AU751855B2 - Assay for screening inhibitors of C4 plant enzymes - Google Patents

Description

WO 99/54495 PCT/AU99/00287 ASSAY FOR SCREENING INHIBITORS OF C 4 PLANT ENZYMES TECHNICAL FIELD The invention described below relates to an assay procedure for screening potential inhibitors of plant enzymes. In particular, the invention relates to an assay procedure which can be used for the high-throughput screening of potential inhibitors of enzymes of the C 4 acid cycle in plants.

BACKGROUND ART The majority of plants can be divided into C 3 and C 4 plants, depending on the mechanism the plant uses to incorporate CO 2 into organic compounds. In C 3 plants, CO 2 is initially added onto a five-carbon compound forming an unstable six carbon compound which dissociates into two stable three carbon compounds, hence the C 3 name. On the other hand, the first stable compound formed in C 4 plants is a four carbon compound. An extra biochemical pathway exists in the leaves of C 4 plants which allows them to fix CO 2 more efficiently and, under certain environmental conditions, to grow more rapidly than their C 3 counterparts. In addition, C 4 plants use water and nitrogen more efficiently than

C

3 plants. Together, these properties enable C 4 plants to compete favourably with many of the world's crops, most of which are C 3 plants for example, wheat, rice, barley and oats.

It follows then that many of the weeds which have an adverse effect on agricultural production throughout the world are C 4 plants. Typical examples are nutgrass (Cyperus rotundus), couch grass (Cynodon dactylon), barnyard grass (Echinochloa spp.), Johnson grass (Sorghum halopense), and goose grass (Eleusine indicia). Nutgrass is a particularly serious global problem being present in more than 100 countries and affecting more than crop species. For efficient agricultural production there is an obvious and pressing need for control of C 4 weed species. To date, however, no herbicide specific for C 4 weeds has been provided.

Crucial to the C 4 acid cycle this being the cycle that fixes CO in C 4 plants are the following enzymes: pyruvate orthophosphate dikinase (pyruvate,Pi dikinase); phosphoenolpyruvate carboxylase; and, NADP-malate dehydrogenase. The pathway involving these enzymes includes the step which incorporates atmospheric CO 2 and creates the products which feed into the sugar-producing Calvin cycle. Interruption of this PCT/AU99/00287 P:OPER\M 199-.027.wo -24/12/99 Received 24 December 1999 -2biochemical pathway should, therefore, adversely affect photosynthesis in C4 plants.

Attempts to develop a C4-specific herbicide have involved designing structural analogues of substrates of the C4 acid cycle enzymes. Those exhibiting inhibitory effects have been further modified to maximise their effect. The only report of a compound which specifically inhibited a C 4 enzyme related to 3 ,3-dichloro-2(dihydroxyphosphinoylmethyl)propenoate which acts on phosphoenolpyruvate carboxylase (see C. L.

D. Jenkins et al., Biochem. Int. 14, 219-226 [1987]; H. G. McFadden et al., Aust. J.

Chem. 40, 1619-1629 [1987]; C. L. D. Jenkins, Plant Physiol. 89, 1231-1237 [1989]; and, H. G. McFadden et al., Aust. J. Chem. 4, 301-314 [1989]). However, the compound was found to have no effect on the growth of C 4 plants. At present, none of the compounds known to inhibit enzymes of the C4 acid cycle has herbicidal activity.

Nevertheless, inhibiting the C4 acid cycle to kill C4 plants remains a promising herbicidal strategy. It has been shown that C4 plants transformed by molecular means (antisense technology) to decrease the level of pyruvate, Pi dikinase or phosphoenolpyruvate carboxylase, enzymes specific to the C4 acid cycle, are incapable of surviving unless grown under high CO, conditions (see J. P. Maroco et al., Plant Physiol.

116, 823-832 [1998]). Therefore, it follows that a compound that inhibits either pyruvate, Pi dikinase or phosphoenolpyruvate carboxylase might be an efficient and selective herbicide, thus preventing the deleterious effect of C4 weeds on C3 crops.

Marine organisms are an abundant source of compounds of benefit to humans. Many pharmaceuticals are isolated from plants or are derivatives of compounds first identified in marine organisms. Compounds of marine origin are also known which are enzyme inhibitors. Thus, it is reasonable to assume that because of the diversity of the compounds produced by marine organisms there are likely to be some that are inhibitors of C 4 acid cycle enzymes.

