Vanilla (Vanilla planifolia Andrews) -  Most healthful spicy orchid in the tropic regions.  Highly regarded for its dried fragrant beans.  One of the second most expensive spices.
  • 3. Aims and Objectives: To establish an efficient reproducible protocol for the in vitro induction of Pineapple and Vanilla plants using shoot tips and nodal segments in MS media supplemented with different combinations and concentrations of plant growth regulators. To optimize the standard tissue cultural condition for the maximum proliferation of in vitro Pineapple and Vanilla plants in different types of alternative matrices instead of Agar and normally available commercial sugar as a carbon source. To find out the standard condition for large scale production of tissue culture generated plantlets using the said alternatives.
  • 4. Materials and Methods: Materials:  Aseptic culture of Ananas comosus and Vanilla planifolia procured from OIST tissue culture laboratory facility as the explants under the present study.  Use commercially available sugar instead of tissue culture grade sucrose.  Use agar and three low cost alternative matrices (coir, bagasse, and luffa sponge).  Agar and luffa sponge - pineapple micropropagation.  Coir and bagasse – vanilla micropropagation. Media: MS basal media (with different nutrient combinations). MS [Murashige and Skoog, 1962] basal media with different combinations and concentrations of growth regulators were used. The nutrient media used in the present study was the conventional Murashige and Skoog media.
  • 5. Methods:  Aseptic cultures of pineapple and vanilla were collected from the OIST plant tissue culture laboratory.  Then the MS basal media with different concentrations and combinations was prepared with the help of conventional MS media procedure protocol.  The low cost alternative matrices were collected from local shops and then made ready to use in micropropagation.  After that the inoculation was done in proper condition at the tissue culture laboratory.  After about 45 days of inoculation, the responses were observed and enlisted in copy.
  • 6. Different concentrations and combinations: P A 1 BA- 0.5mg/l Kin- 0.1mg/l IAA- 0.2mg/l P A 2 BA- 1.0mg/l Kin- 0.2mg/l IAA- 0.4mg/l P A 3 BA- 1.5mg/l Kin- 0.3mg/l IAA- 0.6mg/l P A 4 BA- 2.0mg/l Kin- 0.4mg/l IAA- 0.8mg/l S U C R O S E LS- Tissue culture grade sucrose or Lab Sugar CS- Commercially available sucrose or Common Sugar
  • 7. Results and Discussion PA1CS and PA4CS media was shown poor response (25%). PA2CS and PA3LS media was shown better response (87%). Figure 1: Inoculation of explants of Pineapple (Ananas comosus L Merr.). Figure 2: Inoculation of explants of Pineapple (Ananas comosus L Merr.).
  • 8. All the alternative matrices showed good results except PA2LS media, with the help of low cost alternative matrix bagasse showed very established positive results (100). Figure 3: Inoculation of explants in cost-effective gelling media (Coir and Bagasse) of Vanilla (Vanilla planifolia Andrews).
  • 9. Figure 5: Inoculation of explants in alternative low cost matrix (Coir and Bagasse) of Vanilla (Vanilla planifolia Andrews). Figure 4: Establishment and proliferation of explants in alternative low cost matrix (Luffa Sponge) of Pineapple (Ananas comosus L Merr.).
  • 10. 45 40 40 42 54 49 0 30 0 10 20 30 40 50 60 LS CS LS CS LS CS LS CS PA1 PA2 PA3 PA4 RESPONSE PERCENTAGE (%) MS media with low-cost alternative matrix (Coir) 62 25 37 87 87 75 75 25 0 10 20 30 40 50 60 70 80 90 100 LS CS LS CS LS CS LS CS PA1 PA2 PA3 PA4 RESPONSE PERCENTAGE (%) MS media with conventional gelling agent (Agar) Figure 6: Graphical representation of several responses (%) of in vitro culture of Ananas comosus in different media supplements (PA1LS - PA4CS). Figure 7: Graphical representation of several responses (%) of in vitro culture of Vanilla planifolia in different media supplements (PA1LS - PA4CS) and with the alternative matrix Coir.
