Method for reproducing conifers by somatic embryogenesis using galactose containing compounds as a carbon and energy source

Abstract

A method for reproducing conifers by somatic embryogenesis is disclosed. A galactose-containing compound is used as a carbon source for an embryogenic culture during at least one of the steps of induction, proliferation, and prematuration.

Description

BACKGROUND OF THE INVENTION

[0002] Somatic embryogenesis offers the potential to clonally produce large numbers of plants of many species at low cost. Somatic embryos develop without the surrounding nutritive tissues and protective seed coat found with zygotic embryos, so research has been directed to causing somatic embryos to functionally mimic seeds with regard to efficient storage and handling qualities. The development of techniques for somatic embryogenesis in conifers has greatly improved the ability to culture conifer tissues in vitro and now offers the means to clonally propagate commercially valuable conifers. However, it is necessary to further reduce production costs to make somatic embryogenesis affordable to industry. Thus, there is a need in the technology for improvement of the efficiency of embryo production and of the quality and vigour of plants resulting from somatic embryos from all species of conifers.

BRIEF SUMMARY OF THE INVENTION

[0003] A method for reproducing conifers by somatic embryogenesis is disclosed wherein a galactose-containing compound is used as a carbon source for an embryogenic culture during at least one of the steps of induction, proliferation, and prematuration.

BRIEF DESCRIPTION OF THE FIGURES

[0004] FIG. 1 represents the ability of loblolly pine lines grown on TX maintenance medium to hydrolyze sucrose over time.

[0005] FIG. 2 represents the growth rate of loblolly pine lines grown on TX maintenance medium.

[0006] FIG. 3 represents the growth rate of loblolly pine lines grown on prematuration medium I containing lactose.

[0007] FIG. 4 represents the growth rate of loblolly pine lines grown on prematuration medium II containing lactose.

[0008] FIG. 5 represents the ability of loblolly pine lines grown on prematuration medium I and utilise lactose by breaking it down to produce glucose and galactose.

[0009] FIG. 6 represents the ability of loblolly pine lines grown on prematuration medium II to utilise lactose by breaking it down to produce glucose and galactose.

DETAILED DESCRIPTION

[0010] The following definitions are those consistent with the usage of terms in the present specification.

[0011] Abscisic Acid (ABA) A plant growth regulator in the group of stress hormones.

[0012] Auxin A plant growth regulator which may be natural or synthetic. The main physiological effect of auxin is to stimulate cell elongation. Examples are indole acetic acid (IAA) and 2,4-dichlorophenoxyacetic acid (2,4-D).

[0013] Clone When used in the context of plant propagation, the term refers to a collection of individuals having the same genetic constitution (genotype), and is produced from a culture that arises from an individual explant.

[0014] Conversion The ability of a somatic embryo to germinate (either in vitro or ex vitro) and subsequently develop into an established, autotrophic plant with root and needles.

[0015] Cytokinin A natural or synthetic plant growth regulator such as benzyl adenine (BA). The main physiological effect of cytokinin is to stimulate meristematic cell division.

[0016] Desiccation The drying of an embryo by any means to a moisture content less than that of the original hydrated embryo. Desiccation processes may include (a) mild desiccation, which encompasses moisture contents in the 36-55% moisture content range, and (b) severe desiccation, which occurs at moisture contents less than 36%, usually in the range of about 5-30%. A severely desiccated viable embryo is able to survive freezing, and after rehydration, is able to successfully complete the germination process and convert to a normal autotrophic plant.

[0017] Embryogenic culture A plant cell or tissue culture capable of forming somatic embryos and regenerating plants via somatic embryogenesis.

[0018] Explant Organs, tissues or cells derived from a plant and cultured in vitro for the purposes of starting a plant cell or tissue culture.

[0019] Galactose A hexose of the formula CH2OH.(CHOH)4CHO. It is present in certain gums and seaweeds as a polysaccharide galactan and as a normal constituent of milk.

[0020] Lactose Lactose is a disaccharide (C12H22O11). It yields D-glucose and D-galactose on hydrolysis, which is catalysed by lactase.

[0021] Line This is another term for “clone”.

[0022] Mature embryo A mature embryo is one which is capable of germination to yield a seedling with shoot and root, given the necessary environmental conditions (temperature, light, water, nutrients, etc.). The term implies that the embryo has undergone development through various developmental stages and has reached a size and stage suitable for germination. The embryo contains storage proteins, lipids, and if provided with suitable maturation conditions (e.g. ABA and water stress), will be desiccation tolerant, so may be desiccated prior to germination.

[0023] Megagametophyte A haploid nutritive tissue of gymnosperm seed, of maternal origin, within which the gymnosperm zygotic embryos develop.

[0024] Moisture content The amount of water present in an embryo. This is generally measured by weighing an embryo before and after oven drying (FW and DW, respectively). The preferred manner of expression is percentage weight of water based on the original weight of the embryo, so that the values are always less than 100. MC=((FW−DW)/FW)×100%

[0025] Prematuration The step following the proliferation step and prior to the maturation step, usually involving a gradual reduction in the concentrations of one or more of the hormones auxin and cytokinin and/or a change in water stress and the addition of ABA.

[0026] Proliferation The steps following induction prior to maturation, in which embryogenic cultures divide and grow but do not develop into mature embryo stages. The proliferation step may also be referred to as the maintenance step.

