ORIGINAL RESEARCH article
Sec. Bioprocess Engineering
Volume 6 - 2018 | https://doi.org/10.3389/fbioe.2018.00180
Biochemical Characterization of Kluyveromyces lactis Adenine Deaminase and Guanine Deaminase and Their Potential Application in Lowering Purine Content in Beer
- Microbial Type Culture Collection and Gene Bank, CSIR-Institute of Microbial Technology, Chandigarh, India
Excess amounts of uric acid in humans leads to hyperuricemia, which is a biochemical precursor of gout and is also associated with various other disorders. Gout is termed as crystallization of uric acid, predominantly within joints. The burden of hyperuricemia and gout has increased worldwide due to lifestyle changes, obesity, and consumption of purine-rich foods, fructose-containing drinks, and alcoholic beverages. Some of the therapies available to cure gout are associated with unwanted side-effects and antigenicity. We propose an attractive and safe strategy to reduce purine content in beverages using enzymatic application of purine degrading enzymes such as adenine deaminase (ADA) and guanine deaminase (GDA) that convert adenine and guanine into hypoxanthine and xanthine, respectively. We cloned, expressed, purified, and biochemically characterized both adenine deaminase (ADA) and guanine deaminase (GDA) enzymes that play important roles in the purine degradation pathway of Kluyveromyces lactis, and demonstrate their application in lowering purine content in a beverage. The popular beverage beer has been selected as an experimental sample as it confers higher risks of hyperuricemia and gout. Quantification of purine content in 16 different beers from the Indian market showed varying concentrations of different purines. Enzymatic treatment of beer samples with ADA and GDA showed a reduction of adenine and guanine content, respectively. These enzymes in combination with other purine degrading enzymes showed marked reduction in purine content in beer samples. Both enzymes can work at 5.0–8.0 pH range and retain >50% activity at 40°C, making them good candidates for industrial applications.
Hyperuricemia, an elevated level of uric acid, is an independent risk factor for hypertension, metabolic, and cardiovascular disorders. It also causes painful arthritis known as gout (Chen et al., 2007; Kuwabara, 2016) and it is the most common inflammatory arthritis, affecting 1–2% of the adult population (Richette and Bardin, 2010). Hyperuricemia and gout both occur due to elevated levels of uric acid in the human body. Low urate excretion and higher production of urate, or both conditions, lead to hyperuricemia. Various reports also suggest that epidemiologically, the prevalence of gout and hyperuricemia has increased worldwide, especially in developed countries (Kuo et al., 2015). Numerous factors (modifiable and non-modifiable) like sex, age, race, alcohol consumption, obesity, and lifestyle change regulate hyperuricemia and gout (Choi et al., 2005; Choi and Curhan, 2008; MacFarlane and Kim, 2014). Among these factors, some are modifiable (lifestyle change and alcohol consumption) and their regulation can reduce the prevalence of hyperuricemia and gout (MacFarlane and Kim, 2014). Although many therapies and medications are available for gout treatment, cost-effectiveness and side effects are factors to consider (Cronstein and Terkeltaub, 2006). Despite various medication therapies' availability, a low purine diet and a healthy lifestyle are recommended for all gouty patients (Choi and Curhan, 2004; Choi et al., 2004b). A low purine diet and lifestyle change are considered as some of the alternatives and safe approaches and have the potential to regulate the prevalence of gout and hyperuricemia. The low purine diet recommendation is promising and safe, but it eliminates a wide range of foods and beverages, which makes therapy difficult to be adopted by a major percentage of patients. One of the strategies to make this therapy safe and attractive is to produce the foods and beverages that are low in purine content through the enzymatic application (Trautwein-Schult et al., 2014; Jankowska et al., 2015; Mahor et al., 2016). This gives the patients an option to choose a wide variety of low purine content foods and beverages without any risk of hyperuricemia and gout.
We employed this strategy to produce low purine content beverages through the application of purine degrading enzymes of a GRAS status yeast Kluyveromyces lactis. Our group is working on the enzymes involved in the purine degradation pathway of K. lactis, an industrially important and Food and Drug Administration (FDA)-approved generally regarded as safe (GRAS) status yeast. We have earlier worked on uricase and purine nucleoside phosphorylase of this organism (Kumar, 2012; Mahor et al., 2016). In the present study, we mainly focused on adenine deaminase and guanine deaminase enzymes of the purine degradation pathway of K. lactis and their application in lowering purine content in beverages.