In the absence of an indication that an organism produces a compound having desired properties, identification of useful compounds in marine organisms usually entails the screening of extracts from thousands of organisms. However, the known assays for the above three C4 enzymes, which are spectrophotometric assays, are large-volume assays and are not suitable for the screening of large numbers of samples. There is thus a need for an assay which can be used to screen large numbers of samples for potential inhibitors o f the C4 acid cycle enzymes.

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WO 99/54495 PCT/AU99/00287 -3- SUMMARY OF THE INVENTION The object of the invention is to provide a high-throughput assay which can be used to screen potential inhibitors of enzymes of the C 4 acid cycle in plants.

According to a first embodiment of the invention, there is provided an assay for inhibitors of C 4 acid cycle enzymes of plants, the assay comprising: a) testing for inhibition of at least one of pyruvate orthophosphate dikinase, phosphoenolpyruvate carboxylase or malate dehydrogenase by: i) including a sample containing the potential inhibitor in a test mixture comprising pyruvate orthophosphate dikinase and substrates thereof, phosphoenolpyruvate carboxylase and the substrate bicarbonate, and malate dehydrogenase and the substrate NADH; ii) incubating said test mixture under conditions appropriate for the conversion of pyruvate to malate with oxidation of NADH; and iii) detecting inhibition of at least one of said pyruvate orthophosphate dikinase, phosphoenolpyruvate carboxylase or malate dehydrogenase by comparing the level of NADH or NAD' in said test mixture with the level of NADH or NAD' in a control mixture incubated under the same conditions as in b) testing for inhibition of phosphoenol pyruvate carboxylase or malate dehydrogenase with any sample which contains an inhibitor of at least one of said pyruvate orthophosphate dikinase, phosphoenolpyruvate carboxylase or malate dehydrogenase by: i) including said sample in a test mixture comprising phosphoenolpyruvate carboxylase and substrates thereof, and malate dehydrogenase and the substrate

NADH;

ii) incubating said test mixture under conditions appropriate for the conversion of phosphoenolpyruvate to malate with oxidation of NADH; and iii) detecting inhibition of said phosphoenolpyruvate carboxylase or malate dehydrogenase by comparing the level of NADH or NAD' in said test mixture with the level of NADH or NAD' in a control mixture incubated under the same conditions as in c) testing for inhibition of malate dehydrogenase with any sample which contains an WO 99/54495 PCT/AU99/00287 -4inhibitor of said phosphoenolpyruvate carboxylase or malate dehydrogenase by: i) including said sample in a test mixture comprising malate dehydrogenase, oxaloacetate and NADH or including oxaloacetate in said test mixture from a(ii) or b(ii); ii) incubating said test mixture under conditions appropriate for the conversion of oxaloacetate to malate with oxidation of NADH; and iii) detecting inhibition of said malate dehydrogenase by comparing the level of NADH or NAD in said test mixture with the level of NADH or NAD in a control mixture incubated under the same conditions as in According to a second embodiment of the invention, there is provided an assay for inhibitors of C 4 acid cycle enzymes of plants, the assay comprising: a) testing for inhibition of at least one of pyruvate orthophosphate dikinase, phosphoenolpyruvate carboxylase or malate dehydrogenase by: i) including a sample containing the potential inhibitor in a test mixture comprising pyruvate orthophosphate dikinase and substrates thereof, phosphoenolpyruvate carboxylase and the substrate bicarbonate, and malate dehydrogenase and the substrate NADH; and ii) incubating said test mixture under conditions appropriate for the conversion of pyruvate to malate with oxidation of NADH; iii) detecting inhibition of at least one of said pyruvate orthophosphate dikinase, phosphoenolpyruvate carboxylase or malate dehydrogenase by comparing the level of NADH or NAD in said test mixture with the level of NADH or NAD* in a control mixture incubated under the same conditions as in b) testing for inhibition of phosphoenolpyruvate carboxylase or malate dehydrogenase with any sample which contains an inhibitor of at least one of said pyruvate orthophosphate dikinase, phosphoenolpyruvate carboxylase or malate dehydrogenase by: i) including phosphoenolpyruvate in said test mixture from ii) incubating said test mixture under said conditions used in step and iii) detecting inhibition of said phosphoenolpyruvate carboxylase or malate dehydrogenase by comparing the level of NADH or NAD in said test mixture with the level of NADH or NAD' in a control mixture incubated under the PCT/AU99/00287 P:\OpER\Mj\99c-oo07.o -2412/99 Received 24 December 1999 same conditions as in c) testing for inhibition of malate dehydrogenase with any sample which contains an inhibitor of phosphoenolpyruvate carboxylase or malate dehydrogenase by: i) including oxaloacetate in said test mixture from or b(ii) or including said sample in a test mixture comprising malate dehydrogenase, oxaloacetate and

