- Research article
- Open Access
Structural insights into the substrate tunnel of Saccharomyces cerevisiae carbonic anhydrase Nce103
© Teng et al; licensee BioMed Central Ltd. 2009
- Received: 19 December 2008
- Accepted: 24 October 2009
- Published: 24 October 2009
The carbonic anhydrases (CAs) are involved in inorganic carbon utilization. They have been classified into six evolutionary and structural families: α-, β-, γ-, δ-, ε-, ζ- CAs, with β-CAs present in higher plants, algae and prokaryotes. The yeast Saccharomyces cerevisiae encodes a single copy of β-CA Nce103/YNL036W.
We determined the crystal structure of Nce103 in complex with a substrate analog at 2.04 Å resolution. It assembles as a homodimer, with the active site located at the interface between two monomers. At the bottom of the substrate pocket, a zinc ion is coordinated by the three highly conserved residues Cys57, His112 and Cys115 in addition to a water molecule. Residues Asp59, Arg61, Gly111, Leu102, Val80, Phe75 and Phe97 form a tunnel to the bottom of the active site which is occupied by a molecule of the substrate analog acetate. Activity assays of full length and two truncated versions of Nce103 indicated that the N-terminal arm is indispensable.
The quaternary structure of Nce103 resembles the typical plant type β-CAs of known structure, with an N-terminal arm indispensable for the enzymatic activity. Comparative structure analysis enables us to draw a possible tunnel for the substrate to access the active site which is located at the bottom of a funnel-shaped substrate pocket.
- Substrate Binding Pocket
- Protein Data Bank Code
- Zinc Ligand
- Acetate Molecule
- Hanging Drop Vapor Diffusion Method
Carbonic anhydrase (CA; EC 184.108.40.206) is a zinc containing enzyme which catalyzes a reversible reaction to form bicarbonate from carbon dioxide and water [1, 2]. By facilitating the interconversion between CO2 and bicarbonate in vivo, CA activity was proposed to be required to ensure adequate level of CO2or HCO3- as the substrates for other enzymes . Therefore, CAs have been found to play an essential role in a series of fundamental biological processes such as photosynthesis, respiration, pH homeostasis and ion transport . Based on the origins and structural features, CAs are divided into six classes, termed α, β, γ, δ, ε and ζ, respectively . The α-CAs were found in mammals, algae and prokaryotes to facilitate the exchange of CO2 in the respiratory cycle. The β-CAs were characterized in higher plants, algae and prokaryotes, and those in higher plants have been reported to play a critical role during photosynthesis . The γ-class was first identified in the thermophilic archaeon Methanosarcina thermophila , whereas δ-  and ζ-  class were found in diatom only. Notably, the ε-CAs from bacteria can form a carboxysome .
The β-CAs of known structure form a dimer, tetramer or octamer of identical subunits, with the active site located at the interface of two subunits. Each subunit consists of three parts, an N-terminal arm composed of two or three projecting α-helices, a conserved zinc-binding core consisting of α-β-α units exhibiting a Rossmann fold and an anti-parallel β-sheet and a C-terminal domain that is dominated by α-helices [3, 5, 11–15]. The N-terminal arm of one subunit makes significant contacts with another subunit via domain swapping. The overall structure of the zinc-binding core is relatively conserved, but the zinc-coordinating residues differ in various classes of CA. In β-CA, the zinc ion binds to two cysteines and a histidine, in addition to a water molecule or an aspartate as the fourth ligand. Based on the divergence of the active site, β-CAs were further grouped into two subclasses, the plant type and the cab type .
The budding yeast Saccharomyces cerevisiae encodes a single copy of CA, termed Nce103 after the n on-c lassical e xport pathway where it was identified for the first time . Deletion of NCE103 leads to a growth-defect phenotype under aerobic conditions, but not under anaerobic conditions . The ΔNCE103 strain exhibits an enhanced sensitivity to H2O2 compared to the wild type . However, the restoration of ΔNCE103 is due to the recovery of carbonic anhydrase activity rather than antioxidant activity . Nce103 is an efficient β-CA who shows high CO2 hydrase activity, with a kcat of 9.4 × 105 s-1 and kcat/Km of 9.8 × 107 M-1 s-1.
