Functional Characterization of a Hydroxyacid/Alcohol Hydroxycinnamoyl Transferase Produced by the Liverwort Marchantia emarginata

The aerial organs of most terrestrial plants are covered by a hydrophobic protective cuticle. The main constituent of the cuticle is the lipid polyester cutin, which is composed of aliphatic and aromatic domains. The aliphatic component is a polyester between fatty acid/alcohol and hydroxycinnamoyl acid. The BAHD/HxxxD family enzymes are central to the synthesis of these polyesters. The nature of this class of enzymes in bryophytes has not been explored to date. Here, a gene encoding a fatty ω-hydroxyacid/fatty alcohol hydroxycinnamoyl transferase (HFT) has been isolated from the liverwort Marchantia emarginata and has been functionally characterized. Experiments based on recombinant protein showed that the enzyme uses ω-hydroxy fatty acids or primary alcohols as its acyl acceptor and various hydroxycinnamoyl-CoAs—preferentially feruloyl-CoA and caffeoyl-CoA—as acyl donors at least in vitro. The transient expression of a MeHFT-GFP fusion transgene in the Nicotiana benthamiana leaf demonstrated that MeHFT is directed to the cytoplasm, suggesting that the feruloylation of cutin monomers takes place there.


Introduction
The evolution of plants from marine/aquatic to terrestrial organisms has necessitated the development of a protective outer coat, primarily to prevent water loss [1][2][3]. The material making up this coat typically contains substantial quantities of the polymers cutin and suberin [1,4,5]. Cutin has a high content of the C16 fatty acid ferulic acid and the C18 fatty acid p-coumaric acid linked by esterification to glycerol [1,5,6]. Although cutin is primarily an acylglycerol polymer, varying amounts of certain aromatics (ferulic acid, coumaric acid and caffeic acid) feature in some cutins [1].
The enzymes responsible for acylation belong to the large BAHD/HXXXD acyltransferase family [7], almost all the members of which harbor both the HxxxD and the DFGWG motif. The HxxxD sequence is thought to be involved in enzyme catalysis [8], the DFGWG motif is distal to the active site in space and appears to have a structural function [9,10]. Three functional classes of these enzymes have been identified, namely the alcohol acetyltransferases [11][12][13], the anthocyanin/flavonoid acyltransferases [14][15][16][17][18] and the hydroxycinnamoyl transferases [19][20][21]. Their molecular masses range from 48 to 55 kDa [10]. The enzyme hydroxycinnamoyl-CoA:ω-hydroxyacid/fatty alcohol transferase (HHT) catalyzes the formation of aromatic esters in lipidic polymers. Its activity has been noted in many plant species, both angiosperms and gymnosperms [22,23]. The Arabidopsis thaliana BAHD/HXXXD family acyltransferase, encoded by the gene At5g41040, has been shown to have HHT activity [20,21] and is employed in the formation of suberin aromatics. The suppression of a potato homolog of At5g41040 reduces both the ferulate ester and ω-hydroxy fatty acid contents of suberin,   T  T  T  T  G  T   I  I  I  I  I AtASFT  430  AtDCF  426  AtFACT  432  PtFHT  438  StFHT  470  MeHFT   T  T  T  T  T

