Stevia rebaudiana
Its biological, chemical and agricultural properties

J.E. Brandle, A.N. Starratt and M. Gijzen

Agriculture and Agri-Food Canada,
Southern Crop Protection and Food Research Centre,
1391 Sandford St., London, Ontario N5V 4T3.

 

TABLE OF CONTENTS

Introduction
Biology, Ethnobotany and History of Cultivation
The Chemistry of Stevia Rebaudiana
Biosynthesis of the Sweet Glycosides
Functional and Sensory Properties of Steviol Glycoside Sweeteners
Commercial Extraction of Steviol Glycosides
Safety of Stevia Sweeteners
Crop Production
Conclusion
References

Stevia FAQ

eyes.gif (229 bytes)

INTRODUCTION

The worldwide demand for high potency sweeteners is expected to increase especially with the new practice of blending different sweeteners, the demand for alternatives is expected to increase. The sweet herb of Paraguay, Stevia rebaudiana Bertoni produces, in its leaves, just such an alternative with the added advantage that stevia sweeteners are natural plant products. In addition, the sweet steviol glycosides have functional and sensory properties superior to those of many other high potency sweeteners. Stevia is likely to become a major source of high potency sweetener for the growing natural food market in the future. The task at hand is to convert stevia from a wild plant to a modern crop well suited to efficient mechanized production. For Canada, the necessary steps are the development of seed, seedling and crop production system, including information on optimized crop inputs, weed and disease control, harvest and handling methods and a breeding program aimed at optimizing glycoside content and sensory characteristics. Understanding the biology of the stevia plants and the chemistry and biochemistry of the sweet glycosides are prerequisites for conversion of stevia to a modern crop. This review summarizes the existing literature and provides a baseline for new research.

BIOLOGY, ETHNOBOTANY AND HISTORY OF CULTIVATION

Stevia rebaudiana Bert. is one of 154 members of the genus Stevia and one of only two that produce sweet steviol glycosides (Robinson 1930; Soejarto et al. 1982, 1983). It is native to the valley of the Rio Monday in highlands of Paraguay, between 25 and 26 degrees south latitude, where it grows in sandy soils near streams (Katayama et al. 1976). Stevia was first brought to the attention of Europeans in 1887 when M.S. Bertoni learned of its unique properties from the Paraguayan Indians and Mestizos (Lewis, 1992). Various reports cited by Lewis (1992) indicate that it was long known to the Guarani Indians of the Paraguayan highlands who called it caá-êhê, meaning sweet herb. The leaves were used either to sweeten maté or as a general sweetening agent. Seeds were sent to England in 1942 in an unsuccessful attempt to establish production. The first reports of commercial cultivation in Paraguay were in 1964 (Katayama et al. 1976; Lewis, 1992). A large effort aimed at establishing stevia as a crop in Japan was begun by Sumida (1968). Since then, stevia has been introduced as a crop in a number of countries including Brazil, Korea, Mexico, United States, Indonesia, Tanzania, and, since 1990 Canada (Lee et al. 1979; Donalisio et al. 1982; Goenadi, 1983; Shock 1982; Saxena and Ming 1988; Brandle and Rosa 1992; Fors 1995). Currently stevia production is centered in China and the major market is in Japan (Kinghorn and Soejarto 1985). No large scale mechanized production has been established and stevia sweeteners are not yet found in mainstream food products in most countries of the world. Progress towards large scale commercialization has been slow, largely due to difficulties in producing the crop, the poor quality of stevia extracts and the absence of regulatory approvals essential for stevia sweeteners in the North American and European markets.

Stevia is a member of the Compositae family. It is a small shrubby perennial growing up to 65 cm tall, with sessile, oppositely arranged lanceolate to oblancoelate leaves, serrated above the middle. Trichome structures on the leaf surface are of two distinct sizes, one large (4-5 µm), one small (2.5 µm) (Shaffert and Chetobar 1994b). The flowers are small (7-15 mm), white and arranged in an irregular cyme. The seed is an achene with a feathery pappus (Robinson 1930).

Stevia is an obligate short day plant with a critical day length of about 13 h. Extensive variability within populations for day length sensitivity has been reported (Valio and Rocha 1966; Zaidan et al. 1980). Plants can initiate flowering after a minimum of four true leaves have been produced (Carneiro 1990). Sumida reported the results from a complete diallel cross with 8 parents and found that the amount of selfing ranged between 0 and 0.5%, while outcrossing ranged from 0.7 to 68.7%, indicating that some form of self-incompatibility system is operating (cited in Katayama et al. 1976). The reproductive anatomy of the male and female gametophytes is typical for angiosperms (Shaffert and Chetobar 1992, 1994a). Stevia is diploid and has 11 chromosome pairs, which is characteristic for most of the South American members of the genus (Frederico et al. 1996).

CROP PRODUCTION

Stevia plants can be propagated from cuttings or seed. Since germination rates are poor and seedlings very slow to establish it is best grown as an annual or perrenial transplanted crop. Clonal propagation is practical for small scale production, but is probably not economically viable for large scale stevia production where labor costs are high. The cost of producing vegetatively propagated transplants in Canada is high, so low cost transplants produced from seed is the only viable method on which to base stevia production in Canada. Only production as an annual is possible in most regions of Canada. The discussion of crop production in this review will therefore be limited to seed-based propagation of an annual transplanted crop.

In the temperate latitudes of the Northern hemisphere and South Western Ontario in Canada more specifically, the production cycle for annual stevia begins with the 6-7 week old plants grown from seed, in cells, in heated greenhouses. Seedlings are transplanted to the field in mid to late May. Fertilizer is banded along with the transplants. The crop is irrigated as required. Stevia is slow to establish under Canadian conditions and growth is sluggish until mid July. Most of the leaf yield is accumulated from July until mid to late September. The whole plant is harvested just above ground level, elevated into wagons and then dried. Following drying, the leaves are separated from the stems using a thesher. The leaves are then stored ready for processing.

