2,3(S)-oxidosqualene-cycloartenol cyclases (cycloartenol synthase).

The 2,3(S)-oxidosqualene (OS) cyclases compose a family of biocatalysts that convert (S)-2,3-oxidosqualene (OS) to polycyclic triterpenes. The mammalian (Abe and Prestwich, 1995) and fungal (Shi et al., 1994) OS cyclase (EC 5.4.99.7) produces lanosterol, precursor of cholesterol in vertebrates and of ergosterol in most fungi. The higher plant OS cyclase (EC 5.4.99.8) catalyzes the formation of cycloartenol, precursor of phytosterols (Benveniste, 1986; Nes, 1977). This latter enzyme must break 11 bonds and form 11 new ones to form cycloartenol, which is a pentacyclic cyclopropyl triterpene containing 9 chiral centers. In addition to cycloartenol synthase, higher plants contain other OS-cyclases converting OS into a vast array of pentacyclic triterpenoids (oleanane, ursane, lupane, baccharane, friedelane derivatives). The stereoelectronic factors that understate the catalytic mechanism of these reactions have been discussed elsewhere (Abe et al., 1993). The formation of lanosterol and cycloartenol is initiated in the chair-boat-chair-like conformation of OS whereas the formation of amyrins and related pentacyclic triterpenes is initiated in the chair-chair-chair-like conformation of OS. In all cases the proton-initiated cyclization is postulated to proceed through the following events : i) a series of antiperiplanar 1,2 additions ; 1,2 rearrangements and 1,2 eliminations ; ii) the formation of conformationally rigid and partially cyclized carbocationic intermediates ; iii) stabilization of the developing carbocationic centers on the substrate by negative point charges at the active site of the enzyme (Johnson et al., 1987). As suggested by several authors (Feil et al., 1996; Shi et al., 1994) the electron density required for carbocationic stabilization could arise from anionic and (or) aromatic residues. These cyclization intermediates could be stabilized by cation-Π interactions (Dougherty, 1996). The fact that OS mimics possessing positively charged nitrogen atoms in place of potential carbocation behave as potent inhibitors is consistent with the above views (Taton et al., 1992). Most prokaryotic organisms do not synthesize sterols, but many of them synthesize hopanoids that are derived from pentacyclic triterpenic hydrocarbons which originate from squalene cyclisation owing to squalene-hopene cyclases (Wendt et al., 1997). A 2,3-OS-lanosterol cyclase (lanosterol synthase) gene (ERG7) from S. cerevisiae was isolated and encoded a 83-kDa protein (Corey et al., 1996; Shi et al., 1994). Later on a splendid approach led to the isolation of an Arabidopsis cDNA (ATCYC) encoding a cycloartenol synthase (Corey et al., 1993). This was achieved by functional expression in a yeast mutant lacking lanosterol synthase (GL7) by the use of a chromatographic screen. This cDNA contained a 2277-bp open reading frame encoding a 86-kD protein which was about 35% identical with S. cerevisiae lanosterol synthase and remarkably 46% identity with a Rattus norvegicus lanosterol synthase (Abe and Prestwich, 1995) showing that the plant cycloartenol synthase has more identity with a mammalian than a fungal lanosterol synthase. A single mutation (adenine1362guanine) occurring on the Arabidopsis cycloartenol synthase gene has been shown to confer to cycloartenol synthase the ability to form 25% lanosterol and 21% parkeol in addition to cycloartenol. This mutation leads to a I454V change in the peptidic sequence (Hart et al., 1999). A yeast mutant (erg7) defective in lanosterol synthase was transformed with a plasmid harbouring the cycloartenol synthase cDNA. The transformed yeast was still auxotrophic to ergosterol because cycloartenol is not usable by yeast to make sterols. Erg7 did not need any more ergosterol if transformed with a cycloartenol synthase cDNA possessing the A1362G mutation (Hart et al., 1999). Likewise, a tyrosine-to-threonine mutation was shown to convert the Arabidopsis cycloartenol synthase synthase to an OS cyclase that forms lanosterol as its major product (Herrera et al., 2000). Such experiments have far-reaching evolutionary implications. The corresponding single gene (At2g07050) consists of 18 exons and 17 introns. The Arabidopsis genome sequencing program reveals the presence of a gene (AT3g45130) whose deduced polypeptide sequence possessed 62% identity with the cycloartenol synthase protein and appeared closest to cycloartenol synthase in a phylogenetic tree containing many of the triterpene synthases already known (Fig. 4). The function of the protein encoded by this gene is still unknown.

In recent years a breakthrough has been achieved in the field of triterpene synthases. A cDNA encoding β-amyrin synthase (PGAM) has been characterized in Panax ginseng. Expression of the cDNA in yeast led to formation of a polypeptide capable of converting OS into β-amyrin (Kushiro et al., 1998). A cDNA encoding a lupeol synthase (ATLUP1) has been identified in Arabidopsis after expression in S. cerevisiae (Herrera et al., 1998; Husselstein-Muller et al., 2001). The protein (ATLUP1) encoded by this cDNA was shown to convert OS into lupeol, minor triter-penoid compounds were also identified (Herrera et al.,1998). Another cDNA (ATLUP2) was subsequently cloned from Arabidopsis and expressed in S. cerevisiae (Husselstein-Muller et al., 2001; Kushiro et al., 2000). The transformed S. cerevisiae was shown to cyclize OS into α-, β-amyrins and lupeol (Husselstein-Muller et al., 2001). During parallell experiments performed in another laboratory, taraxasterol, Ψ-taraxasterol, bauerenol, multiflorenol, butyrospermol and tirrucalla-7,21-dienol were identified in addition to α- and β-amyrins and lupeol (Kushiro et al., 2000). Therefore the polypeptide (ATLUP2) encoded by this gene is a novel multifunctional triterpene synthase. Shuffling domain mutagenesis has been done on ATLUP1 and PGAM in order to investigate the region important for protein specificity. The second quarter from the N-terminus of the protein was shown to have a crucial importance in determining the enzymatic process toward lupeol or amyrin (Kushiro et al., 1999). The genome sequencing project has revealed a rather complex situation. ATLUP1 and ATLUP2 are representatives of a small family of five genes (ATLUP1-5), in addition seven genes (ATPEN1-7) whose deduced polypeptide sequences have about 55% identity with the ATLUP family and which could encode triterpene synthases have been also identified (Husselstein-Muller et al., 2001). All genes encoding demonstrated or postulated triterpene synthases have been gathered in the Table 2. Each genomic sequence is labeled with a code and is also characterized by the number of exons and introns. In order to obtain information on evolutionary relationships, a phylogenetic tree was constructed using a heuristic search (Doyle and Gaut, 2000) (Fig. 4). In this tree the prokaryotic hopane synthases from Alicyclobacillus (AAHOP) was considered as reference taxa. According to this tree, the seven pentacyclic triterpene synthases from Arabidopsis (ATPEN1to 7) form a group of genes clearly distinct from the five lupeol synthases (ATLUP1 to 5). Interestingly, the ATLUP subfamily also encompasses the two β-amyrin synthases of Panax ginseng (PGAM) and of Pisum sativum (PSAM) and is clearly distinct from the lupeol synthases from Olea europaea (OELUP) and Taraxacum officinalis (TOLUP) (Kushiro et al., 1999).