Adenine deaminase (ADA) (EC 126.96.36.199.) is also known as adenine amidohydrolase and adenase. It is an intracellular enzyme that deaminates adenine into hypoxanthine with the release of ammonia. ADA is conserved in prokaryotes and lower eukaryotes (Pospísilová et al., 2008). ADA has been reported from Pseudomonas synxantha (Jun and Sakai, 1985), Bacillus subtilis (Nygaard et al., 1996), Leishmania donovani (Kidder and Nolan, 1979), E. coli (Matsui et al., 2001), Azotobacter vinelandii (Heppel et al., 1957), and Arxula adeninivorans (Jankowska et al., 2014). It belongs to the α/β barrel subfamily and most ADAs require metal ions for their catalysis, e.g., P. synxantha and B. subtilis (Jun and Sakai, 1985; Nygaard et al., 1996).
Guanine deaminase (GDA) (EC 188.8.131.52) is a key enzyme of the purine catabolism that belongs to the aminohydrolase family (Schmidt, 1932). It is commonly known as cypin, nedasin, guanase, aminase, guanine aminohydrolase, and guanine aminase. GDA catalyzes guanine and produces xanthine and ammonia via hydrolytic deamination (Lewis and Glantz, 1974; Fernández et al., 2009). It is an irreversible reaction and guanine is reutilized for guanylate nucleotide pools (Fernández et al., 2009). GDA is found in bacteria, lower eukaryotes, plants, and higher eukaryotes (Liaw et al., 2004). GDA has been categorized into two different classes: the aminohydrolases family found in bacterial, fungal, and many eukaryotes and the cytidine deaminase family found in plants and archaea (Ko et al., 2003; Liaw et al., 2004). A number of tissues have not shown a steady level of GDA expression (Scholar and Calabresi, 1973; Kuzmits et al., 1980). Tissue-specific GDA expression suggested that it plays an important role in guanine nucleotide pools (Berger et al., 1985). GDA also has a potential role in cofactor and nucleic acid precursor and signaling pathways. It is a promising drug target for liver and cognitive diseases (Fernández et al., 2010). Similarly, other purine-degrading enzymes (purine nucleoside phosphorylase, xanthine oxidase, and uricase) also play important roles in various disorders (Bzowska et al., 2000; Glantzounis et al., 2005). However, there are very few studies that report ADA and GDA homologs from yeast.
So far, of purine-degrading enzymes, only single yeast A. adeninivorans are characterized (Jankowska et al., 2013, 2015; Trautwein-Schult et al., 2013, 2014). In the present study, we report the biochemical characterization of KlacADA and KlacGDA and their application in lowering purine content in beer. Numerous studies reported that alcohol consumption is strongly associated with gout and the risk of gout attack conceivably depends on the type and dose of alcohol (Choi and Curhan, 2004, 2008; Choi et al., 2004a). The presence of absorbable nucleosides in beer confers a greater risk of gout in comparison to any other alcohol beverages (i.e., wine and spirits).
Previously, we have overexpressed and purified purine nucleoside phosphorylase (Mahor et al., 2016) and xanthine dioxygenase (Mahor et al., 2016, unpublished data) enzymes from K. lactis. Using all these enzymes, we demonstrated that applying an enzyme cocktail (KlacADA, KlacGDA, KlacPNP, and KlacXanA) is able to reduce purines viz. adenine, guanine, inosine, and xanthine content in beer. The enzyme cocktail, along with commercial uricase, was able to reduce overall purine content in beer. The characterization and application of these enzymes support for a method development for low purine content food production.
Materials and Methods
Cloning, Overexpression, and Purification of KlacADA and KlacGDA
Genomic DNA of K. lactis (MTCC 458) was isolated using a Zymo DNA isolation kit (Zymo Research, USA). Amplified products of KlacADA and KlacGDA were cloned into a pET28c vector with N-terminal 6xHis-tag by using NdeI/XhoI restriction sites. Clones pET28c-ADA-DH10β and pET28c-GDA-DH10β were overexpressed in E. coli BL21(DE3) cell and followed by induction with Isopropyl β-D-1-thiogalactopyranoside (IPTG). Positive clones were confirmed by gene-specific PCR amplification, digestion, and followed by sequencing. Best overexpressed clones of KlacADA and KlacGDA were inoculated into 10 mL of primary culture in LB + 50 μg/mL of kanamycin. One percent of primary inoculums were inoculated into 1 L of LB + kanamycin media for a large-scale culture incubated at 37°C, induced with IPTG and incubated at 30 and 25°C, respectively, for 7 and 12 h. Cells were harvested by centrifugation at 4,279 × g for 15 min at 4°C. Pellets of KlacADA and KlacGDA were lysed with lysis buffer (50 mM Tris, 150 mM NaCl, 10 mM imidazole pH 7.0 and 50 mM Tris, 200 mM NaCl, 10 mM imidazole, pH 8.0, respectively), along with protease cocktail inhibitor (1 μL/mL, Sigma- Aldrich), lysozyme 1 mg/mL followed by 30 min incubation. Disruption of cells was done by sonication for 1 h and cell debris separation done by centrifugation at 18,400 × g at 4°C for 45 min. The supernatant of both proteins was loaded into the Ni-NTA column which was pre-equilibrated with buffers. Ni-NTA bound proteins were eluted in several fractions in 50 mM Tris, 150 mM NaCl, 200 mM imidazole, 15% glycerol, pH 7.0 and 50 mM Tris, 200 mM NaCl, 200 mM imidazole, and 10% glycerol pH 8.0, respectively. All fractions of purified proteins were pooled and KlacADA and KlacGDA were dialyzed against 25 mM Tris, 100 mM NaCl, 1 mM DTT, 15% glycerol, pH 7.0 and 50 mM Tris, 100 mM NaCl, 10% glycerol, and pH 8.0 overnight at 4°C. Determining the purified protein concentration was done by UV spectra at 280 nm.