NADH;

ii) incubating said test mixture under said conditions used in step and iii) detecting inhibition of said malate dehydrogenase by comparing the level of NADH or NAD in said test mixture with the level of NADH or NAD in a control mixture incubated under the same conditions as in Other aspects of the invention and the best mode of carrying out the invention will become apparent from a reading of the following detailed description.

DETAILED DESCRIPTION OF THE INVENTION The following abbreviations are used hereafter: ATP adenosine triphosphate AMP adenosine monophosphate Pi inorganic phosphate PPi inorganic pyrophosphate NADH nicotinamide-adenine dinucleotide (reduced form) NAD nicotinamide-adenine dinucleotide (oxidised form) PPDK pyruvate orthophosphate dikinase (EC 2.7.9.1) PEP C phosphoenolpyruvate carboxylase (EC 4.1.1.31) MDH NAD-malate dehydrogenase (EC 1.1.1.37) HEPES N-[2-hydroxyethyl]piperazine-N'-[2-ethanesulfonic acid] OAA Oxaloacetate The term "comprising" as used in the above definition of the embodiments and hereafter denotes a mixture or composition which includes at least the specified components but should not be interpreted as meaning that the mixture or composition consists of only those components. Mixtures and compositions can include other ingredients known to those of skill in the art as normal components of mixtures for the assay of enzymes. Examples of these other ingredients include buffers with a suitable pK, o allow control of the assay mixture within the desired pH range such as HEPES, 2-(N- SAMENUDED

SHEET

IPEAfAUJ PCT/AU99/00287 P:\OPER\MC\99-087.WO -24/1299 Received 24 December 1999 -6- Morpholino)ethanesulphonic acid (MES), 3-N-Morpholino)propanesulphonic acid (MOPS) or Tris(hydroxymethyl)aminomethane (Tris) but excluding phosphate buffers which will interfere with the reaction; reducing agents such as dithiothreitol or P-mercaptoethanol and salts such as the salts of mono and divalent options. For example PPDK is a divalent cation dependent enzyme and requires the presence of a divalent cation, such as Mg2", Ca 2 and Mn 2 PEP C is also divalent cation dependent, being dependent on the presence of a divalent metal cation. Other salts, such as ammonium sulphate may be added to improve the performance of the assay.

The present inventors have found that the activities of the C 4 plant enzymes PPDK and PEP C can conveniently be assayed in a microtitre plate format using the procedures summarised above thus allowing for the screening of a large number of potential inhibitors of these enzymes or of samples suspected of containing inhibitors. The reactions involved in the assay are as follows:

PPDK

Pyruvate ATP Pi phosphenol pyruvate AMP PPi H'

PEPC

Phosphoenol pyruvate HC0 3 oxaloacetate Pi Oxaloacetate NADH H+ malate NAD in which the abbreviations set out above have been used.

The MDH used for the final reaction in the above sequence is preferably not the C 4 plant NADP-dependent enzyme, but is instead the ubiquitous NAD-dependent enzyme.

Use of the ubiquitous NAD-dependent enzyme in assays allows elimination of inhibitors that might have a general effect on plants in not being specific for C 4 plant enzymes.

As NADH is a substrate for the enzyme catalysing the final reaction in the sequence, the progress of the reaction can be measured via the oxidation of NADH which has a maximal absorbance at 340 nm (range, 300-400 nm). Equally, the reaction can be monitored for the production of NAD' by the maximal absorbance of NAD at R proximately 260 nm (range, 230-290 nm). If the latter approach is taken, microtitre AMENDED SHEET !PSA/AUr WO 99/54495 PCT/AU99/00287 -7plates which have little or no UV absorbing properties are required.

With reference to the assay according to the first embodiment of the invention, step (a) of this assay constitutes a primary screening procedure for compounds active against C 4 plant enzymes. Samples identified as containing an active constituent that is, a constituent that reduces the amount of NAD' formed and thus inhibits at least one of PPDK, PEP C or MDH are then subjected to a secondary screening to determine the enzyme specificity of the inhibitor. The secondary screening is done by assaying individual enzymes in accordance with steps and of the first embodiment and/or by carrying out a physiological assay in accordance with the second embodiment of the invention.

