Kobe : High Enzymatic Recovery and Purification of Xylooligosaccharides from Empty Fruit Bunch via Nanofiltration

: Xylooligosaccharides (XOS) are attracting an ever-increasing amount of interest for use as food prebiotics. In this study, we used e ﬃ cient membrane separation technology to convert lignocellulosic materials into a renewable source of XOS. This study revealed a dual function of nanoﬁltration membranes by ﬁrst achieving a high yield of xylobiose (a main component of XOS) from alkali-pretreated empty fruit bunch (EFB) hydrolysate, and then by achieving a high degree of separation for xylose as a monosaccharide product. Alkali pretreatment could increase the xylan content retention of raw EFB from 23.4% to 26.9%, which eventually contributed to higher yields of both xylobiose and xylose. Nanoﬁltration increased the total amount of XYN10Ks_480 endoxylanase produced from recombinant Streptomyces lividans 1326 without altering its speciﬁc activity. Concentrated XYN10Ks_480 endoxylanase was applied to the recovery of both xylobiose and xylose from alkali-pretreated EFB hydrolysate. Xylobiose and xylose yields reached 41.1% and 17.3%, respectively, and when unconcentrated XYN10Ks_480 endoxylanase was applied, those yields reached 35.1% and 8.3%, respectively. The last step in nanoﬁltration was to separate xylobiose over xylose, and 41.3 g.L − 1 xylobiose (90.1% purity over xylose) was achieved. This nanoﬁltration method should shorten the processes used to obtain XOS as a high-value end product from lignocellulosic biomass.

In order to increase the production of XOS, however, the hydrolysates produced by these processes must be refined, and by-products such as monosaccharides and monosaccharide compounds must be separated to increase the purity of XOS [6][7][8]. For example, enzymatic hydrolysis by xylanase produces monosaccharides in addition to XOS, which lowers the concentration of XOS [9]. In our previous study, the microbial production of recombinant endo-1,4-β-xylanase (XYN10Ks_480 endoxylanase) was realized using Streptomyces lividans 1326 expressing an endoxylanase gene from the Kitasatospora sp. strain ID06-480, and the crude enzyme was free from cellulase activity [10]. This strategy enabled the co-production of xylose and XOS from acid-pretreated sugarcane bagasse [10,11]. To increase the yield of XOS, alkali pretreatment is preferable to acid pretreatment, because alkali pretreatment exhibits a minor amount of hemicellulose solubilization compared with the acid process [12]. In addition to sugarcane bagasse, another promising lignocellulosic source is empty fruit bunch (EFB), which is a waste product from palm oil plantations. Today, Indonesia and Malaysia produce approximately 85% of global crude palm oil [13]. However, the palm industry must dispose of about 1.1 tons of EFB per ton of oil produced [14]. As EFB is a non-edible part of the palm plant, it was chosen as useful lignocellulosic waste in this study [15].
The use of commercial enzymes is costly and is one of the obstacles of lignocellulose-based biorefinery technology [16]. Therefore, it is desirable to concentrate on improving total enzymatic activity. Recently, pressure-driven membrane separation processing that uses low levels of energy consumption has been used to recover enzymes and improve subsequent fermentation efficiency [17,18]. In the food industry, membrane operations are applied in the beverage industry (wine, beer, fruit juices, etc.), the dairy industry (whey protein concentration, milk protein standardization, etc.) and, to a lesser extent, in the processing of egg products [19]. In biorefinery, membrane separation has mainly been applied for biofuel recovery, sugar purification, fermentation, hydrolysis, and solvent recycling [20]. Here, the application of membrane processes to recover XOS as ingredients in functional foods from EFB were evaluated. To enhance sugar yields in the enzymatic scarification of insoluble solid fractions, one of the solutions has involved concentrating enzymes by applying membrane separation technologies. The other use of membrane separation has been to increase the purity of XOS to xylose. The purity of commercial XOS ranges from 75% to 95% [8].
The first purpose of this study was to increase the yield of XOS from alkali-pretreated EFB obtained by enzymatic hydrolysis using XYN10Ks_480 endoxylanase produced by S. lividans 1326, expressing an endo-xylanase gene from the Kitasatospora sp. strain ID06-480. This process was subjected to the nanofiltration (NF) membrane concentration process. The second purpose of this study was to investigate the purification procedure for XOS from xylose via the NF separation process. This process demonstrated the dual function of NF by improving both enzymatic yield as well as the purity of the XOS end-product.

