Liquid Culture Systems for in vitro Plant Propagation

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52 Anne Kathrine Hvoslef-Eide et al. g/l pcv % 70 60 50 40 30 20 10 12 10 8 6 4 2 0 0 Fresh weight 1 3 6 8 10 13 Days Packed cell volume (pcv) 1 3 6 8 10 13 Days g/l cluster viability % 4 3,5 3 2,5 2 1,5 1 0,5 0 80 70 60 50 40 30 20 10 0 Dry weight of cells 1 3 6 8 10 13 Days Cluster viability 1 3 6 8 10 13 Days Figure 4: The difference between identical suspension cultures of Cyclamen persicum Mill. in bioreactors (open diamonds) and Erlenmeyer flasks (closed squares) on fresh and dry weight, packed cell volume and cluster viability during a two-week period, showing standard deviations for each measurement. 4.2 General discussion Our system is for batch-culture, where medium is changed once each week as the cultures are diluted and cells are harvested. Such a system is not considered to be optimal with regards to maximum cell growth in such a short period of time. A continuous mode of operation, with a continuous
Bioreactor design for propagation 53 feed of nutrients, where the physiological state of the cells during a run is more uniform, is regarded as the most efficient strategy (Glick and Pasternak, 1998). To see if more optimal nutrient conditions would give homogenous embryo formation, fed-batch systems could be investigated. The pH values during the course of an experiment is a good indicator of the condition of the cells; at first, the pH value will always decrease because the cells will use any ammonium ions first and hence release H + ions into the medium. Later, the medium will be depleted of ammonium, and the cell metabolism will change to use nitrate ions and to release OH - ions in exchange for the negatively charged nitrate. This can then be observed as a rise in pH (Figure 3). The reason the pH value begins to increase again earlier in bioreactors compared to Erlenmeyer flasks (Figure 3) is probably due to the more rapid culture growth in the bioreactors. The uptake of ammonium, compared to nitrate, leading to a reduction in pH value, is faster; the ammonium is depleted more quickly and hence the more rapid rise of pH when the cells begin to take up nitrate ions. A contamination of the bioreactor will usually first be noticeable by an immediate and large change in pH and is a good indicator of culture status. 5. Experiences and recommendations for improvements on bioreactor design The bioreactors described have been used for ten years, and during this time experience about the advantages and limitations of the system, with regard to mechanical considerations as well as measurements, control and software has been gained using cell cultures of various plant genera and cell types. 5.1 Temperature control The bioreactors were constructed to be able to change set point for the different parameters every hour through a 24 h cycle. The temperature control functions well when a constant temperature is required. With alternating day and night temperatures, the regulation seems to be a greater problem. Even though the available interval of temperature regulation is between 15 o C and 35 o C, the available power of the heater limits the temperature range in the same bioreactors to 10 o C during an experiment. Because of the heat exchange from the cold water supply to the bioreactors, it is necessary to regulate the cooling water to the lowest temperature (4 o C), to get the bioreactor temperature as low as 15 o C. Then the heating element is
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LIQUID CULTURE SYSTEMS FOR IN VITRO
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A C.I.P. Catalogue record for this
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Contents Contributing Authors xiii
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Liquid culture systems for in vitro
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Contributing Authors Adelberg, J. 4
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Preface Plant cell, tissue and orga
Page 18 and 19: Chapter 1 General introduction: a p
Page 20 and 21: General introduction 3 2. Cell susp
Page 22 and 23: General introduction 5 rooted in gr
Page 24 and 25: General introduction 7 (Winkelmann
Page 26 and 27: General introduction 9 the bioreact
Page 28 and 29: General introduction 11 (TIS), resu
Page 30 and 31: General introduction 13 Barz W, Rei
Page 32 and 33: General introduction 15 Hohe A, Win
Page 34 and 35: General introduction 17 Shimazu T &
Page 36 and 37: I. Bioreactors
Page 38 and 39: 22 Wayne R. Curtis 1. Introduction
Page 40 and 41: 24 Wayne R. Curtis headspace double
Page 42 and 43: 26 Wayne R. Curtis that is required
Page 44 and 45: 28 Wayne R. Curtis C L y � P O2
Page 46 and 47: 30 Wayne R. Curtis since there is a
Page 48 and 49: 32 Wayne R. Curtis 5 cm 30 cm 30 o
Page 50 and 51: 34 Wayne R. Curtis Pˆ N � � me
Page 52 and 53: 36 Wayne R. Curtis Radial Flow Impe
Page 54 and 55: 38 Wayne R. Curtis CS = Medium diss
Page 56 and 57: 40 Wayne R. Curtis Murashige T & Sk
Page 58 and 59: 42 Anne Kathrine Hvoslef-Eide et al
Page 76 and 77: Chapter 4 Practical aspects of bior
Page 78 and 79: Practical aspects of bioreactor app
Page 94 and 95: Chapter 5 Simple bioreactors for ma
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Page 110 and 111: 96 K. Y. Paek et al. opportunity fo