As indicated above, assays can be performed in 96-well microtitre plates. Plates can have wells with round or flat bottoms and can be made of any material that does not have an appreciable absorbance at the wavelength to be measured (260 or 340 nm). The usual volume of a reaction mixture is about 100 ,l but this can be adjusted to suit the capacity of the microtitre plate. All that is required is that the absorbance value initially attained is significantly different to the background absorbance of the microtitre plate plus the absorbance of the assay mixture minus NADH or NAD'.

A general description of the method of carrying out a primary screening that is, a screening using the assay according to step of the first embodiment of the invention follows. Typical components of mixtures for this assay and the concentrations of components are set out in Table I Table I Assay Mixture Components for a Primary Screen Reagent Typical final Suitable range (mM) concentration (mM) Dithiothreitol 10 1-10 MgSO 4 10 2-10 NaHCO 3 10 2-20 Glucose-6-P 1 0.1-2

(NH

4 )2SO 4 5 0.5-10 NaH 2

PO

4 2.5 0.1-5

NADH

2 0.4 0.2-0.5 HEPES pH 8.0 50 10-200 ATP 1.6 0.5-5 PPDK as required as required PEP C as required as required MDH as required as required Pyruvate 1 0.5-10 WO 99/54495 PCT/AU99/00287 -8- With regard to the enzymes, assay mixtures typically comprise the following: PPDK, 0.005 units; PEC C; 1 unit; and, MDH, 2 units.

Although a pH of 8.0 is given in Table I above, assays can be performed within a pH range of6.0 All mixture components save for at least one of the PPDK substrates are added to wells of a microtitre plate. In addition to test wells to which the test sample is added, positive and negative control wells are also prepared. Positive controls include all assay components save for the test sample. However, an equal volume of test sample solvent (for example, water, methanol, ethanol, DMSO, or mixtures thereof) is added to positive controls. Both test sample and substrate used to initiate the reaction are omitted from the negative control but suitable volumes of the appropriate solvent are added in place of these components. Test wells are typically prepared in duplicate but samples can be tested singly or in greater than two replicates.

After all components have been added to the test and control wells, the plate is usually allowed to equilibrate at room temperature (20-30'C) for 5 minutes to allow dispersion of test samples and control solvent through the reaction mixtures to give a consistent absorbance reading. This equilibration can be for as little as 1 minute but can also be for up to several hours as the enzymes and other assay components are stable. After equilibration, the absorbance at 340 nm (or 260 nm) is measured using a spectrophotometric plate reader. This measurement is defined as the initial absorbance,

A

0 The reaction is started by adding, to all but the negative control wells, the substrate pyruvate to the desired final concentration. Alternatively, the test and positive control assay mixtures can be made with pyruvate and without ATP. The reaction is then initiated with ATP.

Plates are incubated at 20 to 30'C until the reaction is complete as evidenced by a constant reading for the positive controls. This is usually reached after 10 to 60 minutes depending on the amount and activity of the enzymes. The absorbance is then again measured at 340 nm (or 260 nm) to determine the final absorbance, To obtain a percent inhibition for an extract being tested, the difference between Ao and Aend for the test sample is standardised against the difference between A 0 and Aed for the positive control.

WO 99/54495 PCT/AU99/00287 -9- In the individual enzyme approach to secondary screening of sample extracts having inhibitory activity, the first step is to test active samples against PEP C and MDH. This is step of the first embodiment defined above. Typical components of a PEP C/MDH assay mixture are set out in the following table.

Table II Assay Mixture Components for a PEP C/MDH Assay Reagent Typical final Suitable range (mM) Dithiothreitol 10 1-10 MgSO 4 10 2-10 NaHCO 3 10 2-20 Glucose-6-P 1 0.1-2

(NH

4 2

SO

4 5 0.5-10

NADH

2 0.4 0.2-0.5 HEPES pH 8.0 50 10-200 PEP C as required as required MDH as required as required PEP 5 1-10 The PEP C/MDH assay is carried out in essentially the same manner as the primary screening assay. If the reaction is not inhibited, specific inhibition of PPDK by active extracts from the primary screen is indicated.

If inhibition is observed in the PEP C and MDH assay, a further assay is conducted in which active extracts are tested against MDH alone. This second step of the secondary screening corresponds to step of the first embodiment. Typical components of an MDH assay mixture are set out in the following table.