Materials and Microorganisms
The EFB from Elaeis guineensis used in this study was obtained from Oil Palm Mill in Sukabumi, West Java, Indonesia. It was provided in the form of dry fiber. The EFB was ground using a hammer mill (Pallmann Maschinenfabrik GmbH & Co. KG, Zweibrücken, Germany), followed by a disc mill (Swan, Surabaya, Indonesia). Then, it was sieved using 40 and 60 mesh sieves to obtain a material with particle sizes equal to a 40-60 mesh and maintained in sealed plastic bags that were stored in a container.
For alkali pretreatment, 60 g of EFB was soaked in 300 mL of 3% (w/w) sodium hydroxide solution at room temperature for 24 h and was then filtered with Filter 70 (Strix design, Tokyo, Japan) to recover the insoluble EFB solids. The recovered solids were then washed with distilled water until pH neutrality was reached. After the solids were neutralized, they were transferred to an autoclave vessel (1 L working volume) and autoclaved at 130 • C for 8 min under 20 bar. The alkali-pretreated EFB was stored at -20 • C until further use. This method was conducted in the same manner as in our previous report [15]. The recombinant strain used was S. lividans 1326 (NBRC 15675), bearing an expression system of the xylanase gene from Kitasatospora sp. ID06-480, as described previously [10].

Xylanase Production
Recombinant S. lividans 1326 (NBRC 15675) bearing the expression system of XYN10Ks_480 endoxylanase was inoculated into a test tube containing 5 mL of tryptic soy broth (TSB) medium (Becton, Dickinson and Company, Sparks, MD, USA) supplemented with 5 µg/mL of thiostrepton (EMD Chemicals, San Diego, CA, USA), and was then cultured at 28 • C for two days. Then, 1 mL of the seed was inoculated into a 500 mL baffled shaking flask containing 250 mL of TSB medium followed by the addition of 30 g/L glucose (Nacalai, Kyoto, Japan) as a carbon source, 15 g/L tryptone (Nacalai, Kyoto, Japan) as a nitrogen source, and 5 µg/mL of thiostrepton. To induce xylanase production, L-(-)-sorbose (Sigma-Aldrich, St. Louis, MO, USA) was added to the medium to reach a final concentration of 0.05 g/L. Cultivation was performed at 28 • C for three days.
After three days of cultivation, S. lividans 1326 was harvested by centrifugation at 13,000 rpm and 4 • C for 10 min and dialyzed by MEMBRA-CEL ® dialysis tubing with a molecular weight cut-off (MWCO) of 3500 (RC, SERVA Electrophoresis GmbH, Heidelberg, Germany). This was followed by filtration using the following order of filter papers: polycarbonate 0.8 µm, polycarbonate 0.5 µm, and polystyrene 0.22 µm. The solution was then subjected to membrane concentration.

Enzymatic Activity Assay and Protein Assay
The XYN10Ks_480 endoxylanase activity was measured via a dinitrosalicylic acid (DNS) method developed by Miller with modifications [21]. Briefly, the enzymatic reaction consisted of 0.5% w/v beechwood xylan (Sigma-Aldrich, St. Louis, MO, USA), 50 mM sodium acetate buffer (pH 5.0), and 50 µL of the culture supernatant, incubated at 50 • C for 15 min, which was then stopped by the addition of 0.5 mL DNS solution. After being boiled for 5 min in water, the mixture was cooled on ice for 10 min and measured at 540 nm in a UV-VIS spectrophotometer (UVmini-1240, Shimadzu, Kyoto, Japan). One enzyme unit was defined as the amount of enzyme that released 1 µmol of reducing sugar for 1 min of the reaction. A protein assay was performed using a Pierce™ BCA Protein Assay Kit (Thermo Scientific™, Rockford, Illinois, USA).

Membrane Separation Process
RS50, a polyvinylidene fluoride ultrafiltration membrane (UF) with an MWCO of 150,000 Da, sulfonated polyethersulfone NF membrane NTR-7410 (MWCO 3000 Da), and NF membrane NTR-7450 (MWCO 600-800 Da) were obtained from the Nitto Denko Corporation (Osaka, Japan) and cut into 7.5 -cm diameter circles. The RS50 membranes were pretreated by soaking in a 50% (v/v) ethanol solution for 15 min, which was continued in deionized water for 15 min, with a final overnight soaking in deionized water before use. All membranes were used at 400 r/min, 25 • C, with pressures of 0.5 MPa for UF and 2.6 MPa for NF by pressure-driven nitrogen gas inside a flat membrane test cell (diameter, 104 mm; height, 147 mm; working volume, 380 mL; model, C40-B; Nitto Denko Corporation, Osaka, Japan) [22].