S-Adenosylmethionine-sterol-C-methyltransferases.

Sterols from fungi and higher plants differ from vertebrate sterols by the presence of an extra alkylgroup at C-24 (Nes, 2000). Whereas most fungi sterols possess a methyl group at C-24, higher plants contain both 24-methyl- and 24-ethyl sterols. This alkylation of the side chain is catalyzed by S-adenosylmethionine (AdoMet)-sterol-C-methyltransferases (SMTs). In S. cerevisiae, the SMT converts zymosterol into fecosterol (Moore and Gaylor, 1969). In higher plants (and therefore in Arabidopsis), the presence of 24-ethylsterols results from two distinct methyl-transfers from AdoMet (Nes, 2000; Rahier et al., 1984). According to the chemical structures of intermediates of plant sterol biosynthesis and substrate specificity studies, it is generally assumed that cycloartenol (Fig2){ label needed for fig[@id='i1543-8120-38-1-1-f202'] }{ label needed for fig[@id='i1543-8120-38-1-1-f203'] } is the substrate of the first methylation reaction, resulting in 24-methylene cycloartanol (Wojciechowski et al., 1973), whereas 24-methylene lophenol is the preferred substrate for the second methylation, yielding 24-ethylidene lophenol (Fonteneau et al., 1977). Because the chemical structures of 24-methylene cyclartanol and 24-methylene lophenol are very different, it has been suggested that the two methylation ractions would be catalyzed by two different enzymes (Rahier et al., 1986). However, since no plant SMT has been purified so far, the hypothesis of an unique plant SMT catalyzing both alkylations (Nes et al., 1991) should also be considered. The first SMT gene (ERG6) cloned was from S. cerevisiae (Gaber et al., 1989; Hardwick and Pelham, 1994). Later on complete identification was performed by enzymatic assays on the protein derived from ERG6 after expression in E. coli. According to these studies the best substrate of the recombinant enzyme was zymosterol which was methylated to give fecosterol in agreement with previous enzymatic assays performed on microsomes from WT S. cerevisiae (Venkatramesh et al., 1996). A SMT cDNA of 1411 bp has been cloned from an Arabidopsis cDNA library, the deduced amino acid sequence of this cDNA showed three conserved regions found in AdoMet-dependent methyltransferases (Kagan and Clarke, 1994) and 38% identity with ERG6. This cDNA was used to transform a wild-type S. cerevisiae as well as the yeast null mutant erg6, which is deficient in the SMT-zymosterol-C-24 methyltransferase. In both cases, several 24-ethyl and 24-ethylidene sterols were synthetized, indicating that the Arabidopsis cDNA encodes a plant SMT capable of performing two sequencial methylations at C24 and C24-1 of the yeast sterols (Husselstein et al., 1996). Microsomes from erg6 expressing the Arabidopsis SMT were shown to possess AdoMet-dependent sterol-C-methyltransferase activity. Delipidated preparations of these microsomes converted cycloartenol into 24-methylene cycloartanol and 24-methylene lophenol into 24-ethylidene lophenol. The catalytic efficiency of the expressed SMT was 17-times higher with 24-methylene lophenol than with cycloartenol. This result provides evidence that the Arabidopsis cDNA encodes a 24-methylene-lophenol-C-24¹-methyltransferase catalyzing the second methylation step of plant sterol biosynthesis (Bouvier-Navé et al., 1997). This cDNA was named ATSMT2-1. A second cDNA (ATSMT2-2) of 1249 bp was cloned and was shown to encode a protein of 359 amino acids, 82% identical with the protein deduced from ATSMT2-1. Meanwhile two cDNAs from Nicotiana tabacum (NTSMT2-1 and NTSMT2-2) and one from Oriza sativa (OSSMT2) were characterized and were shown to be about 80% identical to the Arabidopsis cDNAs. The cDNA NTSMT2-1 was expressed in erg6 and the corresponding protein was shown to convert 24-methylene lophenol into 24-ethylidene lophenol as efficiently as ATSMT2-1 (Bouvier-Navé et al., 1997). Meanwhile cDNAs from Glycine max (Shi et al., 1995; Shi et al., 1996), Ricinus communis (Bouvier-Navé et al., 1997), Zea mays (Grebenok et al., 1997), N. tabacum and O. sativa (Bouvier-Navé et al., 1998) and Arabidopsis (Diener et al., 2000; Schaeffer et al., 2001) were isolated and characterized. The proteins encoded by these cDNAs are about 80% identical in all possible combinations, but have only 40% identity with SMT2 and 48% identity with ERG6. They constitute therefore a group of cDNAs (SMT1) distinct of the group formed by SMT2. SMT1 from Z. mays (Grebenok et al., 1997), from Arabidopsis (Diener et al., 2000) and from N. tabacum (Bouvier-Navé et al., 1998) were shown to partially restore the abillity of erg6 to make ergosterol. The G.max SMT1 was expressed in E. coli and the recombinant protein was shown to alkylate lanosterol (an unnatural substrate in plants) to give eburicol (Shi et al., 1996). In the presence of AdoMet, delipidated microsomes from erg6 transformed with tobacco SMT1 efficiently converted cycloartenol into 24-methylene cycloartanol, but did not produce any 24-ethylidene lophenol upon incubation with 24-methylene lophenol. This demonstrated that cDNA NTSMT1 (and most probably the other plant SMT of the same group such as ATSMT1) encoded a cycloartenol-C24 methyltransferase (Bouvier-Navé et al., 1998). Sequence alignment of SMT1 and SMT2 reveal three highly conserved domains. One of them (LDXGCGXGGPXRXI) corresponds to the G-rich consensus motif described for all AdoMet-dependent methyltransferases (Kagan and Clarke, 1994). A second (IEATCHAP) and a third (YEW/F/YGWGXSFHF) motives are believed to be typical of methyltransferases acting on a sterol substrate (Bouvier-Navé et al., 1997; Nes, 2000). Whereas SMT2 possess a hydrophobic domain of approximately 25 amino acids at the N-terminal position, SMT1 are devoid of such a hydrophobic domain (Bouvier-Navé et al., 1997). As confirmed by the Arabidopsis sequencing project and the above results, the Arabidopsis genome contains three distinct genes (At5g13710, At1g20330, At1g76090) encoding sterol-C24 methyltransferases(ATSMT1, ATSMT21, ATSMT22 respectively). smt1 mutations, which lack SMT1, were isolated from a transposon Ac transgenic line (Diener et al., 2000). The smt1 plants have pleiotropic defects: poor growth and fertility, root sensitivity to Ca²⁺ ions, and a loss of proper embryo morphogenesis. smt1 was shown to have an altered sterol content. It accumulates cholesterol, has much less 24-ethyl sterols, but its campesterol content is similar to this in control plants, reflecting that methylation of endogenous sterols is still active even in the absence of any functional SMT1 present. Actually, if SMT1 were the only enzyme responsible in planta for the first methylation reaction of cycloartenol to produce 24-methylene cycloartanol, smt1 should be completely deficient for C-24 alkylation. Because the majority of sterols in smt1 plants are alkylated, SMT1 cannot be the only enzyme in Arabidopsis capable of the first C-24 methylation step (Diener et al., 2000). One explanation for the presence of 24-methylated sterols in smt1 is that in the absence of SMT1, these methylations would be performed by SMT21 or SMT22 (that do not ordinarily perform this reaction in the wild type because of their preference for 24-methylene lophenol) even though at a much slower rate. The expression of SMT2 and SMT1 was also studied in plants (Schaeffer et al., 2000; Schaeffer et al., 2001; Schaller et al., 1998). The expression of ATSMT21 was modulated in 35S : :SMT21 Arabidopsis in order to study its physiological function. Plants overexpressing the transgene accumulated sitosterol at the expense of campesterol. These plants displayed a reduced stature and growth that could be restored by brassinosteroid treatment. Plants showing co-suppression of SMT21 were characterized by a high campesterol content and a depletion in sitosterol. Pleiotropic effects on development such as reduced growth, increased branching, and low fertility of high campesterol plants were not modified by exogenous brassinosteroids, indicative of specific sterol requirements to promote normal development. Thus ATSMT21 has a crucial role in balancing the ratio of campesterol to sitosterol in order to satisfy both growth requirements and membrane integrity (Schaeffer et al., 2001).