[0027] Nutrients The inorganic micro- and macro-minerals, vitamins, hormones, organic supplements, and carbohydrates (or any one or more of them) necessary for culture growth and somatic embryo germination.

[0028] Somatic embryo A plant embryo formed in vitro from vegetative (somatic) cells by mitotic division of cells. Early stage somatic embryos are morphologically similar to immature zygotic embryos, and comprise a region of embryonal cells subtended by suspensor cells.

[0029] Somatic Embryogenesis A process of initiation and development of somatic embryos in vitro from somatic cells and tissues.

[0030] Water potential The total water potential to which an organism is subjected in a water-containing matrix. This is a sum of (1) osmotic (solute) potential, (2) gravitational potential resulting from the vertical position of the water, and (3) a suction component (capillary or matric potential).

[0031] Water Stressing The reduction of water potential to which an embryogenic tissue or somatic embryo is controlled during maturation by controlling the environment of the tissue or embryo in order to modify the progress of maturation.

[0032] Zygotic Embryo An embryo derived from the sexual fusion of gametic cells produced by meiosis.

[0033] Somatic embryogenesis in plants is a multistep process consisting of induction, proliferation, maturation (embryo development), and germination and requires that specific culture conditions, including nutrient media compositions, are provided for each step of the multistep process. Thus, in general for most conifers an auxin and cytokinin and a low osmoticum are required in media for induction and proliferation of embryogenic tissues. For further embryo development it is often beneficial to increase the osmotic concentration, and to replace the auxin and cytokinin with abscisic acid (ABA). The effects of different carbohydrates on the different steps of somatic embryogenesis are not clearly understood. For conifers the optimal carbohydrate has thus far been found to be either sucrose or maltose (Iraqi and Tremblay 2001 a, Iraqi and Temblay 2001b, Ramarosandratana et al, 2001).

[0034] Water stress plays an important role in maintaining embryos in a maturation state, and low water content rather than ABA may prevent precocious germination during later stages of development. This is important because precocious germination of embryos during development in seeds would be lethal during desiccation. A conventional way to water stress plant cells grown in vitro is to increase the osmotic concentration of the culture medium through the use of plasmolysing osmotica. For example, increased concentrations of plasmolysing osmotica such as sucrose or mannitol have been used to promote somatic embryo maturation of many plant species.

[0035] Sucrose or maltose are considered to be the most suitable carbon sources for conifers, depending upon the species, for most stages of culture. Lactose has been used as an osmoticum with maltose or sucrose supplements as the carbon source during the conifer maturation step. Lactose or galactose has not been described as a suitable energy source for the induction or maintenance of the immature embryo stages. The newly-discovered fact that embryos of some conifer species can hydrolyze lactose and/or metabolize galactose at certain developmental stages without galactose toxicity, and that this results in improved cultures is an unexpected beneficial result.

[0036] Here, a compound containing galactose as a carbon and energy source in the media is used during early conifer embryogenesis, specifically sugars containing galactose or galactose subunits. The most suitable sugars are galactose or lactose, the choice of which depends on the conifer species being cultured.

[0037] The method is especially well suited to culturing conifers of the family Pinaceae, especially those species including Pinus taeda (loblolly pine), Pinus radiata (radiata pine) and Pseudotsuga menziesii (Douglas fir). The method produces higher induction frequencies.

[0038] The method promotes differentiation of immature embryos in proliferation cultures. These embryos when subsequently transferred to development (maturation) medium show reduced growth of suspensor tissue, improved embryo quality and improved yields of mature embryos. This results in higher numbers of genotypes that can be successfully cultured and cryostored, and results in a higher number of seedlings produced at lower costs than those of prior known methods.

[0039] Diploid cultures of conifers are most readily initiated from zygotic embryos, which are genetically dissimilar from each other. Low osmotic conditions are beneficial for induction from conifers. The sugar most often used for induction is sucrose at about 1% (w/v) concentration. However, the use of galactose-containing compounds, such as galactose and lactose at the induction stage, is now shown to lead to improved induction success. The most suitable concentration may be less than about 6%, and, more particularly, may be less than about 2%, and even more particularly, between about 1% and about 2%, alone or with additional carbon sources. Cytokinin is important to most species, and is usually included with an auxin at concentrations of 5 and 10 μM, respectively.

[0040] Exceptions to the above plant growth regulator (PGR) requirements are Abies spp, which are different from other conifers, and require cytokinin as the sole PGR for induction as well as proliferation.

[0041] Genotype specificity for embryogenic induction occurs in conifers. Also, the induction of somatic embryogenesis is under strong additive genetic control. For conifers, immature zygotic embryos yield somatic embryos more readily than mature zygotic embryos, which are generally more responsive than explants from young seedlings. Cryopreservation of immature somatic embryos in liquid nitrogen is routine for long-term preservation and is used to preserve genotypes while extended field tests are carried out. Following the field trials elite genotypes are then removed from cryogenic storage and bulked up in liquid suspensions for mass propagation. Methods of this invention lead to greater numbers of cryopreserved lines following induction.