Oligomerization of KlacADA and KlacGDA
The oligomeric state of KlacADA and KlacGDA was determined by gel filtration chromatography. Dialysed recombinant proteins were concentrated and KlacADA and KlacGDA were further purified by gel exclusion chromatography by using HiPrep 16/60 Sephacryl S-200 HR column and HiPrep 16/60 Sephacryl S-300 HR column (GE Healthcare Life Sciences), respectively. Further confirmation of results was done by MALDI-TOF analysis. MALDI mass spectra of KlacADA and KlacGDA was generated by using sinapinic acid as a matrix on a mass spectrometer (Agilent Technologies G4226A, US).
Enzymatic Assays of KlacADA and KlacGDA
ADA converts adenine into hypoxanthine with the release of ammonia and KlacADA activity was measured spectrophotometrically monitoring adenine consumption at 254 nm. Enzyme assay was done at 30°C and in 100 mM potassium phosphate buffer pH 6.0. The reaction consisted 200 nmoles of the enzyme, 100 mM of the buffer in 250 μL of the final volume and was incubated for 20 min. The adenine concentration varied from 0 to 1 mM to calculate kinetic parameters. In addition to the above-mentioned assay, we have also determined KlacADA activity through an indirect assay at 30°C under the following assay conditions: 0.1 U xanthine oxidase, 100 mM potassium phosphate buffer pH 6.0, 200 nmoles of enzyme, and 0–1 mM of adenine. Uric acid production was monitored in the assay at 293 nm.
Guanine was converted into xanthine by guanine deaminase. Guanine deaminase activity was determined by monitoring guanine utilization at 250 nm. The assay reaction consisted of 0.5 μM of the enzyme, 100 mM phosphate buffer pH 7.0, and was incubated for 15 min at 25°C. The guanine concentration varied from 0 to 500 μmoles and was stopped at 10, 20, and 30 min to get the linear range. The kinetic parameters of KlacGDA were calculated by non-linear parameters of origin software. KlacGDA activity was also determined by indirect assay by using 0.1U xanthine oxidase in 100 mM phosphate buffer pH 7.0, and 0.5 μM of the enzyme at 25°C. The absorbance was monitored at 293 nm for uric acid production.
Biochemical Properties of KlacADA and KlacGDA
The effect of pH on KlacADA and KlacGDA activity was determined by their measured activity in 100 mM universal buffer (50 mM Tris, 50 mM boric acid, 33 mM citric acid, and 50 mM Na2PO4) (Visser et al., 2010) in a pH range of 3.0–12.0, at 1.0 pH unit interval. Reactions were stopped by the addition of 50 μL of 10 M NaOH and their activity was measured at the 254 and 250 nm, respectively. The optimum temperature of KlacADA and KlacGDA was examined by measuring their activity across a 5–55°C temperature range. The KlacADA and KlacGDA reaction mixtures in 100 mM universal buffer at optimum 6.0 and 7.0 pH levels, respectively, were incubated at 5–55°C with 5°C intervals. The reactions were stopped by adding 50 μL of 10 M NaOH, and absorbance was measured.
To determine the pH stability of KlacADA and KlacGDA, proteins were incubated in a pH range of 3.0–12.0, at 1.0 pH unit interval of universal buffer for 12 h. The enzyme assay was performed under optimum conditions (KlacADA at 25°C, pH 6.0 and KlacGDA at 30°C, pH 7.0) with incubated enzymes and reactions were stopped by 10 M NaOH. Finally, activity was measured at 254 and 250 nm, respectively. The thermostability of KlacADA and KlacGDA were measured by incubating enzymes at 5–55°C for 1–2 h. Enzyme reactions were set with incubated enzymes at their optimum conditions and absorbance was measured at their respective wavelengths.