4,4-dimethyl sterol and 4α-methyl sterol 4-demethylation.

The passage of 24-methylene cyclartanol to end-pathway sterols involves removal of two methyls at position 4 and one methyl at position 14. The steps involved in these operations are depicted in Fig.2.{ label needed for fig[@id='i1543-8120-38-1-1-f202'] }{ label needed for fig[@id='i1543-8120-38-1-1-f203'] } The enzymatic system operating in the removal of the two methyls at C-4 in plants presents profound differences with the fungal or mammalian systems (Pascal et al., 1990; Pascal et al., 1993). In contrast to animals and fungi where the two C-4-methyl group are sequentially removed, a series of results have unequivocally established that two distinct oxidative systems are involved in the removal of the first and the second C4-methyl of phytosterol precursors. The first will act on 24-methylene cycloartanol whereas the second will operate on 24-methylene and 24-ethylidene lophenol (Fig 2){ label needed for fig[@id='i1543-8120-38-1-1-f202'] }{ label needed for fig[@id='i1543-8120-38-1-1-f203'] }. In the case of the first enzymatic system it has been shown that the oxidative conversion of 24-methylene cycloartanol to cycloeucalenol exhibits similar cofactor requirements, and inhibitor sensitivity as do corresponding animal systems. The demethylation is specific for the C-4α methyl group and is initiated by the C-4 methyl oxidase, which converts the methyl group to the alcohol, the aldehyde and finally to the carboxylic acid. This sequential oxidation was shown to require NADH, oxygen and cytochrome b5 as an electron carrier between the terminal oxidase and NADH. It is not inhibited by CO but is susceptible to cyanide, indicating that a cytochrome P-450 is not involved. In the next reaction, the carboxyl group is removed by a second enzyme, the C4 decarboxylase acting on 4α-carboxy-4β,14α-dimethyl-9β,19-cyclo-5α–ergost-24(24¹)-en-3β–ol and resulting in formation of cycloeucalenone possessing a keto group at C-3 (Rondet et al., 1999). A third enzyme, 3-keto reductase, then reduces the keto group of cycloeucalenone to give cycloeucalenol (Pascal et al., 1994). This process is repeated with the second methyl group but the substrate is then 24-methylene or 24-ethylidene lophenol and the product is then episterol or Δ⁷-avenasterol, respectively. Cloning and characterization of ERG25, the S. cerevisiae gene encoding C4-methyl oxidase has been reported (Bard et al., 1996). This gene encodes a 309-amino acid polypeptide showing a C-terminal endoplasmic reticulum (ER) retrieval signal KKXX and three histidine-rich clusters found in eukaryotic membrane bound fatty acid desaturases (Shanklin et al., 1994). A human homologue of ERG25 was cloned and sequenced. It encodes a polypeptide of 293 amino acids with an identity of 38% to ERG25 and contains histidine clusters (Li and Kaplan, 1996). Very recently the functional identification of sterol-4α-methyl oxidase cDNAs from A. thaliana was achieved by complementation of a yeast erg25 mutant lacking sterol-4α-methyl oxidation (Darnet el al., 2001).

Cycloeucalenol obtusifoliol isomerase.

One of the most striking event occurring during sterol biosynthesis is the opening of the cyclopropane ring of cycleucalenol to give obtusifoliol, a step that is restricted to the plant kingdom and catalyzed by an enzyme, the cycloeucalenol-obtusifoliol isomerase or cyclopropyl sterol isomerase (CPI), the catalytic mechanism of which has been thoroughly studied (Heintz and Benveniste, 1974; Rahier et al., 1989) (Fig. 2){ label needed for fig[@id='i1543-8120-38-1-1-f202'] }{ label needed for fig[@id='i1543-8120-38-1-1-f203'] }. Photosynthetic eukaryotes and certain non photosynthetic protists such as Acantamoeba polyphaga (Raederstorff and Rohmer, 1987) or Dictyostelium discoidum (Godzina et al., 2000; Nes et al., 1990) use CPI (EC 5.5.1.9) to convert pentacyclic cyclo-propyl sterols to tetracyclic end-pathway sterols. Arabidopsis CPI was cloned by functional complementation of a S. cerevisiae mutant (Lovato et al., 2000). Expression of an Arabidopsis cycloartenol synthase cDNA in a S. cerevisiae lanosterol mutant (erg7) provided a sterol auxotroph because cycloartenol is not usable by yeast to make ergosterol. This yeast strain was transformed with an Arabidopsis expression library constructed in a yeast vector (pFL61) and sterol prototrophs were selected. A strain accumulating biosynthetic ergosterol was obtained. The novel phenotype was conferred by an Arabidopsis cDNA (CPI) that encoded a 36-kDa protein of 280 amino acids. It was assumed that the S. cerevisiae sterol C4 demethylase complex (Erg25p, Erg26p, and Erg27p) that normally metabolize lanosterol would have sufficiently broad substrate specificity to accept its isomer cycloartenol. Thus cycloartenol would be demethylated at C4 (at least partially) to give small amounts of 31-nor-cycloartenol which was shown to be readily transformed into 31-nor lanosterol (Heintz and Benveniste, 1974), which could then enter the normal yeast sterol pathway (Lovato et al., 2000). CPI is encoded by a unique gene (At 5g50375) possessing 8 exons.

Obtusifoliol-14α-demethylase.