Enzymatic Hydrolysis of Pretreated EFB
The enzymatic saccharification of the pretreated EFB was performed in 50 mL screw cap Corning ® centrifuge tubes (Sigma-Aldrich, Tamaulipas, Mexico). The reaction was started by adding 15% (w/v) of the pretreated EFB (equal to 1.8 g dry basis) into a 6 mL acetate buffer solution (pH 5) for a final volume of 50 mM, following the addition of 3.6 mL NF membrane-concentrated or unconcentrated XYN10Ks_480 endoxylanase from the S. lividans 1326 strain. The solution was increased to 12 mL with the addition of distilled water before incubation at 50 • C with rotation at 70 r/min. The xylose yield was calculated using a xylose equation introduced by Pangsang, and XOS were calculated based on molecular weight [23].

Thin-Layer Chromatography Analysis
Thin-layer chromatography (TLC) analysis was used to identify the hydrolysis products. The hydrolysis products were filtered through a SEPARA ® syringeless filter membrane (Zola Pedrosa, Italy) and detected by TLC. Sample aliquots (1 µL) were spotted four times on a TLC plate (Silica gel 60 F-254; EMD/Merck, Darmstadt, Germany), and developed in a solvent system containing n-butanol, acetic acid, and water (2:1.1:1, v/v/v). Spots were stained using DAAP reagent that contained diphenylamine, aniline, acetone, and phosphoric acid (Merck KGaA, Darmstadt, Germany), which was followed by heating at 120 • C for 15 min. The standard mixture contained xylose, xylobiose, xylotriose, xylotetraose, and xylopentaose, all of which were purchased from Megazyme (Wicklow, Ireland) [11].

Analytical Methods
Compositional analysis of the EFB before and after alkali pretreatment was performed using a standard procedure stipulated by the National Renewable Energy Laboratory (NREL) [24]. A high-performance liquid chromatographic (HPLC) method (Shimadzu, Kyoto, Japan) was used to determine the concentrations of xylose, xylobiose, xylotriose, xylotetraose, and xylopentaose. The standards of these compounds were obtained from Megazyme (Wicklow, Ireland). The HPLC was equipped with a refractive index (RI) detector and a column set of dual series TSKgel G2500PW XL (TOSOH Corporation, Tokyo, Japan) and operated at 80 • C using Milli-Q water as mobile phase at a flow rate of 0.5 mL/min.

Alkali Pretreatment
In this study, EFB was pretreated with alkali (sodium hydroxide) to retain hemicellulose for enzymatic hydrolysis. The chemical compositions of EFB before and after alkali pretreatment were analyzed in accordance with the NREL method [24] and appear in Table 1. A higher xylan content after pretreatment is desirable [1]. The alkali pretreatment increased the xylan content of raw EFB from 23.4% to 26.9%, which would eventually aid in a higher recovery of XOS [25]. The glucan content of raw EFB was also increased from 37.3% to 45.0%, which agreed with results published by Choil et al. [15]. During alkali pretreatment, the biomass amount was decreased; however, carbohydrate content increased, and lignin content was unchanged. This result corresponded with the previous report showing that the alkali pretreatment selectively removed lignin without degrading carbohydrates, thereby enhancing enzymatic hydrolysis [26].

