Expression of human dopamine receptor in potato (Solanum tuberosum) results in altered tuber carbon metabolism
© Skirycz et al; licensee BioMed Central Ltd. 2005
Received: 16 August 2004
Accepted: 09 February 2005
Published: 09 February 2005
Even though the catecholamines (dopamine, norepinephrine and epinephrine) have been detected in plants their role is poorly documented. Correlations between norepinephrine, soluble sugars and starch concentration have been recently reported for potato plants over-expressing tyrosine decarboxylase, the enzyme mediating the first step of catecholamine synthesis. More recently norepinephrine level was shown to significantly increase after osmotic stress, abscisic acid treatment and wounding. Therefore, it is possible that catecholamines might play a role in plant stress responses by modulating primary carbon metabolism, possibly by a mechanism similar to that in animal cells. Since to date no catecholamine receptor has been identified in plants we transformed potato plants with a cDNA encoding human dopamine receptor (HD1).
Tuber analysis of transgenic plants revealed changes in the activities of key enzymes mediating sucrose to starch conversion (ADP-glucose phosphorylase and sucrose synthase) and sucrose synthesis (sucrose phosphate synthase) leading to altered content of both soluble sugars and starch. Surprisingly the catecholamine level measured in transgenic plants was significantly increased; the reason for this is as yet unknown. However the presence of the receptor affected a broader range of enzyme activities than those affected by the massive accumulation of norepinephrine reported for plants over-expressing tyrosine decarboxylase. Therefore, it is suggested that the presence of the exogenous receptor activates catecholamine cAMP signalling in plants.
Our data support the possible involvement of catecholamines in regulating plant carbon metabolism via cAMP signalling pathway.
The catecholamines (dopamine, norepinephrine and epinephrine) are a group of biogenic amines possessing a substituted 3, 4-dihydroxy phenyl ring that are widespread in the animal kingdom; but they have also been detected in plants [1, 2]. The role of catecholamines in plants is poorly documented, but it is clear that they are involved in many aspects of growth and development. They were proposed as precursors for various alkaloids [3, 4] and to be associated with processes such as ethylene production, nitrogen fixation, defence against herbivores, flowering, prevention of 3-indole acetic acid (IAA) oxidation and gibberellin signalling [5, 6]. Analogous with animal cells in which catecholamines stimulate glycogen mobilization a similar role for catecholamines in the regulation of plant carbohydrate metabolism was suggested. Transgenic plants over-expressing tyrosine decarboxylase, which controls an important step of catecholamine synthesis, were characterized by highly increased concentrations of norepinephrine and soluble sugars, whereas starch level was dramatically decreased. Observed changes indicated a positive correlation of norepinephrine with soluble sugars and a negative correlation with starch . The physiological action of catecholamines in animal cells is mediated by their interaction with G-protein coupled receptors that stimulate or inhibit the enzyme adenylyl cyclase (AC). In most animal cells cyclic AMP (cAMP) exerts its effect by activating cAMP dependent, serine-threonine protein kinase (PKA). Recently strong evidence for the occurrence and function of cAMP in higher plants has emerged . It was demonstrated that cAMP levels in tobacco bright yellow 2 (TBY-2) cells are tightly connected to cell cycle progression . The involvement of cAMP in gibberellin and ABA action has also been suggested [10, 11]. Molecular evidence has shown the existence of plant protein kinases containing a high degree of sequence homology with PKA . Moreover, molecular techniques led to the identification of cAMP response element-binding proteins (CREBs) , cyclic nucleotide-gated cation channels  and cAMP binding enzymes . These data strongly indicate the involvement of catecholamines in regulating plant carbohydrate metabolism, possibly by a mechanism similar to that in animal cells. However, this suggestion is limited by the fact that to date no catecholamine receptor has been identified in plants. In the present study we characterize potato plants transformed with a cDNA encoding human dopamine receptor (HD1). The receptor is a rhodopsin-like integral membrane protein of 446 amino acids, seven transmembrane domains and molecular mass of 49 kDa. Our analysis revealed a regulatory effect of HD1 on carbohydrate metabolism including changes in key enzyme activities.
