CA2298882A1 - Transgenic plants using the tdc gene for crop improvement - Google Patents

Abstract

The present invention provides nucleic acid constructs and methods of producing transgenic plants having improved resistance to fungi, bacteria, and/or nematodes, wherein the enhanced resistance arises from enhanced expression of a tryptophan decarboxylase (TDC) gene construct.

Description

TRANSGENIC PLANTS USING THE TDC GENE FOR CROP IMPROVEMENT
This application claims the benefit of U.S. Provision Application No.
60/054,316, filed July 31, 1997.
BACKGROUND OF THE INVENTION
Field of the Invention The present invention relates to transgenic plants having surprisingly improved fungal, bacterial, and/or nematode disease resistance, wherein the enhanced resistance arises from enhanced expression of a tryptophan decarboxylase (TDC) gene.
Summary of the Related Art Crop losses incurred by diseases and pests have a major negative economic impact upon all sectors of agriculture today. Despite attempts to control these losses through various crop husbandry techniques (e.g., crop rotation), breeding of resistant cultivars and application of agrochemicals, losses remain unacceptably high. As of 1987, approximately 37% of all crops produced worldwide are lost to pests such as insects (13%), diseases (12%), and weeds and grasses (12%). Dependence 1 S on agrochemicals is not only expensive, but it is also detrimental to the environment and generally regarded as unhealthy for living creatures. Over the last decade, agricultural biotechnology has provided some solutions for disease and insect management. The most intensive global efforts in agricultural biotechnology today are directed toward the design and implementation of effective transgene-mediated disease and pest resistance strategies.
The tremendous losses incurred by pathogenic fungi on crops worldwide has fueled the interest to develop rational and effective anti-fungal strategies in transgenic plants (for review, see Cornelissen and Melchers (1993) Plant Physiol. 101, 709-712). One of the earliest concepts, and to date, one of the most successful anti-fungal strategies has been to utilize fungal cell wall-degrading enzymes to attack an invading pathogen. Proteins that possess chitinase or [3-glucanase activity have been purified and characterized from numerous plant, fungal, and bacterial sources (Kauffinan et al. (1987) EMBO J. 6, 3209-3212; Legrand et al. (1987) Proc.
Natl. Acad. Sci. USA
84, 6750-6754). The genes that encode for some of these hydrolytic enzymes have been cloned, sequenced, and subsequently overexpressed in transgenic plants. The single, unifying conclusion that has emerged from these numerous studies is that while modest levels of fungal protection can be afforded by overexpression of these enzymes alone, significantly enhanced protection can often be achieved by co-expression of chitinase and ~i-glucanase together. To date, encouraging results have been reported in transgenic tomato against Fusarium solani (Jongedijk et al. (1995) Euphytica 85, 1-8) and in transgenic tobacco against Rhizoctonia solani (Jach et al.
(1995) Plant J. 8, 97-109).
Extensive field testing remains necessary, however, to determine whether these resistance levels are sufficient to confer commercially-significant phenotypes.
An alternative anti-fungal technology that has slowly been gaining attention involves overexpression of small peptides with antimicrobial activity in transgenic plants. Some of these peptides, isolated from non-plant sources such as frog (magainins) and moths (cecropins), form amphipathic a-helices upon association with microbial plasma membranes, insert into the membranes and interact with one another to initiate pore formation, causing cell leakage and eventual cell death (for review, see Boman, H.G. (1991) Cell 6S, 205-207). The expression of cecropins in transgenic tobacco, however, has not led to any significant levels of disease resistance (Florack et al. (1995) Transgenic Res. 4, 132-141). Other antimicrobial peptides, termed defensins (for review, see Broekaert et al. (1995) Plant Physiol. 108, 1353-1358) have been isolated from radish (Terras et al. (1992) ,l. Biol. Chem. 267, 15301-15309) and barley (Mendenez et al. (1990) Eur. J. Biochem.194, 533-539) and feature a more complex three-dimensional structure that includes cysteine-stabilized triple anti-parallel (3 sheets together with an a-helix.
Terras et al. (1995) Plant Cell 7, 573-588, reported very good levels of protection against infection by Alternaria in transgenic tobacco that overexpressed the radish AFP2 protein. A threshold level of AFP2 peptide (which was not easily obtained) in the transgenic plants was required to detect any significant level of disease resistance, however.
Other anti-fungal proteins include ribosome-inactivating proteins (RIP's), which act by inhibiting protein synthesis in target cells by a modification of the 28S
rRNA. RIP's do not affect the ribosomes of the plants in which they are produced, but can be effective against fungal ribosomes. A barley RIP 'under control of a wound-inducible promoter was reported to show increased resistance to Rhizoctonia solani (Logemann et al. (1992) Biotech 10, 305-308). Finally, Alexander et al. (1993) Proc.Natl. Acad. USA 90, 7327-7331, demonstrated that constitutive high-level expression of tobacco PR-la (pathogenesis-related) protein (of unknown activity) in transgenic tobacco resulted in increased resistance to Phytophthora parasitica and Peronospora tabacina.

Manipulation of the plant's own defense system -- systemic acquired resistance (SAR) -- has drawn tremendous attention in recent years. Activation of this complex network of defense-related genes gives rise to protection against a wide range of pathogens, including bacteria, fungi, and viruses. Attempts to utilize the entire complex of defense-related genes in the SAR repertoire include the two-component system, which has been described by de Wit, P.J.G.M.
(1992) Annul Rev.
Phytopathol. 30, 391-418, the application of chemical inducers of SAR like 2,6-dichloroisonicotinic acid (Kessmann et al. (1994) Annul Rev. Phytopathol. 32, 439-459), and the constitutive expression of proposed intermediates (e.g., active oxygen species like hydrogen peroxide) in the signal transduction pathway for SAR that effectively activates the SAR response (Wu et al. (1995) Plant Cell 7, 1357-1368). These approaches hold tremendous potential for conferring broad spectrum disease resistance, but with the exception of chemical inducers of SAR; are in the development phase and remain largely unproven.
Plants produce a rich diversity of secondary metabolites, which do not seem necessary for their basic metabolism, but appear to contribute to their environmental fitness and adaptability.
These secondary compounds are responsible for aroma (monoterpene indole alkaloids) and color {anthocyanins and carotenoids) and are commercial sources of numerous important pharmaceutical (alkaloids) and industrial chemicals. Their importance has encouraged intensive investigation of the regulation and control of the biosynthetic pathways, and more recently, how these pathways can be manipulated through "metabolic engineering," first coined by Bailey, J.E.
(1991) Science 251, 1668-1675, as "the improvement of cellular activities by manipulation of enzymatic, transport, and regulatory functions of the cell with the use of recombinant DNA technology."
The enzymology associated with the biosynthesis of alkaloids has been the subject of much study. The tropical plant, Catharanthus roseus (periwinkle), forms a wide range of terpenoid indole alkaloids (TIA's), some of which have important medicinal applications. The leaf derived alkaloids, vinblastine and vincristine, and the root-derived alkaloids, ajmalicine and serpentine, are valuable drugs for treatment of cardiac/circulatory diseases and tumors, respectively.
It is generally accepted that protoalkaloid production is the first committed step in the TIA pathway of Catharanthus.
Consequently, tryptophan decarboxylase (TDC), the enzyme that catalyzes this bridge reaction between primary (amino acid) and secondary (alkaloid) metabolic pathways, has drawn much attention. TDC catalyzes the decarboxylation and conversion of L-tryptophan into tryptamine.