Seed Production and Quality

Given stevia’s daylength requirements, seed production in the Northern hemisphere would be best situated between 20 and 30E N latitude. The crop could be transplanted in February or March and seed collected in late summer. Flowering under these conditions should occur between 54-104 d following transplanting, depending on the daylength sensitivity of the cultivars used for seed production (Katayama et al. 1979). One-thousand seed weights for stevia seed usually range between 0.15 and 0.30 g and, depending on plant density, seed yields of up to 8.1 kg ha-1 are possible (Carniero 1990). Seed germination is often poor and rates less than 50% are common (Miyazaki and Wantenabe 1974). Given the aforementioned conditions, seed produced on one ha could be enough to supply transplants for up to 200 ha of leaf production. Seed viability and yield are affected by growing conditions during pollination and seed filling. Excessive rainfall during pollination can affect both seed yield and germination (Carneiro 1990, Shuping and Shizhen 1995). Seed is best stored at 0E C, but even under low temperature conditions germination will still decline 50% over three years (Shuping and Shizhen 1995). Sealing of storage containers or using lower temperatures did not prevent the decrease in germination over time.

Cultural Practices

Planting densities ranging from 40,000 to 400,000 plants/ha have been tried in experiments conducted in Japan (Katayama et al. 1976). Leaf yield increased with increasing density up to 83,000 and 111,000 plants ha-1 for the first year of production. The concentration of stevioside in the leaves of stevia increases when the plants are grown under long days (Metvier and Viana 1979). Since glycoside synthesis is reduced at or just before flowering, delaying flowering with long days allows more time for glycoside accumulation. It follows that stevia production would be best situated in a long day environment where vegetative period is longer and steviol glycoside yields will be higher.

Fertility requirements for stevia grown as an annual crop are moderate. Results from Japan demonstrate that, at the point of maximum dry matter accumulation, stevia plants consist of 1.4% N, 0.3% P, and 2.4% K (Katayama et al. 1976). In Ontario total biomass production of 7500 kg ha -1 are possible and of that total, 26% would be roots, 35% stems, and 39% leaves (R. Beyaert pers. comm.). Based on the composition observed by Katayama (1976) such biomass would require approximately 105 kg N, 23 kg P and 180 kg K from both soil and fertilizer. The actual rates of application will vary according to soil type and production environment, and need to be optimized for each specific situation.

Two fungal diseases, Septoria steviae and Sclerotinia sclerotiorum, have been reported in stevia grown in Canada (Lovering and Reeleder 1996; Chang et al. 1997). Septoria disease was characterized by depressed, angular, shiny olive gray lesions, sometimes surrounded by a chlorotic halo, that rapidly coalesce. Sclerotinia disease was characterized by brown lesions on the stem, near the soil line, followed by wilting and eventually by the complete collapse of affected individuals. No means of controlling these diseases have yet been published. Since stevia is very slow to establish and does not compete well with weeds, herbicides or other means will be essential to control weed growth to produce ample yield and a clean crop. The herbicide trifluralin appears to be well tolerated by stevia (Katamaya 1979).

Stevia is harvested just prior to flowering when steviol glycoside content in the leaves is at its maximum (Sumida 1980, Xiang 1983). Following harvest the whole plant is dried and the leaves separated from the stems for further processing (Murai 1988). The stems have very low concentrations of sweet glycosides and are removed to minimize processing costs (Brandle and Rosa 1992). Drying stevia under artificial conditions is affected by a number of factors including loading rate, temperature, and ambient air conditions (Van Hooren and Lester 1992). The effect of drying conditions on glycoside levels or processing quality of the leaves has not been investigated.

Cultivar Development

A variety of plant breeding procedures have been used to improve leaf yield and rebaudioside A concentration in the leaves. Based on cultivar descriptions from Japan, China and Korea and our own work, it appears that sufficient genetic variability exists to make significant genetic gains in leaf yield, rebaudioside A content and the ratio of rebaudioside A to stevioside (Brandle and Rosa 1992; Lee et al. 1979 and 1982; Shizhen 1995; Shyu et al. 1994; Morita 1987). Brandle and Rosa (1992) found that the heritability of stevioside content to be high (83%), based on calculations from a group of half-sib families. Heritabilities for leaf yield (75 %) and leaf to stem ratio (83 %) were also substantial indicating that selection would be effective. Total sweet glycoside concentration in some lines from China was reported to be as high as 20.5%, and a rebaudioside A to stevioside ratio of 9:1 was disclosed in the Japanese patent literature (Shizhen 1995; Morita 1987). Two breeding methods reported by the latter authors were: phenotypic mass selection and, recurrent selection for phenotype where selected plants are intercrossed before another round of selection. Some cultivars such as the high rebaudioside A selection from Japan, and Suweon 2 and 11 from Korea are based on the selection of single plant and because of self-incompatibility they can only be reproduced vegetatively, which limits their utility.

Nakamura and Tamura (1985) studied a population of 300 random individuals and found that total glycoside concentrations at the seedling and harvest stages were not correlated suggesting that early selection for total glycosides would not be effective. However, the proportion of individual glycosides relative to the total was correlated between seedlings and mature plants making early selection for glycoside composition possible. The authors also observed a wide range of variation in the four main glycosides and found that dulcoside A and stevioside, and rebaudioside A and C, were positively correlated with each other. Stevioside and rebaudioside A, and dulcoside and rebaudioside C, were negatively correlated with each other. These correlations can be partially explained by the biosynthetic relationships between the individual glycosides because stevioside is the substrate for the synthesis of rebaudioside A, plants high in rebaudioside A will probably be low in stevioside (Shibata et al. 1991).

THE CHEMISTRY OF THE DITERPENE GLYCOSIDE SWEETENERS

The sweet diterpene glycosides of stevia have been the subject of a number of reviews (Kinghorn and Soejarto 1985, Crammer and Ikan 1986, and Hanson and De Oliveira 1993). Although interest in the chemistry of the sweet principles dates from very early in the century, significant progress towards chemical characterization was not made until 1931, with the isolation of stevioside (Bridel and Lavieille 1931a). Treatment of this substance with the digestive juice of a snail yielded three moles of glucose and one mole of steviol, while acid hydrolysis gave isosteviol (Bridel and Lavieille 1931b). Isosteviol was also obtained when steviol was heated in dilute sulfuric acid. Subsequent studies have led to the isolation of seven other sweet glycosides of steviol. Typical proportions, on a dry weight basis, for the four major glycosides found in the leaves of wild stevia plants is 0.3 % dulcoside, 0.6% rebaudioside C, 3.8 % rebaudioside A and 9.1 % stevioside.