In animals and fungi, the 14α–methyl group is the first of the C14 and C4 methyls to be removed; however in higher plants, the 14α–methyl is removed after one C-4 methyl has disappeared (Fig 2){ label needed for fig[@id='i1543-8120-38-1-1-f202'] }{ label needed for fig[@id='i1543-8120-38-1-1-f203'] }. The mechanism of the 14α–methyl removal involves two oxidation steps leading to an alcohol, then an aldehyde at C-29 and a further oxidative step involving a deformylation leading to formic acid and the sterol product with a typical 8,14-diene (Aoyama et al., 1987). The three steps are catalyzed by a single enzyme, which has been shown to be a cytochrome P-450 (Trzaskos et al., 1986). Lanosterol is the substrate of this enzyme in S. cerevisiae and in mammals (Aoyama et al., 1987; Shyadehi et al., 1996), eburicol would be the preferred substrate in filamentous fungi (Delye et al., 1998), while obtusifoliol is the substrate in higher plants (Taton and Rahier, 1991). Much attention has been payed to the 14α–demethylase since the enzyme is the target of a vast array of compounds having antimycotic effect and used in agriculture (Benveniste and Rahier, 1992) and medicine (Vanden Bossche and Janssen, 1992). These compounds, which are derivatives of pyridine, pyrimidine, imidazole, triazole…interact by their nitrogen sp2 doublet with the protohemic iron of cytochrome P-450 and hamper the access to oxygen. As shown above, the plant pathway differs from fungal and animal pathways downstream of 2(3)-oxidosqualene. No lanosterol is present in plants to serve as substrate for the 14-demethylation step. It is obtusifoliol that is the substrate for 14-demethylation. A thorough enzymological study has defined the stuctural requirements of this enzyme, which was shown to be remarkably specific for the structure of obtusifoliol and which does not use lanosterol (Taton and Rahier, 1991). A panoply of azole derivatives were shown to inhibit this enzyme ; some of them, developed as herbicides, were shown to be specific to obtusifoliol-14-demethylase (OBT14DM) (Benveniste and Rahier, 1992; Salmon et al., 1992). Tobacco calli resistant to phytotoxic azole derivatives have been isolated in mutagenesis experiments. The mechanism of resistance consists of an overproduction of sterols, which is not due to OBT14DM overproduction or modification but to an increase of HMGR enzymatic activity (Gondet et al., 1992; Schaller et al., 1994). cDNAs encoding lanosterol, eburicol and obtusifoliol 14-demethylases have been isolated from mammals (Aoyama et al., 1994), fungi (Kalb et al., 1986) and plants (Bak et al., 1997; Cabello-Hurtado et al., 1999) respectively. They shared a remarkable amino acid identity ranging from 38% to 65% though they belong to widely diverging species. Therefore they were classified in the same family, which is CYP51 (Nelson et al., 1996). A functional Sorghum bicolor OBT14DM was cloned and expressed at high levels in E. coli. The recombinant enzyme was shown to catalyze efficiently the 14α–demethylation of obtusifoliol (Bak et al., 1997). Likewise a Triticum vulgare OBT14DM was expressed in a S. cerevisiae mutant (erg11) defective in lanosterol 14-demethylase. Appropriate engineering of the TvOBT14DM cDNA and of the recipient erg11 mutant allowed to optimize expression (Cabello-Hurtado et al., 1999). Experimental structural informations on the active sites of the fungal, plant, and mammalian CYP51 would greatly facilitate developing more efficient antifungal drugs. However all forms of CYP51 were membrane-bound microsomal enzymes which complicates structural studies of this protein by X-ray crystallography. A soluble CYP51 ortholog has been discovered recently in Mycobacterium tuberculosis (Bellamine et al., 1999). It has been shown to demethylate lanosterol and obtusifoliol and to be inhibited by azole antifungals. E. coli-expressed MTCYP51 has been recently crystallized in the presence of fluconazole and a crystal structure at 2.2 A has been reported (Podust et al., 2001). This new structure provides a basis for rational design of more efficacious antifungal agents or new herbicides (Salmon et al., 1992; Grausem et al., 1995) as well as insight into the molecular mechanism of P450 catalysis. Arabidopsis genome sequencing has revealed the existence of two genes (At2g17330, At1g11680) encoding proteins having 65–75 % identity with an already characterized OBT14DM from Sorghum bicolor (Bak et al., 1997). Both genes possess two exons and an intron. The cDNA (ATCYP51) corresponding to At1g11680 has been cloned and has been shown to be able to sustain growth of the erg11 mutant suggesting ATCYP51 to be a functional sterol 14α–demethylase. Arabidopsis plants were transformed with AtCYP51 in antisense orientation. The resulting transgenic plants showed a semi-dwarf phenotype in the early growth stage. Their obtusifoliol content increased while campesterol and campestanol levels were unchanged (Kushiro et al., 2001). As their 24-ethyl sterols content was not reported, it is still not possible to draw conclusions as to the link between growth reduction and sterol biosynthesis inhibition in these transgenic plants.

Δ^8,14-sterol-Δ¹⁴-reductase.

4α,14α-dimethyl-5α-ergosta-8,14,24(24¹)-trien-3β–ol is the product of the C14 demethylation of obtusifoliol in plants. The following step is the hydrogenation by NADPH of the Δ¹⁴ double bond to give fecosterol (4α–methyl-5α–ergosta-8,24(24¹)-dien-3β–ol) (Fig. 2){ label needed for fig[@id='i1543-8120-38-1-1-f202'] }{ label needed for fig[@id='i1543-8120-38-1-1-f203'] }. The product of the C14 demethylase reaction in S. cerevisiae, 4,4-dimethyl-cholesta-8,14,24-trienol, is reduced at the C-14 position to form 4,4-dimethylcholesta-8,24-dienol by the action of the product of the ERG24 gene (Lorenz and Parks, 1992; Marcireau et al., 1992). ERG24 encoded a protein of 438 amino acids. The C14 reductase is inhibited by Fenpropidine and Fenpropimorph, two fungicides used in agriculture (Baloch and Mercer, 1987). By chromosomal gene disruption a S. cerevisiae defective in 14-reductase has been constructed. This strain was shown to grow in aerobiosis if it beared an additional mutation allowing sterol uptake. In this last growth condition, the cells required a sparking ergosterol supplementation and accumulated 5α-ergosta-8,14-dienol as the end-product of the sterol pathway (Marcireau et al., 1992). Most interestingly it has been shown that the human lamin B receptor exhibited sterol C-14-reductase activity in S. cerevisiae (Silve et al., 1998). In fact, the sterol C14 reduction step and ergosterol prototrophy were restored in lamin B receptor-producing erg24 transformants which lack endogenous C14-reductase. C14 reductase was studied in plants. Rubus fruticosus suspension cell cultures were highly susceptible to A25822B, an azasterol antimycotic agent and accumulated 5α–stigmasta-8,14-dien-3β–ol and 5α–stigmasta-8,14, Z-24(24¹)-trien-3–ol at the expense of Δ5-end pathway sterols (Schmitt et al., 1980). An enzymatic assay for 8,14-sterol 14-reductase was devised allowing to characterize this enzyme and to study its inhibition by analogues of a presumptive carbo-cationic intermediate of the reduction reaction (Taton et al., 1989). Cloning of the gene (FACKEL) encoding this enzyme was performed recently through the isolation of dwarf mutants (EMS and TDNA insertion mutants). FACK-EL (At 3g52940) was isolated and was shown to encode a predicted integral membrane protein of 369 amino acids with eight to nine transmembrane segments related to the vertebrate lamin receptor and several sterol C-14 reduc-tases including S. cerevisiae sterol C-14 reductase (Jang et al., 2000; Schrick et al., 2000). The Arabidopsis protein possessed a signature motif (LLXSGYWGXXRH) of sterol reductases. Functional evidence that FACKEL encoded a sterol C-14 reductase was provided by complementation of erg24 (Schrick et al., 2000). GC/MS analysis confirmed that fk mutations lead to accumulation of Δ8,14-sterol intermediates in the biosynthetic pathway preceding the C-14 reductase step. The sterol profile of fk calli was similar to that of plant cells treated with A25822B (Schmitt et al., 1980; Schaller et al., 1994). The fk mutation resulted also in reduction of brassinosteroid (BRs) content (Jang et al., 2000). However, unlike other BR-deficient mutants, the defect of hypotyl elongation could not be overcome by exogenous BRs (Jang et al., 2000; Schrick et al., 2000). Thorough microscopical and cytological observations indicated that mutations in the FACKEL gene affect body organization of the Arabidopsis seedlings and that FACKEL was required for cell division and expansion and was involved in proper organization of the embryo. These results indicated a novel role for sterols in the embryogenesis of plants (Clouse, 2000).

