Use of corn cob through xylan extraction and its potential use as a substrate for the quantification of xylanase enzymatic activity

R. Uzárraga-Salazar, Yamilet Nallely Reyes-Ramírez, Tania García-Herrera, E. Flores‐Andrade, M. Castillo-Morales
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Abstract

In Mexico, it is estimated that the amount of residues produced by the planting of the ten main crops is approximately 45 million tons of dry matter, of which just over 25 million tons are corn cob. The corn cob contains large amounts of hemicellulose, mainly composed of xylan, which can have various industrial uses. For this reason, in the present study, fresh and dry corn cob was used with two particle sizes: 0.105 mm and 0.42 mm, to carry out an exhaustive alkaline extraction of xylan and where eight fractions of hemicelluloses extracts were obtained. Each of the fractions were subjected to enzymatic hydrolysis for eight hours with a commercial xylanase (Livanol Devisco 1500) and as internal control, beechwood xylan (Sigma Aldrich, X4252) was used, of which only 6.9 ± 2.25 g/L were released. reducing sugars. It was found that the fractions from the steam treatment and the fraction from the alkaline extraction precipitated with alcohol, both for fresh corn cob, were released a quantity of reducing sugars very similar to commercial xylan with 7.10 ± 2.02 and 7.24 ± 0.37 g/L, respectively. Finally, it was possible to determine that although the 8 fractions obtained in the present study can be used as substrates to determine the xylanase enzymatic activity, the best was the fraction of the alkaline extraction since 0.236 ± 0.03 IU/mL were quantified, while for the commercial substrate (beechwood xylan) an activity of 0.287 ± 0.01 IU/mL was obtained.
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利用玉米芯提取木聚糖及其作为底物定量测定木聚糖酶活性的潜力
在墨西哥,据估计,种植十种主要作物所产生的残留物约为4500万吨干物质,其中2500多万吨是玉米芯。玉米芯含有大量的半纤维素,主要由木聚糖组成,具有多种工业用途。为此,本研究以鲜玉米芯和干玉米芯为原料,分别以0.105 mm和0.42 mm两种粒径对木聚糖进行了全碱提取,得到了8个半纤维素提取物组分。用商用木聚糖酶(Livanol desivco 1500)水解8小时,内对照为山毛榉木聚糖(Sigma Aldrich, X4252),其释放量仅为6.9±2.25 g/L。还原糖。结果表明,新鲜玉米芯蒸馏分和碱提醇沉馏分的还原糖释放量与商品木聚糖相似,分别为7.10±2.02和7.24±0.37 g/L。最后可以确定,虽然本研究得到的8个组分都可以作为测定木聚糖酶酶活性的底物,但以碱性提取的组分为最佳,定量为0.236±0.03 IU/mL,而商业底物(山毛榉木聚糖)的酶活性为0.287±0.01 IU/mL。
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