Structure of steviol, isosteviol and stevioside

The structure, stereochemistry and absolute configuration of steviol and isosteviol were established, through a series of chemical reactions and correlations over 20 years after the pioneering work of Bridel and Lavieille (Mosettig and Nes, 1955; Dolder et al. 1960; Djerassi et al. 1961; Mosettig et al. 1963). Structures of these and other diterpenes and diterpene glucosides are presented in Fig. 1. Concurrent studies on the parent glycoside indicated that one D-glucopyranose residue, hydrolyzed under alkaline conditions yielding steviolbioside, was attached to a carboxyl group (Wood et al. 1955) while the other two were components of a sophorosyl group (Vis and Fletcher 1956) bound to the aglycone through a $-glycosidic linkage (Yamasaki et al. 1976). Support for the proposed stereochemistry was achieved by the synthetic transformation of steviol into stevioside (Ogawa et al. 1980). Earlier, several approaches to the in vitro synthesis of steviol had been reported (Cook and Knox 1970; Nakahara et al. 1971; Mori et al. 1972; Ziegler and Kloek 1977). Recently, spectroscopic data concerning stevioside and steviolbioside were published (Van Calsteren et al. 1993).

Other diterpenoid glycosides

Further investigation of extracts of S. rebaudiana leaves resulted in the isolation and identification of seven other sweet diterpenoid glycosides. Kohda et al. (1976) obtained the first two of these, rebaudiosides A and B, from methanol extracts together with the major sweet substance stevioside and steviolbioside, a minor constituent which was first prepared from stevioside by alkaline hydrolysis (Wood et al. 1955). Subsequently, it was suggested that rebaudioside B was an artifact formed from rebaudioside A during the isolation (Kaneda et al. 1977; Sakamoto et al. 1977b). Stevioside has been converted by enzymatic and chemical procedures to rebaudioside A (Kaneda et al. 1977). Further fractionation of leaf extracts led to the isolation and identification, which was aided by 13C NMR spectroscopy, of three other new sweet glycosides named rebaudioside C, D and E (Sakamoto et al. 1977a, 1977b). Both rebaudioside A and rebaudioside D could be converted to rebaudioside B by alkaline hydrolysis showing that only the ester functionality differed (Kohda et al. 1976; Sakamoto et al. 1977b). Dulcosides A and B, the latter having the same structure as rebaudioside C, were reported by another laboratory (Kobayashi et al. 1977).

Methods of diterpenoid glycoside analysis

A wide range of analytical techniques have been employed to assess the distribution and level of sweet diterpenoid glycosides in S. rebaudiana. These include thin layer chromatography (Tanaka 1982; Metivier and Viana 1979; Kinghorn et al. 1984; Nikolova-Damyanova et al. 1994), over pressured layer chromatography (Fullas et al. 1989), droplet counter-current chromatography (Kinghorn et al. 1982), and capillary electrophoresis (Liu and Li 1995; Mauri et al. 1996). Stevioside levels have also been determined enzymatically (Mizukami et al. 1982) and by near infrared reflectance spectroscopy (Nishiyama et al. 1992) in plant strains producing mainly stevioside. The most common analytical method, however, has been high performance liquid chromatography. Although separations have been also achieved using silica gel (Nikolova-Damyanova et al. 1994), hydroxyapatite (Kasai et al. 1987), hydrophilic (Hashimoto et al. 1978), and size exclusion (Ahmed and Dobberstein 1982a,1982b) columns, amino bonded columns have been used most frequently for the analysis of the sweet glycosides (Kinghorn et al. 1984; Liu and Li 1995; Makapugay et al. 1984; Striedner et al. 1991). Amino columns have also been used to measure stevioside and related glycosides in foods and beverages (Chang and Cook 1983; Fujinuma et al. 1986; Kitada et al. 1989). In our laboratories, a carbohydrate cartridge column with a propylamine bonded phase, has been used to analyze the diterpenoid glycosides in more than 4000 stevia leaf samples (W.A. Court unpublished). Stevioside and rebaudioside A have also been analyzed by HPLC after conversion to the p-bromophenacyl esters of steviolbioside and rebaudioside B (Ahmed et al. 1980).

Other constituents

In addition to the sweet diterpenoid glycosides, several other diterpenes have been isolated from stevia. Since these compounds may be part of the waste stream produced during stevia processing, their availability in large quantities could make them into valuble co-products. The first to be characterized were jhanol and austroinulin, previously obtained from other plants, and 6-O-acetylaustroinulin (Sholichin et al. 1980). Also reported were the triterpenes $-amyrin acetate and three esters of lupeol and the sterols stigmasterol and $-sitosterol, previously isolated from leaves by Nabeta et al. (1976). Jhanol, austroinulin, 6-O-acetylaustroinulin and 7-O-acetylaustroinulin as well as stevioside and rebaudioside A have been obtained from stevia flowers (Darise et al. 1983). Eight additional diterpenes, called sterebins A-H, have been isolated from leaves and identified (Oshima et al. 1986, 1988).

Other chemical constituents of stevia have been reported. Rajbhandari and Roberts (1983) identified six flavonoid glycosides in an aqueous methanol extract of leaves: apigenin-4'-O-glucoside, luteolin-7-O-glucoside, kaempferol-3-O-rhamnoside, quercitrin, quercetin-3-O-glucoside and quercetin-3-O-arabinoside and 5, 7, 3'-trihydroxy-3, 6, 4'-trimethoxyflavone (centaureidin). The major identified components in the essential oil were the sesquiterpenes $-caryophyllene, trans-$-farnesene, "-humulene, *-cadinene, caryophyllene oxide and nerolidol and the monoterpenes linalool, terpinen-4-ol and "-terpineol (Fujita et al. 1977). Later, Martelli et al. (1985) identified 54 components of a steam distillate of dried leaves from Brazil. Of these, caryophyllene oxide and spathulenol were the main components, totaling 43%. Interestingly, these substances were not the major components in an essential oil preparation from a fresh sample of cultivated stevia plants from Italy.

BIOSYNTHESIS OF THE SWEET GLYCOSIDES

Steviol glycosides are derived from the mevalonic acid pathway. This is a fundamental metabolic route that provides the two C5 building block molecules, isopentenyl pyrophosphate (IPP) and dimethylallyl pyrophosphate (DMAPP), that are required for synthesis of all isoprenoid compounds (Chappell 1995; McGarvey and Croteau 1995).