Table III Assay Mixture Components for an MDH Assay Reagent Typical final Suitable range (mM) Dithiothreitol 10 1-10

NADH

2 0.4 0.2-0.5 HEPES pH 8.0 50 10-200 MDH as required as required OAA 1 0.5-5 If the MDH reaction is not inhibited, the step 1 result can be interpreted as indicating that the inhibitor acts on either PEP C only, or PEP C and PPDK, but not on MDH.

WO 99/54495 PCT/AU99/00287 Active extracts identified in the primary screen can also be tested using the physiological assay according to the second embodiment. Inhibition of PPDK is first assessed with the physiological assay using the components listed above in Table I and using essentially the same procedure as for the primary screen. Inhibition of PEP C is then tested by adding the substrate, phosphoenol pyruvate, to the reaction mixture. If an inhibitor is specific for PPDK, no inhibition of PEP C is seen at this stage for the extract containing such an inhibitor. If, however, inhibition is seen, the MDH substrate oxaloacetate is added and the effect of the inhibitor on this enzyme assessed. As with the isolated enzyme approach, normal MDH activity indicates that the inhibitor acts on either PEP C only, or PEP C and PPDK, but not on MDH.

With the assays described above, compounds, or at least extracts containing such compounds, can be identified that are specific inhibitors of the C 4 plant enzymes, PPDK and PEP C. The ability to differentiate between inhibitors of these enzymes and inhibitors of MDH allows elimination of those compounds that also act on the more catholic enzyme MDH and thus would not be useful as specific C 4 plant herbicides.

It should be noted that while it is not necessary to subject samples which show no inhibition in step a) to further steps b) and or to subject samples inactive in step b) to step it may be convenient, especially when performing a high throughput assay, to subject all samples to steps b) and c) regardless of whether inhibition is seen in steps a) and b).

Subjecting all samples to all steps may serve as a useful cross check.

The assays according to the invention can be used to screen for potential inhibitors derived from any source including plants, animals, bacteria, fungi and protozoans. Crude aqueous or organic extracts can be tested, typical organic solvents being methanol, ethanol, dimethylsulfoxide (DMSO) or any combination thereof. Extracts can be acidic or basic provided that any alteration of pH of reaction mixtures on addition of extract does not interfere with the progress of reactions. Compounds able to be tested in the assays include any isolated natural or synthetic product, or any combination of compounds whether produced by combinatorial, purification, or synthetic processes.

The C 4 plant enzymes PPDK and PEP C can be prepared by any of the methods known to those of skill in the art. For example, Chapter 3 of Methods in Plant Biochemistry, Vol. 3 (Academic Press Limited, London, England, 1990, pp. 39-72), which is by Anthony R.

Ashton et al. and is entitled "Enzymes of C 4 Photosynthesis", includes summaries of methods WO 99/54495 PCT/AU99/00287 -11for the purification of PPDK and PEP C. The entire content of Chapter 3 of this volume is incorporated herein by cross-reference. MDH is widely available from commercial sources.

Having broadly described the assays according to the invention, the results of application of the assays to the screening of extracts of marine organisms for inhibitors of PPDK and PEP C will now be provided as a non-limiting example of the invention.

Example 1 Screening of Extracts of Marine Organisms Source of Extracts Extracts were obtained from marine organisms collected via diving, trawling, reefwalking or scissors grab from areas on and off the Australian coastline. The organisms, or portions thereof, were freeze-dried prior to addition of ethanol or methanol as the extracting solvent.

Materials and Methods Assays were conducted using 96-well microtitre plates obtained from Sarstedt, South Australia. General assay mixture components were obtained from the following: Sigma Chemical Company, St Louis, MO, USA; Ajax Chemicals, Botany, NSW, Australia; and Boehringer Mannheim Biochemicals, Roche Diagnostics, Basel, Switzerland. PPDK and PEP C were purified from maize and sugar cane as described by Ashton et al. (supra). MDH was obtained from Sigma Chemical Company.

The steps taken in carrying out a primary screen of extracts were as follows: An assay mixture less initiating substrate and extracts was made up as per the second column of Table I and 100 gll added to wells ofa 96-well microtitre plate.

Portions of 10 gl of extract in methanol were added to duplicate wells leaving the last two rows for positive and negative controls. This allowed 40 samples to be tested per plate.

Ten microlitres of methanol was added to the positive and negative control wells.