Transgenic plant selection
Phenotype analysis of HD1 plants revealed significant changes in single tuber mass and tuber number, whereas tubers yield was only slightly changed. Data represent the mean of determination on six individual plants per line. Asterisks (*) indicate values that are significantly different from the wild type plants.
Mean FW per tuber
Tuber number per plant
Tuber weight per plant
69.49 ± 5.5
7.33 ± 1.4
509.3 ± 70.3
50.38 ± 3.0*
10.00 ± 1.2*
503.8 ± 42.7
53.39 ± 18.4
12.66 ± 5.2
675.9 ± 254.6
31.43 ± 10.6*
13.66 ± 3.4*
429.3 ± 125.8
49.73 ± 4.0*
10.50 ± 0.9*
522.1 ± 43.2
In order to develop an easy and reliable assay for the quantitative and qualitative determination of catecholamines in plants, the suitability of gas chromatography coupled to a quadruple mass spectrometer (GCMS) was recently investigated. A sensitive GCMS method based on the analysis of the trimethylsilylated catecholamine derivatives was developed to monitor the presence and concentration of these compounds and related metabolites. Based on the retention times and the mass spectra of standards the presence of dopamine, norepinephrine and a new compound normetanephrine in potato leaves and tubers was clearly detected .
Determination of carbohydrate content in tubers of transgenic plants
Changes in carbohydrate are most likely responsible for the altered phenotype of transgenic HD1 tubers. Reduced tuber mass can be explained by decreased starch content whereas increased tuber number by the increase of soluble sugar concentration.
Sucrose – starch metabolism
Under normal growth conditions the major flux in potato tuber carbon metabolism is the conversion of sucrose through hexose phosphates to starch .
Since HD1 plants were characterized by changed concentrations of both soluble sugars and starch we measured the activities of enzymes involved in this pathway. Sucrose transported from leaves is symplastically unloaded from the phloem and degraded by sucrose synthase (SuSy). ADP-glucose phosphorylase (AGPase) converts glucose-1-phosphate (Glu-1-P) into ADP-glucose, an immediate precursor of starch. Both SuSy and AGPase are considered as key enzymes for starch synthesis .
Activities of AGPase and SuSy were significantly decreased in HD1 plants to 56% and 68% of the wild type level, respectively (Figure 4). In agreement with their roles in starch synthesis, and their proposed coordinated regulation, activities of both enzymes and starch content were all significantly correlated (cor >0.9).
Metabolite analysis of HD1 plants revealed changes in glucose-6-phosphate, fructose-6-phophate and intermediates of TCA cycle. Data represent the mean ± SE of determination on three individual plants per line. Asterisks (*) indicate values that are significantly different from the wild type plants.
4.823 ± 0,52
4.025 ± 0.36
5.605* ± 0.24
10.268* ± 0.79
1,615 ± 0,14
1.301 ± 0.29
2.182* ± 0.27
4.264* ± 0.62
TCA cycle metabolites
21.048 ± 3.09
16.463* ± 1.42
16.295* ± 1.27
20.606 ± 2.05
375.434 ± 27.29
118.433* ± 16.63
153.121* ± 19.25
189.106* ± 16.73
0.744 ± 0.067
2.611* ± 0.124
1.400* ± 0.137
2.653* ± 0.128
76.478 ± 6.29
27.878* ± 3.45
65.754* ± 4.21
63.814* ± 3.56
To establish whether enhanced starch mobilization also contributed to the observed decreases in starch content we measured the activity of starch phosphorylase. In two out of the four examined transgenic lines the activity of starch phosphorylase was significantly increased, further contributing to decreased starch content of HD1 plants (Figure 4)
Moreover HD1 expression led to activation of sucrose phosphate synthase (SPS), responsible for sucrose production. Maximum SPS activity (measured wih saturating substrates, Vmax) only changed in two lines, whilst activity of the enzyme measured in the assay that contained limiting substrate concentration (Vmax/Km) and as a consequence 1/Km increased in all the lines.
