GB2211205A - Method for producing Brassica oleracea by protoplast fusion - Google Patents

Abstract

Brassica oleracea plants containing mitochondria of the Ogura CMS (male sterility) cytoplasm and chloroplasts of normal fertile Brassica oleracea. Method of production by protoplast fusion.

Description

IMPROVEKBNTS IN OR RELATING TO ORGANIC SYSTEMS This invention concerns the development of nev parental lines of Brassica oleracea. The parental lines are used to produce hybrid seed.

Specifically this invention enables a plant breeder to incorporate the desirable quality of cytoplasmic male sterility (COS) into a commercially desirable variety of B oleracea.

Male sterility is of value in B oleracea hybrid seed breeding because normal flowers are self-pollinating. Male sterile lines do not produce viable pollen and cannot self-pollinate. By eliminating the pollen of one parental variety in a cross, a plant breeder is assured of obtaining hybrid seed of uniform quality. At present cytoplasmic male sterility is not readily available in B oleracea varieties. Commercial producers of hybrid seed use nuclear self-incompatibility systems to avoid self-pollination during seed production. This system is inaccurate and results in impure hybrid seed lots. Also, it is time consuming, laborious and thus costly to introduce this genetic system into all breeding lines. In Raphanus sativus a cytoplasm has been discovered that confers male sterility.This cytoplasm is known as Ogura CMS cytoplasm and the DNA from the mitochondria and chloroplasts contained in the cytoplasm is genotypically different from the DNA in the cytoplasm of fertile B oleracea plants. The Ogura type CMS cytoplasm can be introduced in B oleracea by repeated back crosses. In the resulting Ogura CMS B oleracea plants the mitochondria of R sativus result in a CMS phenotype. The presence of the chloroplasts of R sativus however results in chlorosis when the plants are grown at low temperature which consequently results in yield losses. This wakes this type of Ogura CMS B oleracea plant of little use in commercial hybrid seed production.

The present invention provides B oleracea plants having mitochondria of the Ogura CMS cytoplasm and cold tolerant chloroplasts of normal fertile B oleracea. -The plants according to the invention have cytoplasmic male sterility, but will not show chlorosis when grown at low temperature.

The present invention further provides a process of preparing B oleracea plant material having cytoplasmic male sterility and commercially desirable nuclear traits, which do not shov chlorosis when grown at lov temperatures. Such CMS B oleracea plants are obtained by fusion of B oleracea protoplasts having commercially desirable nuclear traits with inactivated or nucleus-free protoplasts of an Ogura CMS B oleracea plant, folloved by regeneration into plants of the thus obtained allogenic cells.

The present invention is particularly suitable for the production of CMS in the following B oleracea varieties: 1 Brassica oleracea L. convar. acephala (DC.) Alef. var. botrytis L.

(cauliflower) 2 Brassica oleracea L. convar. capitata (L.) Alef. var. alba DC (vhite cabbage) 3 Brassica oleracea L. convar. oleracea var. gemmifera DC (Brussels sprouts) 4 Brassica oleracea L. convar. acephala (DC.) Alef. var. sabellica L.

(curly kale) 5 Brassica oleracea L. convar. capitata (L.) Alef. var. sabauda L.

(Savoy cabbage) 6 Brassica oleracea L. convar. capitata (L.) Alef. var. rubra DC. (red cabbage) 7 Brassica oleracea L. convar. acephala (DC.) Alef. var. gongylodes (Kohlrabi) 8 Brassica oleracea L. convar. botrytis (L.) Alef. var. cymosa Duch (broccoli) and more preferably in cauliflower, white cabbage, Brussels sprouts and broccoli as identified above.

The term Ogura CMS cytoplasm as used herein refers to Raphanus sativus originating cytoplasm comprising mitochondrial DNA which confers male sterility to plants. The term Ogura CMS Brassica oleracea plant or plant cell as used herein refers to a Brassica oleracea plant or plant cell comprising Ogura CMS cytoplasm.

The protoplast fusion according to the invention may be accomplished by employing polyethylene glycol (PEG) causing agglutination, in the presence of a fusion buffer, ie a high pB solution to let the membranes fuse. Such somatic hybridisation may be effected under the conditions disclosed by Sundberg et al [Plant Science 43 (1986) 155)1 for the production of interspecific hybrids or modifications thereof. An appropriate procedure is as follows.