Steviol Biosynthesis from Geranylgeranyl Pyrophosphate

Steviol biosynthesis was first investigated over 30 years ago (Fig. 2) (Ruddat et al. 1965; Bennett et al., 1967; Hanson and White 1968). This early work established that the initial steps leading to the steviol glycosides from GGPP are identical to those in gibberellin biosynthesis. Thus, GGPP is converted to ent-copalyl pyrophosphate (CPP) by CPP synthase (also called ent-kaurene synthase A) and ent-kaurene is produced from CPP by ent-kaurene synthase (also called ent-kaurene synthase B). Subsequent oxidation of this product at the C-19 position to ent-kaurenoic acid is assumed to occur via the action of one or more P450 monooxygenases that have yet to be identified (Hedden and Kamiya, 1997). At this point the pathways to the steviol glycosides and the gibberellins diverge. Steviol is produced by further hydroxylation of ent-kaurenoic acid at the C-13 position. This ent-kaurenoic acid 13-hydroxylase has been purified from stevia leaf extracts and partially characterized (Kim et al., 1996a). The native enzyme is a 160 kD homotetramer that requires NADPH and O2 for catalysis.

The Glycan Side Chains

The two oxygenated functional groups of steviol, the C-19 carboxylate and the C-13 alcohol, provide attachment points for the sugar side chains that determine the identity of the 8 different glycosides identified to date. These glycan side chains are comprised predominately of glucose residues but may also contain rhamnose (Fig. 1). The biosynthetic sequence of glycosylations that give rise to the different glycan side chains is still in the early stages of elucidation. At least three distinct glucosyltransferase activities have been identified (Shibata et al. 1991, 1995). Two of these activities have been purified and characterized. Activity I transfers glucose from UDP-glucose to the 13-hydroxy position of steviol to afford steviolmonoside. Activity IIb has a much broader substrate specificity, using steviol, steviolmonoside, steviolbioside, or stevioside as substrate for further glucosylation by UDP-glucose (Shibata et al. 1995).

Compartmentation of Biosynthesis and Storage

Diterpene biosynthesis has been found to occur generally in plastids of plant cells (McGarvey and Croteau 1995; Hedden and Kamiya 1997). There is good evidence that steviol biosynthesis conforms to this pattern and is localized in leaf chloroplasts. High levels of HMG-CoA reductase activity can be extracted from isolated stevia chloroplasts and the ent-kaurenoic acid 13-hydroxylase that converts ent-kaurenoic acid to steviol was purified from the chloroplast stroma (Kim et al. 1996a, 1996b). In contrast, the UDP-glucosyl transferases performing the glycosylations on the steviol skeleton are operationally soluble enzymes, indicating that these reactions happen outside of the chloroplast. Steviol glycosides are transported to the cell vacuole where they are stored. The glycosides accumulate in stevia leaves where they may comprise from 10 to 20% of the leaf dry weight. Thus, a large fraction of total plant metabolism is committed to the synthesis of these structurally complex molecules. The conditions that favoured selection of such high diterpene glycoside producers are not known. Like other plant secondary metabolites, the steviol glycosides may function in a defensive capacity as feeding deterrents or anti-microbial agents against specific herbivores, pests, or pathogens.

FUNCTIONAL AND SENSORY PROPERTIES OF STEVIOL GLYCOSIDE SWEETENERS

Of the four major sweet diterpene glycoside sweeteners present in stevia leaves only two, stevioside and rebaudioside A, have had their physical and sensory properties well characterized. Stevioside and rebaudioside A were tested for stability in carbonated beverages and found to be both heat and pH stable (Chang and Cook 1983). However, rebaudioside A was subject to degradation upon long term exposure to sunlight. Kinghorn and Soejarto (1985) also cite numerous Japanese studies that demonstrate that stevioside is very stable.

Phillips (1989) has summarized the early sensory research. Stevioside was between 110 and 270 times sweeter than sucrose, rebaudioside A between 150 and 320, and rebaudioside C between 40 and 60. Dulcoside A was 30 times sweeter than sucrose. Rebaudioside A was the least astringent, the least bitter, had the least persistant aftertaste and was judged to have the most favourable sensory attributes of the four major steviol glycosides (Phillips 1989, Tanaka 1997). Dubois and Stephanson (1984) have also confirmed that rebaudioside A is less bitter than stevioside and demonstrated that the bitter notes in stevioside and rebaudioside A are an inherent property of the compounds and not necessarily the result of impurities in whole plant extracts. Relative to other high potency sweeteners such as apsartame, bitterness tends to increase with concentration for both stevioside and rebaudioside A (Schiffman et al. 1994). Both stevioside and rebaudioside A are synergistic in mixtures with other high potency sweeteners such as aspartame and are good candidates for inclusion in blends (Schiffman et al. 1995). Although specialty applications may exist for the other glycosides, increasing levels of rebaudioside A in stevia leaves is a clear objective for breeding work.

COMMERCIAL EXTRACTION OF STEVIOL GLYCOSIDES

Most of the commercial processing of stevia leaves occurs in Japan and there are dozens of patents describing methods for the extraction of steviol glycosides. Kinghorn and Soejarto (1985) have categorized the extraction patents into: those based on solvent (Haga et al. 1976), solvent plus a decolorizing agent (Ogawa 1980), adsorption chromatography (Itagaki and Ito 1979), ion exchange (Uneshi et al. 1977), and selective precipitation of individual glycosides (Matsushita and Kitahara 1981). Phillips (1989) has indicated that the most favoured extraction processes involve four steps: aqueous or solvent extraction, ion exchange, precipitation or coagulation with filtration, then crystallization and drying. New methods based on ultra-filtration have been disclosed recently (Tan and Ueki 1994).

SAFETY OF STEVIA SWEETENERS

Stevia sweeteners have a long history of use in South America and now in Japan and there are no reports of adverse effects. Nonetheless, the safety of stevia sweeteners has been the subject of controversy for a number of years (e.g. Bonvie et al. 1997, Pendergast 1991). Planas and Kuc (1968) reported that 5 % solution of stevia leaf extract had a strong anti-fertility effect in both male and female rats. Subsequent studies conducted to confirm this result have all been negative (Sincholle and Marcorelles 1989, Yodyingyuad and Bunyawong 1991). In studies of acute toxicity, a LD50 of 8.2 g kg-1 for a refined stevioside extract was cited by Katayama et al. (1979). An acceptable daily stevioside intake of 7.9 mg kg-1 was suggested by Xili et al. (1992). Yodyingyuad and Bunyawong (1991) reported that neither growth nor reproduction were affected in hamsters fed pure stevioside at levels up to 2.5 g kg-1 day-1 for 4 months. Stevioside and rebaudioside A are both non-cariogenic (Das et al. 1992).