1/Km, correlated well with the sucrose content of transgenic tubers (cor -0.81) (Figure 4).
In contrast to the vast knowledge concerning the role and action of catecholamines in mammals, very little is known about the physiological significance of catecholamines in plants. Since most of the components of animal catecholamine signaling pathway have been also identified in plants (G-proteins, cAMP, PKA homologs) the involvement of catecholamines in plant signalling pathways is possible. Recently, the analysis of transgenic plants over-expressing tyrosine decarboxylase, which accumulate a high quantity of catecholamines, suggested a possible signalling effect on plant primary metabolism. The increase of catecholamines resulted in decreased starch concentration but increased soluble sugars .
Therefore we suggest that the exogenous receptor activates catecholamine action in potato plants. A difference in enzyme activities involved in starch biosynthesis was noted. The sucrose level was comparable in HD1 and TD plants and consistent with enhanced activity of SPS. Activity of starch phosphorylase was significantly increased in both TD and HD1 plants but the decreases in activity for AGPase, SuSy and PGM was seen only for HD1 plants.
Expression of HD1 in potato (Solanum tuberosum) results in altered carbon metabolism
The previously reported positive correlation between catecholamine level and soluble sugars content and negative correlation with starch level for tubers of potatoes over -expressing tyrosine decarboxylase and in tubers stored at 4°C [2, 7], was also found in our study. Expression of a dopamine receptor resulted in increased catecholamine content and was accompanied by decreased starch level and increases of glucose, fructose and sucrose content. It seems likely that the introduced dopamine receptor activates catecholamine action in carbohydrate metabolism. The question now arises whether catecholamine activates starch breakdown or inhibits its synthesis or whether both processes are affected.
In mammalian systems epinephrine and norepinephrine regulate glycogen turnover by stimulating glycogen mobilization and inhibiting glycogen synthesis. This appears similar in potato, with decreased starch content in HD1 tubers being a consequence of both inhibition of starch synthesis and enhanced starch mobilization. AGPase and SuSy, two key enzymes involved in starch biosynthesis, showed 44% and 32% decreases in their activities respectively. Also the activity of PGM was significantly decreased; we have not determined the contribution of the different isoforms (cytosolic and plastidial) to the observed changes. Increased content of hexose-6-phosphates demonstrates that a direct inhibition of AGPase, rather than a substrate shortage may cause inhibition of starch synthesis. Alternatively the increased hexose phosphate levels may be due to increased starch degradation in response to elevated catecholamine levels. This is supported by the increased activity of starch phosphorylase in two of four transgenic lines. The inhibition of starch synthesis and accumulation of hexose phosphates was accompanied by an increase of sucrose synthesis. Two factors should be taken into consideration. First, that SPS is subject to allosteric activation by Glc-6-P and inhibition by Pi. Second, elevated catecholamine content led to a decrease of SPS Km suggesting increase of the enzyme catalytic activty. Sucrose phosphate synthase has many potential sites of phosphorylation and three of them were shown to influence its catalytic activity. In spinach leaf, phosphorylation of Ser 158 is responsible for enzyme downregulation in darkness, phosphorylation of Ser 229 enables binding of 14-3-3 proteins and down- regulates the enzyme whereas phosphorylation of Ser 424 under stress conditions stimulates SPS activity. There is a growing body of correlative evidence that the potato tuber SPS is regulated in an analogous manner to the leaf enzyme .
Since the level of 14-3-3 proteins was not changed in any of the transgenic lines (data not shown) it is thus suggested that enzyme phosphorylation targeted to the stress site is responsible for its activity enhancement in HD1 plants.
In mammals the action of epinephrine and norepinephrine is mediated by phosphorylation of enzymes involved in glycogen mobilization and synthesis. Very recent studies reported direct evidence that enzymes of starch metabolism (amylopectin synthesis) are regulated by protein phosphorylation and indicate a wider role for protein phosphorylation in the control of starch anabolism and catabolism . Therefore, it is possible that catecholamine action in plants could also involve phosphorylation of enzymes involved in starch metabolism.
Catecholamines – the new stress hormones in plants?