Page 112 and 113: 98 K. Y. Paek et al. disadvantages
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104 K. Y. Paek et al. cosmetics, wh
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106 K. Y. Paek et al. protocol, mor
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108 K. Y. Paek et al. use. In order
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110 K. Y. Paek et al. a b c d e f F
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112 K. Y. Paek et al. a b c d e f F
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114 K. Y. Paek et al. Escalona M, L
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116 K. Y. Paek et al. Son SH & Paek
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118 Seppo Sorvari et al. economical
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120 Seppo Sorvari et al. membrane w
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122 Seppo Sorvari et al. 3. Results
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124 Seppo Sorvari et al. D.O. 160 1
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Chapter 8 Cost-effective mass cloni
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Cost-effective mass cloning of plan
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144 Eun-Joo Hahn & Kee-Yoeup Paek 1
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146 Eun-Joo Hahn & Kee-Yoeup Paek F
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148 Eun-Joo Hahn & Kee-Yoeup Paek T
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150 Eun-Joo Hahn & Kee-Yoeup Paek 3
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152 Eun-Joo Hahn & Kee-Yoeup Paek E
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Chapter 10 Control of growth and di
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Control of growth and differentiati
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Chapter 11 Temporary immersion syst
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Temporary immersion system: a new c
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198 Elio Jiménez González 1. Intr
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200 Elio Jiménez González Several
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202 Elio Jiménez González Figure
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204 Elio Jiménez González exploit
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206 Elio Jiménez González weeks i
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208 Elio Jiménez González germina
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210 Elio Jiménez González Escalan
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Chapter 13 Use of growth retardants
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Use of growth retardants for banana
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Chapter 14 Somatic embryo germinati
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Somatic embryo germination of Psidi
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Somatic embryo germination of Psidi
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232 Tino Hempfling & Walter Preil N
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234 Tino Hempfling & Walter Preil 3
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236 Tino Hempfling & Walter Preil F
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238 Tino Hempfling & Walter Preil F
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240 Tino Hempfling & Walter Preil 4
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242 Tino Hempfling & Walter Preil R
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244 C. Damiano et al. Over the last
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246 C. Damiano et al. 2.2 Temporary
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248 C. Damiano et al. Table 3: Wate
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250 C. Damiano et al. hyperhydricit
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Chapter 17 Optimisation of growing
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Optimisation of growing conditions
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264 Katerina Grigoriadou et al. cul
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266 Katerina Grigoriadou et al. 2.4
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268 Katerina Grigoriadou et al. mic
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270 Katerina Grigoriadou et al. of
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272 Katerina Grigoriadou et al. 4.
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274 Katerina Grigoriadou et al. Tei
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276 Ch. Wawrosch et al. possesses s
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278 Ch. Wawrosch et al. 3. Results
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280 Ch. Wawrosch et al. References
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Chapter 20 Propagation of Norway sp
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Propagation of Norway Spruce 285 2.
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Propagation of Norway Spruce 287 su
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Propagation of Norway Spruce 289 5.