Substrate Specificity of KlacADA and KlacGDA
Substrate specificity of enzymes was measured through the HPLC method. Standards of the substrate and expected products in 2 mM concentration were run on an SCL-10AV HPLC system (Shimadzu, Japan), equipped with a SIL-10AD injector and a UV spectrophotometric detector. Each of the substrates was treated with KlacADA and KlacGDA in optimum conditions and incubated for 30 min. Post incubation, reaction mixtures were heated to 100°C to stop the reaction, centrifuged for 15 min and the supernatant was separated. Ten microliters of the sample was injected into in a Lichrospher 100 RP-18 column (LichroCART® 250-4, Merck), at 0.5 mL/min run at 35°C, and UV-absorbance spectra were collected at 254 nm. The solvent system used for separation was 100 mM sodium phosphate buffer + 10% methanol. The buffer pH was 2.3, maintained by 100 mM phosphoric acid. Chromatograms were analyzed in the absence and presence of enzymes which revealed that KlacADA and KlacGDA can consume a wide range of substrates.
Purine Content Quantification in Beers
Pure purine compounds (adenosine, guanosine, inosine, xanthosine, adenine, guanine, hypoxanthine, xanthine, and uric acid) in a wide range of concentrations (0–5 mM) were run on the HPLC system to generate a standard curve, using the parameters mentioned earlier. Different beer samples designed with code words were run on HPLC without any pre-treatment. Analysis of HPLC chromatograms revealed the presence of different purines. The identity of each purine was determined by the retention times obtained for each individual pure purine compound chromatogram and was further confirmed by LC-ESI-MS analysis.
Reduction of Purine Content in Beer by Enzymatic Reaction
Standards (adenine, hypoxanthine, guanine, and xanthine) in 2 mM concentrations were dissolved in a phosphate buffer and were run on the HPLC system. HPLC parameters were the same as mentioned previously. To examine enzyme potential for purine reduction initially, the pure substrate was treated with KlacADA and KlacGDA in 1.0 U at room temperature. HPLC chromatograms showed a decrease in adenine and guanine peaks and a corresponding increase in hypoxanthine and xanthine peaks. Beer samples treated with KlacADA and KlacGDA (1.0 U) at room temperature were run on the HPLC system. Chromatograms of enzymatically treated and untreated beer samples revealed that both KlacADA and KlacGDA were able to lower adenine and guanine content in beer. Retention time of standards was used to determine the identity of the compounds and peak value was used for quantification, and further confirmation was done by LC-ESI-MS analysis.
Finally, beer was treated with an enzyme cocktail (KlacADA, KlacGDA, KlacPNP, KlacXanA in 1.0 U) along with uricase 0.2 U (commercially available as Candida utilis uricase), incubated for 1.5 h, and the sample was run on HPLC by using similar parameters as mentioned before. The enzymatic cocktail lowered the purine content in beer. The identification of purine compounds was done in a similar manner as mentioned above.
Identification of KlacADA and KlacGDA
The gene coded for ADA in K. lactis (gene ID KLLAOE2317) was found by a BLAST search with other available sequences. It is located from position 2,064,516–2,065,583 on the E-chromosome of K. lactis with no introns. The KlacADA sequence showed a high degree of similarity with the ADA of Kluyveromyces marxianus (76%) and AAH of S. cerevisiae (66%), whereas the human, E. coli, bovine, and murine ADAs showed a 24, 28, 24, and 24% degree of similarity, respectively (Figure S1). This similarity goes well with the statement that lower eukaryotes have adenine deaminase rather than adenosine deaminase. The gene coding for GDA (gene ID. KLLAOD9492), located on chromosome D from position 1,643,703–1,645,193, was found by a BLAST search with fungal and higher eukaryotes GDAs sequences. Sequence similarity results revealed that KlacGDA shares a 69% sequence similarity with K. marxianus GDA, whereas S. cerevisiae GDA (51%), human GDA (37%), and E. coli GDA (35%) have less sequence similarity (Figure S2).
Cloning, Expression, and Purification of KlacADA and KlacGDA
The genomic DNA of K. lactis MTCC 458 was isolated by using a DNA isolation Kit (Zymo Research, USA). Amplified ada and gda genes were cloned into a pET28c vector with a NdeI/XhoI site carrying N-terminal 6xHis-tag. To overexpress enzymes, genes were further cloned into BL21(DE3) cells and induced with 0.300 and 0.150 mM of IPTG, respectively. Overexpressed proteins KlacADA and KlacGDA were purified through a Ni-NTA column in several fractions. Purified fractions of proteins were pooled and further purified by gel filtration chromatography. SDS-PAGE results indicated that proteins were purified to >95% homogeneity. The KlacADA can be stored at 4°C in 25 mM Tris, 100 mM NaCl, 15% glycerol and pH 6.0, and KlacGDA can be stored at 4°C in 50 mM Tris, 100 mM NaCl, 10% glycerol and pH 7.0, respectively, for a month.