We overexpressed, purified and crystallized the full length Nce103, but failed optimizing the crystal to diffraction quality. After performing a multiple sequence-alignment, we deduced the first non-conserved 13 residues of Nce103 might interfere the crystal packing (Figure 1). Thus, we constructed the truncated version Nce103ΔN13 which enabled us to determine its crystal structure at 2.04 Å resolution.
Two subunits form a very tight homodimer with a buried interface of 3,027 Å2, bringing the two zinc binding pockets close to each other. The juxtaposition of the two β2 strands at an angle of 120° results in the formation of an eight-strand β-sheet running through the core of the homodimer. Via domain swapping, the N-terminal arm of one molecule reaches both the zinc binding core and the C-terminal subdomain of the second molecule in the asymmetric unit, creating a broad and deep groove. The overall structure of the homodimer is reminiscent of a saddle (Figure 2A).
The zinc binding site
An acetate molecule in the substrate binding pocket
A hydrophilic tunnel that passes a bottleneck consisting of Phe97, Leu102, Gly111 and Asp59 is the only access to the active site of Nce103. In the substrate binding pocket, there is a flat trilobed piece of density, reminiscent of an acetate molecule (Figure 3A), which is an analog of the substrate bicarbonate as reported previously . In both active sites of the two subunits, the acetate molecule is finely complementary to the pocket from both the viewpoints of shape and charge (Figure 3B). Moreover, the acetate is stabilized by five hydrogen bonds with the amide nitrogens of residue Gly117 and three water molecules (Figure 3B). On the surface of the homodimer, there are four flat but slightly longer pieces of electron density which are well fitted with four molecules of ethylene glycol. Both acetate and ethylene glycol were introduced during crystallization.
Comparison between the active sites of Nce103 and β-CAs from other species
A proposed tunnel of substrate
Using the program CAVER, we added hydrogen atoms to the Nce103 structure and calculated a solvent accessible pathway starting from the acetate ion to the outside bulky solvent. The tunnel profile is a graph of cross section radius (radius of maximally inscribed ball) versus tunnel length measured from its deepest place to the outside (Figure 4B). We speculate that this calculated pathway can mimic the possible substrate diffusion tunnel . The two tunnels in the homodimer point to the opposite directions towards the surface (Figure 4C). It is worth noting that this tunnel is funnel-shaped, widely open toward the solvent but has a narrow gorge (cross section radius ~2.1 Å) in the vicinity of the acetate ion, suggesting that the linear CO2 (with a length of ~3.3 Å) molecule can freely diffuse toward the active sites, consistent with the diffusion-control catalytic mechanism of β-CAs. The gorge of the funnel is lined by several hydrophobic residues (Phe75, Phe97 and Leu102) on one side and polar residues (Asp59 and Arg61) on the other (Figure 4D). The distribution of hydrophobic and polar residues creates an ideal microenvironment for the diffusion of both nonpolar CO2 and negatively charged HCO3-. Furthermore, all these residues are highly conserved among β-CAs from other species, suggesting a potential role of these residues in assisting the substrate approaching the active site (Figure 1).
Activity assays indicated that the N-terminal arm of Nce103 is indispensable
In the pathogenic fungus Cryptococcus neoformans, the N-terminal domain of the β-CA (Can2) is formed by four antiparallel α-helices . It is reported that the N-terminal extension has a strong interaction with a surface groove which is located on the top of the active site of an adjacent monomer within the dimer. So, the N-terminal extension might mediate a regulation mechanism or protein/protein interaction . The shorter N-terminal extension of Nce103 does not contain those residues necessary to interact with the active site in Can2 (Figure 1). To further validate the putative contribution of the N-terminal arm to the activity of Nce103, we constructed another truncated version of Nce103 which contains residues His51-Lys221, designated as Nce103ΔN50. During purification, both Nce103ΔN13 and Nce103ΔN50 were not stable at pH 8.5 (data not shown), despite Nce103ΔN50 remained dimeric in solution. Therefore, the Nce103 homodimer is mainly sustained by the interactions of the hydrophobic groups of the zinc binding core, instead of the swapped N-terminal arms.