[0042] Embryogenic cultures of conifers are usually maintained on a medium similar to the induction medium, which typically includes an auxin, a cytokinin and a low concentration of sugar. The method of maintenance (or proliferation) depends upon the intended use of the culture. A common way to maintain cultures is on semi-solidified medium in Petri dishes. These stationary cultures are sub-cultured every 2-4 weeks to prevent browning and death. Liquid culture is more suitable for maintaining conifer cultures in a rapidly proliferating state for large scale propagation.

[0043] Pine embryogenic tissue, when grown on abscisic acid (ABA) in the presence of sucrose, undergoes a disorganised growth phase, prior to organised growth. Such cultures do not readily undergo further development with ABA and a low osmotic concentration, perhaps because they are too juvenile to respond to ABA. Replacing the sucrose with lactose or galactose at the proliferation step has the benefit of reducing disorganised growth, and leads to the production of well-organised immature embryos with enlarged embryonal regions. This effect is more pronounced than with maltose. When transferred to maturation medium these lactose/galactose embryos have a greater propensity to develop to mature embryo stages than those grown on other sugars, including maltose, and disorganised suspensor tissue proliferation is inhibited. The result is that mature embryos are produced in higher yields than with other known methods, and the mature embryos are of greater uniformity. They are also of better quality and thus are vigorous during subsequent germination. All of the latter lead to greater numbers of plants recovered at the end of the process.

[0044] In order to encourage the production of mature developmental stages of conifer somatic embryos, immature somatic embryos must be transferred from a medium containing hormones to stimulate proliferation to an environment containing ABA and ideally a raised osmotic concentration. A gradual transition to these growth conditions is often beneficial. Thus, prior to ABA treatments, immature somatic embryos may be transferred to a prematuration medium containing no, or reduced, plant growth regulators. Charcoal may be beneficial.

[0045] Following the maturation step it is often desirable to desiccate the somatic embryos. A moisture content of less than 55% is beneficial to producing high storage reserves and inducing desiccation tolerance. In addition to promoting germination, desiccation reduces production costs by providing a means of storing somatic embryos. For optimal efficiency, mature somatic embryos can be produced continuously year round, then stored and pooled with somatic embryos from subsequent production runs. They can then be germinated synchronously to provide plants of uniform age and size for planting during a suitable growing season.

[0046] Post-germinative growth of conifer somatic embryos occurs without the benefit of the haploid megagametophyte, which is a major organ for storage of both lipids and proteins within the conifer seed. Conifer somatic embryos therefore require nutrients, usually in the form of PGR-free media supplied at half strength and containing 1-3% sucrose for further growth into autotrophic plants.

[0047] The process of the present invention is not limited to any single basal culture medium. Any well known medium or modification may be used, however we have found the formulation below to work well for many conifers as described in the following sections.

TABLE A
TX medium basal salts
               Amount per liter
Basal salts    Medium, mg
Major
KNO3           950.00
KH2PO4         170.00
MgSO4.7H2O     925.00
CaCl2.2H2O     211.00
Minor
KI             4.15
H3BO3          31.0000
ZnSO4.7H2O     43.0000
MnSO4.H2O      21.0000
Na2MoO4.2H2O   1.5000
CuSO4.5H2O     0.5000
CoCl2.6H2O     0.1300
Iron
FeSO4.7H2O     27.8
Na2EDTA        37.2
Vitamins
Thiamine-HCl   0.1000
Pyridoxine-HCl 0.1000
Nicotinic acid 0.5000
Myo-Inositol   100

EXAMPLES

[0048] Examples Assessing Loblolly Pine Somatic Embryogenesis

Example 1

Effect of Carbon Source on Induction of Loblolly Pine

[0049] Female gametophytes containing the immature zygotic embryos were used as explants. The cones were surface sterilized in 10% bleach solution for 15 min. They were rinsed 3 times with sterile water, air dried and stored in polyethylene bags at 4° C. until used. Seeds were sterilized in 3% hydrogen peroxide containing 0.1% Tween 20 and rinsed in sterile deionized water. Megagametophytes containing the immature embryos were plated on TX medium (Table A) supplemented with 2.2 mg/l 2,4-D, 1 mg/l BA and 0.3% Phytagel and containing either 1% sucrose, or 1.5% lactose and 0.025% glucose.

[0050] Cultures were maintained on the two media by subculturing the embryogenic tissue every 10 to 14 days to fresh media. All cultures were incubated at 23° C. in the dark. The results of the induction are presented in Table 1.

TABLE 1
Effect of carbon source on Loblolly pine induction success
Treatment  % induction
TX sucrose 1.46
TX lactose 6.85

[0051] Induction success was greater than three times higher when medium containing lactose was used.

Example 2

Effect of Carbon Source on Solid Maintenance of Loblolly Pine

[0052] Tissue induced on sucrose from Example 1 was further maintained on the semi-solid TX medium containing 1% sucrose, and tissue induced on lactose was maintained on semi-solid TX medium containing 1.5% lactose and 0.025% glucose. The tissue morphology of the lines induced on lactose was different from the ones induced on sucrose. Tissue induced on lactose-containing medium consisted of more early-stage immature embryos and a limited amount of suspensor type of surrounding tissue. Predominantly suspensor type tissue and very few embryos were observed in the tissue induced on sucrose. In order to further increase the proliferation rate, 0.5% sucrose was added to the TX 1.5% lactose-containing medium in place of 0.025% glucose. This medium provided a reasonable bulk-up rate, and growth of embryos was more synchronized than in the 1% sucrose medium.