Functional Analysis
The molecular mass of the recombinant MeHFT protein, as estimated from its migration through an SDS polyacrylamide gel was ~71 kDa (including the 20.4 kDa His-tag) (Figure 3), which is in line with that of most BAHD acyltransferases. The experiments run to test its ability to accept a range of thioester donors (p-coumaroyl CoA, caffeoyl CoA and feruloyl CoA) and acyl acceptors (16-hydroxypalmitic acid, hexadecanoic acid and a range of primary alcohols [C6, C7, C10, C12, C14, C16, C20, C22]) showed that when recombinant MeHFT was provided with feruloyl CoA and 1-dodecanol, a single prominent HPLC peak was observed ( Figure 4A). MS/MS analysis of this reaction product revealed it to be a molecular ion [M+H] + with an m/z of 363.3, consistent with it being a complex of ferulate with C12 ( Figure 4B). The presence of an additional fragment with an m/z of 177.1 implied the presence of a feruloyl moiety in the reaction product. No products were generated from a control reaction run with the protein obtained from the culture of E. coli carrying an empty pET32a plasmid ( Figure 4A). When C10 was provided as the acyl acceptor, the activity of the recombinant MeHFT provided with caffeoyl CoA as a substrate was only ~38% of that recorded when feruloyl CoA was provided and ~43% when using p-coumaroyl CoA ( Table 1). The data implied that the preferred acyl donor of MeHFT was feruloyl CoA. With feruloyl-CoA as the acyl donor, a comparison of 15 aliphatic substrates as potential acyl acceptors (Table 1) showed that 1-decanol, 1-dodecanol and 1-tetradecanol were similarly effective as acceptors. The recombinant enzyme showed a level of activity when provided with the short-to-mid-chain fatty alcohols (C6, C7, C10, C12, C14) but none when provided with the long chain fatty alcohols (C20, C22).

Functional Analysis
The molecular mass of the recombinant MeHFT protein, as estimated from its migration through an SDS polyacrylamide gel was~71 kDa (including the 20.4 kDa His-tag) (Figure 3), which is in line with that of most BAHD acyltransferases. The experiments run to test its ability to accept a range of thioester donors (p-coumaroyl CoA, caffeoyl CoA and feruloyl CoA) and acyl acceptors (16-hydroxypalmitic acid, hexadecanoic acid and a range of primary alcohols [C6, C7, C10, C12, C14, C16, C20, C22]) showed that when recombinant MeHFT was provided with feruloyl CoA and 1-dodecanol, a single prominent HPLC peak was observed ( Figure 4A). MS/MS analysis of this reaction product revealed it to be a molecular ion [M + H] + with an m/z of 363.3, consistent with it being a complex of ferulate with C12 ( Figure 4B). The presence of an additional fragment with an m/z of 177.1 implied the presence of a feruloyl moiety in the reaction product. No products were generated from a control reaction run with the protein obtained from the culture of E. coli carrying an empty pET32a plasmid ( Figure 4A). When C10 was provided as the acyl acceptor, the activity of the recombinant MeHFT provided with caffeoyl CoA as a substrate was only~38% of that recorded when feruloyl CoA was provided and~43% when using p-coumaroyl CoA ( Table 1). The data implied that the preferred acyl donor of MeHFT was feruloyl CoA. With feruloyl-CoA as the acyl donor, a comparison of 15 aliphatic substrates as potential acyl acceptors (Table 1) showed that 1-decanol, 1-dodecanol and 1-tetradecanol were similarly effective as acceptors. The recombinant enzyme showed a level of activity when provided with the short-to-mid-chain fatty alcohols (C6, C7, C10, C12, C14) but none when provided with the long chain fatty alcohols (C20, C22).       Experiments designed to identify the optimal reaction conditions for recombinant MeHFT showed that the enzyme preferred a temperature of 40 • C and a pH of 7.5. At this temperature and pH optimum, recombinant MeHFT, when provided with~0.1 mM feruloyl-CoA as the acyl donor, was associated with comparable K cat /K m ratios in the presence of 1-decanol (3181 M −1 s −1 ) and 1-dodecanol (3015 M −1 s −1 ) ( Table 1). When provided with 0.1 mM 1-decanol and feruloyl-CoA the K cat /K m rose to 3928 M −1 s −1 , a value comparable to that achieved by HFTs isolated from higher plants [26]. These measurements suggested that, in the presence of a non-limiting supply of CoA thioester, MeHFT is effective in catalyzing transferuloylation on aliphatic monomers, at least in vitro. Just as is the case with AtFACT, MeHFT recognized feruloyl-CoA, caffeoyl-CoA and p-coumaroyl-CoA as an acyl donor, although its preference was for feruloyl-CoA, while that of AtFACT was for caffeoyl-CoA [31]. The substrate preferences of AtHHT1/ASFT, StHFT and PtHFT are the same as that of MeHFT.