Oligomeric States of KlacADA and KlacGDA
There are a few reports of an oligomeric form of ADA (Jankowska et al., 2015). To confirm the oligomeric state of KlacADA, we performed gel exclusion chromatography. A single dominant peak at 60 mL, which corresponds to 46 kDa molecular weight, indicates a monomeric form of KlacADA (Figure 1A), while a single peak of KlacGDA corresponding to 106 kDa suggests a dimeric form of it (Figure 1B). These results were very well-correlated with MALDI-TOF analysis (Figure S3).
Figure 1. Gel exclusion chromatography elution profiles of KlacADA and KlacGDA. (A) KlacADA in HiPrep 16/60 Sephacryl S-200 HR column. The inset graph shows the elution profile of standard molecular weights from the same column ribonuclease (13.7 kDa), carbonic anhydrase (29 kDa), BSA (67 kDa), conalbumin (75 kDa), (left panel) and SDS-PAGE profile of KlacADA with protein ladder (right panel). (B) KlacGDA in HiPrep 16/60 Sephacryl S-300 HR column. The inset graph shows the elution profile of standard molecular weights from the same column ribonuclease (13.7 kDa), carbonic anhydrase (29 kDa) ovalbumin (44 kDa), conalbumin (75 kDa), alcohol dehydrogenase (150 kDa) (left panel) and SDS-PAGE profile of KlacGDA with protein ladder (right panel).
Biochemical Properties of KlacADA and KlacGDA
The optimum pH of the KlacADA and KlacGDA was determined using a universal buffer with different pH ranges. It was observed that KlacADA is able to work at a pH range of 4.0–8.0 with an optimum pH of 6.0 (Figure 2A), and KlacGDA can work at pH 6.0–9.0 with an optimum pH of 7.0 (Figure 3A). KlacADA and KlacGDA are able to work across a wide temperature range with an optimum temperature of 30°C (Figure 2C) and 25°C (Figure 3C), respectively. KlacADA worked in pH range of 4.0–8.0 with >50% activity (Figure 2B), whereas KlacGDA retained >40% catalytic activity at a pH range of 5.0–9.0 (Figure 3B). The enzymes were moderately thermostable in nature; KlacADA retained >85% activity after incubation at 5–40°C (Figure 2D), while KlacGDA retained >50% activity after incubation at the same range of temperature for 1.5 h (Figure 3D).
Figure 2. Biochemical properties of KlacADA. (A) Optimum pH of KlacADA. (B) Effect of pH on KlacADA stability. (C,D) Optimum temperature and thermostability of KlacADA. The experiments were done in triplicates and representing values are means of them. The activity of enzymes measured in optimum conditions and maximum activity was defined as having a relative activity of 100%. Standard deviation represented by error bars.
Figure 3. Biochemical properties of KlacGDA. (A) Optimum pH of KlacGDA. (B) pH stability of KlacGDA. (C,D) Optimum temperature and thermostability of KlacGDA. The experiments were done in triplicates and representing values are means of them. The activity of enzymes measured in optimum conditions and maximum activity was defined as having a relative activity of 100%. Standard deviation represented by error bars.
Kinetic Analysis of KlacADA and KlacGDA
Purified KlacADA was enzymatically active and capable of utilizing purines. As adenine was the preferred substrate of KlacADA, we determined its kinetic parameters and observed that KlacADA has KM 680 ± 4.6 μM and kcat 8.1 ± 1.3 s−1 with 1.1 × 104 M−1s−1 efficiency. KlacGDA's preferred substrate is guanine. The kinetic parameters of KlacGDA for guanine are KM 83 ± 2.7 μM and kcat 7.3 ± 1.2 s−1, respectively, with 0.87 × 106 M−1s−1 catalytic efficiency (Table 1).
Substrate Specificity of KlacADA and KlacGDA
Substrate specificity of enzymes was examined by the HPLC-UV method using their respective natural substrates, various purines, and their analogs. As expected, adenine was the preferred substrate for KlacADA, but it is also able to utilize 2,6-diaminopurine, 6-chloropurine, and traces of flavin adenine dinucleotide (FAD), in decreasing order of substrate preference, whereas other compounds showed no detectable activity (Table 2). In the case of KlacGDA, guanine is the preferred substrate. KlacGDA activity has been examined for other purines (adenine, adenosine, xanthine, hypoxanthine, thioguanine, guanosine, and 8-azaguanine) but it could degrade only 6-thioguanine and 8-azaguanine 13.7 and 23.2%, respectively (Table 3).