In mammalian systems, catecholamines serve as stress hormones increasing as a result of stress. In order to see whether or not a similar response occurs in plants, leaves of potato plants were wounded and catecholamines levels prior to and 5, 10 and 13 min after wounding were determined. Although the data varied, there was a consistent increasing trend in concentration of dopamine, norepinephrine and normetanephrine . Very recently a similar increase in norepinephrine was measured in potato leaves subjected to ABA and water stress treatment. Activities of both tyrosine hydroxylase (1.5 and 1.7 fold) and tyrosine decarboxylase (2.33 and 1.2fold) were increased . Under normal growth conditions the major flux in potato tuber carbon metabolism is the conversion of sucrose through hexose phosphates to starch . During environmental perturbations like wounding [23, 24] water stress , high temperature  and hypoxia [27, 28] this balance is disturbed and, consequently, large changes in tuber metabolite levels occur. Elevated temperature or water stress leads to increased respiration, a decline in 3-phosphoglycerate (3PGA), inhibition of AGPase and consequently an inhibition of starch synthesis. Decreased starch was accompanied by a stimulation of sucrose synthesis caused by increased hexose posphate levels and activation of SPS via protein phosphorylation. The activity of SuSy was decreased whereas starch mobilization was suggested to increase. These changes in carbohydrate metabolism and carbohydrate content are very similar to those observed in HD1 plants, making it conceivable that catecholamines might play a role in plant stress responses by modulating tuber primary carbon metabolism.
Introducing humane dopamine receptor into plant cells can be considered as controversial but the obtained data would argue for the value of our approach.
Vast changes in the activities of key enzymes mediating carbon metabolism of potato tuber (in HD plants) led to a dramatic reduction of starch but increased sucrose content. The relation between catecholamine, primary carbon metabolism and stress seems possible. We speculate that similarly to situation in animal cells expression of HD1 in potato resulted in activation of the cAMP mediated signalling pathway. This can be supported by the result obtained for potato plants expressing another isoform of human dopamine receptor, HD2. In contrast to HD1, HD2 receptor does not affect activity of adenylate cyclase in animal cells.
Similarly plants expressing HD2 showed no changes in carbohydrate metabolism (data not shown). The obvious next step would be further investigation of our plants with respect to their kinase activity as well as cAMP levels. In parallel we have made efforts to identify a plant dopamine receptor.
Potato plants (Solanum tuberosum L. cv. Desiree) obtained from "Saatzucht Fritz Lange KG" (Bad Schwartau, Germany) were cultivated in a greenhouse in soil under 16 h light (22°C) and 8 h dark (15°C) regime. Plants were grown in individual pots and watered daily. For analysis, the leaves were harvested at noon from 30-day-old greenhouse grown plants and the tubers were harvested in September, 3 months after the transfer of the tissue culture plants to the greenhouse.
Construction of a transgenic plant
The 1.3 kb SmaI, XbaI cDNA encoding HD1 from Homo sapiens ((kindly provided by Marc G.Caron (Duke University, Medical Center); [EMB: XX55760])), was ligated in the sense orientation into the same restriction site of the plant binary vector under the control of the 35S CaMV promoter and Nos terminator. The vector was introduced into the Agrobacterium tumefaciens strain C58C1:pGV2260 and the integrity of the plasmid was verified by restriction enzyme analysis. Young leaves of wild-type potato S. tuberosum L.(cv. Desiree) were transformed with A. tumefaciens by immersing leaf explants in bacterial suspension. A. tumefaciens inoculated leaf explants were subsequently transferred to callus induction medium and shoot regeneration medium. Transgenic plants were pre-selected by using PCR with the primers for the respective phosphotransferase (kanamycin resistance) gene and then selected by northern blot analysis with a HD1 specific cDNA fragment as probe.
