Agrobacterium tumefaciens-mediated transformation of greenhouse-grown Brassica rapa ssp oleifera

被引:21
作者
Kuvshinov, V [1 ]
Koivu, K [1 ]
Kanerva, A [1 ]
Pehu, E [1 ]
机构
[1] Univ Helsinki, Dept Plant Prod, SF-00014 Helsinki, Finland
关键词
Brassica rapa ssp Oleifera; Brassica campestris; Agrobacterium tumefaciens; transformation; turnip rape;
D O I
10.1007/s002990050659
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Greenhouse-grown plants of turnip rape Brassica rapa ssp. oleifera (syn. B. campestris) cv. Valtti and Sisu were transformed by Agrobacterium tumefaciens infection. Of the three A. tumefaciens strains tested (C58C1, EHA105 and LBA4404), LBA4404 gave the best results. Segments excised from one to two upper internodes of an inflorescence-carrying stem served as explants for the Agrobacterium infection. Cultivation of the explants horizontally during the first 3 days of co-cultivation with A. tumefaciens following immediate selection of transformed tissue of the stem segments placed vertically basal side down were critical. Use of silver nitrate (5-10 mg/l) in the culture medium and Micropore (3 M) paper tape for sealing plates was also beneficial. Transgenic shoots were recovered using either hygromycin or kanamycin (20-25 mg/l) selection. Hygromycin was preferable, as the proportion of 'escapes' was 90% under kanamycin and 10% under hygromycin selection. Regeneration was achieved by culturing the explants for 3-6 days on 0.5 mg/l of 2,4-di-chlorophenoxyacetic acid and 1-2 weeks on 2-3 mg/l of 6-benzyl aminopurine with/without 0.05 mg/l a-naphthaleneacetic acid. Recovered shoots were then cultured on hormone-free MS medium. This culture program gave 60-80% shoot regeneration. Regenerants were tested by histological beta-glucuronidase staining and Southern blotting. The recovery rate of transgenic shoots was 4-9% of the number of explants used in the experiments.
引用
收藏
页码:773 / 777
页数:5
相关论文
共 23 条
[1]   NEW PLANT BINARY VECTORS WITH SELECTABLE MARKERS LOCATED PROXIMAL TO THE LEFT T-DNA BORDER [J].
BECKER, D ;
KEMPER, E ;
SCHELL, J ;
MASTERSON, R .
PLANT MOLECULAR BIOLOGY, 1992, 20 (06) :1195-1197
[2]  
CHI GL, 1990, PLANT CELL REP, V9, P195, DOI 10.1007/BF00232178
[3]   IMPROVED HIGH-LEVEL CONSTITUTIVE FOREIGN GENE-EXPRESSION IN PLANTS USING AN AMV RNA4 UNTRANSLATED LEADER SEQUENCE [J].
DATLA, RSS ;
BEKKAOUI, F ;
HAMMERLINDL, JK ;
PILATE, G ;
DUNSTAN, DI ;
CROSBY, WL .
PLANT SCIENCE, 1993, 94 (1-2) :139-149
[4]  
DEBLAERE R, 1985, NUCLEIC ACIDS RES, V13, P4777, DOI 10.1093/nar/13.13.4777
[5]   AGROBACTERIUM-MEDIATED TRANSFER OF ANTISENSE CHALCONE SYNTHASE CDNA TO GERBERA-HYBRIDA INHIBITS FLOWER PIGMENTATION [J].
ELOMAA, P ;
HONKANEN, J ;
PUSKA, R ;
SEPPANEN, P ;
HELARIUTTA, Y ;
MEHTO, M ;
KOTILAINEN, M ;
NEVALAINEN, L ;
TEERI, TH .
BIO-TECHNOLOGY, 1993, 11 (04) :508-511
[6]   TRANSFORMATION OF BRASSICA-NAPUS WITH AGROBACTERIUM-TUMEFACIENS BASED VECTORS [J].
FRY, J ;
BARNASON, A ;
HORSCH, RB .
PLANT CELL REPORTS, 1987, 6 (05) :321-325
[7]  
Gallagher S.R., 1992, GUS PROTOCOLS USING
[8]  
HACHEY JE, 1991, PLANT CELL REP, V9, P549, DOI 10.1007/BF00232329
[9]   A BINARY PLANT VECTOR STRATEGY BASED ON SEPARATION OF VIR-REGION AND T-REGION OF THE AGROBACTERIUM-TUMEFACIENS TI-PLASMID [J].
HOEKEMA, A ;
HIRSCH, PR ;
HOOYKAAS, PJJ ;
SCHILPEROORT, RA .
NATURE, 1983, 303 (5913) :179-180
[10]   NEW AGROBACTERIUM HELPER PLASMIDS FOR GENE-TRANSFER TO PLANTS [J].
HOOD, EE ;
GELVIN, SB ;
MELCHERS, LS ;
HOEKEMA, A .
TRANSGENIC RESEARCH, 1993, 2 (04) :208-218