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Tryptamine and secologanin, another secondary compound, are then condensed to form strictosidine, the precursor for all TIA's in Catharanthus.
For microbes and plants alike, the rate-limiting enzyme for tryptophan biosynthesis has been identified to be anthranilate synthase (AS), a heterodimeric enzyme composed of an a and (3 subunit, which catalyzes the conversion of chorismate to anthranilate. Tryptophan has been demonstrated to be a negative feedback regulator of the microbial enzyme. In microbes, when tryptophan levels are sufficiently high, tryptophan binds to an allosteric site on the a subunit, thereby inactivating the enzyme. Although similar observations have not been made for the plant enzyme, other studies suggest that AS is the rate-limiting enzyme for tryptophan biosynthesis. Plant mutants characterized by elevated tryptophan levels (~3-fold) have been found to contain amino acid changes in their anthranilate synthase coding regions.
More recently, biochemical studies with the two purified anthranilate synthase a subunits (ASaI and ASa2) from Ruta graveolens, and molecular analysis of the genes that encode these proteins have provided some new insight into the complexities of tryptophan biosynthesis. R.
graveolens, like C. roseus, is a medicinal plant which produces a large number of tryptophan-derived monoterpenoid indole alkaloids. Bohlmann et al (1996) Plant Physiol. 111, 507-514, separately purified the ASaI and ASa2 subunits from E. coli strains designed to overexpress the two proteins.
They noted that while the ASa2 enzyme was completely feedback inhibited by ~10 mM tryptophan, the activity of the ASa 1 enzyme was essentially unaffected by tryptophan levels approaching I00 mM. They further demonstrated that ASaI (but not ASa2) transcript levels and enzyme activity were dramatically induced in Ruta cultures that had been exposed to fungal elicitors. They concluded that ASaI and ASa2 participate equally in the housekeeping role of maintaining appropriate tryptophan levels. However, upon exposure to fungal elicitors that induce the TIA
pathway, the tryptophan feedback-resistant ASaI becomes responsible for supplying the copious amounts of tryptophan that will be required for conversion into tryptamine and ultimately, indole alkaloids. Thus, the tryptophan-resistant ASal becomes a specific enzyme for secondary metabolism.
In 1988, De Luca et al. (1988) Plant Physiol. 86, 447-450, noted that TDC
enzymatic activity was highly regulated in germinating seedlings, supporting similar observations made in cell suspension cultures. Later, De Luca et al. (1989) Proc. Natl. Acad. USA 86, 2582-2586, described the cloning and characterization of a TDC cDNA clone from Catharanthus seedlings. The availability of the TDC gene as a nucleic acid probe has helped to elaborate the developmental and environmental cues that affect TDC expression during plant growth and in cell suspensions. For example, Pasquali et al. (1992) Plant Mol. Biol. 18, 1121-1131, reported that TDC steady-state transcript levels were most abundant in roots, moderately abundant in leaves and barely detectable in the flowers and stems of 3-month-old Catharanthus plants. They further demonstrated that TDC
expression in cell suspension cultures was down-regulated by addition of auxin, but strongly induced by treatment with fungal elicitors. This report, along with others (Roewer et al. ( 1992) Plant Cell Rep. 11, 86-89; Berlin et al. (1993) Transgenic Res. 2, 336-3444; Goddijn et al. (1992) Plant Mol.
Biol. 18, 1113-1120; and Goddijn et al. (1995) Transgenic Res. 4, 315-323), helped establish the importance of TDC as the first committed step in TIA biosynthesis.
Given its pivotal role in TIA biosynthesis in plants, efforts were initiated to overexpress TDC
in transgenic plants for the purpose of increasing tryptamine levels. Songstad et al. (1990) Plant Physiol. 94, 1410-1413, placed the TDC cDNA under control of the strong, constitutive cauliflower mosaic virus (CaMV) 35S RNA promoter and introduced this transgene into tobacco. Transgenic tobacco lines were recovered which accumulated up to 250 times their normal levels of tryptamine {in excess of 1 mg/gram fresh weight [gfw]) with no apparent deleterious effect on plant growth and development.
In contrast to tobacco, transgenic canola, which overexpressed the same TDC
transgene, exhibited a very striking phenotype. Chavadej et al. (1994) Proc. Natl. Acad.
USA 9I, 2166-2170, reported that their best transgenic canola line never expressed >9% of the TDC-specific activity and only accumulated 2% of the tryptamine found in the most active transgenic tobacco line. Despite the relatively low TDC activity and tryptamine levels, the pool of available soluble tryptophan for tryptophan-derived indole glucosinolate production was so depleted that glucosinolate levels were reduced in all tissues, especially in mature seeds where glucosinolates accumulated to only 3% of that which were found in non-transformed seeds. Thus, TDC effectively out-competed the indole glucosinolate biosynthetic enzymes for available tryptophan by diverting it to the production of tryptamine.
In TDC-expressing potato, tryptamine accumulation was found to be very tissue specific (Yao et al. (1995) Plant Cell 7, 1787- 1799). While tryptamine accumulated to high levels in the leaves of transgenic potato plants, tryptamine was undetectable in the tubers and was only detected WO 99/06581 PCTlUS98/16033 after wounding or fungal elicitor treatment. The re-direction of tryptophan into tryptamine resulted in a dramatic decrease in the levels of soluble tryptophan, phenylalanine, and phenylalanine derived phenolic compounds, including chiorogenic acid, the major soluble phenolic ester in potato tubers.
This 2-3-fold reduction in phenoiic esters led to reduced synthesis of polyphenolic compounds like lignin because of a limited supply of phenolic monomers. This in turn led to altered cell wall structures in the tubers, which proved to increase susceptibility of the tubers to infection by Phytophthora infestans.
Thomas et al. (1995) Plant Physiol. 109, 717-720, extended the observations made by Songstad and co-workers in TDC-expressing tobacco when they reported that tryptamine-accumulating tobacco plants adversely affected whitefly development and reproduction. Bemisia tabaci, the sweet potato whitefly, was used to test the effects of tryptamine on insect feeding and development. Whitefly emergence tests revealed that pupae emergence (to adulthood) on TDC-expressing plants was typically reduced 3 to 7-fold relative to control plants. They speculated that tryptamine may exert its anti-whitefly effects) during either larval and pupal development and/or adult selection of a leaf for feeding and oviposition.
Pasquali et al., supra, and Roewer et al. (1992) Plant Cell Rep. 11, 86-89, noted that enzymes in the Catharanthus TIA biosynthetic pathway, including TDC, were coordinately induced upon exposure to fungal elicitors. A short report by Miyagawa et al ( 1994) Biosci. Biotech.
Biochem. 58, 1723-1724, detected the presence of fluorescent compounds deposited at the site of infection by powdery mildew in barley. One of these compounds, tryptamine, was suggested to be acting as an anti-fungal agent.
However, this collection of observations answered neither the question of whether tryptamine, normally only a precursor in the TIA biosynthetic pathway, could itself contain broad-spectrum anti-fungal activity, nor what levels could be attained in planta to be sufficient to confer enhanced resistance to infection by fungal pathogens. To date, the answers to these questions have remained elusive.
SUMMARY OF THE INVENTION
We have surprisingly discovered that tryptamine can effectively inhibit in vitro and in vivo growth of both phytopathogenic bacteria and fungi. Furthermore, tryptamine is shown herein to inhibit phytopathogenic nematodes. As a result, the present invention affords constitutive expression in plants of the gene encoding tryptophan decarboxylase (TDC), the enzyme that converts tryptophan to tryptamine, to confer enhanced resistance to infection to a broad spectrum of phytopathogenic fungi, bacteria, and nematodes. Similarly the AS gene can boost this pathway, making more tyrptamine.
The present invention further provides a gene construct containing a promoter and a DNA
sequence encoding a protein with tryptophan decarboxylase activity and/or AS
activity.
The invention also provides transgenic plants and multicellular plant tissue having enhanced fungal and/or bacterial disease resistance andlor nematode resistance, wherein the enhanced resistance is a result of expression of a TDC andlor AS transgene.
The foregoing merely summarizes certain aspects of the invention and are not intended, nor should they be construed, as limiting the invention in any manner. All patents, patent applications, and publications are hereby incorporated by reference in their entirety.
BRIEF DESCRIPTION OF THE DRAWINGS
Figure 1. Chimeric (A) E35S::TDC::nos and (B) UBQ3::TDC::nos constructs. A DNA
fragment containing the duplicated enhancer region, promoter, transcription initiation site and 5' untranslated region (UTR) from the CaMV 35S RNA region was fused to the 5' UTR
of the TDC
cDNA from plasmid pTDCS. A second DNA fragment containing the promoter, transcription initiation site and S' UTR from the Arabidopsis thaliana UBQ3 gene was fused to the 5'UTR of the TDC cDNA from plasmid pTDCS. A DNA fragment containing the polyA addition signal from the nopaline synthase gene (nos) is responsible for transcript maturation at the 3' end in both transgenes.
Figure 2. Flowers from tryptamine-accumulating petunias show enhanced resistance to infection by Botrytis cinerea. Newly opened flowers from greenhouse petunias (3 flowers/line) were detached, placed in water and then inoculated with a freshly prepared Botrytis spore suspension (in 0.005% Tween 20 to discourage spore clumping) containing 0.25 x 103 or 1 x 103 spores/ml. After the flowers were sprayed to the point of runoff with an atomizer, the inoculated flowers were placed in a humidity chamber and incubated at room temperature for 4 days. Disease progression was monitored daily (up to 97 h) using a disease rating scale ranging from 0 to 5 where 0 = uninfected;
1= 1-15 small, necrotic lesions; 2 =15-30 larger, necrotic lesions; 3 =
lesions begin to coalesce; 4 = lesions almost fully coalesced; and 5 collapsed flower.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
The present inventors have surprisingly discovered (as is demonstrated in the Examples, infra) that enhanced TDC expression can confer on plants resistance to a broad spectrum of both bacterial, fungal, and nematode phytopathogens. In accordance with this discovery, the present invention comprises methods and nucleic acid constructs for enhancing resistance in plants to phytopathogenic bacteria, fungi, and nematodes by transforming plant cells with the gene coding for tryptophan decarboxylase (TDC). Although the invention is not limited by any theory of action, we believe that enhanced TDC expression results in enhanced phytopathogenic resistance through increased levels of tryptamine and/or alkaloids produced therefrom. The invention further comprises transgenic plant tissue thereby produced.
In a frst aspect, the invention provides nucleic acid constructs comprising the TDC gene.
Any plant TDC gene can be used. Upon transformation of plant cells, these constructs are useful for conferring enhanced fungal, bacterial, and/or nematode resistance to a wide variety of plants and against a broad spectrum of phytopathogenic fungi, bacteria, and nematodes.
In another embodiment of this aspect, the invention provides nucleic acid constructs comprising an AS {preferably ASal) and a TDC transgene. Any plant AS gene can be used.
Conferral of resistance to bacterial, fungal and nematode phytopathogens by overexpression of tryptamine (and/or alkaloids produced therefrom) can be enhanced by ensuring a constant, sufficient supply of its precursor, tryptophan. Published observations on the anthranilate synthase a subunits (ASaI and ASa2) indicate that constitutive expression of the Ruta ASal subunit in heterologous plants can circumvent the normal regulatory mechanisms in transformed cells and lead to elevated tryptophan levels. We have found that co-transformation with ASal and ASa2 led to enhanced levels of tryptophan and an increased amount of tryptamine. Co-introduction of constitutively-expressed AS {preferably ASaI) and TDC transgenes should provide increased tryptophan levels for immediate conversion into tryptamine. A single plasmid harboring both constitutively-expressed transgenes can be viewed as portable expression cassette for increasing tryptamine levels in virtually any plant. Alternatively, an AS transgene could be used by itself.
In plants, tryptophan biosynthesis is believed to reside exclusively in the plastid; no cytosolic localization is implicated. This conclusion has been solidified by the observation that all the genes in the tryptophan biosynthesis pathway that have been cloned to date encode proteins that contain a recognizable transit peptide at their N-terminus to direct the proteins to the organelle. No gene has thus far been cloned which lacks this feature, thus bolstering the argument that tryptophan biosynthesis is exclusively plastid-localized. Therefore, expression of the TDC gene in the plastid will result in better substrate availability (as well as higher TDC activity as is generally associated with plastid gene expression), which should lead to higher levels of tryptamine accumulation.
Accordingly, the nucleic acid constructs according to this aspect of the invention will further comprise targeting regions at the 3' and 5' ends, which regions target the constructs according to the invention to the plant nucleus or plastid.
In this aspect of the invention, any plant promoter can be operatively linked to the TDC
and/or ASa 1 genes. In a preferred embodiment, the constructs according to this aspect of the invention will preferably be operatively linked to the UBQ3, UBQ10, CaMV 35S
RNA, or the enhanced version of the CaMV 35S RNA (E35S) promoter. In another preferred embodiment, the constructs further comprise a pUC-based vector containing the 3' flanking region of the nopaline synthase gene (hos) from Agrobacterium tumefaciens. The promoters of the UBQ3 and UBQIO
genes, members of the polyubiquitin gene family in Arabidopsis thaliana, have been described by Norns et al., Plant Mol. Biol. 21:8995-8906 (1993).
Where more elegant control of tryptamine production within the plant is desirable, one or both of the transgenes can be fused and thereby operationally linked to tissue-specific promoters.
For example, in petunia, one or both of the transgenes can be fused to petal-specific promoters to confer resistance to infection by Botrytis cinerea.
Constructs according to this aspect of the invention can also comprise a selectable marker gene, expression of which by the transformed cell enables one to identify and isolate the transformed cell or cells from amongst other cells. Any plant selectable marker gene known in the art can be used in the present invention. In a preferred embodiment, the selectable marker gene is the nptII
(neomycin phosphotransferase II) or hph (hygromycin phosphotransferase) gene.
Cells expressing these preferred selectable marker genes are resistant to kanamycin (for nuclear nptIl transformation) and hygromycin (for nuclear transformation) or glyphosate (for plastid hph transformation) and can be selected for by exposing cells subject to transformation (by, e.g., biolistic delivery) to media containing the minimum level of kanamycin, hygromycin, or glyphosate that kill untransformed cells. Of course, the agent to which transformed cells are subject for selection purposes should correspond to the selectable marker gene employed in the transformation.