Northern blot analysis
Total RNA was prepared from frozen plant material using the guanidinium hydrochloride method. Following electrophoresis (1.5% (w/v) agarose, 15% formaldehyde (w/v)), RNA was transferred to nylon membranes (Hybond N, Amersham, UK). Membranes were hybridised overnight at 42°C in 250 mmol sodium phosphate buffer (pH 7.2) containing 7% (w/v) SDS, 1% (w/v) bovine serum albumin (BSA) and 1 mM EDTA. Radioactively labelled full-length cDNA was used as a hybridisation probe. Filters were washed three times in 1 × SSC containing 0.5% (w/v) SDS at 65°C (highly stringent condition) or in the same buffer but at 42°C (medium stringent condition) for 30 min.
Western blot analysis
Proteins were extracted from frozen plant material using extraction buffer E (100 mM Hepes-NaOH, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 1 mM EGTA, 20%glycerol (v/v), 0.5 mM PMSF, 70 mM beta-mercaptoethanol) supplemented either with 0.1% or 1% TritonX- 100 (v/v). The assessment of the expression of HD1 gene by means of western blot analysis using rabbit IgG anti HD1 protein was conducted as described previously. Briefly, solubilised protein was run on 12% SDS polyacrylamide gels (w/v) and blotted electrophoretically onto nitrocellulose membranes (Schleicher and Schuell). Following transfer, the membrane was sequentially incubated with blocking buffer (5% (w/v) dry milk), and then with antibody directed against the HD1 protein (1:2000 dilution). Formation and detection of immune complexes were performed as previously described . Alkaline phosphatase-conjugated goat ant rabbit IgG at a dilution of 1:1500 was used as a secondary antibody.
Determination of starch and soluble sugar contents
Potato tuber slices and leaf discs were extracted with 80% ethanol-50 mM HEPES KOH, pH 7.4, at 80°C. The supernatant was used for enzymatic analysis of glucose, fructose and sucrose . For starch measurement, extracted plant material was homogenized in 0.2N KOH, and following incubation at 95°C was adjusted to pH 5.5 with 1N acetic acid. Starch was hydrolyzed with amyloglucosidase, and the released glucose was determined enzymatically.
Tissue extraction for catecholamine content measurement
Frozen plant tissue (400 mg) was powdered in liquid nitrogen and extracted with methanol (4 ml per g-1 fresh weight), heated for 15 min at 70°C, and centrifuged (5 min., 12000 g). Samples were diluted with water to 50% methanol concentration and extracted with chloroform (1:1 v/v). A portion of the water phase was dried under vacuum and used for derivatisation . Ribitol was used as an internal standard added directly to the sample homogenate (30 μg g-1 fresh weight).
GC – MS analysis
The dried extracts were incubated in pyridine/methoxyamine (20 mg mL-1) at 37°C for 90 min and then acidic protons were derivatised with N-Methyl- N-trimethylsilyltrifluoroacetamide (MSTFA) at 37°C for 90 min. 2 μl of sample was used for analysis . A HP quadrupole mass spectrophotometer (HP 5972A), combined with a gas chromatograph HP 6890 and autosampler (all Hewlett Packard, Germany) and equipped with 30 m HP – 5MS, fused silica capillary column, was used. Injection temperature was 230°C, with the interface set to 250°C and the ion source adjusted to 180°C. The carrier gas used was helium set at a constant flow rate of 1 ml min-1. The temperature program was 5 min isothermal heating at 70°C, followed by a 5°C min-1 oven temperature ramp to 310°C and final 1 min heating at 310°C. The system was then temperature equilibrated for 6 min at 70°C prior to injection of the next sample. Mass spectra were recorded at 2 scan s-1 with an m/z 50 – 600 scanning range. The chromatograms and mass spectra were evaluated using the MSD ChemStation program (Hewlett Packard, Germany). As standards, dopamine, norepinephrine, normetanephrine, L-Dopa, tyramine and tyrosine (Sigma) were used. The recovery samples were spiked with dopamine, norepinephrine, normetanephrine, L-Dopa, tyramine and tyrosine; the estimated recoveries were 80, 93, 85, 95, 82, 90%, respectively. The following ions were used for quantification: ribitol 307; 319, L-Dopa 218; 267; 368, dopamine 174; 338; 426, norepinephrine 174; 355, 514, normetanephrine 174; 297; 456, tyramine 174; 264; 338, tyrosine 218; 280, 354. The amounts of catecholamines were determined from the ratio of peak areas of catecholamines to peak area of the internal standard (ribitol).