Quantification of Purine Content in Beers
Pure purine compounds were used as standards for method optimization. The identification of each purine compound was done according to its relative retention time, and further confirmation was done by LC-ESI-MS analysis. Quantification of the purine content of 16 selected beers that are available in the Indian market revealed that all beers contain different purines like hypoxanthine, adenine, guanosine, guanine, xanthosine, inosine, and uric acid. Overall, the purine content in different beers varied from 91.5 to 339.2 μmol/L, with the brand Beer-KS (<8% of alcohol) being the highest purine-containing beer among 16 different beers (Table 4).
Lowering the Purine Content in a Beer
Initial experiments were performed to examine the ability of KlacADA and KlacGDA to reduce the adenine and guanine content in phosphate buffers spiked with these substrates. KlacADA and KlacGDA degraded their respective substrates, and it was observed that with a reduction in adenine, there is a corresponding increase in hypoxanthine (Figure S4A), a similar reduction in guanine and a corresponding increase in xanthine (Figure S4B). Similar results were also obtained in beer samples treated with KlacADA and KlacGDA (Figure 4). HPLC chromatograms showed that adenine concentration in beer dropped 66–67% and guanine concentration in beer dropped from 68.8 μMol/L to a minimal amount that was difficult to measure (Figure 4). It is evident from analysis that beer samples contain varying concentrations of different purines viz. hypoxanthine, inosine, adenine, guanine, and xanthine. To examine the feasibility of reducing overall purine content, a cocktail of enzymes (KlacADA, KlacGDA, KlacPNP, KlacXanA, and commercial uricase from C. utilis) was used for treating beer samples. It was observed that the overall purine content of beer decreased. The retention time and LC-ESI-MS analysis revealed that the appeared peak corresponds to allantoin (Figure 5). We have successfully demonstrated that a cocktail of purine degrading enzymes was able to lower the purine content in beer and converted it into a more soluble form that is easy to excrete from the human body.
Figure 4. Chromatogram of beer sample before and after the enzyme treatment. (A) The chromatogram shows purine content in beer before (dotted black line) and after KlacADA enzyme reaction (solid gray line). (B) The chromatogram shows purine content in beer before (dotted back line) and after KlacADA enzyme reaction (solid gray line). Beer sample treated with 0.5 U of KlacADA and KlacGDA enzymes. In the panel, A adenine peak (1) was decreased and hypoxanthine peak (3) was increased. In the panel, B guanine (2) peak was decreased and xanthine (3) peak intensity was increased suggesting the conversion of adenine and guanine into hypoxanthine and xanthine, respectively. (C) LC-ESI-MS analysis of purines in beer: 1- Adenine, 2- Guanine, 3- Hypoxanthine, 4- Xanthine, expected and observed the molecular mass of purines.
Figure 5. Chromatogram of beer sample before and after the enzyme cocktail treatment. The chromatogram shows purine content in beer before (dotted back line) and after KlacADA, KlacGDA, KlacPNP, KlacXanA, and uricase from Candida utilis enzyme reaction (solid gray line). Beer treated with the enzyme cocktail showed a decrease in the adenine, guanine, hypoxanthine, xanthine, and uric acid peaks. EC A (Adenine deaminase), G (Guanine deaminase), P (Purine nucleoside phosphorylase), X (Xanthine dioxygenase) cloned in E. coli, and U (commercial uricase).
During the evolutionary process, the loss of human urate oxidase resulted in an increased risk of prevalence to hyperuricemia and gout. Changes in modern lifestyles and diet further enhanced the higher risk of hyperuricemia and gout. Various studies reported that the occurrence of gout has increased worldwide and is dominant in developed countries. Worldwide, cases of gout increased from 0.3 to 6 cases per 1,000 person-years (Kuo et al., 2015). Hyperuricemia and gout are age-associated disorders and are also risk factors for hypertension, metabolic, renal, and cardiovascular diseases. Medications as well as socioeconomic, lifestyle and dietary factors influence the uric acid level in the human body and determine the risk of gout. As 33% of uric acid comes from the diet, consumption of low purine content food and beverages could help to maintain serum uric acid level in humans.
Alcoholic beverages such as beer, spirits, and wine all have different levels of risk of gout. Various studies showed that beer confers the highest risk of gout among all alcoholic beverages (Choi, 2004; Choi and Curhan, 2004, 2008; Choi et al., 2010). One of the reasons for beer's association with gout is the presence of high levels of the nucleoside in beer (Gibson et al., 1984; Puig and Fox, 1984). Some studies reported that two or more servings of beer per day increased the risk of gout by a factor of 2.5 as compared to non-beer drinkers (Choi and Curhan, 2004).