Pezzuto and co-workers (1985) reported that metabolically activated steviol is mutagenic, a result that has been confirmed in another more recent study (Matsui et al. 1996). Kinghorn and Soejarto (1985) and Kinghorn (1992) conducted two reviews of the literature related to safety of stevia sweeteners and concluded that stevia leaves and stevioside are safe for human consumption. However, the activated steviol metabolite that is mutagenic has not yet been identified and it is not known if the activation of steviol actually occurs in humans (Procinska et al. 1991, Matsui et al. 1996). Matsui et al. (1996) concluded that further work is required to determine what risk steviol glycosides pose to humans.

CONCLUSION

Stevia represents a new opportunity for researchers and farmers alike. A great deal of information relating to production practices and disease control is required to optimize annual transplant production for Canada. Such basic things as herbicide and fungicides registration, optimum planting and harvest times, fertilizer recommendations are all essential. Since markets exist for stevia now, production and optimization must occur in parallel. The production of remarkably high levels of one class of secondary metabolite is of significant interest for chemists, biochemists and geneticists and may prove to be a foundation for the production of new metabolites in the future. Because the safety of stevia for human consumption remains controversial, there is a clear need for further experimentation with respect to the metabolic fate of steviol glycosides.

REFERENCES

Ahmed, M. S., Dobberstein, R. H. and Farnsworth, N. R. 1980. Stevia rebaudiana. I. Use of p-bromophenacyl bromide to enhance ultraviolet detection of water-soluble organic acids (steviolbioside and rebaudioside B) in high-performance liquid chromatographic analysis. J. Chromatogr. 192: 387-393.

Ahmed, M. S. and Dobberstein, R. H. 1982a. Stevia rebaudiana. II. High-performance liquid chromatographic separation and quantitation of stevioside, rebaudioside A and rebaudioside C. J. Chromatogr. 236: 523-526.

Ahmed, M. S. and Dobberstein, R. H. 1982b. Stevia rebaudiana. III. High-performance liquid chromatographic separation and quantitation of rebaudiosides B, D, and E, dulcoside A, and steviolbioside. J. Chromatogr. 245: 373-376.

Bennett, R. D., Lieber, E. R., and Heftmann, E. 1967. Biosynthesis of steviol from (-)-kaurene. Phytochemistry 6: 1107-1110.

Bonvie, L., Bonvie, B., and Gates, D. 1997. The stevia story, a tale of incredible sweetness and intrigue. B.E.D. Publications, Atlanta.

Brandle, J.E., and Rosa, N. 1992. Heritability for yield, leaf:stem ratio and stevioside content estimated from a landrace cultivar of Stevia rebaudiana. Can. J. Plant Sci. 72: 1263-1266.

Bridel, M. and Lavieille, R. 1931a. Le principe à saveur sucrée du Kaà-hê-é (Stevia rebaudiana) Bertoni. Bull. Soc. Chim. Biol. 13: 636-655.

Bridel, M. and Lavieille, R. 1931b. Le principe sucré du Kaà-hê-é (Stevia rebaudiana Bertoni). II. L’hydrolyse diastasique du stévioside. III. Le stéviol de l’hydrolyse diastasique et l’isostéviol de l’hydrolyse acide. Bull. Soc. Chim. Biol. 13: 781-796.

Carneiro, J.W.P. 1990. Stevia rebaudiana (Bert.) Bertoni, production of seed. M.Sc Thesis, State University of Maringa, Brazil (English abstr.).

Chang, S. S. and Cook, J. M. 1983. Stability studies of stevioside and rebaudioside A in carbonated beverages. J. Agric. Food Chem. 31: 409-412.

Chang, K.F., Howard, R.J. and Gaudiel R.G. 1997. First report of stevia as a host for Sclerotinia sclerotiorum. Plant Disease 81: 311.

Chappell, J. 1995. Biochemistry and molecular biology of the isoprenoid biosynthetic pathway in plants. Annu. Rev. Plant Physiol. Plant Mol. Biol. 46: 521-547.

Cook, I. F. and Knox, J. R. 1970. A synthesis of steviol. Tetrahedron Lett. 4091-4093.

Crammer, B. and Ikan, R. 1986. Sweet glycosides from the stevia plant. Chem. Brit. 22: 915-916.

Darise, M., Kohda, H., Mizutani, K., Kasai, R. and Tanaka, O. 1983. Chemical constituents of flowers of Stevia rebaudiana Bertoni. Agric. Biol. Chem. 47: 133-135.

Das, S., Das, A.K., Murphy, R.A., Punwani, I.C., Nasution, M.D., and Kinghorn, A.D. 1992. Evaluation of the cariogenic potential of the intense natural sweeteners stevioside and rebaudioside A. Caries Res. 26: 363-366.

Djerassi, C., Quitt, P., Mosettig, E., Cambie, R. C., Rutledge, P. S. and Briggs, L. H. 1961. Optical rotatory dispersion studies. LVIII. The complete absolute configurations of steviol, kaurene and the diterpene alkaloids of the garryfoline and atisine groups. J. Amer. Chem. Soc. 83: 3720-3722.

Dolder, F., Lichti, H., Mosettig, E. and Quitt, P. 1960. The structure and stereochemistry of steviol and isosteviol. J. Amer. Chem. Soc. 82: 246-247.

Donalisio, M.G.R., Duarte, F.R., Pinto, A.J.D.A., and Souza, C.J. 1982. Stevia rebaudiana. Agronomico 34: 65-68.

DuBois, G.E. and Stephenson, R.A. 1984. Diterpenoid sweeteners. Synthesis and sensory evaluation of stevioside analogues with improved organoleptic properties. J. Med. Chem 28:93-98.

Fors, A. 1995. A new character in the sweetener scenario. Sugar J. 58: 30.

Frederico, A.P., Ruas, P.M., Marinmorlaes, M.A., Ruas, C.F. and Nakajima, J.N. 1996. Chromosome studies in some Stevia (Compositae) species from southern Brazil. Braz. J. Genet. 19: 605-609.

Fujinuma, K., Saito, K., Nakazato, M., Kikuchi, Y., Ibe, A. and Nishima, T. 1986. Thin layer chromatographic detection and liquid chromatographic determination of stevioside and rebaudioside A in beverages and foods following reverse phase column chromatography. J. Assoc. Off. Anal. Chem. 69: 799-802.

Fujita, S., Taka, K. and Fujita, Y. 1977. Miscellaneous contributions to the essential oils of the plants from various territories. XLI. The components of the essential oil of Stevia rebaudiana. Yakugaku Zasshi 97: 692-694; Chem. Abstr. 87: 122621v (1977).