The sequence and structure of the constituent elements of the nucleic acid constructs according to this aspect of the invention are publicly available, and constructs according to this aspect of the invention can be made by routine, art recognized techniques.
Exemplary methods are described, e.g., in Example l, infra.
In a second aspect, the invention provides methods for enhancing the resistance of plants to phytopathogenic fungi, bacteria, and nematodes. In a preferred embodiment, the method comprises transforming plant tissue with a construct according to the first aspect of the invention. In another embodiment, when co-transformation with both the TDC and ASa 1 genes is desired, the two genes can be on separate expression vectors and co-transformed simultaneously or sequentially.
Transformation can be accomplished in either the nucleus or the plastid, as determined by the targeting regions of the nucleic acid construct. Details of plastid transformation can be found, e.g., in co-pending international application PCT/US98/**** (WO 99/*****), entitled, "Improved Plastid Transformation Of Higher Plants And Production Of Transgenic Plants With Herbicide Resistance," filed July 23, 1998, and U.S. Application Serial No. 08/899,061, filed July 23, 1997.
Any of the numerous methods for transformation can be used, e.g., Agrobacterium (for nuclear transformation), PEG treatment, electroporation, and biolistic delivery. Preferably, biolistic delivery is employed.
In a third aspect, the invention provides transgenic plant tissue that expresses the TDC gene and/or the ASal gene. As used herein, "plant tissue" includes a plant cell or cells, multicellular plant tissue, and whole plants. Transgenic plants according to this aspect of the invention can be made according to the second aspect of the invention using nucleic acid constructs according to the first aspect of the invention. When cells (e.g., cell suspensions or calli) or plant tissue samples (e.g., leaf or other plant parts) are transformed and selected, whole plants can be obtained using standard, art recognized methods of culturing and growth.
All plants are suitable for transformation with the TDC gene according to the invention.
Agricultural and horticultural plants are of considerable importance, but many are susceptible to microbial infection, requiring extensive application of chemicals for disease control. A reduction in chemical applications because of increased plant resistance is always desirable for worker safety and environmental reasons.
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The present invention will now be illustrated by examples that are provided solely for purposes of illustration and are not intended, nor should they be construed to be limiting in any way.
Those skilled in the art will appreciate that variations and modifications of the following can be made without exceeding the scope or spirit of the invention.
EXAMPLES
Example 1 Construction of TDC- and/or AS-containing constructs To increase tryptamine production throughout the entire plant, the TDC gene was preferably placed under the control of two very active, constitutively expressed promoters. The CaMV 35S
RNA promoter from the CaMV genome is a very well-characterized promoter for expression of transgenes in both dicotyledonous and monocotyledonous plants. The enhanced version (Kay et al., (1987) Science 236, 1299-1302,) of the CaMV 35S RNA promoter (E35S) was preferably used. A
second promoter, UBQ3, is derived from Arabidopsis thaliana and normally directs expression of a member of the polyubiquitin gene family. The present inventors have determined that this promoter directs high levels of reporter gene expression throughout the entire plant in transgenic petunias.
Both promoters were moved into a pUC-based vector already containing the 3' flanking region of the nopaline synthase gene (nos) from Agrobacterium tumefaciens.
This DNA sequence element possesses the recognition site for polyA addition to the transcript.
Also already resident on this plasmid was a multi-cloning site region containing a number of unique restriction enzyme sites for insertion of additional DNA sequence elements. The CaMV 35S and UBQ3 promoters were moved into this plasmid (while maintaining a number of unique restriction sites between the promoter and the nos 3' sequence element) to create plasmids pSANl4 and pSAN151, respectively.
The TDC gene was originally cloned from Catharanthus roseus, or vinca (De Luca et al., ( 1989), supra. A 1.75 kbp fragment containing the full-length cDNA was cloned from a cDNA
library by immunodetection methods. The TDC cDNA contains an open reading frame coding for a protein of 500 amino acids, corresponding to a molecular mass of ~56 kDa.
The cDNA from plasmid pTDCS (De Luca et al., 1989, supra) was removed by digestion with Pst I and Xho 1, the single-strand overhangs at each end removed by treatment with T4 DNA
polymerase, and cloned into the Sma I sites of plasmids pSANl4 and pSANI S 1 to create plasmids pSAN213 and pSAN247, *rB