Example 3

Effect of Carbon Source on Liquid Maintenance

[0053] Suspension cultures of loblolly lines LP1, LP2, LP3, LP4 and LP5 were started with 2 g of tissue introduced to 50 ml of TX liquid medium containing different sugars—1% sucrose, 1.5% maltose, or 1.5% lactose. These cultures were maintained in the same liquid media for 2 weeks by weekly transfers to fresh maintenance medium containing the above sugars. Then, 2 g of tissue produced in each maintenance medium was transferred to prematuration media I, containing the same carbon source as the maintenance media. After one week, 1.5 g of tissue from each prematuration medium I was transferred to prematuration media II containing the same sugars. After the 4 week period in liquid media, early stage somatic embryos were collected and plated on ½ LV maturation medium containing 120 μM ABA and 6.0% sucrose and 1% Phytagel. Eight to ten weeks later, mature somatic embryos were counted and treatments were evaluated based on the number of somatic embryos per gram fresh weight (SE/g FW). Table 2 summarises the tissue yield at the end of the 4-week period and the number of mature somatic embryos produced for each line.

TABLE 2
Effect of carbon source on growth rate
and yield of somatic embryos.
		Average amount of tissue
		produced after 4 weeks in
	Carbon source	liquid (FW g)	# SE/g FW ± sd
	1% Sucrose	592.06	126 ± 20
	1.5% Maltose	204.45	209 ± 28
	1.5% Lactose	18.63	393 ± 10

[0054] The highest growth rate was observed when sucrose was used for the entire 4-week liquid period. The lowest amount of tissue was obtained when lactose was used as sole carbon source. However, tissue cultured in lactose-containing media produced the highest number of SE/g FW. This significantly reduces production costs, as about 60% less maturation cultures are required to produce a target number of embryos.

Example 4

Effect of Lactose During the Prematuration Steps

[0055] Prematuration for loblolly pine may be performed in two steps:

[0056] 1. Prematuration I requires reduction of hormones either by reducing the auxin and cytokinin concentrations to optimally about {fraction (1/20)} of the concentration of proliferation step, or by adding charcoal at about 0.01 to 1%, or a combination of both.

[0057] 2. Prematuration II follows prematuration I and requires an addition of ABA at concentrations of about 5 to 120 μM, preferably 90 μM and no auxin and cytokinins.

[0058] In order to further understand the effect of lactose on somatic embryo development, liquid maintenance cultures were started in TX medium containing 1% sucrose as in Example 3. Three lines were used in this experiment, LP2, LP3 and LP4. After the proliferation step, 2 g of the tissue was transferred for one week to prematuration medium I containing different concentrations of lactose—1.5%, 3% and 6%. After that, 1.5 g of tissue produced in the lactose-containing media was further cultured for a week in prematuration medium II containing the same amount of lactose. The summary of the results is presented in Table. 3.

TABLE 3
Effect of lactose at the prematuration step.
	Mean grams FW
	at the end of
Carbon source	prematuration stage	Mean # SE/g FW ± sd
1% Sucrose to 1.5% lactose	121.90	106 ± 9
1% Sucrose to 3% lactose	216.47	209 ± 7
1% Sucrose to 6% lactose	149.13	169 ± 10

[0059] The highest numbers of somatic embryos were obtained when 3% lactose was used for the last two weeks of the liquid prematuration step.

Example 5

Carbohydrate Metabolism

[0060] In order to understand the effect of sucrose and lactose on somatic embryo development, all media required for the liquid stage (maintenance, prematuration I and II) were analysed for sucrose, glucose, lactose, and galactose. Two lines were used in this experiment: LP3 and LP6.

[0061] Both lines completely hydrolysed sucrose at day 5 during the first week of culture in TX maintenance medium. A similar pattern in the ability of the lines to hydrolyse sucrose was observed after transferring the tissue to the same medium for an additional week of culture. FIG. 1 represents an average of the results for both lines. The growth rates of the lines during the two-week period followed a similar pattern (FIG. 2). Line LP3, however, metabolised more glucose and at the end of the 2-week period no glucose was detectable in the medium. This same line produced the largest amount of tissue (1278.18 g) at the end of the 4 week-liquid period when sucrose was used as sole carbon source.

[0062] After transferring the tissue to the prematuration medium I containing lactose, both lines maintained a similar growth pattern (FIG. 3). During the second week in lactose, at the prematuration II stage, both lines showed a significant increase in the growth rates (FIG. 4). When media were analysed for the presence of glucose and galactose (FIGS. 5 and 6), detectable amounts of glucose and galactose were observed for both lines. A decrease of the amount of lactose was also detected. It is clear that both lines were capable of utilising lactose (Table 4). Data presented in FIG. 6 also provide grounds to conclude that the lines were not only capable of metabolising lactose but also of utilising galactose, as a significant amount of “missing” galactose was registered at day 7 in comparison to day 5 (where the glucose amounts in the medium were the same).