The protoplast fusion according to the invention is conveniently effected in a protoplast fusion solution (FS-1), containing a buffer such as tris(hydroxymethyl)aminomethanehydrochloride, an osmoticum eg a carbohydrate such as mannitol, sorbitol, glucose or sucrose, and potassium and calcium salts. The pH can range from 5.2 to 10, and is preferably about 7.2. The protoplasts of different origin are mixed and concentrated, conveniently to a final density of 10" to 106 protoplasts per ml.

The protoplast mixture should then be left undisturbed for at least 10 minutes to allow the cells to settle at the bottom of the petri dish.

The mixture is then treated with polyethyleneglycol (PEG), preferably having a molecular weight from 1500 to 6000. In general good results are obtained when eg employing an aqueous solution comprising 40Z by weight of PEG (FS-2) at a volume ratio FS-1 to FS-2 of from 10:1 to 1:1.

FS-2 comprises conveniently an osmoticum and a calcium salt. The cells are incubated in FS-2 for 1 to 20 minutes depending on the fragility of the cells.

The fusion is accomplished by washing eg twice, with fusion solutions containing PEG, in a lower concentration than in PS-2, an osmoticum (eg glucose or sorbitol) in a concentration giving a lower osmolarity than FS-2 and a magnesium salt.

Temperatures at which the fusion procedure is suitably carried out range between 200 and 240C, preferably 220C.

The concentration of PEG in the "washing solutions" is gradually decreased with each consecutive washing step (see eg Example 9 and fusion solutions 3 and 4).

Each vashing step should take at least 2 minutes to allow the protoplasts to adjust slowly to the lower osmolartiy of the medium, to avoid bursting of the cells.

After the washing steps have been accomplished the fused protoplasts are placed in an appropriate culture medium. The density of the protoplasts should be in the range of from 105 to 106 protoplasts per ml.

Alternatively such protoplast fusion can be carried out by employing electric current.

For the purpose of electrofusion, chains of protoplasts, consisting of lines of max 8 cells, eg 5 cells, are subjected to a direct current (DC)-pulse ranging from eg 400 to 1000V/cm with a pulse duration of eg 10 to 50 ps. The thus fused protoplasts are conveniently retained for some time in the electric field eg 1 to 2 seconds, before the electric field is turned off to give the protoplasts some time to regain their round shape.

The chains of protoplasts may be prepared in a manner known per se, by subjecting the protoplasts to an alternating current (AC)-electric field. Optimal conditions are determined by varying the alternating field frequency, eg around 1 MHz, and the voltage up to 150 V/cm, so that the cells are lined up within a few minutes.

The thus obtained fusion products may be regenerated in the presence of non-fused parental protoplasts, or after optical selection from the culture. Such optical selection may be performed by micro-manipulation of the cells, eg according to the procedure disclosed by Patnaik et al, Plant Science Letters 24 (1982) 105, for the manual isolation and identification of plant heterokaryons, or by using a cell sorter, eg according to the procedure disclosed by Glimelius et al, Plant Science 45 (1986) 133, for the selection and enrichment of plant protoplast heterokaryons by cell sorting.

When employing the selection strategy, the parental protoplasts are for example stained with fluorescent dyes, eg fluorescein isothiocyanate whereby, where one of the fusion partners is of leaf origin, autofluorescence of the chlorophyll may be used for selection.

The thus obtained fusion products are cultivated in an appropriate culture medium comprising a well-balanced nutrient supply for protoplast growth, containing micro- and macro-elements, vitamins, amino acids and small amounts of carbohydrates, eg various sugars such as glucose. Glucose serves as a carbon source as well as an osmoticum. The culture medium comprises plant hormones (auxins and cytokinins) which are able to regulate cell division and shoot regeneration. Examples of suitable auxins are naphtyl acetic acid (NAA), 2,4-dichlorophenoxyacetic acid (2,4-D) and indoleacetic acid (IAA). Examples of suitable cytokinins include benzyl aminopurine (BAP) and zeatin (Zea). In general NAA and 2,4-D are used in combination vith BAP to initiate cell division. The ratio auxin/cytokinin must then be high, eg greater than 1.

After 7 to 10 days the concentration of auxins is conveniently diluted by addition of the same culture medium, but without or substantially less auxins. Typical star-shaped microcalli will in general have developed after 3 - 4 veeks. Such microcalli vill then be transferred to a regeneration medium to initiate shoot formation, preferably after adaptation in an intermediate regeneration medium to differences in composition and physical properties betveen the culture medium and the regeneration medium.