Fullas, F., Kim, J., Compadre, C. M. and Kinghorn, A. D. 1989. Separation of natural product sweetening agents using overpressured layer chromatography. J. Chromatogr. 464: 213-219.

Goenadi, D.H. 1983. Water tension and fertilization of Stevia rebaudiana Bertoni on Oxic Tropudalf (English abstr.). Menara Perkebunan. 51: 85-90.

Haga, T., Ise, R., and Kobayashi, T. 1976. A method for purifying stevioside (English abstr.). Jap. Patent 51-131900.

Hanson, J. R. and De Oliveira, B. H. 1993. Stevioside and related sweet diterpenoid glycosides. Nat. Prod. Rep. 10: 301-309.

Hanson, J.R., and White, A.F. 1968. Studies in terpenoid biosynthesis II. The biosynthesis of steviol. Phytochemistry 7: 595-597.

Hashimoto, Y., Moriyasu, M., Nakamura, S., Ishiguro, S. and Komuro, M. 1978. High-performance liquid chromatographic determination of Stevia components on a hydrophilic packed column. J. Chromatogr. 161: 403-405.

Hedden, P., and Kamiya, Y. 1997. Gibberellin biosynthesis: enzymes, genes and their regulation. Annu. Rev. Plant Physiol. Plant Mol. Biol. 48: 431-460.

Itagaki K., and Ito, T. 1979. Purification of stevioside (English abstr.). Jap. Patent 54-041898.

Kaneda, N., Kasai, R., Yamasaki, K. and Tanaka, O. 1977. Chemical studies on sweet diterpene-glycosides of Stevia rebaudiana: conversion of stevioside into rebaudioside-A. Chem. Pharm. Bull. 25: 2466-2467.

Kasai, R., Yamaguchi, H. and Tanaka, O. 1987. High-performance liquid chromatography of glycosides on a new type of hydroxyapatite column. J. Chromatogr. 407: 205-210.

Katayama O., Sumida, T, Hayashi, H. and Mitsuhashi H. 1976. The practical application of Stevia and research and development data (English translation). I.S.U. Company, Japan. 747 pp.

Kim, K.K., Sawa, Y., and Shibata, H. 1996a. Hydroxylation of ent-kaurenoic acid to steviol in Stevia rebaudiana Bertoni- Purification and partial characterization of the enzyme. Arch. Biochem. Biophys. 332: 223-230.

Kim, K.K., Yamashita, H., Sawa, Y., and Shibata, H. 1996b. A high activity of 3-hydroxy-3-methylglutaryl coenzyme A reductase in chloroplasts of Stevia rebaudiana Bertoni. Biosci. Biotech. Biochem. 60: 685-686.

Kinghorn, A.D. 1992. Food ingredient safety review: Stevia rebaudiana leaves. Herb Research Foundation, Boulder.

Kinghorn, A. D., Nanayakkara, N. P. D., Soejarto, D. D., Medon, P. J. and Kamath, S. 1982. Potential sweetening agents of plant origin. I. Purification of Stevia rebaudiana sweet constituents by droplet counter-current chromatography. J. Chromatogr. 237: 478-483.

Kinghorn, A. D. and Soejarto, D. D. 1985. Current status of stevioside as a sweetening agent for human use. Pages 1-52 in H. Wagner, H. Hikino and N. R. Farnsworth, eds. Economic and medicinal plant research. Academic Press, London.

Kinghorn, A. D., Soejarto, D. D., Nanayakkara, N. P. D., Compadre, C. M., Makapugay, H. C., Hovanec-Brown, J. M., Medon, P. J. and Kamath, S. K. 1984. A phytochemical screening procedure for sweet ent-kaurene glycosides in the genus Stevia. J. Nat. Prod. 47: 439-444.

Kitada, Y., Sasaki, M., Yamazoe, Y. and Nakazawa, H. 1989. Simultaneous determination of stevioside, rebaudioside A, and C and dulcoside A in foods by high-performance liquid chromatography. J. Chromatogr. 474: 447-451.

Kobayashi, M., Horikawa, S., Degrandi, I. H., Ueno, J. and Mitsuhashi, H. 1977. Dulcosides A and B, new diterpene glycosides from Stevia rebaudiana. Phytochemistry 16: 1405-1408.

Kohda, H., Kasai, R., Yamasaki, K., Murakami, K. and Tanaka, O. 1976. New sweet diterpene glucosides from Stevia rebaudiana. Phytochemistry 15: 981-983.

Lee, J.I., Kang, K.K., and Lee, E.U. 1979. Studies on new sweetening resource plant stevia (Stevia rebaudiana Bert.) in Korea. I. Effects of transplanting date shifting by cutting and seeding dates on agronomic characteristics and dry leaf yields of stevia (English abstr.). Res. Rep. ORD 21: 171-179.

Lee, J.I., Kang, K.H., Park, H.W., and Ham, Y.S. 1982. New high rebaudioside - A stevia variety "Suweon 11" (English abstr.). Res. Rep. ORD 24: 186-188.

Lewis, W.H. 1992. Early uses of Stevia rebaudiana (Asteraceae) leaves as a sweetener in Paraguay. Econ. Bot. 46: 336-337.

Liu, J. and Li, S. F. Y. 1995. Separation and determination of Stevia sweeteners by capillary electrophoresis and high performance liquid chromatography. J. Liq. Chromatogr. 18: 1703-1719.

Lovering, N.M. and Reeleder, R.D. 1996. First report of Septoria steviae on stevia (Stevia rebaudiana) in North America. Plant Disease 80: 959.

Makapugay, H. C., Nanayakkara, N. P. D. and Kinghorn, A. D. 1984. Improved high-performance liquid chromatographic separation of the Stevia rebaudiana sweet diterpene glycosides using linear gradient elution. J. Chromatogr. 283: 390-395.

Martelli, A., Frattini, C. and Chialva, F. 1985. Unusual essential oils with aromatic properties-I. Volatile components of Stevia rebaudiana Bertoni. Flav. Frag. J. 1: 3-7.

Matsui, M., Matsui, K., Kawasaki, Y., Oda, Y., Noguchi, T., Kitagawa, Y., Sawada, M., Hayashi, M., Nohmi, T., Yoshihira, K., Ishidate, M., Jr, and Sofuni, T. 1996. Evaluation of the genotoxicity of stevioside and steviol using six in vitro and one in vivo mutagenicity assays. Mutagenesis 11: 573-579.

Matsushita, K., and Kitahara, T. 1981 Separation of stevioside and rebaudioside A by crystallization (English abstr.). Jap. Patent 56-121454.