TABLE 4
Sugar utilisation summary
	Amount of sugar in media at
Sugar	the start, %	% sugar missing (utilised)
Sucrose	1.0	30
Lactose	1.5	12

Example 5.1

Effect of Galactose During Proliferation and Prematuration Steps on Loblolly Pine

[0063] The finding that loblolly pine cultures were capable of utilising galactose is unique. In order to further investigate these phenomenon two lines, LP1 and LP3, were cultured on semi-solid TX medium containing 1.0% lactose and 0.5% sucrose. Cultures were maintained by subculturing the embryogenic tissue every 10 to 14 days to fresh media. All cultures were incubated at 23° C. in the dark. Suspension cultures were initiated as described in Example 3, however, TX medium was supplemented with either 1% sucrose, 1.5% maltose, 1.5% lactose, or 0.75% galactose. These cultures were maintained in liquid media for 4 weeks by weekly transfers to fresh maintenance or prematuration media. After the 4˜week period, 1 ml of the liquid medium containing 0.1 g of tissue consisting of early stage somatic embryos was plated on each 10 mm plates containing ½ LV maturation medium. This medium contained 120 μM ABA and 6.0% sucrose and 1% Phytagel. Eight to ten weeks later, mature somatic embryos were counted and treatments were evaluated based on the number of somatic embryos per gram fresh weight (Table 5).

TABLE 5
Effect of galactose and galactose-containing sugars on SE yield
			Amount of tissue at
			the end of the
	Carbon source	Line	preculture II stage	# SE/g FW
	Sucrose	LP1	121.22	11 ± 3
		LP3	1278.18	100 ± 6
	Maltose	LP1	232.18	106 ± 4
		LP3	118.22	160 ± 5
	Lactose	LP1	28.9	1060 ± 17
		LP3	8.78	110 ± 7
	Galactose	LP1	59.45	216 ± 8
		LP3	8.65	172 ± 5

[0064] The results show that all lines were able to produce mature embryos after culturing in sucrose medium. However, they performed differently when maltose, lactose or galactose was used as a carbon source. Line LP1 produced over 1000 embryos when cultured in lactose-containing TX medium and only 11 embryos when sucrose was used as a carbon source. Although a reduction in embryo yield was observed when the same line was cultured in galactose-containing TX media, the number of embryos produced by LP1 when galactose was used as the carbon source was significantly higher than the number obtained on sucrose- or maltose-containing TX media. Line LP3 produced more embryos after culturing in TX galactose-containing media. Again, the lowest embryo yield was observed when sucrose was used as carbon source. These results suggest that different lines require different types of sugar as a carbon source for their optimum performance, but galactose-containing sugars are superior.

[0065] Examples Assessing Radiata Pine Somatic Embryogenesis

Example 6

Effect of Carbon Source on Induction of Radiata Pine

[0066] Female gametophytes containing immature zygotic embryos were used as explants. The cones were surface sterilised in 10% bleach solution for 15 min. They were rinsed 3 times with sterile water, air dried and stored in polyethylene bags at 4° C. until used. Seeds were sterilised in 3% hydrogen peroxide containing 0.1% Tween 20 and rinsed in sterile deionized water. Megagametophytes containing the immature embryos were plated on MSG (standard radiata pine medium containing sucrose, Table B) and on TX medium (Table A) supplemented with 2.2 mg/l 2,4-D, 1 mg/l BA and 0.3% Phytagel and containing 1.5% galactose and 0.5% sucrose. Casein hydrolysate was reduced to 1000 mg/l (TXR medium).

TABLE 8
MSG basal salts
               Amount per liter
Basal salts    Medium, mg
Major
KNO3           100
KH2PO4         170
MgSO4.7H2O     370
CaCl2.2H2O     440
KCl            745
Minor
KI             0.83
H3BO3          6.2
MnSO4.H2O      16.9
ZnSO4.7H2O     8.6
Na2MoO4.2H2O   0.25
CuSO4.5H2O     0.025
CoCl2.6H2O     0.025
Iron
FeSO4.7H2O     27.8
Na2EDTA        37.3
Vitamins
Thiamine-HCl   0.1
Pyridoxine-HCl 0.1
Nicotinic acid 0.5

[0067] Cultures were maintained on the two media by subculturing the embryogenic tissue every 10 to 14 days to fresh media. All cultures were incubated at 23° C. in the dark. Suspension cultures were initiated as 2 g of tissue were introduced to 50 ml of TXR liquid medium containing 1.0% sucrose. These cultures were maintained in liquid media for 40-48 days by transfers to fresh maintenance medium every 10 to 14 days.

[0068] One ml of TXR medium containing 0.1 g tissue consisting of early stage somatic embryos was plated on modified ½ LV maturation medium (Table C) in which glutamine was reduced to 500 mg/l and casein hydrolysate to 1000 mg/l. In addition, 120 μM ABA, 6.0% sucrose and 1% Phytagel were added. Twelve to fourteen weeks later, mature somatic embryos were counted and treatments were evaluated based on the number of somatic embryos per gram fresh weight.

[0069] The results of the induction are presented in Table 6. Induction success was greater than three times higher when galactose was used as a carbon source and subsequent yields of mature embryos from these tissues were almost double.