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Propagation of Norway Spruce 291 bl
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Propagation of Norway Spruce 293 H
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296 M. Vágner et al. 1995). In liq
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298 M. Vágner et al. maturation pe
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300 M. Vágner et al. mature somati
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302 M. Vágner et al. Acknowledgeme
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304 Christopher Hunter & Lionel Lev
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314 Michel Petitprez et al. 1. Intr
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316 Michel Petitprez et al. 2.2 QTL
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318 Michel Petitprez et al. Figure
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320 Michel Petitprez et al. Table 1
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322 Michel Petitprez et al. Gentzbi
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324 F. Afreen et al. 1. Introductio
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326 F. Afreen et al. precotyledonar
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328 F. Afreen et al. Dry mass (mg/e
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330 F. Afreen et al. under photoaut
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332 F. Afreen et al. Figure 3: a) C
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334 F. Afreen et al. the plant qual
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Chapter 25 Potential of flow cytome
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Potential of flow cytometry 339 dis
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Potential of flow cytometry 341 Fig
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Potential of flow cytometry 343 tha
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Chapter 26 Somatic embryogenesis of
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Somatic embryogenesis of Gentiana 3
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Chapter 27 Induction and growth of
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Induction and growth of tulip 361 a
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Induction and growth of tulip 363 T
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Chapter 28 Micropropagation of Ixia
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Micropropagation of Ixia 367 for PA
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Micropropagation of Ixia 369 Biomas
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Micropropagation of Ixia 371 Figure
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Chapter 29 Micropropagation of Rosa
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Micropropagation of Rosa 375 The BA
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Micropropagation of Rosa 377 Platfo
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Micropropagation of Rosa 379 3. Res
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Micropropagation of Rosa 381 The ro
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Micropropagation of Rosa 383 4. Dis
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Micropropagation of Rosa 385 Murash
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Chapter 30 Mass propagation of coni
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Mass propagation of conifer trees 3
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Chapter 31 Potentials for cost redu
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Potentials for cost reduction 405 c
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Potentials for cost reduction 407 c
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Potentials for cost reduction 409 s
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Potentials for cost reduction 411 N
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Potentials for cost reduction 413 G
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Chapter 32 A new approach for autom
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A new approach for automation 417 (
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A new approach for automation 419 p
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A new approach for automation 421 T
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A new approach for automation 423 D
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426 B. McAlister et al. 1. Introduc
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428 B. McAlister et al. 2.2 Multipl
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430 B. McAlister et al. Table 2: Mu
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432 B. McAlister et al. rest time -
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434 B. McAlister et al. Figure 3: M
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436 B. McAlister et al. Average mul
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438 B. McAlister et al. Table 4: Co
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440 B. McAlister et al. Semi-solid
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442 B. McAlister et al. Escalona M,
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444 Jeffrey Adelberg including Host
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446 Jeffrey Adelberg BioSystems (Ho
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448 Jeffrey Adelberg more prolific
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450 Jeffrey Adelberg vessel of liqu
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452 Jeffrey Adelberg Figure 4: Labo
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454 Jeffrey Adelberg constituted a
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456 Jeffrey Adelberg Acknowledgemen
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Chapter 35 Aeration stress in plant
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Aeration stress in plant tissue cul
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476 Hans R. Gislerød et al. 1. Int
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478 Hans R. Gislerød et al. biorea
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480 Hans R. Gislerød et al. A low
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482 Hans R. Gislerød et al. Table
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484 Hans R. Gislerød et al. common
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486 Hans R. Gislerød et al. can be
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488 Hans R. Gislerød et al. 4.1 Li
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490 Hans R. Gislerød et al. 4.3 Ca
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492 Hans R. Gislerød et al. Morten
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494 Han Bouman & Annemiek Tiekstra
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V. Biomass for Secondary Metabolite
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510 E. Gontier et al. 1. Introducti
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512 E. Gontier et al. 2. Materials
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514 E. Gontier et al. developed dra
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516 E. Gontier et al. 3.3 Establish
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518 E. Gontier et al. Fresh weight
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520 E. Gontier et al. 3.5 Effect of
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522 E. Gontier et al. 3.6 Scale up
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524 E. Gontier et al. Lorenzo JC, G
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526 Dirk Wilken et al. 1. Introduct
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528 Dirk Wilken et al. running at 6
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530 Dirk Wilken et al. described a
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532 Dirk Wilken et al. packed cell
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534 Dirk Wilken et al. bioactive co
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536 Dirk Wilken et al. Fowler MW (1
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Chapter 40 Cultivation of root cult
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Cultivation of root cultures of Pan
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Chapter 41 Optimisation of Panax gi
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Optimisation of Panax ginseng liqui
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558 S. M. Nalawade et al. performan
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560 S. M. Nalawade et al. Plantlets
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562 S. M. Nalawade et al. leaves on
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564 S. M. Nalawade et al. roots (Fi
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Chapter 43 Production of taxanes in
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Production of taxanes 569 2. Materi
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Production of taxanes 571 Figure 2:
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Production of taxanes 573 various T
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Acknowledgments The editors thank t
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578 Contents 130, 131, 133, 134, 13
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580 Contents poplar, see Populus Po
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582 Contents bubble aerated 165 bub
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584 Contents ginsenoside content, p
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586 Contents plant growth regulator
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588 Contents -free microcorms 71 -f
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