Preparation and analysis of samples for enzyme activities
Tissue was harvested, weighed and immediately frozen in liquid N2. 0.5 g ± 0.1 g tissue was homogenised in a chilled mortar in 2 ml of an extraction buffer containing 30 mM HEPES-NaOH, pH 6.9, 10 mM DTT, 1 mM MgSO4, 0.5 mM EDTA, 0.5% (w/v) BSA and 0.5% (w/v) PVP at 4°C. The homogenate was centrifuged at 16000 g for 10 min and the supernatant desalted using Sephadex G-25 columns. Enzyme activities were determined using the following published methods; SPS ; AGPase ; SuSy, PK ; PGM ; starch synthase ; PGI, enolase ; UGPase ; hexokinase  and starch phosphorylase as described by .
3.9. Statistical analysis
The t-tests were performed using the algorithm embedded into Microsoft Excel. The term significant is used when P < 0.05.
This work was supported by grant No. 3P06A 01523 from State Research Committee (KBN).
- Smith TA: Phenethylamine and related compounds in plants. Phytochemistry. 1977, 16: 9-16. 10.1016/0031-9422(77)83004-5.View ArticleGoogle Scholar
- Szopa J, Wilczyński G, Fiehn O, Wenczel A, Willmitzer L: Identification and quantification of catecholamines in potato plants (Solanum tuberosum) by GC-MS. Phytochemistry. 2001, 58: 315-320. 10.1016/S0031-9422(01)00232-1.PubMedView ArticleGoogle Scholar
- Guinaudeau H, Bruneton J: Isoquinoline alkaloids. Alkaloids and Sulphur Compounds. Methods in Plant Biochemistry. Edited by: Watermann PG, Dey PM, Harborne JB. London, Academic Press; 1993, 8: 373-419.Google Scholar
- Smith TA: Plant amines. Secondary Plant Products, Encyclopedia of Plant Physiology New Series. Edited by: Bell EA, Charlwood BV. Berlin, Springer Verlag, 1980, 8: 433-440.View ArticleGoogle Scholar
- Dai YR, Michaels PJ, Flores HE: Stimulation of ethylene production by catecholamines and phenylethylamine in potato cell suspension cultures. Plant Growth Regul. 1993, 12: 219-222. 10.1007/BF00027201.View ArticleGoogle Scholar
- Kuklin AI, Conger BV: Catecholamines in plants. Journal of Plant Growth Regulation. 1995, 14: 91-97. 10.1007/BF00203119.View ArticleGoogle Scholar
- Świędrych A, Stachowiak J, Szopa J: The catecholamine potentates starch mobilization in transgenic potato tubers. Plant Physiol Biochem. 2004, 42: 103-109. 10.1016/j.plaphy.2003.11.002.PubMedView ArticleGoogle Scholar
- Richards H, Das S, Smith CJ, Pereira L, Geisbrecht A, Devitt NJ, Games DE, van Geyschem J, Gareth Brenton A, Newton RP: Cyclic nucleotide content of tobacco BY-2 cells. Phytochemistry. 2002, 61: 531-537. 10.1016/S0031-9422(02)00266-2.PubMedView ArticleGoogle Scholar
- Ehsan H, Reichheld JP, Roef L, Witters E, Lardon F, Van Bockstaele D, Van Montagu M, Inze D, Van Onckelen H: Effect of indomethacin on cell cycle dependent cyclic AMP fluxes in tobacco BY-2 cells. FEBS Lett. 1998, 422: 165-169. 10.1016/S0014-5793(97)01610-4.PubMedView ArticleGoogle Scholar
- Duffus CM, Duffus JH: A possible role for cyclic AMP in gibberellic acid triggered release of alpha-amylase in barley endosperm slices. Experientia. 1969, 25: 581.PubMedView ArticleGoogle Scholar
- Godoy JA, Lunar R, Torres-Schumann S, Moreno J, Rodrigo RM, Pintor-Toro JA: Expression, tissue distribution and subcellular localization of dehydrin TAS14 in salt-stressed tomato plants. Plant Mol Biol. 1994, 26: 1921-1934. 10.1007/BF00019503.PubMedView ArticleGoogle Scholar