Ten microlitres of water, the solvent for the initiating substrate, was added to the negative control wells.

Assay mixtures with control solvents and samples were equilibrated at room temperature (26 C) to allow dispersion of sample and solvent.

An initial absorbance reading at 340 nm was taken for each well using a Spectra plate reader (Wallac Oy, Turku, Finland).

Ten microlitres of the initiating substrate, pyruvate, in water was added to all wells except the WO 99/54495 PCT/AU99/00287 12negative control wells. This gave a final pyruvate concentration in the 120 1l assay mixture of 4 mM.

The complete reaction mixtures were incubated for 20 to 30 minutes at room temperature.

After this period, a baseline absorbance was reached in the positive control wells due to exhaustion of the NADH, the baseline absorbance being due to the plastic of the microtitre plate and the residual absorbance of the reaction mixture.

A final absorbance reading (And) was then taken, again at 340 nm.

Percent inhibition in samples was determined by standardising the difference in initial absorbance and final absorbance of the test sample against the difference in initial absorbance and final absorbance of the positive control.

Secondary screening assays were carried out in a similar fashion.

Results The results presented in Table IV were obtained in a primary screen of 40 test extracts.

Table IV Primary Screening Results Extract Average Initial Average Final inhibition Number Absorbance Absorbance 2001 1.0215 0.3185 8.2 2002 0.9515 0.198 1.6 2003 0.9275 0.191 3.9 2004 1.1185 0.4635 14.5 2005 1.2945 1.2915 99.6 2006 0.9675 0.2165 2050 0.9765 0.4465 30.8 2051 0.959 0.202 1.2 2052 0.9625 0.207 1.4 2053 1.4055 1.509 113.5 2007 1.0485 0.3565 9.7 2008 0.971 0.2075 0.3 2009 1.0795 0.7535 57.4 2011 1.029 0.992 95.2 2012 1.0505 0.394 14.3 2013 1.0195 0.276 2.9 2057 0.985 0.2465 3.6 2058 0.9795 0.2315 2.3 2060 0.986 0.2105 -1.2 2061 1.014 0.227 -2.7 2014 1.0185 0.3545 13.3 2015 0.964 0.217 2016 1.126 0.4515 11.9 2017 0.9685 0.2145 1.6 2018 0.973 0.88 87.9 2019 1.1195 0.4245 9.3 WO 99/54495 PCT/AU99/00287 13- 2065 2066 2067 2068 2020 2022 2023 2025 2028 2029 2071 2072 2076 2077 0.945 1.029 0.9595 0.9635 0.944 0.9055 0.998 1.0285 0.9505 0.9575 1.5085 1.0095 0.9555 0.9415 0.1985 0.299 0.191 0.2175 0.211 0.726 0.245 0.2785 0.2165 0.203 1.746 0.294 0.215 0.1845 4.7 -0.3 2.6 4.3 76.6 1.7 2.1 4.2 131.0 6.6 3.3 1.2 On the basis of the results obtained in the primary screen, a secondary screen using the isolated enzyme approach was conducted using selected extracts. The results of this screen are presented in Table V.

Table V Secondary Screening Results: PEP C and MDH Activity Extract Number Average Initial Average Final Inhibition Absorbance Absorbance 2005 1.3625 0.507 -1.8 2011 1.09 1.0795 98.8 2018 1.025 0.989 95.7 2053 1.3785 1.4685 110.7 2071 1.6295 1.578 93.9 As the secondary screen indicated that some extracts were active against PPDK and PEP C, or PEP C and/or MDH, certain extracts were tested against MDH alone. The results of these assays are presented in Table VI.

Table VI Secondary Screening Results: MDH Activity Extract Number Average Initial Average Final Inhibition Absorbance Absorbance 2005 1.346 0.4895 -1.4 2011 1.0995 0.3745 14.2 2018 1.018 0.2565 9.9 2053 1.307 1.4165 113 2071 1.815 1.7745 95.2 The results presented in Tables IV to VI show the following: extract 2005 contains a -14substance that is active against PPDK only; extracts 2011 and 2018 contain substances that are active against either PPDK and PEP C, or PEP C only; and, extracts 2053 and 2071 contain substances that are active against MDH and are thus not specific for C 4 enzymes.

A secondary screening was also conducted with selected extracts from Table IV using the physiological assay. Extracts 2053 and 2071 were not tested in this assay as non-specific inhibition was determined in the isolated enzyme assay. No further measurements were needed for extract 2005 after the addition of PEP as this sample had reached its background level at this point.