Δ⁸-Δ⁷-sterol isomerase.

When the 14α–methyl group is removed and the 14 double bond is reduced, the resulting Δ⁸-sterols are isomerized to Δ⁷-sterols in mammals, fungi, and higher plants. This process is catalyzed by a Δ⁸-Δ⁷-isomerase. The reaction involves two steps : first a protonation of the 8 double bond leading to an intermediate bearing a carbocation at C8 then the elimination of a proton at C7 leads to the Δ⁷-sterol (Akhtar et al., 1970; Goad et al., 1969). From enzymatic assays and biogenetic considerations it appears that zymosterol, fecosterol and 4α–methyl-5α–stigmasta-8, Z-24(24¹)-dien-3β–ol are the substrates of this enzyme in vertebrates (Yamaga and Gaylor, 1978), S. cerevisiae (Yabuzaki et al., 1979) and higher plants (Taton et al., 1987) respectively. A mutant (erg2) defective in Δ⁸-Δ⁷-sterol isomerase was described for S. cerevisiae (Barton et al., 1974). The erg2 mutation leads to the accumulation of sterols containing the Δ⁸-double bond. ERG2, the gene encoding the Δ⁸-Δ⁷-sterol isomerase (SI) was cloned by functional complementation of erg2 (Arthington et al., 1991). Later, SI-encoding genes were isolated from the rice blast fungus Magnaporthe grisea and the maize pathogen Ustilago maydis (Keon et al., 1994). Genetic and biochemical evidence showed that ERG2 would encode an enzyme catalyzing conversion of Δ⁸-sterols to Δ⁷-sterols. Recently a S. cerevisiae mutant defective in the internalization step of endocytosis was shown to contain defects in ERG2 leading to a lack of Δ⁸-Δ⁷-isomerase activity (Munn et al., 1999). A murine SI encoding cDNA has been cloned by functional complementation of the corresponding deficiency (erg2) in S. cerevisiae. The amino acid sequence deduced from the cDNA open reading frame was shown to be highly similar to human emopamil-binding protein (EBP), a protein which is the target for neuroprotective drugs (Silve et al., 1996). A yeast strain in which the SI coding sequence has been replaced by that of human EBP or its murine homologue, recovered the ability to convert Δ⁸-sterols to Δ⁷-sterols both in vivo and in vitro. Interestingly, the amino acid sequence deduced from the murine (SI) or human (EBP) failed to reveal any striking similarity with S. cerevisiae Erg2p (13% identity). Mutations in the gene encoding Homo sapiens SI were shown to cause X-linked dominant Conradi-Hunermann syndrome (Braverman et al., 1999). Alanine scanning mutagenesis was used to identify residues in the four putative transmembrane α-helices of human EBP that are required for Δ⁸-Δ⁷-sterol isomerase catalytical activity and binding of inhibitors. Out of 64 ala-nine mutants of EBP mutants H77A, E81A, T126A, N194A, W197A, contained less than 10% end-pathway 5,7-sterols. Therefore amino acids H77, E81, T126, N194 and W197 should play an important role in sterol Δ⁸-Δ⁷ isomerization (Moebius et al., 1999). An Arabidopsis Δ⁸-Δ⁷-sterol isomerase cDNA has been isolated by functional complementation of the corresponding S. cerevisiae sterol mutant (erg2). The full length Arabidopsis cDNA that complement the erg2 mutation contained an open reading frame encoding a protein of 223 amino acids sharing 35% amino acid identity to the Mus musculus SI and the H. sapiens EBP and very low identity (less than 15%) with Erg2p. The sigma ligands, haloperidol, ifenprodil and verapamil inhibited the production of ergosterol in wild-type S. cerevisiae and in the erg2 mutant complemented with the Arabidopsis SI (Grebenok et al., 1998). The Arabidopsis protein contained three transmembrane segments and presented several structural and biochemical similarities with the mammalian EBP. It is encoded by an unique gene (At1g20050) possessing 4 exons and 3 introns.

Δ⁷-sterol-C5(6)-desaturase.