- Lawton MA, Yamamoto RT, Hanks SK, Lamb CJ: Molecular cloning of plant transcripts encoding protein kinase homologs. Proc Natl Acad Sci USA. 1989, 86: 3140-3144.PubMedPubMed CentralView ArticleGoogle Scholar
- Katagiri F, Lam E, Chua NH: Two tobacco DNA-binding proteins with homology to the nuclear factor CREB. Nature. 1989, 340: 727-730. 10.1038/340727a0.PubMedView ArticleGoogle Scholar
- Leng Q, Mercier RW, Fao W, Berkowitz GA: Cloning and first functional characterization of a plant cyclic nucleotide-gated cation channel. Plant Physiol. 1999, 121: 753-61. 10.1104/pp.121.3.753.PubMedPubMed CentralView ArticleGoogle Scholar
- Laukens K, Roef L, Witters E, Slegers H, Van Onckelen H: Cyclic AMP affinity purification and ESI-QTOF MS-MS identification of cytosolic glyceraldehydes 3-phosphate dehydrogenase and two nucleoside diphosphate kinase isoforms from tobacco BY-2 cells. Planta. 2002, 214: 510-20. 10.1007/s004250100644.View ArticleGoogle Scholar
- Fernie AR, Willmitzer L, Trethewey NR: Sucrose to starch: a transition in molecular plant physiology. Trends in Plant Science. 2002, 7: 36-41. 10.1016/S1360-1385(01)02183-5.View ArticleGoogle Scholar
- Geigenberger P: Regulation of sucrose to starch conversion in growing potato tubers. J Exp Bot. 2003, 54: 457-465. 10.1093/jxb/erg074.PubMedView ArticleGoogle Scholar
- Tauberger E, Fernie AR, Emmermann M, Renz A, Kossmann J, Willmitzer L, Trethewey RN: Antisense inhibition of plastidial phosphoglucomutase provides compelling evidence that potato tuber amyloplasts import carbon from the cytosol in the form of glucose-6-phosphate. Plant J. 2000, 23: 43-53. 10.1046/j.1365-313x.2000.00783.x.PubMedView ArticleGoogle Scholar
- Fernie AR, Tauberger E, Lytovchenko A, Roessner U, Willmitzer L, Trethewey RN: Antisense repression of cytosolic phosphoglucomutase in potato (Solanum tuberosum) results in severe growth retardation, reduction in tuber number and altered carbon metabolism. Planta. 2002, 214: 510-520. 10.1007/s004250100644.PubMedView ArticleGoogle Scholar
- Lunn J, Mac Rae E: New complexities in the synthesis of sucrose. Curr Opin Plant Biol. 2003, 6: 208-214. 10.1016/S1369-5266(03)00033-5.PubMedView ArticleGoogle Scholar
- Tetlow IJ, Wait R, Zhenxiao L, Akkasaeng R, Bowsher CG, Esposito S, Kosar-Hashemi B, Morell MK, Emes MJ: Protein phosphorylation in amyloplast regultes starch branching enzyme activity and protein-protein interactions. Plant Cell. 2004, 16: 694-708. 10.1105/tpc.017400.PubMedPubMed CentralView ArticleGoogle Scholar
- Świędrych A, Lorenc-Kukuła K, Skirycz A, Szopa J: The catecholamine biosynthesis route in potato is affected by stress. Plant Physiol Biochem. 2004, 42: 593-600. 10.1016/j.plaphy.2004.07.002.PubMedView ArticleGoogle Scholar
- Hajirezaei MR, Sonnewald U, Viola R, Carlisle S, Dennis D, Stitt M: Transgenic potato plants with strongly decreased expression of pyrophosphate:fructose-6-phosphate phosphotransferase show no visible phenotype and only minor changes in metabolic fluxes in their tubers. Planta. 1994, 192: 43-55.Google Scholar