TABLE C
1/2 LV medium basal salts
               Amount per liter
Basal salts    Medium, mg
Major
NH4NO3         825.00
KNO3           950.00
KH2PO4         170.00
MgSO4.7H2O     925.00
CaCl2.2H2O     11.00
Minor
KI             4.1500
H3BO3          31.0000
ZnSO4.7H2O     43.0000
MnSO4.H2O      21.0000
Na2MoO4.2H2O   1.3000
CuSO4.5H2O     0.5000
CoCl2.6H2O     0.1300
Iron
FeSO4.7H2O     27.8
Na2EDTA        37.2
Vitamins
Thiamine-HCl   0.1000
Pyridoxine-HCl 0.1000
Nicotinic acid 0.5000
Myo-Inositol   100

[0070]

TABLE 6
Effect of carbon source on radiata pine induction success
				Embryo yield
	Treatment	% induction	% cryopreserved	(#SE/gFW)
	MSG	10.03	100	213
	TXR	26.07	100	405

Example 7

Effect of Carbon Source on Somatic Embryo Development of Radiata Pine Embryos in Liquid Cultures

[0071] Tissue induced on MSG containing sucrose was further maintained on MSG sucrose medium, and tissue induced on TXR galactose was maintained on TXR medium containing galactose as described in Example 6. The tissue morphology of the lines induced on galactose was different from that induced on sucrose. Tissue induced on galactose-containing medium consisted of more early stage immature embryos and a limited amount of suspensor type of surrounding tissue, whereas predominantly suspensor type tissue and very few embryos were observed in the tissue induced on sucrose. The lines used in this study were RP1, RP2, RP3, and RP4.

[0072] Suspension cultures were initiated as described in Example 6. These cultures were maintained in liquid media for 20-28 days by transfers to fresh maintenance medium every 10 to 14 days. Up to five fold increase of the tissue was estimated at the end of each 10 to 14 day transfer.

[0073] In order to study the effect of galactose on embryo development after the proliferation stage, 2 g tissue was further transferred to 250 ml flasks, containing 50 ml of TXR prematuration medium I supplemented with either 1.0% sucrose or 3.0% galactose. As with loblolly pine cultures, prematuration I requires reduction of hormones either by reducing the auxin and cytokinin concentrations to optimally about {fraction (1/20)} of the concentration of proliferation step, or by adding charcoal at about 0.01 to 1%, or a combination of both.

[0074] After the 10-14 day period, 1.5 g tissue was transferred to 250 ml flasks containing 50 ml TXR prematuration medium II to which either 1.0% sucrose or 3.0% galactose and 90 μM ABA were added.

[0075] Early stage somatic embryos were collected after 10 to 14 days and matured on modified ½ LV maturation medium as described in Example 6. Results are shown in Table 7.

TABLE 7
Tissue and somatic embryo yield.
	Grams FW at the end of
Carbon source	proliferation stage (from 1.5 g)	# SE/g FW ± sd
Sucrose	11.05 ± 2	213.3 ± 6
Galactose	9.5 ± 2	405.3 ± 10

[0076] Tissue growth increased more than 5 times when galactose was used as a carbon source and the number of mature somatic embryos at the end of maturation was doubled.

[0077] Examples Assessing Douglas Fir Somatic Embryogenesis

[0078] The culture medium for Douglas fir was TX medium (see Table A) with the following additives: glutamine 100 mg., Casein hydrolysate 100 mg., and pH 5.8. The following compounds were added into the basal medium for Douglas fir somatic embryo development at different stages:

[0079] 1) Induction medium: 18 μM 2,4-D and 9 μM BA, phytagel 0.28%, sucrose 1%

[0080] 2) Solid maintenance medium: 9 μM 2,4-D and 4.5 μM BA, phytagel 0.28%, sucrose 1%.

[0081] 3) Liquid maintenance and bulking-up medium: 9 μM 2,4-D and 4.5 μM BA, different carbon sources for experiments.

[0082] 4) Liquid pre-treatment medium: 20 (first week) or 30 μM ABA (second week), 10% PEG4000 (first week) or PEG1500 (second week), different carbon sources as described in examples below.

[0083] 5) Solid maturation media: TX (Table A) plus 0.02% NH4NO3

[0084] Medium I. 40 μM ABA, 10% PEG 1500, maltose 2.5%, phytagel 0.6%

[0085] Medium II. 60 μM ABA, 10% PEG1500, maltose 2.5% and sucrose 1%, phytagel 0.8%

[0086] Medium III. 70 μM ABA, 6% PEG1500, sucrose 6%, phytagel 1%.

[0087] Embryogenic tissue was induced from immature zygotic embryos. The cones and seeds were surface-sterilised as described for pines, and embryos were dissected out from megagametophytes. The embryos, with the attachment of suspensors to their megagametophytes, were placed on the surface of induction medium. The culture was kept in darkness at 23° C. Embryogenic tissue was sub-cultured once every two weeks onto solid maintenance medium.

Example 8

Effects of Carbohydrates on Liquid Maintenance of Douglas Fir Embryogenic Tissue

[0088] Embryogenic tissue of Douglas fir was collected from solid maintenance culture and one gram of tissue was transferred into a 200 ml flask containing 50 ml TX (see Table A) liquid maintenance medium. The liquid maintenance medium was supplied with different sugars (Table 8).