respectively (Figure 1). This effectively fused the 5' UTR region of the TDC
gene to the S' UTR
regions of the transcripts of the gene promoters. Since these constructs were to be introduced via particle bombardment, there was no direct requirement to transfer them to a T-DNA-based plant vector like pBINl9. Also, since the TDC-containing plasrnids were to be co-bombarded with a second plasmid containing a plant selectable marker gene like nptll (neomycin phosphotransferase I 1 ) or hph (hygromycin phosphotransferase), no marker gene was added to the TDC-containing plasmid.
Several gene constructs containing the ASal gene alone or in combination with the TDC
gene were constructed. Construct pSAN368 contains the ASaI gene driven by the UBQ10 promoter and, constructs pSAN369 and pSAN310 contained in addition to the ASa1 gene the TDC gene driven by the UBQ3 pormoter.
Example 2 Transformation of Petunia with TDC gene The TDC transgenes were introduced into petunia by particle bombardment.
Briefly, two plasmids, one containing the TDC transgene and the second containing an nptll transgene, were co-precipitated in equivalent amounts onto ~ 1 pm M-10 tungsten particles. The DNA coated particles were then bombarded into petunia leaf explants that had been placed on a nutrient agar media. After two successive bombardments, the leaf explants were allowed to recover on the nutrient media for four to five days. After recovery, the leaf explants were cut into small pieces and placed onto selective agar media containing kanamycin. Kanamycin-resistant transformed shoots were regenerated and shoots were transferred to fresh media and rooted in the absence of kanamycin.
Small leaf samples were excised from in vitro-maintained plantlets and cell-free extracts prepared for HPLC analysis of tryptophan and tryptamine content. In untransformed petunia plantlets that were maintained under in vitro conditions, tryptamine levels were approximately 4 ~,g per gram fresh weight (pg/gfw) of leaf tissue. In TDC-expressing petunias, transgenic lines accumulated in excess of 300 mg/gfw, approaching 100-fold over endogenous levels.
Example 3 Inhibition of fungal pathogens by arvptamine isolates of several phytopathogenic fungi were grown on nutrient agar media under conditions that encouraged sporulation. Conidiospore suspensions were prepared from Fusarium WO 99/06581 PCT/US98/Ib033 solani, Fusarium graminearum, Thielaviopsis basicola, and Botrytis cinerea.
For Phytophthora parasitica zoospores were prepared from liquid culture. For Rhizoctonia solani R2, a preparation of mycelial fragments (avg. length of 4 cells) substituted for the spores. In a 96-well microtiter plate, 1 x 103 spores (except where noted), either germinated or non-germinated, in 50 lcl 0.005% Tween 20 were added to 50 p.l aliquots of serially-diluted tryptamine prepared in potato dextrose broth.
Microtiter plates were covered and incubated at room temperature with gentle shaking for 24-48 h.
After 48 h, the lowest concentration of tryptamine which inhibited all fungal growth was designated the minimum inhibitory concentration (MIC ) value. In some cases, spores were pre-incubated to allow germination to occur before exposure to tryptamine. The results are shown in Table 1.
Table 1 Tryptamine minimum inhibitory concentration (MIC) values for fungal phytopathogens Phytopathogen MIC9 (mg/ml) Phytophthora parasitica (vinca) non-germinated (1 x 102) 0.25 germinated (1.5 x 102) 0.25-0.50 Phytophthora parasitica (petunia) non-germinated NAb germinated (2 x 10z) 0.25-0.50 Fusarium solani non-germinated > 1.00 germinated 0.25-0.50 Fusarium graminearum non-germinated >0.50 germinated NA