The results of the physiological assay are presented in the Table VII below.

The results presented in Table VII affirm the earlier results. That is, extract 2005 contains a substance that is active against PPDK only while extracts 2011 and 2018 contain substances which are active against PPDK and PEP C.

Table VII Secondary Screening Results: Physiological Assay S' 15 Extract Initial Final Final Final No. Absorbance Absorbance Inhibition Absorbance Inhibition Absorbance Inhibition (after (PPDK) (after PEP (PEP C) (after

(MDH)

pyruvate addition) oxaloacetate addition) additinn~ 20 2005 1.3845 1.433 106.1 0.6905 6.4 2011 0.991 1.008 102.3 0.971 94.4 0.3495 2.3 2018 0.9495 0.929 97.3 0.8965 95.1 0.3 6.2 2053 2071 It will be appreciated that many changes can be made to the assays as exemplified above without departing from the broad ambit and scope of the invention.

Throughout this specification and claims which follow, unless the context requires otherwise, the word "comprise", and variations such as "comprises" or "comprising", will be understood to imply the inclusion of a stated integer or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps.

The reference to any prior art in this specification is not, and should not be taken an acknowledgment or any form of suggestion that the prior art forms part of the cpmmon general knowledge in Australia.

Claims (14)

1. A multiscreening assay for identifying inhibitors of a plant C 4 acid cycle enzyme selected from pyruvate orthophosphate dikinase, phosphoenolpyruvate carboxylase and both enzymes, the multiscreening assay comprising at least three screens: a) a first screen for testing for inhibition of at least one of pyruvate orthophosphate dikinase, phosphoenolpyruvate carboxylase and malate dehydrogenase by: i) including a sample containing the potential inhibitor in a test mixture comprising pyruvate orthophosphate dikinase and substrates thereof, phosphoenolpyruvate carboxylase and the substrate bicarbonate, and malate dehydrogenase and the substrate NADH; ii) incubating said test mixture under conditions appropriate for the conversion of pyruvate to malate with oxidation of NADH; and iii) detecting inhibition of at least one of said pyruvate orthophosphate dikinase, phosphoenolpyruvate carboxylase and malate dehydrogenase by comparing the level of NADH or NAD in said test mixture with the level of NADH or NAD in a control mixture incubated under the same conditions as in a)(ii); 20 b) a second screen for testing for inhibition of phosphoenolpyruvate carboxylase or malate dehydrogenase with any sample which contains an inhibitor from said first screen by: i) including said sample in a test mixture comprising phosphoenolpyruvate carboxylase and substrates thereof, and malate dehydrogenase and the substrate NADH; ii) incubating said test mixture under conditions appropriate for the S* conversion of phosphoenolpyruvate to malate with oxidation of NADH; and iii) detecting inhibition of said phosphoenolpyruvate carboxylase or 0 ~malate dehydrogenase by comparing the level of NADH or NAD in P:\OPER\MJC\33988-99 claims.doc-12A7/02 -16- said test mixture with the level of NADH or NAD in a control mixture incubated under the same conditions as in and c) a third screen for testing for inhibition of malate dehydrogenase with any sample which contains an inhibitor from said second screen by: i) including said sample in a test mixture comprising malate dehydrogenase, oxaloacetate and NADH or including oxaloacetate in said test mixture from a)(ii) or b)(ii); ii) incubating said test mixture under conditions appropriate for the conversion of oxaloacetate to malate with oxidation of NADH; and iii) detecting inhibition of said malate dehydrogenase by comparing the level of NADH or NAD in said test mixture with the level of NADH or NAD in a control mixture incubated under the same conditions as in c)(ii), wherein said inhibitor is identified by detecting inhibition at least in a)(iii) or b)(iii), but substantially no inhibition detected in c)(iii). *o oo