Carbonic anhydrase is an important enzyme in inorganic carbon utilization. Here we provide the X-ray structure of S. cerevisiae β-carbonic anhydrase Nce103 at 2.04 Å resolution. The quaternary structure of Nce103 resembles the typical β-CAs of known structure. Comparative structure analysis enabled us to find a possible moving path of the substrate analog acetate toward the active site, and to calculate a funnel-shaped tunnel for the diffusion of the substrate/product. Furthermore, the activity assays indicated the N-terminal arm is indispensable for the enzymatic activity.
Cloning, expression and purification
The open reading frame of the NCE103/YNL036W gene was amplified by PCR using the genomic DNA of S. cerevisiae strain S288C as the template. An additional sequence coding for a six-histidine tag was introduced at the 5' end of the gene during PCR amplification. Then the PCR product was cloned into a pET29a-derived vector between Nco I and Not I restriction sites. Expression was done at 37°C using the transformed E. coli Rossetta (DE3) strain and 2× YT medium (OXOID LTD.) supplemented with 30 μg/ml kanamycin and chloramphenicol, respectively. When the cell culture reached an OD600 nm of 0.6, protein expression was induced with 0.2 mM IPTG (BBI) and the cells were grown for a further 4 hr. Cells were collected by centrifugation, resuspended in 30 ml buffer containing 200 mM NaCl, 20 mM Tris-HCl, pH 8.5. Cells were lysed by three cycles of freezing/thawing followed sonication. His-tagged proteins were purified using a Ni2+ affinity column. Eluted protein was further purified by gel filtration using a Superdex™ 75 column (GE Healthcare Bioscience) equilibrated in 200 mM NaCl, 20 mM β-mercaptoethanol and 20 mM Tris-HCl, pH 8.5. The purity of the pooled fractions was checked by SDS-PAGE.
The truncated NCE103 without the sequence coding for the N-terminal 13 or 50 residues (Nce103ΔN13 and Nce103ΔN50) were amplified, respectively. PCR products were purified using the DNA gel extraction kit (V-gene, China) and inserted into pET29a-derived vector. The mutant proteins (Nce103ΔN13 and Nce103ΔN50) were overexpressed and purified as described above, except that Nce103ΔN13 for crystallization was purified in 20 mM acetate buffer, pH 4.6.
Crystallization of Nce103ΔN13
Crystals of Nce103ΔN13 were obtained by the hanging drop vapor diffusion method at 16°C. In each drop of crystallization, 2 μl protein sample at 4 mg/ml in the buffer of 40 mM NaCl, 20 mM sodium acetate, pH 4.6 and 20 mM β-mercaptoethanol was mixed with 1 μl reservoir solution (20% PEG4000, 0.1 M sodium citrate, pH 5.6, 0.1 M sodium acetate, 20% ethylene glycol) and equilibrated against 0.5 ml reservoir solution. Crystals at a maximal size of 100-200 μm appeared within 6 days.
Data collection and structure determination
Crystal parameters, data collection and structure refinement statistics.
Unit cell (Å), (°)
A = 60.57, b = 155.73, c = 89.69 α = β = γ = 90.00
Resolution range (Å)
Resolution range (Å)
Number of protein atoms
Number of water atoms
RMSDe bond lengths (Å)
RMSD bond angles (°)
Mean B factors (Å2)
Most favored (%)
Additional allowed (%)
Enzymatic activity measurements
The assay was performed at 25°C and repeated twice by the changing pH/dye indicator method at pH 7.5 . The 2× buffer indicator solution and enzyme of 100 μl contained (final concentrations): 25 mM HEPES, 100 μM phenol red (pH 7.5, λ max = 558 nm), 100 mM sodium sulfate and 2 μM enzyme. The reaction was initiated by addition of 100 μl CO2 (aq) to 100 μl of a 2× buffer indicator solution containing enzyme. The activity of Nce103 was measured at pH 7.5. A negative control was included in each set of measurements. The absorption at 558 nm was monitored for 20 sec at an interval of 1.5 sec using Beckman-DU 800 (Beckman Coulter LTD.).
This work was funded by the projects 2006CB910202 and 2006CB806501 from the Ministry of Science and Technology of China, and the grant 30470366 from Chinese National Natural Science Foundation.
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