Δ⁷-Sterol products of the Δ⁸-Δ⁷-sterol isomerase are transformed into Δ⁵-sterols through two reactions : the first one involves a desatura-tion step at C5 leading to a Δ^5,7-sterol, then the Δ⁷-double bond of Δ^5,7-sterols is reduced to give Δ⁵-sterols (Fig. 2){ label needed for fig[@id='i1543-8120-38-1-1-f202'] }{ label needed for fig[@id='i1543-8120-38-1-1-f203'] }. Insertion of the 5,6-double bond has been shown to involve stereospecific removal of the 5 (4-proR in MVA) and 6 (5-proS in MVA) hydrogen atoms during ergosterol biosynthesis in S. cerevisiae (Bimpson et al., 1969). The same stereospecificity is seen during the insertion of the 5,6-double bond during sterol biosynthesis in rat liver, higher plants and Ochromonas malhamensis (Goodwin, 1979). The close similarity of fatty acid desaturation in rat liver microsomes to the introduction of the sterol 5,6-double bond has been pointed out (Reddy et al., 1977). Both systems require NADH and molecular oxygen, and involve a cyanide-sensitive factor ; they both abstract cis-oriented hydrogens, occur in the microsomes and are inhibited by cyanide and thiol-blocking agents, but not by carbon monoxide. Further evidence of this came witth the demonstration of the participation of cytochrome b5 in the conversion of cholest-7-en-3-ol into cholesta-5,7-dien-3-ol (Osumi et al., 1979). The characterization of a Δ7-sterol C5(6)-desaturase from Zea mays has been reported (Taton and Rahier, 1996). This desaturase presents features similar to those reported for rat liver and yeast. It is strongly inhibited by cyanide, is sensitive to 1,10-phenanthroline and to salicylhydroxamic acid, but is insensitive to carbon monoxide, thereby suggesting the involvment of a metal ion, presumably iron, in an enzyme-bound form in the desaturing system (Taton and Rahier, 1996). More recently the ERG3 gene from S. cerevisiae has been cloned by complementation of an erg3 mutant defective in C5-sterol desaturase. The functional gene contained an open reading frame of 365 amino acids. Gene disruption demonstrated that ERG3 is not essential for cell viability (Arthington et al., 1991). A nuclear and recessive mutant of Arabidopsis affected in sterol biosynthesis (ste1) has been isolated and identified. This mutant accumulated Δ⁷-sterols (24R)-24-ethyl-5α-cholest-7-en-3-ol, and (24ξ)-24-methyl-5-cholest-7-en-3β-ol at the expense of the normally occurring campesterol and sitosterol. It has been suggested that ste1 is defective in the sterol-C5-desat-urase (Gachotte et al., 1995). To check this hypothesis ste1 was transformed with ERG3 encoding a Δ⁷-sterol-C5-desaturase from yeast, which resulted in partial recovery of wild-type sterol composition. To definitely identify ste1, homologous complementation was necessary. To this end an Arabidopsis cDNA encoding a Δ⁷-sterol-C5-desat-urase was isolated and characterized by functional complementation of erg3. This was achieved by transformation of erg3 with an Arabidopsis cDNA library inserted in a yeast vector (pFL61). Transformants were screened for cycloheximide resistance and resistant clones were analyzed to determine their sterol profile. The presence of ergosterol was detected in one clone in which a plasmid containing a cDNA of 1141bp was found. The 1141 cDNA allowed the deduction of an open reading frame of 843 bp encoding a 281 amino acid polypeptide (Gachotte et al., 1996). Three histidine-rich motifs (HX₃H, HX₂HH and HX₂HH) and three transmembrane segment were found in the Arabidopsis polypeptide and are also present in Erg3p as well as in Nicotiana tabacum (Husselstein et al., 1999) and Homo sapiens (Husselstein et al., 1999; Matsushima et al., 1996; Nishi et al., 2000) orthologues. Histidine-rich motifs are also characteristic of many membrane-bound fatty acid desaturases from higher plants (Shanklin et al., 1994). Overexpression of the Arabidopsis desaturase cDNA driven by a 35S promoter in transgenic ste1 plants led to full complementation of the mutant. This result demonstrated that STE1 was the impaired component in the desaturation system. The ste1-derived open reading frame has been cloned by RT-PCR. Alignment of the wild-type with the ste1 derived protein sequences revealed a single amino acid substitution : T114 in the wild-type is changed to I114 in Ste1p. The presence of this mutation in the mutant STE1 genomic sequence demonstrated that the change of the T114 to I was necessary and sufficient to create the leaky allele ste1 (Husselstein et al., 1999). The role of 15 residues in the reaction catalyzed by Arabidopsis Δ⁷-sterol-C5(6)-desaturase (5-DES) was investigated using site-directed mutagenesis and expression of the mutated enzymes in an erg3 S. cerevisiae strain defective in 5-DES. One group of mutants was affected in the eight invariant histidine residues from three histidine-rich motifs. Replacement of these residues by leucine completely eliminated the desaturase enzymatic activity both in vivo and in vitro (Taton et al., 2000) in agreement with the hypothesis that the function of histidine-rich motifs would be to provide the ligands for a presumed catalytic Fe center, as previously proposed (Shanklin et al., 1994). Another group of mutants was affected in residue 114 based on previous observations indicating that mutant T114I (ste1) was deficient in 5-DES. It was shown that the enzyme T114I had an 8-fold higher Km and 10-fold reduced catalytic efficiency. Conversely, the functionally conservative substituted mutant enzyme T114S displayed a 28-fold higher Vmax value and an 8-fold higher Km value than the wild-type enzyme. The data suggested that T114 strongly affected the reactivity of the desaturase and gave clues to get engineered 5-DES with much higher performances (Taton et al., 2000). Deuterated 7-cholestenol analogues were used as mechanistic probes for wild-type and mutated Δ⁷-sterol-C5(6)-desaturase. Deuterium kinetic isotopic effects for the removal of 6α- and 5α-hydrogens were measured. The observed pattern of isotope effects allowed Rahier (2000) to propose a mechanism for the desaturation of cholest-7-en-3β-ol. The Arabidopsis 5-DES considered above is encoded by one gene (At3g02580). Sequencing of Arabidopsis genome has revealed the existence of a second gene (At3g02590), the deduced protein sequence of it having 80% identity with Ste1p. Both genes possess three exons and two introns. Screening of about 50,000 M2 seeds of an EMS mutant population allowed the isolation of 43 dwarf mutants. Two of them (dwf7-1 and dwf7-2) were biochemically complemented by brassinolide (BR) and early BR biosynthetic precursors. Furthermore, results from feeding studies with ¹³C-labeled MVA and mevastatin and from sterol analysis suggested that the defective step was specifically the Δ⁷-sterol C5(6) desaturation. Sequencing revealed a premature stop codon in exon1 (dwf7-2) and in exon 3 (dwf7-1) of the the 5-DES gene confirming that dwf7-1 and dwf7-2 were null alleles of STE1. This work showed for the first time that the reduction of BR biosynthesis in dwf7 was due to a shortage of substrate sterols (campesterol) and was the direct cause of the dwarf phenotype (Choe et al., 1999b). An extremely dwarf mutant (bul1-1) of Arabidopsis was recently isolated and shown to contain as much as 90% of Δ⁷-sterols and less than 2% of Δ⁵-sterols. It was therefore defective in the Δ⁷-sterol-C5-desaturation step leading to brassinosteroid biosynthesis. Cellular characterization and rescue experiments with brassinosteroids demonstrated the involvment of the 5-DES in brassinosteroid-dependent plant growth processes (Catterou et al., 2001a). Indirect immunofluorescence of α-tubulin in bul1-1 revealed a total lack of the parallel microtubule organization that is typical of elongating cells in the wild-type. Rescue experiments with brassi-nosteroids and subsequent molecular analyses suggested that a brassinosteroid-responsive pathway exists, which allows microtubule nucleation/organization and cell elongation without activation of tubulin gene expression (Catterou et al., 2001b).