The Subcellular Localization of MeHFT
The pattern of expression of the p35S::MeHFT-GFP trangene in the N. benthamiana leaf is shown in Figure 5. The clear result was that the translation product was deposited in the cytoplasm.  (Table 1). When provided with 0.1 mM 1-decanol and feruloyl-CoA the Kcat/Km rose to 3928 M −1 s −1 , a value comparable to that achieved by HFTs isolated from higher plants [26]. These measurements suggested that, in the presence of a non-limiting supply of CoA thioester, MeHFT is effective in catalyzing transferuloylation on aliphatic monomers, at least in vitro. Just as is the case with AtFACT, MeHFT recognized feruloyl-CoA, caffeoyl-CoA and p-coumaroyl-CoA as an acyl donor, although its preference was for feruloyl-CoA, while that of AtFACT was for caffeoyl-CoA [31]. The substrate preferences of AtHHT1/ASFT, StHFT and PtHFT are the same as that of MeHFT.

The Subcellular Localization of MeHFT
The pattern of expression of the p35S::MeHFT-GFP trangene in the N. benthamiana leaf is shown in Figure 5. The clear result was that the translation product was deposited in the cytoplasm.

Plant Materials
M. emarginata thallus was raised under a 12 h photoperiod and a constant temperature of 25 °C. Harvested thalli were snap-frozen in liquid nitrogen and stored at −80 °C. Nicotiana benthamiana plants were soil-grown for 5-6 weeks under a 12 h photoperiod, with a day/night temperature regime of 24 °C/22 °C.

Reagents
All chemicals and reagents required were purchased from either Sigma-Aldrich (St. Louis, MO, were soil-grown for 5-6 weeks under a 12 h photoperiod, with a day/night temperature regime of 24 • C/22 • C.

Reagents
All chemicals and reagents required were purchased from either Sigma-Aldrich (St. Louis, MO, USA) or Energy Chemical (Shanghai, China), unless otherwise noted. Feruloyl CoA, p-coumaroyl CoA and caffeoyl CoA were synthesized from ferulic acid, p-coumaric acid and caffeic acid, respectively, using liverwort 4-coumarate CoA ligase [35], then purified using an LC-18 SPE column (Supelco Inc., Bellefonte, PA, USA), following the recommendation of Beuerle and Pichersky [36]. The products were checked for purity using a spectrophotometric assay.

Phylogenetic Analysis of the MeHFT Sequence
A phylogenetic analysis involving the MeHFT sequence and certain selected related plant proteins was carried out using routines implemented in MEGA v5.1 software. [37]. The Neighbor-Joining method was applied, and a bootstrap analysis, based on 1000 replicates, was performed to give statistical support for the derived clade structure.

Gene Isolation, Recombinant Protein Expression and Purification
Total RNA from two month old M. emarginata thallus was extracted using a CTAB-based method [38], and reverse transcribed with the help of a PrimeScript™ RT Master Mix Kit (Takara Bio, Inc., Shiga, Japan) according to the supplier's protocol. The full length cDNA produced by MeHFT was amplified from a cDNA template using PrimeSTAR HS DNA polymerase (Takara) driven by the primer pair MeHFT-F/-R (sequences given in Table 2). The full length clone was subcloned into pMD19-T (Takara, Japan) and then transformed into Escherichia coli DH5a. Plasmids from positive transformants were extracted with Plasmid Mini Kit (Omega Bio-Tek, Norcross, GA, USA) and fully sequenced. The plasmids was then double-digested with SacI and XhoI (Takara, Japan), and ligated into the corresponding cleavage sites of pET32a (Novagen, Darmstadt, Germany) in order to generate a transgene which encoded a His-tagged version of MeHFT. To heterologously express this transgene, it was transferred into competent E. coli BL21 (DE3) cells Expression of the transgene was induced by the addition of 0.5 mM isopropyl β-D-1-thiogalactopyranoside to the culture medium, and the cells were held at 16 • C for 16 h. Recombinant protein was purified from the medium by passage through a Ni-NTA Sefinose His-bind column (Bio Basic Inc., Markham, ON, Canada), following Gao et al. [35]. The concentrations and approximate molecular masses of the recombinant protein were determined as described elsewhere [39].