Thielaviopsis basicola non-germinated 0.25 germinated 0.25 Botrytis cinerea non-germinated 0.50 germinated NA

Phytopathogen MICa (mg/mI) Rhizoctonia solani R2 mycelial fragments (1 x >I.00 102) a MIC: minimum tryptanune concentration required to inhibit all fungal growth after 48 hours.
b not assayed As can be observed in Table 1, non-germinated spores from the vinca isolate of Phytophthora parasitica were inhibited by 0.25 mglml tryptamine. Germinated spores from both Phytophthora isolates were sensitive to 0.25-0.50 mg/ml tryptamine. Similar results were observed for Thielaviopsis basicola (germinated and non-germinated spores). Regarding the Fusarium species, non-germinated spores from F. graminearum were somewhat sensitive to tryptamine while those from F. solani were considered insensitive. However, germinated spores from F. solani were sensitive. Also, growth from nongerminated spores of Botrytis cinerea were inhibited by 0.50 I O mg/ml tryptamine. Rhizoctonia solani mycelial fragments were unaffected by 1 mg/ml tryptamine.
In general, nearly all the fungi exhibited some level of sensitivity to treatment with tryptamine.
Example 4 Fungicidal and Fungistatic activity of tryptamine To determine whether tryptamine's mode of action was fungicidal or fungistatic, Botrytis cinerea spores were exposed to toxic levels of tryptamine for various times, then diluted to sub-lethal concentrations to permit growth. If the spores now germinated and grew, then tryptamine's effect was considered to be fungistatic. If no growth was observed, the effect was concluded to be fungicidal.
In a 96-well microliter plate, 1 x 10~ Botrytis spores (in 50 ~.1 0.005% Tween 20) were treated with serial dilutions of tryptamine. The experiment was set up with three treatments. One treatment was incubated at room temperature and the wells were scored for growth after 48 h and 96 h. The second treatment was incubated at room temperature for 22 h, the wells scored for growth, then diluted 4-fold with 0.5X potato dextrose broth before continuing incubation for another 48 h and a final reading for growth. The third and last treatment was incubated at room temperature for 46 h, the wells scored for growth, then diluted 4-fold with 0.5X potato dextrose broth before continuing incubation for another 48 h and a final reading for growth.
As can be observed in Table 2, Botrytis spores maintained in 0.50 mg/mI
tryptamine throughout the entire experiment (growth noted at 46 and 94 h) showed essentially no growth while all growth was inhibited at 1 mg/ml. Botrytis spores exposed to I mg/ml tryptamine for 22 h showed no growth, but when diluted to 0.25 mg/ml, germinated and grew normally over the next 48 h.
Similarly, spores exposed to 2 mg/ml for 22 h showed no growth, but when diluted to 0.5 mg/ml, germinated and grew, albeit relatively poorly. These results indicated that exposure to tryptamine concentrations as high as 2 mg/ml for 22 h was not toxic to Botrytis. Spores exposed to 0.5 mg/ml tryptamine for 46 h showed little growth, but when diluted to 0.12 mg/ml, grew normally. However, spores exposed to I mg/ml and 2 mg/ml tryptamine showed no growth after 46 h, and after 4-fold dilution, either grew very poorly (1 mg/ml reduced to 0.25 mg/ml} or not at all (2 mg/ml reduced to 0.5 mg/ml) over the next two days. These results suggested that tryptamine was indeed killing the Botrytis spores. Thus, it appears as though tryptamine can act as both a fungistatic and fungicidal compound (at least against Botrytis), being fungicidal only when the concentration and exposure period are high enough and long enough, respectively.
Table 2 T'ryptamine acts primarily as a fungistatic agent against Botrytis cinerea rather than a fungicidal one Initial Duration Reduced Duration Concentration (hours) Growth' Concentration (hours) Growth (pg/mi) 0.00 46 + NA 48 +