  • 11. 45 0 100 45 46 38 51 0 0 20 40 60 80 100 120 LS CS LS CS LS CS LS CS PA1 PA2 PA3 PA4 RESPONSE PERCENTAGE (%) MS media with low-cost alternative matrix (Bagasse) 48 47 47 48 29 0 38 35 0 10 20 30 40 50 60 LS CS LS CS LS CS LS CS PA1 PA2 PA3 PA4 RESPONSE PERCENTAGE (%) MS media with low-cost alternative matrix (Luffa Sponge) Figure 8: Graphical representation of several responses (%) of in vitro culture of Vanilla planifolia in different media supplements (PA1LS - PA4CS) and with the alternative matrix Bagasse. Figure 9: Graphical representation of several responses (%) of in vitro culture of Ananas comosus in different media supplements (PA1LS - PA4CS) and with the alternative matrix Luffa Sponge.
  • 12. Discussion: During the establishment and proliferation stage, maximum responses were observed in liquid media using bagasse as an alternative cost-effective matrix, followed by coir and luffa sponge.  Cost reduction was maximum in coir matrix followed by bagasse and luffa sponge concerning conventional agar media. Liquid media has many advantages over solid media such as efficient nutrient uptake, lower cost, and dilution of excreted material (Smith and Spoomer, 1995; Aitcken-Christie et al. 1995). When the liquid media is supported by solid, biodegradable, fibrous matrices, the nutrients can diffuse easily through it and vitrification can be prevented (Gangopadhyay et al., 2002). Among the three alternatives, cost-effective gelling agents tested, minimum greening was observed in media with luffa sponge.
  • 13. This cost reduction was attributed to the replacement of tissue culture grade sucrose (3%) with table sugar (3%) which reduced the cost of carbon source by almost 97%. The carbon source such as tissue culture grade sucrose that is often used in the micropropagation of plants in the laboratory contributes about 34% of the production cost (Demo et al., 2008). Sucrose has been reported as a source of both carbon and energy (Bridgen, 1994). There is reported success in reducing the 90% cost of tissue culture banana plants by replacing sucrose. In the plant propagation medium Kaur et al., (2005) substituted sucrose with table sugar which reduced the cost of the medium considerably by 96.8% similar to the present study and Prakash et al., (2002) reported the reduction in the cost of the medium by 78 to 87% using common sugar.
  • 14. Conclusions: • PA2CS (BA- 1.0mg/l, Kin- 0.2mg/l, IAA- 0.4mg/l and Commercial Sucrose- 30gm/l) and PA3LS (BA- 1.5mg/l, Kin- 0.3mg/l, IAA- 0.6mg/l and tissue culture grade sucrose- 30gm/l) are the best media so far tested for optimum micropropagation of pineapple in in vitro system with the convention gelling matrix, agar. • In the case of using alternative matrices with the same combinations and concentrations used in the agar matrix, bagasse (PA2LS) showed a better comparative result than the coir and luffa sponge. • I hope, this investigation will provide an emphasis on the technical knowhow of tissue culture methods of pineapple and vanilla plants especially the use of commercially available sucrose over tissue culture grade sucrose and also the using of alternative low-cost biodegradable matrices such as coir, bagasse, luffa sponge, etc. over conventional gelling matrix agar for the researchers and industrialists in future.