TABLE 8
Growth of Douglas fir tissue (fold, mean ± SD) in suspension
maintenance/bulking-up cultures for 3 weeks.
Cell line DF-2 was used in this experiment.
Major carbon sources	Additional glucose (%)	Tissue growth
0.5% galactose	0	68.64 ± 4.58
0.5% galactose	0.025	97.02 ± 2.67
1% lactose	0	1.40 ± 0.14
1% lactose	0.025	2.75 ± 0.24
0.5% mannitol	0	1.60 ± 0.13
0.5% mannitol	0.025	3.34 ± 0.22
0.5% glucose	0	223.14 ± 15.4
1% sucrose	0	100.94 ± 12.0
1% maltose	0	85.01 ± 1.71

[0089] The tissue was drained, weighed and sub-cultured once per week. During a culture period of three weeks, the highest tissue growth was found in the culture with glucose as the major carbon source. The media containing sucrose, maltose and galactose also supported a fast tissue growth. With these latter sugars, tissue increased to 68 to 100 fold in three weeks. Tissue grew little in the media containing lactose or mannitol. Supplement of a small amount of glucose in the media containing galactose, lactose or mannitol respectively increased tissue growth (Table 8) and this increase of tissue growth corresponded to the amount of glucose supplied into the media (data not shown). Similar results were obtained within two cell lines, DF-7A and DF-2.

[0090] Thus, among the tested sugars, glucose resulted in the fastest tissue growth. Sucrose, maltose and galactose were all good carbon sources for tissue growth. Lactose and mannitol have to be used in combination with other carbon sources such as glucose, in order to achieve a good tissue growth.

Example 9

Osmolarity and Carbon Metabolism in Liquid Maintenance

[0091] After a one-week liquid maintenance culture, the osmolarity of culture medium showed little change when lactose or mannitol was used as the major carbon source while the medium containing either galactose or glucose decreased from 22% to 32% (Table 9). More change of medium osmolarity occurred during week 2 than week 1. The medium osmolarity changed little when lactose or mannitol was used in the media.

TABLE 9
Medium osmolarity (mmol/kg, mean ± SD) and changes
before and after a one-week tissue inoculation.
	Osmolarity before	Osmolarity after
Carbohydrates	inoculation	inoculation	Change (%)
0.5% galactose	71.67 ± 1.15	48.67 ± 0.58	−32.09
1% lactose	93.33 ± 0.58	94.67 ± 1.15	1.44
0.5% mannitol	76 ± 1	71.67 ± 1.15	−5.70
0.5% glucose	77.67 ± 0.58	54.67 ± 1.53	−29.61

[0092] Sugars in the media were quantified with the method of enzymatic BioAnalysis that can quantify the specific carbohydrates in trace amount. In the medium, glucose decreased sharply, up to 94.4%, while galactose decreased about 80.6%. Little changes were found with lactose or mannitol after a one-week culture (Table 10).

TABLE 10
Changes of carbohydrates in Douglas fir suspension
media after tissue (DF-7A), inoculation for one week.
Major carbon	Sugar	Before use
source	analyzed	(%)	After use (%)	Decreased (%)
0.5% glucose	Glucose	0.5	0.0278	94.44
0.5% galactose	Galactose	0.5	0.097	80.6
1% lactose	Lactose	1	0.99	0.01
0.5% mannitol	Mannitol	0.5	0.5	0

[0093] The results of this study show that glucose is an easily-consumable carbon source for Douglas fir tissue. Galactose can be utilised slowly. Lactose and mannitol are not metabolised by Douglas fir tissue.

Example 10

Effects of Carbohydrates in Suspension Cultures on Embryo Yield

[0094] In pre-treatment media, ABA was the only plant hormone present in the media and polyethylene glycol (PEG) was added as a non-permeable osmoticum to stimulate and synchronize embryo maturation. It was a common phenomenon that tissue grew more after being transferred from maintenance media containing other carbon sources into the pre-treatment medium containing maltose as the major carbon source. Tissue grew faster during the first week and then slowed down in the second week (Table 11).

[0095] After pre-treatment, about 0.1 g tissue was plated onto a piece of filter paper on the surface of solid maturation medium I. After two weeks, the tissue was transferred with the filter paper to medium II and then medium III after three additional weeks. The maturation culture was kept in darkness, 23° C. for 8 weeks and then 12° C. for one week. Embryos were evaluated after this nine-week maturation. During evaluation only mature embryos with a normal shape and at least three well-developed cotyledons were scored.

TABLE 11
Douglas fir tissue growth (fold, mean ± SD) during pre-maturation
treatments (pt) and embryo maturation.
					Yield of
Carbon source					embryos (started
in maintenance	Growth - Pt	Growth - Pt	Total	Mature	with one gram of
& pre-treatment	week 1	week 2	growth	embryos/pp	tissue at P1)
A* & A	4.9 ± 0.28	2.4 ± 0.28	11.76	75 ± 23.3	8017
A & m**	7.1 ± 0.85	2.3 ± 0.14	16.33	105 ± 27.81	15586
B & B	4.75 ± 1.06	1.9 ± 0.28	9.025	61.38 ± 19.64	5035
B & m	7.7 ± 0.74	2.4 ± 0.6	18.48	82.33 ± 12.5	13830
C & C	6.85 ± 0.64	2 ± 0.8	13.7	53 ± 25.23	6600
C & m	8.5 ± 0.62	2.2 ± 0.4	18.7	96.75 ± 20.65	16446
D & D	9.9 ± 0.57	2.3 ± 0.21	22.77	62 ± 15.4	12834
D & m	9.4 ± 0.6	2.4 ± 0	22.56	105.75 ± 20.36	21686
Suc & m	6.6 ± 0.2	4.92 ± 0.28	32.472	50.5 ± 19.27	14906
*A: 0.5% galactose, B: 0.5% galactose + 0.01% glucose, C: 0.5% galactose + 0.025% glucose, D: 0.5% galactose + 0.05% glucose
**m - 1% maltose, suc - 1% sucrose,

[0096] Galactose and a small amount of glucose supplement in liquid maintenance culture combined with maltose in pre-treatment showed the highest embryo yield either in the total number or on the yield per gram of tissue.