0.12 46 + NA 48 +

0.25 46 + NA 48 +

0.50 46 +I- NA 48 +/-1.00 46 - NA 48 -2.00 46 - NA 48 0.00 22 + 0.00 48 +

0.12 22 + p,03 4g +

0.25 22 + 0.06 48 +

0.50 22 +/- 0.12 48 +

1.00 22 - 0.25 48 +

2.00 22 - 0.50 48 +/-Initial Duration Reduced Duration Concentration (hours) Growth' Concentration (hours) Growth (pg/ml) 0.00 46 + 0.00 48 +

0.12 46 + 0.03 48 +

0.25 46 + 0.06 48 +

0.50 46 +/- 0.12 48 +

1.00 46 - 0.25 48 +/-2.00 I 46 I - ~ 0.50 I 48 j where + represents normal growth; +~- represents dramatically reduced growth;
and - represents no visible growth.
b not applicable Example 5 Inhibition of phytobacteria by tryptamine In a series of experiments similar to those described in Example 3, a collection of phytopathogenic bacteria were tested for their sensitivity to tryptamine.
Cultures of Agrobacterium tumefaciens, Erwinia amylovora, Erwinia carotovora, Pseudomonas cichorii, Pseudomonas syringae, and Xanthomonas campestris were grown to saturation density. After dilution and growth for 7-8 h, cells from log-phase cultures were treated with tryptamine. Log-phase cells were grown in LB broth at 28°C (ODs9o = 0.05 -0.15) and 50 ~tl of cells added to 50 ~.l of serial dilutions of tryptamine made in LB broth. Microtiter plates were incubated overnight at 28°C. The following day, the lowest concentration of tryptarnine which inhibited all bacterial growth was recorded as the minimum inhibitory concentration (MIC) value. Table 3 shows the results.
Table 3 Tryptamine minimum inhibitory concentration (MIC) values for bacterial phytopathogens Phytopathogen MICe (mg/ml) Agrobacterium tumefacien0.50-1.00 Erwinia amylovora >1.00 Erwznia carotovora >1.00 Pseudomonas cichorii0.25-0.50 Pseudomonas syringae0.50-1.00 Phytopathogen MICa (mg/mI) Xanthomonas campestris0.25-0.50 a MIC: minimum tryptamine concentration required to inhibit all bacterial growth after 24 hrs.
P. cichorii and X. campestris cells exhibited greatly reduced growth in the presence of 0.25 mg/ml tryptamine, and no growth at 0.5 mg/ml. A. tumefaciens and P. syringae cells showed dramatically reduced growth at 0.5 mg/ml and were completed inhibited by 1 mg/ml. In contrast, both Erwinia strains grew, albeit more slowly, in the presence of 1 mg/ml tryptamine and were considered to be relatively resistant. Overall, the results in Table 3 clearly support the notion that tryptamine possesses anti-bacterial properties. Taken together with the in vitro anti-fungal results presented in Examples 3 and 4, tryptamine exhibits impressive broad spectrum, of antimicrobial properties.
Example 6 Tryptamine tissue distribution and tryptophan dependence in transgenic petunia Three TDC-expressing transgene petunia lines were produced and carefully evaluated for their tryptamine levels and disease resistance characteristics. Petunia line PE-261 contains the TDC
gene under control of the E35S promoter while lines PE-310 and PE-312 contain the TDC gene under control of the UBQ3 promoter. Tryptamine levels were measured in the leaf tissue of both in vitro and greenhouse-grown plants. Leaf tissue from in vitro and greenhouse plants and petal tissue from greenhouse plants (all ~10-20 mgs fresh weight) were excised and homogenized in 0.2 ml cold 50 mM Na3P04, pH 7.4 buffer. Cell debris was removed by centrifugation at 10,000 x g for 5 min at 4 °C. The cleared supernatant was moved to a fresh tube and assayed for tryptamine content by HPLC using a fluorescence detector (excitation at 278 nm and emission at 360 nm).
Known amounts of authentic tryptamine (Sigma) were chromatographed to construct a standard curve for the determination of tryptamine levels in the experimental samples.
The results are presented in Table 4.
Table 4 Tryptamine accumulation in TDC-expressing petunias Tr'YPtamine, pg/gfw' Line ~