Enzymatic Assay and Kinetics Determination
Each 50 µL enzymatic assay reaction comprised 1 µg recombinant protein, along with 50 µM of either p-coumaroyl-CoA, caffeoyl-CoA or feruloyl-CoA and 20 µM acyl acceptor (see below) in 0.1 M Tris-HCl buffer, pH 7.5. The reactions were initiated by the addition of the recombinant protein, held at 40 • C for 20 min, and terminated by the addition of 50 µL acetonitrile. After centrifugation (12,000× g, 20 min) to remove any precipitated protein, a 20 µL aliquot of the mixture was injected into an HPLC device equipped with C18 reverse-phase column (4.6 × 250 mm Agilent, Santa Clara, CA, USA). The material was eluted by passing a mixture of 0.2% v/v glacial acetic acid in water (A) and acetonitrile (B) provided at a flow of 0.8 mL min −1 . In the period 0-5 min, the eluate was composed of 85% A, 15% B; from 5 to 25 min, the proportion of B was raised linearly to 100%; from 25 to 35 min, the eluate was 100% B; and from 35 to 40 min, the proportion of B was lowered linearly to 15%. UV absorption was monitored at 330 nm.
The reaction kinetics of the recombinant MeHFT was tested in two sets of experiments. In the first, the recombinant enzyme was provided with 0.1 mM 1-decanol and a range of concentrations of feruloyl-CoA in 0.1 M Tris-HCl buffer (pH 7.5), while in the second, the feruloyl-CoA concentration was fixed at 0.1 mM and the 1-decanol concentration was varied. Both sets of experiment utilized 1 µg purified protein, and were held at 40 • C for 10 min. Kinetic data were calculated on the basis of the Michaelis-Menten equation, using Graphpad Prism 5 software (www.graphpad.com). The quantity of reaction product was calculated based on a standard calibration curve.

The Subcellular Localization of MeHFT
The MeHFT sequence was inserted into pGWB5 (p35S::GL2-GFP) (www.thermofisher.com) for the purpose of determining the subcellular localization of MeHFT. After its amplification driven by primer pair attB1-MeHFT-F/R (Table 2), the sequence was introduced into pDONR207 (Invitrogen, Carlsbad, CA, USA) using the BP reaction, as recommended by the manufacturer. Correct insertion was verified by sequencing. Following validation by sequencing, the construct was transferred into pGWB5 via the LR reaction, and the recombined pGWB5 plasmid was transferred into Agrobacterium tumefaciens strain EHA105 using the freeze/thaw method. To achieve its transient transformation in the N. benthamiana leaf, a 0.1 mL aliquot of the overnight Ag. tumefaciens culture was seeded into 10 mL yeast extract peptone medium containing 50 mg/L of both kanamycin and rifamycin. The cultures were shaken (200 rpm) and held at 28 • C until their OD 600 reached about 0.5. The cells were then harvested by centrifugation (2000× g, 20 min), rinsed in 50 mM MES/KOH (pH 5.6), 2 mM Na 3 PO 4 , 28 mM glucose, 100 mM acetosyringone, then re-suspended in the same buffer to an OD 600 of 1.0. The resuspended cells and p19 were mixed in a 1:1 ratio and the mixture incubated for 3 h at 25 • C, then infiltrated with a syringe into the base of a N. benthamiana leaf [39]. After two days, the fluorescence of the leaf hypodermis was inspected by laser confocal microscopy (Model LSM 700, Carl Zeiss AG, Oberkochen, Germany). The micrscope was equipped with both 495-570 nm (GFP) and 650-760 nm (chlorophyll) band pass filters. Image data were visualized using ZEN 2009 software (CarlZeiss AG).

Conclusions
This represents the first report of the in vitro functionality of a bryophyte HFT. The identification of a member of the BAHD family in as basal a land plant as the liverwort M. emarginata may reveal new insights into the diversity of acyltransferases.