For shoot formation the ratio auxin/cytokinin in the regeneration medium should conveniently be lov, eg belov 1:10. In general it will be preferred to employ the auxin IAA in combination with the cytokinins Zea and BAP for shoot regeneration.

The regeneration media, BR-1 and BR-2 are relatively poor oedia compared to the culture medium. They contain less vitamins, the content of carbon source is lower, they comprise solely sucrose and xylose as carbon source, and do not contain amino acids and coconut milk. The regeneration media also have a higher viscosity than the culture medium.

BR-1 is semi-solid and contains the grovth regulators NAA, 2,4-D and BAP, vith the ratio of auxin to cytokinin being less than 1. BR-2 contains Zea and BAP and optionally IAA.

After 4 - 6 veeks regeneration in BR-1 medium calli of approximately 3mm in diameter are transferred to BR-2 regeneration medium containing a low sucrose concentration. At this stage shoots will develop within 2 3 weeks.

The obtained shoots are then rooted on a basic medium, MS, without additional hormones.

The nuclear DNA and cell organelle DNA of the thus obtained plantlets may then be identified in a manner known per se, eg employing suitable restriction endonucleases and comparing the thus obtained DNA digest pattern of the fusion products with that of the parental lines.

Brassica oleracea protoplasts and inactivated or nucleus-free protoplasts of an Ogura CMS Brassica oleracea plant, employed herein as starting material may be obtained in a manner known per se from the corresponding plant cells.

Cell wall-free cells, ie protoplasts are obtained from green plant material eg leaf material, and/or from white plant material eg etiolated seedlings, cell suspension cultures, roots or bleached plant material, according to conventional methods, eg according to the method disclosed by Glimelius, Physiologia Plantarum 61 (1984) 38, for the regeneration of hypocotyl protoplasts.

Where optical selection of the fusion products is intended the starting materials will be conveniently selected from a green plant or where they are from white plant material they will advantageously be stained to facilitate selection.

The inactivated or nucleus-free protoplasts of an Ogura CMS Brassica oleracea plant are obtained in a manner known per se from corresponding Ogura CMS Brassica oleracea plant cells or protoplasts, eg by irradiation or by standard methods known for the removal of the nucleus from cell material such as centrifugation.

The inactivation of the nucleus by irradiation can be effected with the aid of gamma, UV or X-rays.

Where irradiation is effected with an X-ray source, nucleus inactivat ion will in general be obtained by applying a dose of eg 10 krad/min for 3 to 20 minutes.

The appropriate X-ray dosage may for example be established by determining the minimum level of X-ray irradiation killing 100X of the protoplast population: the percentage of dead cells is estimated by counting the number of formed colonies after 10 - 20 days in culture.

To obtain optimal conditions for the development of cell colonies at low density, it is desirable to use a feeder layer, a pre-conditioned culture medium, or an appropriate cell rescue procedure. Upon determination of the minimum dosage required for the inactivation of cell divisions, the protoplasts are exposed to five increments of X-ray level: the minimum dosage, 10 and 20 krad above and below the minimum dosage.

The thus obtained protoplasts are then introduced in the process of the invention.

Satisfactory nucleus inactivation in general may also be achieved by gamma irradiation with 60Co at a dose of 3 - 30 krad.

Nucleus elimination may also be carried out by incubation of pro to plasts in high osmotic medium to obtain nucleus free subprotoplasts.

An appropriate method for the removal of nuclei by ultracentrifugation suitable for the preparation of the nucleus-free protoplast starting material of the invention is disclosed by Spangenberg in the EURO PEAN JOURNAL OF CELL BIOLOGY 39 (1985) 41-45. Cytochalasine-B is advantageously added to facititate the release of the nuclei from the cells.

Ogura CMS Brassica oleracea plants may be obtained by classical breeding techniques from B oleracea and CMS Raphanus sativus (see introductory part of this application).

It will be appreciated that the Brassica plants of the invention may be employed as starting material for the preparation of other Brassica oleracea varieties having the desired mitochondria of the Ogura CMS cytoplasm and chloroplasts of normal fertile B oleracea and optionally additional desirable traits by in vitro and/or crossing techniques.

Such in vitro and crossing techniques are known in the art by the skilled breeder.