Leaf, Tissue Leaf, GreenhousePetal, Greenhouse culture V26 4 <1.4 6 Tryptamine, pg/gfw Li -ne Leaf, Tissue Leaf, GreenhousePetal, Greenhouse culture ~g tryptamma per gram fresh weight of tissue As can be seen, under tissue culture conditions, the tryptamine levels ranged from 141-310 pg/gfw.
However, under greenhouse conditions, the levels decreased approximately 4-fold for all three lines to 42-80 ~g/gfw. It is especially worth noting that this decrease can most likely be attributed to a reduction in the level of available tryptophan in the cell. The levels of tryptophan in the leaves of the untransformed V26 control and each of the transgenic lines dropped ~4-fold when plants were transferred to the greenhouse. In all three transgenic lines, the ratio of tryptamine to tryptophan content in the cells remained unchanged. These results strongly support the idea that tryptophan availability may be a crucial limiting factor in the production of tryptamine within the leaf.
As further evidence that tryptophan availability is rate-limiting for the in planta production of tryptamine in the transgenic petunias, the following experiment was devised. Stem cuttings from an untransformed V26 plant and line PE-261 were placed into tubes containing either water or 1 mg/ml tryptophan, and then incubated at room temperature for three days to permit uptake. After 3 days, leaf tissue samples were assayed for tryptophan and tryptamine levels.
The results are presented in Table 5.
Table 5 Tryptamine production in TDC-expressing petunias is limited by tryptophan availability Line Treatment Tf'YPtophan, T~-yptamine, p,glgfw ,uglgfw V26 Water 42 2,g Tryptophan18,026 3.3 PE-261 Water 11 81 PE-261 Tryptophan2,785 2,263 As can be observed in Table 5, the V26 control samples in either water or tryptophan accumulated the same low level of tryptamine (3-4 mglgfw), even though tryptophan levels were dramatically higher in the tryptophan-treated sample (nearly 70-fold higher). Line PE-261 in water showed the expected levels of tryptophan and tryptamine (81 mg/gfw). However, when PE-261 was supplied with exogenous tryptophan, tryptamine levels soared to 2,263 mg/gfw, a 28-fold increase over the water treated sample. Interestingly, the level of tryptophan in the tryptophan-treated PE-261 line remained 7-fold below the V26 sample treated with tryptophan suggesting that the conversion of tryptophan to tryptamine was extremely efficient and rapid. Taken together, these results provided convincing evidence that the in plants production of tryptamine by TDC is limited by tryptophan availability.
Example 7 Transgenic TDC-expressing Petunia resistance to powdery mildew Greenhouse-grown petunia lines PE-261, PE-310, PE-312 and an untransformed V26 control were inoculated on their leaf surface with a 5 ~.1 droplet containing 103 powdery mildew spores. The third leaf {from the top) on each of five shoots of a single plant was inoculated. Each line was represented by four plants (for a total of 20 inoculation sites). Disease progression was monitored for approximately two weeks by recording the percentage of inoculated sites infected and measuring the diameter of the fungal colony with calipers to calculate their size (area). The results are displayed in Table 6.
Table 6 Line Disease incidencesDisease severityb a percent infecrion of inoculated sites relative to an untransformed control assigned a value of 100 b relative colony size (area) compared to an untransforcned control assigned a value of 100 In all three transgenic lines, disease incidence was reduced compared to inoculated, untransformed controls. The incidence of disease was reduced 2-fold for PE-312 and approximately 3-fold for lines PE-261 and PE-310. The reduction in disease incidence correlated well with the tryptamine levels in the leaf {lowest in PE-312, 42 ~.g/gfw, and highest in PE-261, 80 Itg/gfw).
Moreover, disease severity was also reduced compared to the untransformed control line. For lines PE-310 and PE-312, disease severity was reduced approximately 9-fold while disease severity for PE-261 was reduced nearly 17-fold. Taken together, these data strongly support the argument that tryptamine-accumulating petunias show enhanced resistance to infection by powdery mildew. It is especially worth noting that reductions in both disease incidence and severity correlated extremely closely with tryptamine amounts in the leaf tissue of the three different lines. It should also be mentioned that the in vitro sensitivity of powdery mildew to tryptamine remains unknown since this pathogen is an obligate parasite and cannot be assayed by our usual method.
Example 8 Transgenic TDGexpressing Petunia resistance to Botrytis cinerea We also evaluated whether the flower petals from the TDC-expressing petunia Lines showed increased resistance to infection by Botrytis cinerea. Flower petals were measured for their tryptamine content and shown to contain between 300 and 600 ug/gfw tryptamine.
The high levels of tryptamine in the petals is directly attributable to two factors, a higher concentration of available tryptophan and promoter activity. The CAMV 35S promoter is known to be extremely active throughout the entire petunia flower. Moreover, we have discovered that the UBQ3 promoter is even more active than the 35S promoter in petunia flowers, especially in a mature flower which is fully opened.
To assess Botrytis resistance in the petal, newly opened flowers from greenhouse plants were detached and placed into tubes containing water. A Botrytis spore suspension of 250 spores/ml was sprayed to the point of runoff and the inoculated flowers placed into a humidity chamber at room temperature. The rate of disease progression was then followed for 4-5 days and petals scored on a scale of 0 (uninfected) to 5 (flower collapse). Within 25 h, the untransformed control petals began to show necrotic lesions caused by Botrytis. These lesions rapidly expanded so that by 97 h, most flowers had totally collapsed. In contrast, the three transgenic lines showed only mild levels of infection (small, isolated lesions) after the 4-day period. At higher inoculum levels (103 spores/ml), the V26 control and PE-261 lines showed equal susceptibility to infection by Botrytis. However, lines PE-3I0 and PE-312 still exhibited greatly reduced rates of infection by Botrytis. After 97 h, PE-310 flowers still showed only a small number of isolated lesions. Disease symptoms were only slightly more advanced in PE312 flowers as the lesions were more numerous and larger.
As previously noted in the powdery mildew experiments, there was a tight correlation between tryptamine levels and the degree of Botrytis resistance achieved. The strongest (PE310) and weakest (PE-261) Botrytis-resistant lines contained the highest (592 wg/gfw) and lowest (310 p.g/gfw) amounts of tryptamine, respectively. Moreover, it now appears that the in vitro studies presented in Example 3 provided meaningful results as it was predicted that 500 p.g/ml tryptamine would be required to inhibit Botrytis (compare to the petal values of 310-592 ug/gfw). Taken together with the powdery mildew results, a very unifying and consistent picture emerges that shows that tryptamine can confer enhanced levels of disease resistance against fungal pathogens, and that the degree of resistance achieved is directly dependent upon the in planta tryptamine concentration.
Example 9 Sensitivity of nematodes to tryptamine Experiments similar to those described in Example 3 were designed to test the effect of tryptamine on phytopathogenic nematodes. Larvae of the Root Knot nematode (Meloidogyne hapla) were exposed to various concentrations of tryptamine to test their sensitivity. A suspension of nematodes was prepared by extracting them from soil around heavily infected tomato plants. In a 24-well plate, 100-150 root-knot nematodes were added in a volume of 285 pl, next 215 pI of tryptamine solution was added to each well. The final concentrations of tryptamine were based on a 500 p.I volume. Microtiter plates were covered and incubated at 25 C with gentle shaking for 48 h. At 48 h the number of mobile and immobile nematodes in each well was counted in a counting chamber using a dissecting microscope.
As can be observed in Table 7, tryptamine is very active against the root-knot nematodes.
Nematodes were immobilized at 3I wg/ml, a concentration readily achieved in transgenic plants (see Example 6).
Table 7 Number Tr of nematodes tamine conc (m l l yp . Mobile Immobile g m ) Experiment 1 0.125 17 118 0.250 7 170 0.500 6 177 Number of nematodes 1.0 2 181 Experiment 2 0.016 100 4 0.031 6 113 0.062 7 87 0.125 I 0 145 To determine if TDC-expressing plants are resistant to nematodes, leaf disks of transgenic petunia lines were inoculated with the foliar nematode Aphelenchoides fragariae. Briefly, leaf disks (2.1 cm diameter) were cut from surface sterilized greenhouse grown leaves of the transgenic V26 petunia lines (PE-310 and PE-312) and the non-transgenic control. Disks were placed onto wet filter paper in a mufti-well dish (1 disk/well) and then inoculated with a drop containing 50 A. fragariae nematodes that had been raised on a sterile tobacco callus culture. Inoculated disks were incubated for eighteen days at mom temperature and then the number of nematodes per well was quantified.
Although, there was an increase in nematode population in each well, the two transgenic lines (PE-310, PE-312) showed only a slight increase (from 50 to 74 or 67 respectively) while the non-transgenic control increased four fold (from 50 to 194).
We have shown that two unrelated plant pathogenic nematode species are sensitive to tryptamine either by direct contact in solution (M. hapla) or by feeding on transgenic petunia that overexpresses TDC (A. fragariae). These species were selected solely on the basis of being readily available and should not represent a biased sample. We conclude that tryptamine is a generally effective nematicide. Therefore, TDC transgenic plants of any species overexpressing the TDC
and/or AS gene should be resistant to nematodes, as long as the target tissue has adequate amounts of tryptamine. In the plants we have tested, tryptophan and tryptamine levels are low in the roots.
Therefore, to protect roots from nematodes it may be necessary to use an AS
gene to boost tryptophan and tryptaxnine levels in roots. In the case of root pathogenic nematodes such as Meloidogyne sp. and Heterodera sp., they induce special plant structures for feeding. These specialized feeding cells act as plant metabolic sinks. These specialized feeding cells may have enough tryptophan for the TDC gene to produce a concentration of tryptamine that is efficacious to root feeding nematodes, even without the booster affect of an AS gene.
Example 10 Botrytis cinerea resistance in other transgenic plant species Several other plant species (poinsettia cv. Angelika, geranium Designer Scarlet, lisianthus and another bedding plant) were transformed with the TDC gene. A measurable increase in tryptamine was found in transgenic poinsettia and geranium lines. Transgenic poinsettia lines demonstrated resistance to Botrytis cinerea in a leaf disk assay. Briefly, twelve leaf disks (8 mm in diameter) from each tissue culture-maintained transformed lines (and an untransformed control) were punched out with a cork borer and placed onto moistened Whatman 3M paper inside a sterile plastic bioassay dish. A freshly-prepared suspension ofBotrytis spores (103 spores in 2.5 ul) was then pipetted onto the leaf disk surface. The humidity chamber was sealed and the leaf disks left at 20°C
to permit disease development. For the next 3-14 days (timeline is species-dependent), disease progression was monitored and recorded as percentage of leaf disks infected.
Transgenic geranium lines demonstrated resistance to Botrytis cinerea infection when flowers were inoculated.
In at least one transgenic plant species we observed increased tryptophan and tryptamine concentration when the ASITDC combination was used.