This study reports the characterization of purine degrading enzymes KlacADA and KlacGDA, the quantification of purine content in different beers from the Indian market, and examines the application of KlacADA and KlacGDA in lowering purine content in beer. Finally, we demonstrated that the application of a cocktail of enzymes (KlacADA, KlacGDA, KlacPNP, KlacXanA with commercial uricase) was successful in lowering purine content in beers.
KlacADA and KlacGDA were cloned, overexpressed, and purified from E. coli with His-tag. A gel filtration chromatogram revealed that KlacADA and KlacGDA exist as a monomer and dimer, respectively, monodispersed in solution. The monomeric form of KlacADA is similar to A. adeninivorans ADE (Jankowska et al., 2014). KlacADA showed an optimum pH of 6.0 while maximum ADEs showed an optimum pH range of 6.0–9.0, e.g. C. fasciculate (pH 6.0), A. adeninivorans (pH 6.5–7.0), S. cerevisiae (pH 7.0), S. pombe (pH 6.7), and P. synxantha (pH 9.0) (Kidder et al., 1977; Jun and Sakai, 1985; Pospísilová et al., 2008). ADEs showed a diverse range of optimum temperatures. For example, S. cerevisiae, S. pombe, P. synxantha, A. adeninivorans, and E. coli showed optimum temperatures of 30–37, 33, 40–45, 40, and 60°C respectively (Kidder et al., 1977; Jun and Sakai, 1985; Pospísilová et al., 2008; Jankowska et al., 2014). It was found that KlacADA's optimum temperature is 30°C, which is nearer to S. cerevisiae and S. pombe. Some studies reported that ADEs have ~30% activity in the 5.0–8.0 pH range (Kidder et al., 1977; Jun and Sakai, 1985). A. adeninivorans ADE is stable at 30°C up to 24 h in the HEPES buffer, ranging from 7.5 to 8.5 (Jankowska et al., 2014). KlacADA's pH stability was tested in the universal buffer and found that it can work at a wide pH range of 5.0–9.0. C. fasciculate ADA is a thermostable enzyme and retained 90% activity at up to 55°C for 1 h (Kidder et al., 1977). ADE of C. utilis was an unstable protein and lost 50% of activity within 10 min at 37°C. A. adeninivorans ADE retained 70% of activity after 1 h at 40°C (Jankowska et al., 2014). KlacADA is moderately thermostable and able to work at 5–40°C with >70% activity and able to work across wide pH range.
Allam et al. (1981) reported that ADE has only a natural substrate, adenine, but other studies showed that ADE can also hydrolyze 6-halogenpurines (Abbondandolo et al., 1971; Jun and Sakai, 1985). It was observed that KlacADA is able to consume adenine, 2,6-diaminopurine, 6-chloropurine, and 8-azaguanine. It was described that adenine deaminase can consume various structurally related cyclic compounds as substrates (Hartenstein and Fridovich, 1967). The kinetic parameters of KlacADA for adenine are KM 680 ± 4.6 μM, kcat 8.1 ± 1.3 s−1, with a catalytic efficiency of 1.1 × 104 M−1s−1. The KM value of ADEs has been reported from 40 different clones (wild-type and mutants), which lay in the range of 0.09–2.2 mM (Brenda Database). KlacADA lies in the mentioned range and is more catalytically efficient in comparison to many ADEs, such as E. coli, Burkholderia sp., P. aeruginosa (Goble et al., 2011; Kamat et al., 2011).
The optimum pH of GDA ranges from 5.5 to 9.0 in the different organisms and it was found that KlacGDA's optimum pH was 7.0, which is comparable to the pH of humans and Camellia sinesis. GDA is a moderately thermostable enzyme that can work actively up to 55°C (Trautwein-Schult et al., 2014). It was observed that KlacGDA's optimum temperature was 25°C, which is comparable with the optimum temperature of O. cuniculus (Ujjinamatada et al., 2006). KlacGDA is a pH-stable protein and retained ~50% activity at pH 5.0–9.0. The pH stability data suggest that KlacGDA has a broad range of pH stability in comparison to A. adeninivorans GDA (Trautwein-Schult et al., 2014). Various studies reported that GDA is a thermostable enzyme; Rattus norvegicus GDA retained 67% at 70°C (Kim and Kimm, 1982) and Human liver GDA is active up to 55°C (Kimm and Lee, 1985). In our study, it was found that KlacGDA has >40% activity at a range of 5–40°C, which is comparable to human liver GDA (Gupta and Glantz, 1985). Guanine and ammeline are natural substrates for GDA. Besides these two substrates, GDA is also able to catalyze other analogs (6-thioguanine and 8-azaguanine). We found the KlacGDA consumes guanine with high efficiency but is unable to consume other purines except for the 6-thioguanine and 8-azaguanine. KlacGDA has higher KM as compared to the reported KM of human liver, A. adeninivorans, C. sinensis, and R. norvegicus (Kimm and Lee, 1985; Negishi et al., 1994; Trautwein-Schult et al., 2014).
