Effects of ascorbic acid and embryogenic microspore selection on embryogenesis in white cabbage (Brassica oleracea L. var. capitata)

Journal of Horticultural Science and Biotechnology

Volumn 90, Issue 6, 2015, Pages 607-612

  Zeng, Aisong ^a   Yan, Jiyong ^a   Song, Lixiao ^a   Gao, Bing ^a   Li, Jianqi ^b  

^a INSTITUTE OF PLANT PROTECTION   (China)

^b Qingdao Bioivy Crop Science Co Ltd   (China)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84946567465     PISSN: 14620316     EISSN: None     Source Type: Journal    
DOI: 10.1080/14620316.2015.11668722     Document Type: Article

References (26)

1. ASIF, M., EUDES, F., GOYAL, A., AMUNDSEN, E., RANDHAWA, H. and SPANER, D. (2013). Organelle antioxidants improve microspore embryogenesis in wheat and Triticale. In Vitro Cellular & Developmental Biology – Plant, 49, 489–497.
2. ATHAR, H.R., KHAN, A. and ASHRAF, M. (2008). Exogenously applied ascorbic acid alleviates salt-induced oxidative stress in wheat. Environmental and Experimental Botany, 63, 224–231.
3. CAO, M. Q., CHARLOT, F. and DORÉ, C. (1990). Embryogenesis and plant regeneration in sauerkraut cabbage (Brassica oleracea L. subsp. capitata) by in vitro culture of isolated microspores. Comptes Rendus de l’ Academie des Sciences Paris, Serie III, 310, 203–209.
4. COUMANS, M. and ZHONG, D. (1995). Doubled-haploid sunflower (Helianthus annuus) plant production by androgenesis: fact or artifact? Part 2. In vitro isolated microspore culture. Plant Cell, Tissue and Organ Culture, 41, 203–209.
5. GILL, S. S. and TUTEJA, N. (2010). Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiology and Biochemistry, 42, 909–930.
6. GLAND, A., LICHTER, R. and SCHWEIGER, H. G. (1988). Genetic and exogenous factors affecting embryogenesis in isolated microspore culture of Brassica napus L. Plant Physiology, 132, 613–617.
7. GU, H.H., HAGBERG, P. and ZHOU, W. J. (2004). Cold pretreatment enhances microspore embryogenesis in oilseed rape (Brassica napus L.). Plant Growth Regulation, 42, 137–143.
8. HABIBI, N., SUTHAR, P. K. and PUROHIT, S. D. (2009). Role of PGRs and inhibitors in induction and control of somatic embryogenesis in Themeda quadrivalvis. Indian Journal of Experimental Biology, 47, 198–203.
9. HESLOP-HARRISON, J., HESLOP-HARRISON, Y. and SHIVANNA, K.R. (1984).The evaluation of pollen quality and of further appraisal of the fluorochromatic (FRC) test procedure. Theoretical and Applied Genetics, 67, 367–375.
10. HOSEINI, M., GHADIMZADEH, M., AHMADI, B. A. J. and SILVA, T. (2013). Effects of ascorbic acid, a-tocopherol, and glutathione on microspore embryogenesis in Brassica napus L. In Vitro Cellular & Developmental Biology – Plant, 50, 26–35.
11. HUANG, B., BIRD, S., KEMBLE, R., SIMMONDS, D., KELLER, W. and MIKI, B. (1990). Effects of culture density, conditioned medium and feeder cultures on microspore embryogenesis in Brassica napus L. cv. Topas. Plant Cell Reports, 8, 594–597.
12. KIM, M., PARK, E.J., AN, D. J. and LEE, Y. W. (2013). High-quality embryo production and plant regeneration using a two-step culture system in isolated microspore cultures of hot pepper (Capsicum annuum L.). Plant Cell, Tissue and Organ Culture, 112, 191–201.
13. KOTT, L.S., POLSONI, L., ELLIS, B. and BEVERSDORF, W. D. (1988). Autotoxicity in isolated microspore cultures of Brassica napus. Canadian Journal of Botany, 66, 1665–1670.
14. LEIST, M. (1997). The shape of cell death. Biochemical and Biophysical Research Communications, 236, 1–9.
15. LICHTER, R. (1982). Induction of haploid plants from isolated pollen of Brassica napus. Zeitschrift fur Anorganische und Allgemeine Chemie, 105, 427–434.
16. MARASCHIN, S.F., GAUSSAND, G., PLIDO, A., OLMEDILLA, A., LAMERS, G., KORTHOUT, H., SPAINK, H. P. and WANG, M. (2005). Programmed cell death during the transition from multinucleate structures to globular embryos in barley androgenesis. Planta, 221, 459–470.
17. PECHAN, P.M., KELLER, W.A., MANDY, F. and BERGEROA, M. (1988). Selection of Brassica napus L. embyogenic microspores by flow sorting. Plant Cell Reports, 7, 396–398.
18. RODRÍGUEZ-SERRANO, M., BÁRÁNY, I., PREM, D., CORONADO, M.J., RISUENO, M. C. and TESTILANO, P. S. (2012). NO, ROS, and cell death associated with caspase-like activity increase in stress-induced microspore embryogenesis of barley. Journal of Experimental Botany, 63, 2007–2024.
19. RUDOLF, K., BOHANEC, B. and HANSEN, M. (1999). Microspore culture of white cabbage, Brassica oleracea var. capitata L: genetic improvement of non-responsive cultivars and effect of genome doubling agents. Plant Breeding, 118, 237–241.
20. SORIANO, M., CISTUÉ, L. and CASTILLO, A. M. (2008). Enhanced induction of microspore embryogenesis after n-butanol treatment in wheat (Triticum aestivum L.) anther culture. Plant Cell Reports, 27, 805–811.
21. VARNIER, A. L., JACQUARD, C. and CLEMENT, C. (2009). Programmed cell death and microspore embryogenesis. In: Advances in Haploid Production in Higher Plants. (Touraev,A., Forster, B. P. and Jain, S. M., Eds.). Springer, Dordrecht, The Netherlands. 147–154.
22. YUAN, S.X., LIU, Y. M., FANG, Z. Y., YANG, L.M., ZHUANG, M., ZHANG, Y. Y. and SUN, P. T. (2012). Effects of pH, MES, and ara-binogalactan-proteins on microspore cultures in white cabbage. Plant Cell, Tissue and Organ Culture, 110, 69–76.
23. YUAN, S.X., LIU, Y. M., FANG, Z. Y., YANG, L.M., ZHUANG, M., ZHANG, Y. Y. and SUN, P. T. (2011). Effect of combined cold pretreatment and heat shock on microspore cultures in broccoli. Plant Breeding, 130, 80–85.
24. ZENG, A. S., YAN, J. Y., SONG, L.X., GAO, B., ZHANG, Y. X., LI, J.Q., LIU, H.H., HOU, X. L. and LI, Y. (2015). Induction and development of microspore-derived embryos in broccoli ? white-headed cabbage hybrids microspore culture. Euphytica, 203, 261–272.
25. ZHOU, H., ZHENG, Y. and KONZAK, C. F. (1991). Osmotic potential of media affecting green plant percentage in wheat anther culture. Plant Cell Reports, 10, 63–66.
26. ZUR, I., DUBAS, E., GOLEMIEC, E., SZECHYNSKA-HEBDA, M., GOLEBIOWSKA, G. and WEDZONY, M. (2009). Stress-related variation in antioxidative enzymes activity and cell metabolism efficiency associated with embryogenesis induction in isolated microspore culture of Triticale (? Triticosecale Wittm.). Plant Cell Reports, 28, 1279–1287.