Claims

1. A method for reproducing conifers by somatic embryogenesis wherein a galactose-containing compound is used as a carbon source for an embryogenic culture during at least one of the steps of induction, proliferation, and prematuration.

2. The method of claim 1 wherein the galactose-containing compound is a sugar with galactose comprising one or more of the sub-units.

3. The method of claim 2 wherein the galactose-containing sugar is selected from the group consisting of monosaccharides, disaccharides, oligosaccharides, and polysaccharides.

4. The method of claim 3 wherein the galactose-containing sugar is lactose.

5. The method of claim 1 wherein the galactose-containing compound is less than about 6% of the nutrient medium.

6. The method of claim 1 wherein the nutrient medium is gelled or liquid.

7. The method of claim 1 wherein the conifers are selected from the family Pinaceae.

8. The method of claim 7 wherein the conifers are selected from the genera Pinus, Picea and Pseudotsuga.

9. The method of claim 8 wherein the conifer is Pinus taeda or a hybrid thereof.

10. The method of claim 8 wherein the conifer is Pseudotsuga menziesii.

11. The method of claim 8 wherein the conifer is Pinus radiata.

12. The method of claim 1 in which the embryogenic culture is cultured in at least one prematuration medium comprising a galactose-containing compound and then transferred to a maturation medium to produce cotyledonary stage embryos suitable for germination.

13. The method of claim 12 wherein the prematuration medium contains less auxin and less cytokinin than the nutrient medium used during proliferation.

14. The method of claim 12 wherein the prematuration medium further comprises abscisic acid.

15. The method of claim 3 wherein the galactose-containing sugar is supplemented with additional sugars.

16. The method of claim 15, wherein the additional sugars are readily metabolized.

17. The method of claim 16, wherein the additional sugars are selected from the group consisting of sucrose, glucose, and fructose.

18. The method of claim 1 wherein the galactose-containing compound is more than about 1% of the nutrient medium.

19. The method of claim 1 wherein the embryogenic culture contains early stage embryos.

20. The method of claim 1 wherein the galactose-containing compound is less than about 2% of the nutrient medium.

21. The method of claim 1 wherein the galactose-containing compound is between about 1% and about 6% of the nutrient medium.

22. The method of claim 1 wherein the nutrient medium further comprises an auxin and a cytokinin.

23. A method for reproduction by somatic embryogenesis of conifers selected from the group consisting of Pinus taeda and hybrids, Pinus radiata, and Pseudotsuga menziesii which comprises: using a galactose-containing compound during at least one of the steps of induction, proliferation, and prematuration.

24. The method of claim 23 wherein the galactose-containing compound is a sugar with galactose comprising one or more of the sub-units.

25. The method of claim 24 wherein the galactose-containing sugar is selected from the group consisting of monosaccharides, disaccharides, oligosaccharides, and polysaccharides.

26. The method of claim 25 wherein the galactose-containing sugar is lactose.

27. The method of claim 23 wherein the galactose-containing compound is less than about 6% of the nutrient medium.

28. The method of claim 23 wherein the nutrient medium is gelled or liquid.

29. The method of claim 23 wherein the conifer is Pinus taeda or a hybrid thereof.

30. The method of claim 23 wherein the conifer is Pseudotsuga menziesii.

31. The method of claim 23 wherein the conifer is Pinus radiata.

32. The method of claim 23 in which the embryogenic culture is cultured in at least one prematuration medium comprising a galactose-containing compound and then transferred to a maturation medium to produce cotyledonary stage embryos suitable for germination.

33. The method of claim 32 wherein the prematuration medium contains less auxin and less cytokinin than the nutrient medium used during proliferation.

34. The method of claim 32 wherein the prematuration medium further comprises abscisic acid.

35. The method of claim 24 wherein the galactose-containing sugar is supplemented with additional sugars.

36. The method of claim 35, wherein the additional sugars are readily metabolized.

37. The method of claim 36, wherein the additional sugars are selected from the group consisting of sucrose, glucose, and fructose.

38. The method of claim 23 wherein the galactose-containing compound is more than about 1% of the nutrient medium.

39. The method of claim 23 wherein the embryogenic culture contains early stage embryos.

40. The method of claim 23 wherein the nutrient medium further comprises an auxin and a cytokinin.

41. The method of claim 23 wherein the galactose-containing compound is less than about 2% of the nutrient medium.

42. The method of claim 23 wherein the galactose-containing compound is between about 1% and about 6% of the nutrient medium.

43. A method for reproducing conifers by somatic embryogenesis which comprises: growing conifer cells on a nutrient medium comprising a galactose-containing compound, an auxin, and a cytokinin to produce an embryogenic culture.