Abstract
The effects of temporary immersion system (TIS) culture on the growth and quality of Siraitia grosvenorii plantlets were investigated. The TIS promoted the growth and quality of S. grosvenorii plantlets. Proliferation rate, shoot length, fresh weight (FW) and dry weight (DW) of shoots, and total biomass production were significantly (P ≤ 0.05) higher in the TIS than in gelled and liquid medium, respectively. The TIS also decreased callus formation at the base of shoots. Callus diameter was significantly (P ≤ 0.05) lower in the TIS (3.30 mm) than in gelled medium (6.31 mm) and liquid medium (6.77 mm), respectively. FW (50.83 mg) and DW (7.08 mg) of callus in the TIS were also significantly (P ≤ 0.05) lower than those in gelled medium (80.00 and 10.56 mg, respectively) and liquid medium (218.75 and 23.75 mg, respectively). During rhizogenesis, minimal callus was evident at the base of shoots in the TIS, with a well-developed root system. However, the plantlets in gelled medium just produced thick, brown and easily broken roots with obvious callus and fewer secondary roots. The natural-like plantlets of S. grosvenorii obtained in the TIS would probably have positive effects on ex vitro rooting and transplanting in large-scale commercial production.
Abbreviations
- BAP:
-
6-Benzylaminopurine
- DW:
-
Dry weight
- ETR:
-
Electron transfer rate
- Fv/Fm:
-
Maximal photochemical efficiency of PSII
- FW:
-
Fresh weight
- MS:
-
Murashige and Skoog (1962) (medium)
- NAA:
-
Naphthalene acetic acid
- PA:
-
Photoautotrophic micropropagation
- PM:
-
Photomixotrophic micropropagation
- TIS:
-
Temporary immersion system
References
Akihisa T, Hayakawa Y, Tokuda H, Banno N, Shimizu N, Suzuki T, Kimura Y (2007) Cucurbitane glycosides from the fruits of Siraitia grosvenorii and their inhibitory effects on Epstein-Barr virus activation. J Nat Prod 70(5):783–788
Alonso NP, Wilken D, Gerth A, Jahn A, Michael H, Kerns G, Perez AC, Jimenez E (2009) Cardiotonic glycosides from biomass of Digitalis purpurea L. cultured in temporary immersion systems. Plant Cell Tiss Organ Cult 99:151–156
Alvard D, Cote F, Teisson C (1993) Comparison of methods of liquid medium culture for banana micropropagation. Plant Cell Tiss Organ Cult 32:55–60
Cabasson C, Alvard D, Dambier D, Ollitrault P, Teisson C (1997) Improvement of citrus somatic embryo development by temporary immersion. Plant Cell Tiss Organ Cult 50:33–37
Dai YF, Liu CJ (1999) Fruits as medicine: a safe and cheap form of traditional Chinese food therapy. Pelanduk, Malaysia
Escalona M, Samson G, Borroto C, Desjardins Y (2003) Physiology of effects of temporary immersion bioreactors on micropropagated pineapple plantlets. In Vitro Cell Dev Biol-Plant 39:651–656
Etienne H, Berthouly M (2002) Temporary immersion systems in plant micropropagation. Plant Cell Tiss Organ Cult 69:215–231
Jackson MB (2003) Aeration stress in plant tissue cultures. Bulg J Plant Physiol Special issue:96–109
Konoshima T, Takasaki M (2002) Cancer-chemopreventive effects of natural sweeteners and related compounds. Pure Appl Chem 74(7):1309–1316
Lin R, Wang RZ (1980) The whole plantlets obtained of Siratia grosvenorii via plant tissue culture. Guihaia 1 11 [in Chinese]
Lin W, Li QQ, Peng HW, Xue JJ, Liang S, Huang LY (2003) Problem and solution of tissue cultured seedling cultivation of Siratia grosvenorii. Guangxi Agri Sci 4:74–75 [in Chinese]
Lorenzo JC, Gonzalez BL, Escalona M, Teisson C, Borroto C (1998) Sugarcane shoot formation in an improved temporary immersion system. Plant Cell Tiss Organ Cult 54:197–200
Martre P, Lacan D, Just D, Teisson C (2001) Physiological effects of temporary immersion on Hevea brasiliensis callus. Plant Cell Tiss Organ Cult 67:25–35
McAlister B, Finnie J, Watt MP, Blakeway F (2005) Use of the temporary immersion bioreactor system (RITA) for production of commercial Eucalyptus clones in Mondi Forests (SA). Plant Cell Tiss Organ Cult 81:347–358
Murashige T, Skoog F (1962) A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol Plant 15:473–479
Roels S, Noceda C, Escalona M, Sandoval J, Canal MJ, Rodriguez R, Debergh P (2006) The effect of headspace renewal in a temporary immersion bioreactor on plantain (Musa AAB) shoot proliferation and quality. Plant Cell Tiss Organ Cult 84:155–163
Shi H, Hiramatsu M, Komatsu M, Kayama T (1996) Antioxidant property of Fructus Momordicae extract. Biochem Mol Biol Int 40(6):1111–1121
Thomas YDS, Surminski KS, Lieberei R (2008) Plant regeneration via somatic embryogenesis of Camptotheca acuminata in temporary immersion system (TIS). Plant Cell Tiss Organ Cult 95:163–173
Tsang KY, Ng TB (2001) Isolation and characterization of a new ribosome inactivating protein, momorgrosvin, from seeds of the monk’s fruit Momordica grosvenorii. Life Sci 68(7):773–784
Wawrosch C, Kongbangkerd A, Kopf A, Kopp B (2005) Shoot regeneration from nodules of Charybdis sp.: a comparison of gelled liquid and temporary immersion culture systems. Plant Cell Tiss Organ Cult 81:319–322
Yan HB, Liang CX, Yang LT, Li YR (2010) In vitro and ex vitro rooting of Siratia grosvenorii, a traditional medicinal plant. Acta Physiol Plant 32:115–120
Yang SH, Yeh DM (2008) In vitro leaf anatomy, ex vitro photosynthetic behaviors and growth of Calathea orbifolia (Linden) Kennedy plants obtained from semi-solid medium and temporary immersion systems. Plant Cell Tiss Organ Cult 93:201–207
Zhang MJ, Zhao DD, Ma ZQ, Li XD, Xiao YL (2009) Growth and photosynthetic capability of Momordica grosvenori plantlets grown photoautotrophically in response to light intensity. HortScience 44(3):757–763
Zobayed FA, Zobayed SMA, Kubota C, Kozai T, Hasegawa O (1999) Supporting material affects the growth and development of in vitro sweet potato plantlets cultured photoautotrophically. In Vitro Cell Dev Biol-Plant 35:470–474
Acknowledgments
This research was financially supported by the Innovation Foundation for PhD of Guangxi University (200810593090101D020), and the Research Foundation granted by the Guangxi Academy of Agricultural Sciences (200814 JI), Nanning, Guangxi, China. Comments and suggestions on the manuscript from the editor, the associate editor and three anonymous reviewers are gratefully acknowledged. We are also grateful to Prof. Toyoki Kozai in Japan and Dr. Manoj Kumar Srivastava from India for their kind help in going through and polishing the manuscript.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Yan, H., Liang, C. & Li, Y. Improved growth and quality of Siraitia grosvenorii plantlets using a temporary immersion system. Plant Cell Tiss Organ Cult 103, 131–135 (2010). https://doi.org/10.1007/s11240-010-9752-2
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11240-010-9752-2