Characterization of XYN10Ks_480 Endoxylanase for Membrane Selections
Alkali-pretreated EFB was enzymatically hydrolyzed by XYN10Ks_480 endoxylanase produced by recombinant S. lividans 1326 to obtain XOS and xylose. SDS-PAGE had previously shown that a protein band at 49 kDa belonged to the endo-1,4-β-xylanase GH-family 10 [10]. Thus, NTR-7410 with an MWCO of 3 kDa was selected as a membrane that could be used to concentrate the xylanase [22]. The NF membrane separation process was applied to 350 mL of the culture supernatants of recombinant S. lividans 1326. Aliquots of culture supernatant, membrane retentate, and membrane permeate were used to measure XYN10Ks_480 endoxylanase activity and protein content.
The results of XYN10Ks_480 endoxylanase activity and protein content are listed in Table 2. Both XYN10Ks_480 endoxylanase activity and protein assay in the membrane retentate were increased compared with those in the culture supernatant. The specific activity of XYN10Ks_480 endoxylanase in the culture supernatant was similar to that in the membrane retentate. This indicated that XYN10Ks_480 endoxylanase had retained its enzyme stability even after a pressure of 2.6 MPa was applied to the system (specific activity: 6.8-6.9 U/mg). This corresponded with previous results, showing that a pressure of more than 100 MPa had slightly inactivated the xylanase activity of Dictyoglomus thermophilum [27].

230
The primary hydrolysate from alkali-pretreated EFB using concentrated XYN10Ks_480 231 endoxylanase produced by recombinant S. lividans 1326 was subjected to sequential membrane NFs 232 to refine and concentrate the XOS from xylose. The liquor was first subjected to an RS50 UF 233 membrane to remove the macromolecules and to recover the sugar solution [28]. The UF permeate

239
The value of xylobiose against xylose achieved a maximum value of 90.1%, which compares with 240 commercial XOS that range from 75% to 95% [8]. The NTR-7450 NF membrane, as previously 241 described, produced concentrated sucrose while simultaneously separating glucose and fructose,

242
and was also sufficient for the separation of xylobiose from xylose [28].

243
Membrane separation is a promising process for refining and concentrating XOS due to high 244 recovery, low energy, and a simple procedure that does not require other chemicals as a solvent 245 [6,8]. The efficient co-production of xylobiose and xylose from alkali-pretreated EFB was achieved

Concentration and Separation of Xylobiose by Nanofiltration
The primary hydrolysate from alkali-pretreated EFB using concentrated XYN10Ks_480 endoxylanase produced by recombinant S. lividans 1326 was subjected to sequential membrane NFs to refine and concentrate the XOS from xylose. The liquor was first subjected to an RS50 UF membrane to remove the macromolecules and to recover the sugar solution [28]. The UF permeate contained 8 g.L −1 xylose and 11.2 g.L −1 xylobiose (xylopentaose was a minuscule fraction, less than 1 g.L −1 ). The application of NTR-7450 NF to increase xylobiose and separate xylose was repeated four times, with dilutions (up to five-fold) simultaneously administered three times, as described in Figure 3. As a result, the NTR-7450 NF membrane produced concentrated xylobiose at 41.3 ± 6.3 g.L −1 for a recovery rate of 42.4% and decreased xylose to 4.1 ± 0.3 g.L −1 for a recovery rate of 5.8%. The value of xylobiose against xylose achieved a maximum value of 90.1%, which compares with commercial XOS that range from 75% to 95% [8]. The NTR-7450 NF membrane, as previously described, produced concentrated sucrose while simultaneously separating glucose and fructose, and was also sufficient for the separation of xylobiose from xylose [28].

Conclusions
A method was successfully developed to purify XOS from a primary hydrolysate of alkali-pretreated EFB using concentrated XYN10Ks_480 endoxylanase produced by recombinant S. lividans 1326. An NF membrane performed the dual function of concentrating xylanase and purifying the XOS fraction. As a result, an efficient co-production of xylobiose and xylose from alkali-pretreated EFB was achieved via an integration between XYN10Ks_480 endoxylanase production from a recombinant strain and membrane separation technology. At first, alkali pretreatment retained xylan content ranging from 23.4% to 26.9% from raw EFB, which would eventually contribute to higher yields of xylobiose and xylose. The NF step was used to increase the total amount of XYN10Ks_480 endoxylanase produced from recombinant S. lividans 1326 without altering its specific activity. By applying the concentrated XYN10Ks_480 endoxylanase, both xylobiose and xylose from alkali-pretreated EFB hydrolysate were recovered (xylobiose and xylose yields reached 41.1% and 17.3%, respectively) in higher yields compared with the use of unconcentrated XYN10Ks_480 endoxylanase (with xylobiose and xylose yields that reached 35.1% and 8.3%, respectively). Then, NF was used to separate xylobiose over xylose, and a 41.3 g.L −1 yield of xylobiose (90.1% purity over xylose) was achieved. Future works should focus on large-scale applications for industrial approaches.