Solutions employed in the experiments: a) TVL solution 0.3M sorbitol 0.O5M CaCl2.2H20 pH = 5.6 - 5.8 b) Enzyme solution 0.6 - 1X cellulysin O.1X macerate dissoloved in BR-1 but with 2 x sucrose concentration, no agarose and 10 x concentration 2,4-D pH = 5.4 - 5.8 c) W5 solution (1L) 18.4g CaCl2.2H20 9.0g NaCl l.Og glucose 0.8g KCl pH = 5.6 - 5.8 d) CPV16s (1L) 16% sucrose 0.0272 g KH2PO4 0.1010 g KNO3 1.4800 g CaCl2.2H20 0.2460 g MgSO4.2H2O 0.00016 g KI 0.000025 g CuSO4.5H20 pH = 5.5 - 5.8 e) Fusion solution-1 (FS-1) 0.15 M sorbitol 0.03 M CaCl2.2H20 0.075M KCl 0.05 M tris(hydroxymethyl)aminomethanehydrochloride pH = 7.2 f) Fusion solution-2 (FS-2) 30-40% PEG (mw 1500) 0.3 M glucose 50 mM CaCl2.2H2O g) Fusion solution-3 (FS-3) 13.3% PEG (mw 1500) 0.1 M glucose 0.067 N sorbitol 0.067 M CaCl2.2H20 h) Fusion solution-4 (FS-4) 6.7% PEG (mw 1500) 0.05 N glucose 0.083 H sorbitol 0.083 N CaCl2.2H20 Table 1: COMPOSITION OF THE MEDIA (mg/l) MS BC-1 BC-2 BR-1 BR-2 KNO3 1900 1900 1900 2500 2500 NH4NO3 1650 600 600 250 250 MgSO4.2H20 370 300 300 250 250 KH2PO4 170 170 170 - - CaCl2.2H20 440 600 600 300 300 KCl - 300 300 - NaH2PO4.H2O - - - 150 150 (NH4)2SO4 - - - 134 134 KI 0.83 0.75 0.75 0.75 0.75 MnSO4.4H20 22.3 10 10 10 10 H3B03 6.2 3 3 3 3 ZnSO4.2H20 8.6 2 2 2 2 NaMoO4.2H2O 0.25 0.25 0.25 0.25 0.25 CuSO4.5H2O 0.025 0.025 0.025 0.025 0.025 KS BC-1 BC-2 BR-1 BR-2 CoCl2.6H20 0.025 0.025 0.025 0.025 0.025 Fe-EDTA 43 43 43 43 43 Thiamine-HCl 0.1 10 10 10 10 Pyridoxine-HCl 0.5 1 1 1 1 Nicotinic acid 0.5 1 1 1 1 Ascorbic acid - 2 2 - Sodiumpyruvat - 20 20 - Citric acid - 40 40 - - Maleic acid - 40 40 - - Fumaric acid - 40 40 - - Glycine 2 - - - Fructose - 250 250 - Ribose - 250 250 - Xylose - 250 250 250 250 Hannose - 250 250 - Rhamnose - 250 250 - Cellobiose 250 250 - Sorbitol - 250 250 - Hannitol - 250 250 - Inositol 100 100 100 100 100 Sucrose ** 250 250 70000 5000 Glucose - 68400 68400 - Casamino acid - 250 250 - Coconut water* - 20 20 - Agarose . - - - 2000 4000 Agar 6000 - - - NAA - 0.1 0.1 0.1 2,4-D - 1 - 0.1 IAA - - - - (0.1) Zeatin - - - - 1 BAP - 0.5 0.5 0.5 0.5 * ml/l ** see examples EXAMPLES Example 1:Seed sterilisation and ger.ination Seeds of Brassica oleracea, Delira type cauliflower with CMS cytoplasm from Raphanus sativus CMS Ogura (hereinafter designated B oleracea A 61043) are briefly dipped in 20% alcohol and sterilised in a 1% sodium hypochlorite solution for 20 minutes on a gyrotary shaker at 160 rpm at 220C. Afterwards extensive rinsing with sterile distilled water is required. The seeds are placed on the MS nutrient medium (see Table 1), with 1% sucrose and without hormones. To obtain green sterile plantlets, the seeds are grown on replica plates in the light (3000 lux), 16hr photoperiod at 220C. Sterile shoots are subcultured under the same conditions in plastic containers.

To obtain white tissue for protoplast isolation, eg hypocotyls, the seeds are grown in petri plates in the dark at 22 C.

Example 2: Analagous to the procedure of Example 1, seeds of Brassica oleracea, cultivar SG 121(atcauliflower) are sterilised and germinated.