Mauri, P., Catalano, G., Gardana, C. and Pietta, P. 1996. Analysis of Stevia glycosides by capillary electrophoresis. Electrophoresis 17: 367-371.

McGarvey, D.J., and Croteau, R. 1995. Terpenoid metabolism. Plant Cell 7: 1015-1026.

Metivier, J. and Viana, A. M. 1979. Determination of microgram quantities of stevioside from leaves of Stevia rebaudiana Bert. by two-dimensional thin layer chromatography. J. Exp. Bot. 30: 805-810.

Miyazaki, Y., and Watanabe, H. 1974. Studies on the cultivation of Stevia rebaudiana Bertoni; On the propogation of the plant (English abstr.). Jap. J. Trop. Agric. 17: 154-157.

Mizukami, H., Shiiba, K. and Ohashi, H. 1982. Enzymatic determination of stevioside in Stevia rebaudiana. Phytochemistry 21: 1927-1930.

Mori, K., Nakahara, Y. and Matsui, M. 1972. Diterpenoid total synthesis-XIX. (±)-Steviol and erythroxydiol A: rearrangements in bicyclooctane compounds. Tetrahedron 28: 3217-3226.

Morita, T. 1987. Dried leaves (English abstr.). Jap. Patent 62-96025

Mosettig, E. and Nes, W. R. 1955. Stevioside. II. The structure of the aglucone. J. Org. Chem. 20: 884-899.

Mosettig, E., Beglinger, U., Dolder, F., Lichti, H., Quitt, P. and Waters, J. A. 1963. The absolute configuration of steviol and isosteviol. J. Amer. Chem. Soc. 85: 2305-2309.

Murai, N. 1988. Stevia drying system (English abstr.) Jap. Patent 63-258553.

Nabeta, K., Kasai, T. and Sugisawa, H. 1976. Phytosterol from the callus of Stevia rebaudiana. Agric. Biol. Chem. 40: 2103-2104.

Nakahara, Y., Mori, K. and Matsui, M. 1971. Diterpenoid total synthesis. Part XVI. Alternative synthetic routes to (±)-steviol and (±)-kaur-16-en-19-oic acid. Agric. Biol. Chem. 35: 918-928.

Nakamura, S. and Tamura, Y. 1985. Variations in the main glycosides of stevia. Jap. J. Trop. Agric. 29:109-115.

Nikolova-Damyanova, B., Bankova, V. and Popov, S. 1994. Separation and quantitation of stevioside and rebaudioside A in plant extracts by normal-phase high performance liquid chromatography and thin-layer chromatography: a comparison. Phytochem. Anal. 5: 81-85.

Nishiyama, P., Alvarez, M. and Vieira, L. G. E. 1992. Quantitative analysis of stevioside in the leaves of Stevia rebaudiana by near infrared reflectance spectroscopy. J. Sci. Food Agric. 59: 277-281.

Ogawa, T. 1980. Decolorization and purification of a stevia sweet component (English abstr.). Jap. Patent 55-111768.

Ogawa, T., Nozaki, M. and Matsui, M. 1980. Total synthesis of stevioside. Tetrahedron 36: 2641-2648.

Oshima, Y., Saito, J. and Hikino, H. 1986. Sterebins A, B, C and D, bisnorditerpenoids of Stevia rebaudiana leaves. Tetrahedron 42: 6443-6446.

Oshima, Y., Saito, J. and Hikino, H. 1988. Sterebins E, F, G and H, diterpenoids of Stevia rebaudiana leaves. Phytochemistry 27: 624-626.

Pendergast, W.R. 1991. GRAS Affirmation Petition Number 2G0390.

Pezzuto, J.M., Compadre, C.M., Swanson, S.M., Nanayakkara, N.P.D., and Kinghorn, A.D. 1985. Metabolically activated steviol, the aglycone of stevioside, is mutagenic. Proc. Natl. Acad. Sci. USA 82: 2478-2482.

Phillips, K.C. 1989. Stevia: steps in developing a new sweetener. Pages 1-43 in T.H. Grenby ed. Developments in sweeteners, Volume 3. Elsevier Applied Science, London.

Planas, G.M., and Kuc, J. 1968. Contraceptive properties of Stevia rebaudiana. Science. 162: 1007.

Procinska, E., Bridges, B.A., and Hanson, J.R. 1991. Interpretation of results with the 8-azaguanine resistance system in Salmonella typhimurium: no evidence for direct acting mutagenesis by 15-oxosteviol, a possible metabolite of steviol. Mutagenesis 6: 165-167.

Rajbhandari, A. and Roberts, M. F. 1983. The flavonoids of Stevia rebaudiana. J. Nat. Prod. 46: 194-195.

Robinson, B.L. 1930. Contributions from the Gray Herbarium of Harvard University. The Gray Herbarium of Harvard University, Cambridge.

Ruddat, M., Heftmann, E., and Lang, A. 1965. Biosynthesis of steviol. Arch. Biochem. Biophys. 110: 496-499.

Sakamoto, I., Yamasaki, K. and Tanaka, O. 1977a. Application of 13C NMR spectroscopy to chemistry of natural glycosides: rebaudioside-C, a new sweet diterpene glycoside of Stevia rebaudiana. Chem. Pharm. Bull. 25: 844-846.

Sakamoto, I., Yamasaki, K. and Tanaka, O. 1977b. Application of 13C NMR spectroscopy to chemistry of plant glycosides: rebaudiosides-D and -E, new sweet diterpene-glucosides of Stevia rebaudiana Bertoni. Chem. Pharm. Bull. 25: 3437-3439.

Saxena, N.C., and Ming, L.S. 1988. Preliminary harvesting characteristics of stevia. Phys. Prop. Agric. Mat. Prod. 3: 299-303.

Schiffman, S.S., Pecore, S.D., Booth, B.J., Losee, M.L., Carr, B.T., Sattely-Miller, E., Graham, B.G., and Warwick, Z.S. 1994. Adaptation of sweeteners in water and in tannic acid solutions. Phys. Behavior 55: 547-559.

Schiffman, S.S., Booth, B.J., Carr, B.T., Losee, M.L., Sattely-Miller, E., and Graham, B.G. 1995. Investigation of synergism in binary mixtures of sweeteners. Brain Res. Bull. 38: 105-120.

Schock, C.C. 1982. Experimental cultivation of Rebaudi's stevia in California. University of California Agronomy Progress Report No. 122.