Δ^5,7-sterol Δ⁷-reductase (Δ7-SR) catalyzes the reduction of the Δ⁷-double bond of the Δ^5,7-sterols into Δ⁵-sterols. This step occurs only in vertebrates and higher plants. A microsomal preparation from seedlings of Zea mays catalyzed the NADPH dependent reduction of the Δ ⁷-bond of Δ^5,7-cholestadienol (Taton and Rahier, 1991). Novel 6-aza-B-homosteroids were shown to strongly inhibit (Δ⁷-SR) and to behave as analogues of a high energy carbocationic intermediate occurring during the reaction (Rahier and Taton, 1996). The gene encoding the Δ⁷-SR was cloned by transformation of wild-type S. cerevisiae with a cDNA library of Arabidopsis constructed in the yeast vector pFL61 and the subsequent selection of cells producing Δ⁵-sterols at the expense of ergosterol (a Δ^5,7-sterol) by nystatin selection. These cells were selected due to their resistance to nystatin, a polyene fungicide that is highly toxic to ergosterol producing cells. This clever strategy allowed recovery of a plasmid bearing a 1290-bp cDNA open reading frame, which encoded a protein of 430 amino acids that had significant sequence identity (32%) with Arabidopsis sterol Δ¹⁴-reductase and the previously reported LLXSGWWGXXRH signature of sterol reductases. Cholesta-5,7-dien-3β-ol was shown to be reduced in vitro to cholesterol by an enzymic preparation from a yeast strain expressing the Arabidopsis (Δ⁷-SR) (Lecain et al., 1996). Screening of a population of dwarf mutants led to a series of mutants (dwf5) presenting a defect in the gene encoding the Δ⁷-SR. dwf5 plants display the characteristic dwarf phenotype typical of BR mutants. This phenotype included small, round, dark-green leaves, and short stems, pedicels, and petioles. dwf5 mutants were biochemically complemented with exogenous BRs. Metabolite tracing with ¹³C-labeled precursors in dwf5 and sterol analysis suggested a deficiency in a Δ⁷-SR activity. In particular sterol analysis showed that Δ^5,7-campestenol (a possible substrate of Δ⁷-SR) accumulated. Surprisingly, the major compound analyzed was shown to be 5α-ergost-7-en 3β-ol. To explain this result authors suggested that a Δ⁵-reductase (det2) acting downstream of campesterol could reduce the Δ⁵ double bond of Δ^5,7-sterols which accumulated in dwf5. Deficiency in Δ7-SR activity was verified by DNA sequencing showing that all six independent alleles contained loss-of-function mutations in the Δ7-SR gene. The dwf5 plant could be restored to wild type by ectopic overexpression of the wild-type copy of the gene (Choe et al., 2000). This gene (At1g50430) was shown to contain 13 exons and 12 introns. The Smith-Lemli-Opitz syndrome (SLOS) is an inborn disorder of sterol metabolism. All patients suffer from mental retardation. The SLOS gene has been shown to be a Δ⁷-SR (EC 1.3.1.21) required for the de novo cholesterol biosynthesis. The protein encoded by the Homo sapiens Δ⁷-SR has 35% identity with the Arabidopsis Δ⁷-SR (Moebius et al., 1998). Results showed also that defects in the Δ⁷-SR gene (several missense, nonsense, and splice site mutations) caused the SLOS (Fitzky et al., 1998).

Δ⁵-sterol Δ²⁴-reductase(isomerase) catalyzes the reduction of the Δ²⁴ double bond of the side chain of sterols. This reaction uses a substrate possessing one double bond in animals and in higher plants. In animals this substrate is desmosterol, a Δ²⁴⁽²⁵⁾ sterol, whereas in higher plants, substrates are 24-methylene cholesterol and isofucosterol (Fig. 2){ label needed for fig[@id='i1543-8120-38-1-1-f202'] }{ label needed for fig[@id='i1543-8120-38-1-1-f203'] } and Δ24(24¹)-sterols are probably isomerized in Δ²⁴⁽²⁵⁾-sterols prior to be reduced. However, reduction of the Δ²⁴ double bond proceeds on sterols possessing two conjugated double bonds such as ergosta-5,7,22,24-tetraen-3β-ol in S. cerevisiae and other organisms producing ergosterol. The ERG4 gene provides the enzyme that reduces the double bond at C24(24¹), the final step in ergosterol biosynthesis. Disruption of ERG4 led to a mutant (erg4) which was able to grow similarly to the wild-type showing that the C24 reductase was not essential for viability (Lai et al., 1994). As discussed earlier (Lees et al., 1995), the sterols accumulated in erg4 mutants (e.g. ergosta-5,7,22,24-tetraen-3β-ol) are similar in structure to ergosterol and could fulfil functions normally attributed to ergosterol. The diminuto mutant (dim) was initially isolated as a slowly growing dwarf Arabidopsis mutant with greatly reduced fertility (Klahre et al., 1998). The DIM gene was cloned, and genomic analysis and gene expression studies strongly suggested that dim did not produce any DIM protein. The DIM gene (AT3g19820), also referred to as DWF1 (Choe et al., 1999b) or CBB1 (Kauschmann et al., 1996), is composed of two exons and one intron. Both the mutant phenotype and gene expression could be rescued by the addition of exogenous BRs. Analysis of endogenous sterols demonstrated that dim accumulated 24-methylene cholesterol but was deficient in campesterol, an earlier precursor of BR and in BRs as well. Feeding experiments using deuterium-labeled 24-methyl-enecholesterol and 24-methyl desmosterol confirmed that DIM/DWF1 is involved in both the isomerization and reduction of the 24(241) bond and encoded a sterol C24(241) reductase isomerase (S24REDISO). Transient expression of a green fluorescent protein-DIM/DWF1 fusion protein and biochemical experiments showed that DIM/DWF1 is an integral membrane protein that most probably is associated with the ER (Klahre et al., 1998). Several dwf1 alleles were also characterized. 7 of 10 dwf1 mutations were shown to directly affect a flavin adenin dinucleotide binding domain conserved in various oxidoreductases (Choe et al., 1999b). The proteic sequence of S24REDISO from Arabidopsis was shown to have 41% identity with an Homo sapiens ortholog (seladin-1) but no significant identity with ERG4. No ortholog of S24REDI has been reported in the S. cerevisiae genome. Thus the C24 reduction step seems to be performed by completely different enzymatic systems in higher plants and animals on one hand and in S. cerevisiae (and probably most fungi) on the other hand. The human DIM/DWARF1 homolog seladin-1 has been shown to confer resistance to Alzheimer's disease-associated neurodegeneration and oxidative stress (Greeve et al., 2000). This exciting result would attribute a novel role of cholesterol in neurodegenerative diseases. However the involvment of seladin-1 in cholesterol biosynthesis has not been demonstrated so far. Finally mutations in the 3β-hydroxysterol Δ²⁴-reductase gene were shown to cause desmosterolosis, an autosomal recessive disorder of cholesterol biosynthesis (Waterham et al., 2001).

Sterol-Δ²²-desaturase.