  • 15. References: 1. Babbar, S. B., and Jain, N. (1998). `Isubgol' as an alternative gelling agent in plant tissue culture media. Plant cell reports, 17(4), 318–322. 2. Be L.V. and Debergh P.C. 2005. Potential low-cost micropropagation of pineapple (Ananas comosus). South African Journal of Botany 72(2006):191-194. 3. Bhojwani S.S., and Razdan M.K., 2005. Plant tissue culture: Theory and practice, a revised Edition, Reed Elsevier India Pvt. Ltd. 4. Bridgen M. P., 1994. A review of plant embryo culture. Hort. Sci. 29: 1243-1245. 5. Chauhan U., Singh A.K., Godani D., Handa S., Gupta P.S., Patel S. and Joshi P. 2018. Some natural extracts from plants as low cost alternatives for synthetic PGRs in rose micropropagation. Journal of Applied Horticulture, 20(2): 103-111. 6. Daud N., Taha R.M., Noor N.N.M. and Alimon H. 2011. Provision of low cost media options for in vitro culture of Celosia sp. African Journal of Biotechnology, 10(80): 18349-18355. 7. Demo P, Kuria P, Nyenda AB, Kahangi EM (2008). Table sugar as an alternative low-cost medium component for in vitro micro-propagation of potato (Solanum tuberosum L.). Afr. J. Biotechnol. 7: 2578-2854. 8. Dipak D. Kadam, Amit A. Chhatre, Shivaji A. Lavale and Nalini A. Shinde. 2018. Low-Cost Alternatives for Conventional Tissue Culture Media. Int.J.Curr.Microbiol.App.Sci. 7(04): 2523-2529. 9. Dutta I., Bhadra J., Ghosh P., Saha B. and Datta S. 2013. An Efficient and Cost Effective Protocol for In vitro Propagation of Pineapple. Journal of Ornamental Plants, 3(4): 229-234. 10. Ganapathi, T.R., Mohan, J.S.S., Suprasanna P., Bapat V.A. and Rao P.S. 1995. Current Science 68(6): 646-650. 11. Gangopadhyay G., Das S., Mitra S.K., Poddar R., Modak B.K., Mukherjee K.K. (2002). Enhanced rate of multiplication and rooting through the use of coir in aseptic liquid culture media. Plant Cell Tissue Organ Cult. 68: 301-310.
  • 16. 12. Gangopadhyay G., Roy S.K. and Mukherjee K.K. 2009. Plant response to alternative matrices for in vitro root induction. African Journal of Biotechnology 8(13):2923-2928. 13. Gangopadhyay, G., Bandyopadhyay, T., Basu Gangopadhyay, S. and Mukherjee, K.K. 2004. Luffa sponge-a unique matrix for tissue culture of philodendron. Curr Sci. 86: 315-319. 14. Jain R., and Babbar S. B. (2006). Xanthan gum: an economical substitute for agar in plant tissue culture media. Plant cell reports, 25(2), 81–84. 15. Kadam DD, Chhatre AA, Lavale SA and Shinde NA. Low-cost Alternatives for Conventional Tissue Culture Media. Int. J. Curr. Microbiol. App. Sci. 2018;7(4) (pp.2523-29). 16. Kaur, R., Gautam, H. and Sharma, D.R. (2005). A LOW COST STRATEGY FOR MICROPROPAGATION OF STRAWBERRY (FRAGARIA × ANANASSA DUCH.) CV. CHANDLER. Acta Hortic. 696, 129-133. 17. Murashige, T., Skoog, F., 1962. A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiologia Plantarum 15, 473– 497. 18. Prakash S., Hoque M.I. and Brinks T. 2002. Culture media and containers in low-cost options for tissue culture technology in developing countries. Proc. of Tech. in Food and Agricultural, Austria, Vienna.pp.29-40. 19. Raghu A.V., Martin G., Priya V. and Geetha S.P. 2007. Journal of Plant Sciences 2(6): 592-599. 20. Roy S.K., Gangopadhyay G., Bandyopadhyay T., Modok B.K., Datta S. and Mukherjee K.K. 2006. Enhancement of in vitro microcorm production in Gladiolus using alternative matrix. African Journal of Biotechnology. 12: 1204 -1209. 21. Saraswathi M.S., Uma S., Kannan G., Selvasumathi M., Mustaffa M.M. and Backiyarani S. 2016. Cost-effective tissue culture media for large-scale propagation of three commercial banana (Musa spp.) varieties, The Journal of Horticultural Science and Biotechnology, 91:1, 23-29. 22. Smith M.A.L. and Spoomar L.A. 1995. Vessels, gels, liquid media and support systems. P. 371-405. In: Aitken–Christie J, T. Kozai, M.A.L. Smith (eds) Automation and environmental control in plant tissue culture. Kluwer Academy Publication, Dordreeht.
  • 17. CRÉDITOS: Esta plantilla para presentaciones es una creación de Slidesgo, e incluye iconos de Flaticon, e infografías e imágenes de Freepik