(a) deposited Dec. 8, 1987 at the American Type Culture Collection under ATCC designation number 40399.

Example 3: Isolation of protoplssts Four week old sterile shoots of plant material according to Example 1 are cut into small pieces and preplasmolysed for approximately 1 hour in TVL solution in the dark.

TVL solution is removed and a check for bacterial contamination of the plant material is done, by means of culturing a part of the incub ated TVL solution over night in bacterial medium at 220C.

To the material is added an enzyme solution, containing 0.6 - 1X cellulysin and 0.1X macerase and the material incubated for 16 hours in the dark at 220C.

The suspension is then filtered through nylon mesh (70cm) and washed with half volume of CPV16s solution by centrifugation at 750 rpm for 7 minutes. This results in floatation of the intact protoplasts. The protoplasts are collected and rinsed first with V5 solution and then washed with fusion solution-l by centrifugation at 500rpm for 5 minutes.

Example 4: Eight day old hypocotyls of the plant material according to Example 1 are isolated according to the process of Example 3, except that during the enzyme treatment lug/ml of fluorescein isothiocyanate is added. In this way stained protoplasts suitable for hand or machine selection are obtained.

Example 5: Seeds of Brassica oleracea, cultivar SG 121 (cauliflower) are sterilised and germinated according to the procedure of Example 1, and 4 week old sterile shoots thereof are then treated according to the procedure of Example 3, to give protoplasts of B oleracea, cultivar SG 121.

Example 6: Seeds of B oleracea, cultivar SG 121 (cauliflower) are sterilised and germinated according to the procedure of Example 1, and 8 day old hypocotyls thereof are then treated according to the procedure of Exam- ple 3, except that during the enzyme treatment lpg/ml of fluorescein isothiocyanate is added to give stained protoplasts suitable for hand or machine selection.

Example 7: Irradiation of protoplasts Freshly isolated protoplasts according to Example 3 are plated in a 6 cm petri dish in VS solution (2ml). The protoplasts are irradiated using an X-ray source (Baltobloc CE 100), at a dose of 10 krad/min, for 5 to 20 minutes. After irradiation, the inactivated protoplasts are diluted in fusion solution-l before being used for fusion experiments.

Example 8: Cytoplast isolation by ultracentrifugaton A gradient consisting of lOml water saturated with sucrose and a top layer of 4ml 1.5H sorbitol, containing 0.5X dimethyl sulfoxide (DHSO) and 30pg/ml cytochalasine-B and 2ml (= 1 x 106) protoplasts according to Example 3 in fusion solution-1 are loaded on top thereof. The material is subjected to centrifugation for 15 minutes at 40,000 x g at 250C, to give nucleus-free cytoplasts of B oleracea A 61043.

Example 9: Fusion procedure Protoplasts according to Examples 5 and 7 are mixed 1:1 in a final concentration of 5 x 105 protoplasts (pps)/ml fusion solution-1 in a sterile chamber under sterile air flow.

Droplets of 200us are placed in an uncoated petri dish (5-7 droplets per 6cm petri dish), and are allowed to settle for 15 minutes. (The sterile air flow is turned off to avoid disturbance of the settling protoplasts.) Fusion solution-2 (25 - 100p1 per droplet) is added to induce agglutination for 3 - 7 minutes.

The sterile air flow is turned on again, and the solution is replaced by fusion solution-3 for 5 minutes. Then the solution is replaced by fusion solution-4 for 5 minutes. Finally the fusion solutions are replaced with 1.5ml culture medium (BC-1).

Example 10: Selection and grovth of fusion products Fused cells, which can be recognised visually by the presence of double fluorescence are picked up with a micromanipulator.

Hybrids or cybrids are cultured in Biopor filter membranes, diameter 1.1cam or 3cm with pore width of 0.45 - 3pm, containing 100 to 105 cells per ml of culture medium. The filters are placed in a petri dish containing 2-2.5ml feedercells (105 per ml) and the material is incubated at 220C in the dark.

When 20% of the cells are dividing, culture medium-2 is added.

When typical star-shaped microcalli have developed, they are transferred to regeneration medium (BR-1) in coated petri dishes and cultured at 220C and 500 lux for 4 - 6 weeks.

Example 11: Stained hypocotyl protoplasts according to the procedure of Example 4 are irradiated according to the procedure of Example 7. Thus obtained inactivated, stained protoplasts are fused with the protoplasts accord ing to Example 5 and the fused protoplasts then selected employing a cell sorter equipped with a mercury lamp (HB 100) for tvo parameter fluorescence sorting.