Ergosterol from S. cerevisiae, most fungi and several algae, and stigmasterol : (24S)-24-ethyl-cholesta-5, E-22-dien-3β-ol from most higher plants possess a double bond at C-22. Δ²²-sterols are not present in vertebrates. This double bond results from a desaturation step. This step is the antepenultimate during ergosterol biosynthesis, it is probably the last step of plant sterol biosynthesis. The substrate of Δ²²-desaturase is ergosta-5,7,24(24¹)-trien-3β-ol in yeast, which is transformed into ergosta-5,7,22,24(24¹)-tetraen-3-ol by yeast microsomes. This reaction has been shown to involve molecular oxygen, NADPH, and is inhibited by CO and metyrapone. Thus it involves a cytchrome P-450 species (Hata et al., 1983). The gene (ERG5) encoding this reaction has been recently cloned by complementation of an erg5 mutant (Skaggs et al., 1996). The deduced amino acid sequence (538 amino acid residues) presented general features common to most cytochrome P-450 open reading frames and exhibits the highest homology with some animal cytochrome P-450 proteins of the family 2. Surprisingly, the highest homology was not with CYP51A1 (lanosterol-14-demethylase) (Skaggs et al., 1996). Thus ERG5 is the first member of the CYP61 family. Enzymatic properties and inhibition by azole antifungal agents of CYP61 have been studied. Results revealed CYP61 to have a similar affinity to azole drugs (fluconazole, keto-conazole) when compared with data available for CYP51 (Kelly et al., 1997). The results of gene disruption demonstrated that ERG5 is not essential for cell viability suggesting that the Δ22 would not be essential. Most biosynthetic studies show that sitosterol would be the substrate for a C-22 desaturase leading to stigmasterol (Benveniste, 1986; Nes, 1977). Very little is known about this step in higher plants, since the in vitro conversion of sitosterol to stigmasterol has never been shown enzymatically. Arabidopsis is remarkable among higher plants since it was shown to contain brassicasterol (ergosta-5, E-22-dien-3-ol) in addition to stigmasterol, indicating that both 24-methyl and 24-ethyl sterols could be substrates of the C-22 desaturase. No cDNA encoding this proteins from Arabidopsis (or any other higher plant) has been reported so far.

Sterol esterification.

Steryl esters are present in all plants (Dyas and Goad, 1993) and are most often localized in the cytoplam of plant cells. They accumulate also as lipid bodies in the elaioplasts of the tapetum in developing Brassica napus anthers (Hernandez-Pinzon et al., 1999; Wu et al., 1999). In most cases sterols are esterified by fatty acids but in some plants (Oriza sativa) sterols are esterified by phenylpropanoids and especially by ferulic acid (Akihisa et al., 2000). A large number of studies have established that phytosterol and phytostanol fatty acid esters have serum cholesterol-lowering properties and are inhibitors of cholesterol absorption in human small intestine (Gylling et al., 1999; Jones, 1999; Normén et al., 2000). Triterpene and phytosteryl ferulates from rice bran have been shown to have anti-inflammatory effects against 12-O-tetradecanoylphorbol-13-acetate-induced inflammation in mice (Akihisa et al., 2000). Two enzymatic systems are involved in sterol esterification : In mammals cellular cholesterol is esterified by a fatty acid CoA derivative and this step is catalyzed by an acylCoA cholesterol acyltransferase (ACAT) (Farese Jr, 1998; Lin et al., 1999; Yang et al., 1997), whereas blood cholesterol is esterified by a fatty acid from lecithin using a lecithin cholesterol acyltransferase (LCAT) (Jonas, 2000; Peelman et al., 1999). In S. cerevisiae ergosterol is esterified by two polypeptides encoded by two ACAT related genes (Yang et al., 1996). Deletion of both ACAT genes resulted in a viable cell with undetectable esterified sterol (Yang et al., 1996). ACAT and LCAT are completely different proteins and their aminoacid sequences have no significant identity. The enzymatic system operating in higher plants is still not clearly defined. The reaction seems to be associated with the microsomal fraction that is able to convert phytosterols into steryl esters (Bouvier-Navé and Benveniste, 1995). However, several acyl donors : triacylglycerol (Zimowski and Wojciechowski, 1981), diacylglycerol (Garcia and Mudd, 1978), and lecithin (Bouvier-Navé and Benveniste, 1995; Garcia and Mudd, 1978) have been reported so far. Still, no cDNA encoding a sterol acyltransferase has been characterized. A polypeptide from Arabidopsis possessing 25% identity with the human ACAT1 was shown to be in fact a diacylglycerol acylCoA acyltransferase (DGAT) (Bouvier-Navé et al., 2000). The Arabidopsis genome sequencing program has revealed the existence of several candidate genes encoding proteins having significant identity (higher than 25%) with human LCAT.

Sterol glycosylation.

Extensive reviews on sterol glycosylation have been published (Ullmann et al., 1993; Wojciechowski, 1991). This reaction consists of the reaction of free sterols with UDP-glucose to give sterylglyco-sides and UDP in the presence of a UDP-glucose :sterol glucosyltransferase. This reaction has been shown to be associated with membranes in higher plants and more precisely with the plasma membrane in Zea mays (Hartmann-Bouillon and Benveniste, 1978). Such a reaction plays an important role in eukaryotic organisms. It is obvious that the attachment of a glycosyl moiety to the sterol backbone alters the physical properties of this lipid. Such changes have been studied with artificial membranes (Grunwald, 1975; Webb et al., 1995). To evaluate the impact of these changes in the living cell a genetic approach would be needed. For this purpose isolation and characterization of sterol glycosyltransferases from eukaryotes have been undertaken. A purified enzyme (Warnecke and Heinz, 1994) has been used for the cloning of a corresponding cDNA from oat. Amino acid sequences derived from the amino terminus of the purified protein and from peptides of a trypsin digestion were used to construct oligonucleotide primers for PCR experiments. Screening of oat and Arabidopsis cDNA libraries with amplified labeled DNA fragments resulted in the isolation of sterol glucosyltransferase-specific cDNAs with inserts lenghts of ca. 2.3 kb for both plants. These cDNAs encode polypeptides of 608 (oat) and 637 (Arabidopsis) amino acid residues with molecular masses of 66kDa and 69kDa, respectively (Warnecke et al., 1997). Genes from S. cerevisiae, Pichia pastoris, Candida albicans, Dyctiostelium discoidum (Warnecke et al., 1999) and cDNAs from oat (Avena sativa) and Arabidopsis (Warnecke et al., 1997) have been cloned and were expressed in E. coli. In vitro enzyme assays with cell-free extracts of transgenic E. coli strains showed that the genes encoded UDP-glucose :sterol glucosyltransferases which can use different sterols such as cholesterol, sitosterol, and ergosterol as sterol acceptors. The genes from Arabidopsis (At3g07020 and At1g43620) are composed of 14 exons and 13 introns.

Conversion of campesterol into brassinosteroids will be developed in another chapter of this book.