- Geigenberger P, Reimholz R, Geiger M, Merlo L, Canale V, Stitt M: Regulation of sucrose and starch metabolism in potato tubers in response to short term water deficit. Planta. 1997, 20: 502-518. 10.1007/s004250050095.View ArticleGoogle Scholar
- Geigenberger P, Geiger M, Stitt M: High-temperature inhibition of starch synthesis is due to inhibition of ADPGlc pyrophosphorylase by decreased levels of 3PGA in growing potato tubers. Plant Physiol . 1998, 117: 1307-1317. 10.1104/pp.117.4.1307.PubMedPubMed CentralView ArticleGoogle Scholar
- Dixon WL, ap Rees T: Identification of the regulatory steps in glycolysis in potato tubers. Phytochemistry. 1980, 19: 1297-1301.View ArticleGoogle Scholar
- Geigenberger P, Fernie AR, Gibon Y, Christ M, Stitt M: Metabolic activity decreases as an adaptive response to low internal oxygen in growing potato tubers. Biological Chemistry. 2000, 381: 723-740. 10.1515/BC.2000.093.PubMedView ArticleGoogle Scholar
- Stitt M, Lilley RM, Gerhart R, Heldt WW: Metabolite levels in specific wells and subcellular compartments of plant leaves. Met Enzymol. 1994, 174: 518-552.View ArticleGoogle Scholar
- Szopa J, Rose KM: Cleavage of the 190-kDa subunit of DNA-dependent RNA polymerase I yields small polypeptides capable of degrading DNA. J Biol Chem. 1986, 261: 9022-9028.PubMedGoogle Scholar
- Toroser D, Huber SC: Protein phosphorylation as a mechanism for osmotic-stress activation of sucrose-phosphate synthase in spinach leaves. Plant Physiol. 1997, 114: 947-955. 10.1104/pp.114.3.947.PubMedPubMed CentralView ArticleGoogle Scholar
- Müller-Röber B, Sonnewald U, Willmitzer L: Inhibition of the ADP-glucose pyrophosphorylase in transgenic potatoes leads to sugar-storing tubers and influences tuber formation and expression of tuber storage protein genes. EMBO J. 1992, 11: 1229-1238.PubMedPubMed CentralGoogle Scholar
- Sweetlove LJ, Burrell MM, ap Rees T: Starch metabolism in tubers of transgenic potato (Solanum tuberosum) with increased ADPglucose pyrophosphorylase. Biochem J. 1996, 320: 493-498.PubMedPubMed CentralView ArticleGoogle Scholar
- Takamiya S, Fukui T: Phosphoglucomutase from potato tubers. Chemical and catalytic properties. J Biochem. 1978, 84: 569-74.PubMedGoogle Scholar
- Abel GJ, Springer F, Willmitzer L, Kossmann J: Cloning and functional analysis of a cDNA encoding a novel 139 kDa starch synthase from potato (Solanum tuberosum L.). Plant J. 1996, 10: 981-991. 10.1046/j.1365-313X.1996.10060981.x.PubMedView ArticleGoogle Scholar
- Ainsworth C, Burrell M: Adenosine diphosphate glucose pyrophosphorylase genes in wheat: differential expression and gene mapping. Planta. 1995, 197: 1-10. 10.1007/BF00239933.PubMedView ArticleGoogle Scholar
- Zrenner R, Salanorbat M, Willmitzer L, Sonnewald U: Evidence of the crucial role of sucrose synthase for sink strength using transgenic potato plants (Solanum tuberosum L.). Plant J. 1995, 7: 97-107. 10.1046/j.1365-313X.1995.07010097.x.PubMedView ArticleGoogle Scholar
- Renz A, Merlo L, Stitt M: Partial purification from potato tubers of three fructokinases and three hexokinases which show differing organ and developmental specifity. Planta. 1993, 19: 156-165.Google Scholar
- Steup M: Starch degradation enzymes. Methods in Plant Biochemistry. London. Academic Press, 1990, 3: 103-128.Google Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.