Claims (24)

We claim:

1. A transgenic plant tissue having improved resistance to fungi, bacteria, nematodes or combinations thereof, comprising a plant tissue whose cells are transformed with and express a TDC transgene.

2. A transgenic plant tissue having improved resistance to fungi, bacteria, nematodes or combinations thereof, comprising a plant tissue whose cells are transformed with and express an AS transgene.

3. The transgenic plant tissue according to claim 2, wherein the AS transgene is the AS.alpha.1 transgene.

4. The transgenic plant tissue according to claim 1, wherein the plant cells are cotransformed with and express an AS transgene.

5. The transgenic plant tissue according to claim 4, wherein the AS transgene is the AS.alpha.1 transgene.

6. The transgenic plant tissue according to any one of claims 1 to 5 wherein plant tissue plastids are transformed with a TDC transgene, an AS transgene, or both.

7. The transgenic plant tissue according to claim 6, wherein the AS transgene is the AS.alpha.1 transgene.

8. A nucleic acid construct comprising a TDC gene operatively linked to the promoter.

9. A nucleic acid construct comprising a TDC gene operatively linked to the CaMV 35S
RNA promoter.

10. A nucleic acid construct comprising a TDC gene and an AS gene.

11. The nucleic acid construct according to claim 10, wherein the AS gene is the AS.alpha.1 gene.

12. The nucleic acid construct according to claim 10, wherein the TDC gene is operatively linked to the UBQ3 promoter.

13. The nucleic acid construct according to claim 10, wherein the TDC gene is operatively linked to the CaMV 35S RNA promoter.

14. The nucleic acid construct according to claim 10, wherein the AS gene is operatively linked to the UBQ10 promoter.

15. A method of enhancing resistance to phytopathogenic bacteria, fungi, and/or nematodes in a plant tissue, the method comprising transforming the plant tissue with a nucleic acid construct according to claim 8.

16. A method of enhancing resistance to phytopathogenic bacteria, fungi, and/or nematodes in a plant tissue, the method comprising transforming the plant tissue with a nucleic acid construct according to claim 9.

17. A method of enhancing resistance to phytopathogenic bacteria, fungi, and/or nematodes in a plant tissue, the method comprising transforming the plant tissue with a nucleic acid construct according to claim 10.

18. A method of enhancing resistance to phytopathogenic bacteria, fungi.
and/or nematodes in a plant tissue, the method comprising transforming the plant tissue with a nucleic acid construct according to claim 11.

19. A method of enhancing resistance to phytopathogenic bacteria, fungi, and/or nematodes in a plant tissue, the method comprising transforming the plant tissue with a nucleic acid construct according to claim 12.

20. A method of enhancing resistance to phytopathogenic bacteria, fungi, and/or nematodes in a plant tissue, the method comprising transforming the plant tissue with a nucleic acid construct according to claim 13.

21. A method of enhancing resistance to phytopathogenic bacteria, fungi, and/or nematodes in a plant tissue, the method comprising transforming the plant tissue with a nucleic acid construct according to claim 14.

22. A method of enhancing resistance to phytopathogenic bacteria, fungi, and/or nematodes in a plant tissue, the method comprising transforming the plant tissue with the TDC gene.

23. A method of enhancing resistance to phytopathogenic bacteria, fungi, and/or nematodes in a plant tissue, the method comprising transforming the plant tissue with the AS gene.

24. The method according to claim 23, wherein the AS gene is the AS.alpha.1 gene.