From the literature survey, we could not find any report on purine content analyses of beer samples available from the Indian market. Purine content in beer may depend on the source of raw material used, strain selection, and downstream processing. So, before treating with enzymes, a quantification of purine content was done in different beers available in the Indian market. It was observed that hypoxanthine, adenine, guanine, guanosine, inosine, and uric acid were present in different beers and hypoxanthine was high in each beer in comparison to the purine content in beer from the UK and Japan. Hypoxanthine is the most harmful purine in the context of gout.
The beer samples treated with KlacADA and KlacGDA showed a reduction in the amount of adenine and guanine, respectively. Furthermore, the beer was treated with an enzyme cocktail and it was observed that the overall purine content of beer was reduced significantly. This is a preliminary study which demonstrated the application of an enzymatic approach to low purine content beverage production. Further studies are required to develop a method for industrial applications of this approach. A similar approach could also be developed for lowering purine content in other kinds of foods. Currently, our group is exploring strategies to make low purine content food affordable. We believe, using yeast strain harboring engineered enzymes like KlacADA, KlacGDA, KlacPNP, and KlacXanA for the production of beer could be an attractive and cost-effective approach for creating low purine content beverages and foods. The application of this approach may be beneficial to hyperuricemic and gouty patients in maintaining healthy life styles.
GP conceived and coordinated the study. DM designed and carried out experiments. DM and GP analyzed the data and wrote the paper. All authors reviewed results and approved the final version of the manuscript.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
This work was supported by a project, Expansion and Modernization of Microbial Type Culture Collection and Gene Bank (MTCC), jointly supported by the Council of Scientific and Industrial Research (CSIR) Grant No. BSC0402 and Department of Biotechnology (DBT) Govt. of India Grant No. BT/PR7368/INF/22/177/2012. DM is a graduate student, recipient of UGC fellowship.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fbioe.2018.00180/full#supplementary-material
Figure S1. Amino acid sequence alignment of KlacADA with the adenine deaminases of S. cerevisiae, K. marxianus, and adenosine deaminases (ADAs) of Human, E. coli, Bos Taurus, and Mus musculus. Highly Conserved regions are highlighted in red boxes, conservative substitutions are also boxed. The amino acid similarity figure was generated by using the ESPript 3.
Figure S2. Amino acid sequence alignment of KlacGDA with the guanine deaminases of Human, S. cerevisiae, E. coli, and K. marxianus. Highly Conserved regions are highlighted in red boxes, conservative substitutions are also boxed. The amino acid similarity figure generated by using the ESPript 3.
Figure S3. MALDI-TOF profile of KlacADA and KlacGDA. (A) MALDI-TOF analysis of KlacADA revealed the monomeric form of it. (B) MALDI-TOF profile of KlacGDA revealed the monomeric and dimeric form of it.
Figure S4. HPLC chromatograms of KlacADA and KlacGDA with the standards. (A) Adenine treated with the KlacADA (solid gray line), HPLC chromatograms showed the reduction in adenine peak (solid black line) and corresponding elevation in hypoxanthine peak (dotted gray line). (B) Guanine treated with the KlacGDA (solid gray line), HPLC chromatograms showed the reduction in guanine peak (solid black line) and corresponding elevation in xanthine peak (dotted gray line).
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Keywords: Kluyveromyces lactis (K. lactis), hyperuricemia, gout, purine, high-performance liquid chromatography (HPLC), beer
Citation: Mahor D and Prasad GS (2018) Biochemical Characterization of Kluyveromyces lactis Adenine Deaminase and Guanine Deaminase and Their Potential Application in Lowering Purine Content in Beer. Front. Bioeng. Biotechnol. 6:180. doi: 10.3389/fbioe.2018.00180
Received: 02 June 2018; Accepted: 12 November 2018;
Published: 29 November 2018.
Edited by:Angela F. Jozala, Universidade de Sorocaba, Brazil
Reviewed by:Helen Treichel, Universidade Federal da Fronteira Sul, Brazil
Yasushi Ogasawara, Hokkaido University, Japan
Copyright © 2018 Mahor and Prasad. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Gandham S. Prasad, email@example.com
†Present Address: Durga Mahor, TU Delft, Applied Sciences, Biotechnology, Delft, Netherlands