The fluorescence excitation beam of the cell sorter is set betveen 488nm and 500nm. The emission beam coming from the excited cells is split by "dichroic"mirrors into two light beams: one vith vavelengths betveen 560 and 610no, representing the autofluorescence of the chloroplasts, and the other with vavelengths betveen 500 and 560nm, represen- ting the fluorescein isothiocyanate fluorescence. Two photomultipliers are used to measure these signals. The sheath fluid (carrier fluid used in the cell sorter to dilute the protoplast sample into a continuous liquid stream) contains autoclaved and degassed V5 medium.

The sorting is based on the principle that fluorescence of non-fused parental cells shov only single fluorescence (red fluorescence of leaf mesophyll protoplasts or fluoresceine isothiocyanate yellov/green fluorescence of the stained hypocotyl protoplasts) vhile fused cells vill shov double fluorescence (red and yellov/green).

Sorted hybrids or cybrids are cultured in a manner identical to that used for cells selected by micromanipulation.

Example 12: The entire fusion mixture according to Example 9 is kept in the petri dish in which the fusion vas performed and cultured in the dark at 220C. After 1-2 days the cells are pipetted and transferred to a coated petri dish. After about 7-14 days when lOX of the cells are dividing, two volumes of culture medium-2 (BC-2) are added. After 10 days another volume of BC-2 is added. The cells are still cultured in the dark at 220C. After 2 - 4 weeks, when the cells have formed typical, star shaped microcalli, they are transferred to regeneration medium-l. The microcalli are cultured in lov light intensity (500 lux), 16 hour photoperiod at 220C.

Example 13: Plant regeneration The calli according to Example 10 and Example 12, having developed to a size of 2-Smn in diameter are transferred to regeneration medium-2 (BR-2) and cultured at 220C and 3000 lux, 16 hour photoperiod. Shoots of about lcm are transferred to MS medium with 1X sucrose without hormones and rooted on the same MS medium.

Example 14: Molecular analysis of the fusion products a) Nuclear DNA composition Characterisation of the nuclear composition of the fusion products is effected by using specific DNA probes. A O.9kb Kpn 1/Bam HI fragment of the beta-tubulin gene of Arabidopsis thaliana hybridises vith various bands in an endonuclease digest pattern of nuclear DNA of the CMS donor, B oleracea A 61043. This pattern is specific for B oleracea A 61043 and differs from the B oleracea breeding lines that'are used as acceptor for the CKS trait (figure 1A).

b) Hitochondrial DNA composition Characterisation is effected with pBO 604 DNA, a clone containing a 1.5 kbp Sac I fragment from the mitochondrial DNA of Ogura CMS cytoplasm of Raphanus sativus. This clone gives hybridisation signals with restriction endonuclease digests of mitochondrial DNA from Ogura CMS cytoplasms of B oleracea, A 61043 but not vith mitochondrial DNA from fertile cytoplasm of B oleracea breeding lines (figure 1B).

c) Chloroplast DNA composition The DNA present in the chlorosis sensitive chloroplasts of the Ogura CKS cytoplasm is characterised with the probe lambda Bcp 17. This clone contains a 4.5 kpb Xho I/Sac I fragment from Ogura CMS chloroplast DNA.

The clone hybridises with a 57.5 kpb band in the Sal I digest of Ogura CMS chloroplast DNA and with a 9.9 kbp band in the Sal r digest of chloroplast DNA from fertile cytoplasms in B oleracea breeding lines (figure 1C).

The figures 1A, 1B and 1C are accurate hand drawn copies of photographs.

Claims (3)

1CMS Brassica oleracea plants containing mitochondria of the Ogura CMS cytoplasm and chloroplasts of normal fertile Brassica oleracea.

2 CMS Brassica oleracea plants according to claim 1 which are selected from the group consisting of cauliflower, white cabbage, Brussels sprouts and broccoli.

3 Process of preparing CMS Brassica oleracea plants of claims 1 and 2 which comprises: a) fusing protoplasts of B oleracea having commercially desirable traits with inactivated protoplasts or nucleus-free protoplasts of an Ogura CMS B oleracea plant followed by regeneration of the thus obtained allogenic cells.

b) employing the CMS B oleracea cells or plants obtained according to process a) of this claim or the progeny thereof as starting material for the preparation of CMS B oleracea plants of claims

1 and 2 by in vitro and/or crossing techniques.