2. A multiscreening assay for inhibitors of a plant C 4 acid cycle enzyme selected from pyruvate orthophosphate dikinase, phosphoenolpyruvate carboxylase and both .o o enzymes, the multiscreening assay comprising at least three screens: a) a first screen for testing for inhibition of at least one of pyruvate orthophosphate dikinase, phosphoenolpyruvate carboxylase or malate dehydrogenase by: including a sample containing the potential inhibitor in a test mixture comprising pyruvate orthophosphate dikinase and substrates thereof, phosphoenolpyruvate carboxylase and the substrate bicarbonate, and malate dehydrogenase and the substrate NADH; and ii) incubating said test mixture under conditions appropriate for the conversion of pyruvate to malate with oxidation of NADH; iii) detecting inhibition of at least one of said pyruvate orthophosphate dikinase, phosphoenolpyruvate carboxylase or malate dehydrogenase by comparing the level of NADH or NAD in said test mixture with P:\OPER\MJC33988-99 claims doc-12/07/02 -17- the level of NADH or NAD in a control mixture incubated under the same conditions as in a)(ii); b) a second screen for testing for inhibition of phosphoenolpyruvate carboxylase or malate dehydrogenase with any sample which contains an inhibitor from said first screen by: i) including phosphoenolpyruvate in said test mixture from a)(ii); ii) incubating said test mixture under said conditions used in step a)(ii); and iii) detecting inhibition of said phosphoenolpyruvate carboxylase or malate dehydrogenase by comparing the level of NADH or NAD+ in said test mixture with the level of NADH or NAD in a control mixture incubated under the same conditions as in and c) a third screen for testing for inhibition of malate dehydrogenase with any sample which contains an inhibitor from said second screen by: i) including oxaloacetate in said test mixture from a)(ii) of b)(ii) or including said sample in a text mixture comprising malate dehydrogenase, oxaloacetate and NADH; ii) incubating said test mixture under said conditions used in step a)(ii); S. and S 20 iii) detecting inhibition of said malate dehydrogenase by comparing the level of NADH or NAD in said test mixture with the level of NADH or NAD in a control mixture incubated under the same S* conditions as in a)(ii); wherein said inhibitor is identified by detecting inhibition at least in a)(iii) 25 or b)(iii), but substantially no inhibition in c)(iii).

3. An assay according to claim 1 or claim 2 wherein the malate dehydrogenase is a ubiquitous NAD-dependent enzyme.

4. An assay according to any one of claims 1 to 3 wherein the level of NADH in one or more of the test mixture is compared to the level of NADH in the corresponding P:\OPER\MJC\33988-99 claimisdoc-12/07/02 -18- control mixture by comparing the relative absorbances of the mixtures at one or more wavelengths in the range of 300 to 400 nm.

An assay according to claim 4 wherein the absorbence is measured at a wavelength of 340 nm.

6. An assay according to any one of claims 1 to 3 wherein the level of NAD in the corresponding control mixture by comparing the relative absorbances of the mixtures at one or more wavelengths in the range of 230 to 290 nm.

7. An assay according to claim 6 wherein the absorbence is measured at a wavelength of about 260 nm. o

8. An assay according to any one of claims 1 to 7 wherein said assay is performed 15 using a microtitre plate formate.

9. An assay according to any one of claims 1 to 8 wherein step a) is performed with a pH in the range of 6.0 to

10. An assay according to any one of claims 1 to 9 wherein, in the first screen, one of *oo the substrates for pyruvate orthophosphate dikinase is added last to the test mixture and control as an initiator. oooo

11. A method for inhibiting the C 4 acid cycle in a C 4 plant including the step of applying to said C 4 plant, or to a locus thereof, an inhibitor of one or more C 4 acid cycle enzymes identified in accordance with the assay defined in any one of claims 1 to

12. A method for inhibiting the C 4 acid cycle in a C 4 plant including the step of applying to said C 4 plant, or to a locus thereof, an inhibitor specific to pyruvate orthophosphate dikinase identified in accordance with the assay defined in any one P:\OPER\MJC33988-99 claims.doc-12/07/02 -19- of claims 1 to 10, said inhibitor being contained within a sample which shows inhibition at step a)(iii) but substantially no inhibition at step b)(iii).

13. A method for inhibiting the C 4 acid cycle in a C 4 plant including the step of applying to said C 4 plant, or to a locus thereof, an inhibitor acting on phosphoenolpyruvate carboxylase only or on phosphoenolpyruvate carboxylase and pyruvate orthophosphate dikinase, but which does not act on malate dehydrogenase, said inhibitor being identified in accordance with the assay defined in any one of claims 1 to 10, and being contained within a sample which shows inhibition at steps a)(iii) and b)(iii), but substantially no inhibition at step c)(iii).

14. An assay according to claim 1 or claim 2 substantially as hereinbefore described with reference to the Examples. DATED this 12 th day of July 2002 Australian Institute of Marine Science AND James Cook University of North Queensland By DAVIES COLLISON CAVE Patent Attorneys for the Applicant