Shaffert, E.E. and Chetobar, A.A. 1992. Development of the male gametophyte in Stevia rebaudiana (English abstr.). Buletinul Academiei de Schtintse A Republica Moldava 6: 3-9.

Shaffert, E.E. and Chetobar, A.A. 1994a. Development of the female gametophyte in Stevia rebaudiana (English translation). Buletinul Academiei de Schtintse A Republica Moldava 6: 10-18.

Shaffert, E.E. and Chetobar, A.A. 1994b. Structure, topography and onogeny of Stevia rebaudiana (English abstr.). Botanicheskii Zhurnal 79: 38-48.

Shibata, H., Sonoke, S., Ochiai, H., Nishihashi, H., and Yamada, M. 1991. Glycosylation of steviol and steviol-glucosides in extracts from Stevia rebaudiana Bertoni. Plant Physiol. 95: 152-156.

Shibata, H., Sawa, Y., Oka, T., Sonoke, S., Kim, K.K. and Yoshioka, M. 1995. Steviol and steviol-glycoside. Glucosyltransferase activities in Stevia rebaudiana Bertoni. Purification and partial characterization. Arch. Biochem. Biophys. 321: 390-396.

Shizhen, S. 1995. A study on good variety selection in Stevia rebaudiana. Scientia Agricultura Sinica 28: 37-41.

Shuping, C., and Shizhen, S. 1995. Study on storage technique of Stevia rebaudiana seed (English abstr.). Acta Agronomica Sinica 21: 102-105.

Shyu, YT, Liu, S.Y., Lu, H.Y., Wu, W.K. Su, C.G. 1994. Effects of harvesting dates on the charateristics, yield and sweet components of stevia (Stevia rebaudiana Bertoni) lines. J. Agric. Res. China 43:29-39.

Sholichin, M., Yamasaki, K., Miyama, R., Yahara, S. and Tanaka, O. 1980. Labdane-type diterpenes from Stevia rebaudiana. Phytochemistry 19: 326-327.

Sincholle, D. and Marcorelles, P. 1989. Study of the anti-androgenic activity of extracts of Stevia rebaudiana Bertoni (English abstr.). Med. Plants and Phytotherapy 23: 282-287.

Soejarto, D.D., Compadre, C.M., Medon, P.J., Kamath, S.K., and Kinghorn, A.D. 1983. Potential sweetening agents of plant origin. II. Field search for sweet-tasting Stevia species. Econ. Bot. 37: 71-79.

Soejarto, D.D., Kinghorn, A.D., and Farnsworth, N.R. 1982. Potential sweetening agents of plant origin. III. Organoleptic evaluation of stevia leaf herbarium samples for sweetness. J. Nat. Prod. 45: 590-599.

Striedner, J., Czygan, F.-C. and Braunegg, G. 1991. Contributions to the biotechnological production of sweeteners from Stevia rebaudiana Bertoni. I. A method for the serial analysis of diterpene glycosides by HPLC. Acta Biotechnol. 11: 495-499.

Sumida, T. 1968. Reports on Stevia rebaudiana Bertoni M. introduced from Brazil as a new sweetness resource in Japan. Misc. Pub. Hokkaido Natl. Exp. Sta. 2: 69-83.

Sumida, T. 1980. Studies on Stevia rebaudiana Bertoni as a new possible crop for sweetening resource in Japan (English summary). J. Cent. Agric. Exp. Stn. 31: 1-71.

Tan, S., and Ueki, H. 1994. Method for extracting and separating sweet substances of Stevia rebaudiana Bertoni (English abstr.). Jap. Patent 06-007108.

Tanaka, O. 1982. Steviol-glycosides: new natural sweeteners. Trends Anal. Chem. 1: 246-248.

Tanaka, O. 1997. Improvement of taste of natural sweeteners. Pure Appl. Chem. 69:675-683

Uneshi, H., Ise R., and Kobayashi, T. 1977. Purification of a stevia sweetening agent (English abstr.). Jap. Patent 54-030199.

Valio, I.F.M. and Rocha, R.F. 1966. Effect of photoperiod and growth regulators on growth and flowering of Stevia rebaudiana Bertoni. Jap. J. Crop Sci. 46:243-248.

Van Calsteren, M.-R., Bussière, Y. and Bissonnette, M. C. 1993. Spectroscopic characterization of two sweet glycosides from Stevia rebaudiana. Spectroscopy 11: 143-156.

Van Hooren, D.L., and Lester, H.R. 1992. Stevia drying in small scale bulk tobacco kilns. In Methods to utilize tobacco kilns for curing, drying and storage of alternate crops, final report. Ontario Ministry of Agriculture and Food, Delhi.

Vis, E. and Fletcher, H. G. 1956. Stevioside. IV. Evidence that stevioside is a sophoroside. J. Amer. Chem. Soc. 78: 4709-4710.

Wood, H. B., Allerton, R., Diehl, H. W. and Fletcher, H. G. 1955. Stevioside. I. The structure of the glucose moieties. J. Org. Chem. 20: 875-883.

Xiang, Z.P. 1983. Stevia (partial English translation). General Bureau of State Farms, Heilongjiang, China.

Xili, L., Chenggjiany, B.C., Eryi, X., Reiming, S., Yuengming, W., Haodong, S., and Zhiyan, H. 1992. Chronic oral toxicity and carcinogenicity study of stevioside in rats. Food Chem. Tox. 30: 957-965.

Yamasaki, K., Kohda, H., Kobayashi, T., Kasai, R. and Tanaka, O. 1976. Structures of stevia diterpene-glycosides: application of 13C NMR. Tetrahedron Lett. 1005-1008.

Yodyingyuad, V., and Bunyawong, S. 1991. Effects of stevioside on growth and reproduction. Human Reprod. 6: 158-165.

Zaidan, L.B.P., Dietrich, S.M.C., and Felippe, G.M. 1980. Effect of photoperiod on flowering and stevioside content in plants of Stevia rebaudiana Bertoni. Jap. J. Crop Sci. 49: 569-574.

Ziegler, F. E. and Kloek, J. A. 1977. The stereocontrolled photoaddition of allene to cyclopent-1-ene-1-carboxaldehydes. A total synthesis of (±)-steviol methyl ester and isosteviol methyl ester. Tetrahedron 33: 373-380.

eyes.gif (229 bytes)

|Top of Document | FAQ Table of Contents |SCPFRC HomePage | SCPFRC Site Map |

 

Last Revised: Saturday, January 29, 2000 11:36:01 AM