• 한국미생물·생명공학회지
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• 제43권4호
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• pp.330-335
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• 2015

Bacillus agaradhaerens 균주의 효소를 정제하여 그 특성을 확인하였다. 균주가 생산하는 xylanase를 70% ammonium sulfate로 침전하고 CM-sepharose ion exchange chromatography와 ultrafiltration(PM-10)을 행하여 16.7%의 수율과 6.7배의 정제도를 지니는 효소를 얻을 수 있었으며 SDS-PAGE를 통하여 23 kDa의 분자량을 갖는 효소임을 확인하였다. 효소의 최적 pH는 6.0으로서 sodium phosphate buffer에서 24시간까지 안정하였으며, 최적반응온도는 $60^{\circ}C$, EDTA의 첨가 시 효소활성이 증가되었고 $40^{\circ}C$에서 24시간까지 안정하였다. 효소는 xylan만을 기질로 이용할 수 있었으며 Birchwood xylan에 대하여 최대 활성을 나타내었고 $V_{max}$는 $49,724{\mu}M/min$, $K_m$은 6.08 mg/ml로 확인되었다.

• Asian-Australasian Journal of Animal Sciences
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• 제16권3호
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• pp.394-402
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• 2003

Individual and combined supplementation of phosphorus-adequate, wheat-based broiler diets with exogenous phytase and xylanase was evaluated in three experiments. The effects of the enzyme combination in lysine-eficient diets containing wheat and sorghum were more pronounced than those of the individual feed enzymes. The inclusion of phytase plus xylanase improved (p<0.05) weight gains (7.3%) and feed efficiency (7.0%) of broilers (7-28 days post-hatch) and apparent metabolisable energy (AME) by 0.76 MJ/kg DM. Phytase plus xylanase increased (p<0.05) the overall, apparent ileal digestibility of amino acids by 4.5% (0.781 to 0.816); this was greater than the responses to either phytase (3.6%; 0.781 to 0.809) or xylanase (0.7%; 0.781 to 0.784). Absolute increases in amino acid digestibility with the combination exceeded the sum of the individual increases generated by phytase and xylanase for alanine, aspartic acid, glutamic acid, glycine, histidine, isoleucine, phenylalanine, threonine, tyrosine and valine. These synergistic responses may have resulted from phytase and xylanase having complementary modes of action for enhancing amino acid digestibilities and/or facilitating substrate access. The two remaining experiments were almost identical except wheat used in Experiment 2 had a higher phytate concentration and a lower estimated AME content than wheat used in Experiment 3. Individually, phytase and xylanase were generally more effective in Experiment 2, which probably reflects the higher dietary substrate levels present. Phytase plus xylanase increased (p<0.05) gains (15.4%) and feed efficiency (7.0%) of broiler chicks from 4-24 days post-hatch in Experiment 2; whereas, in Experiment 3, the combination increased (p<0.05) growth to a lesser extent (5.6%) and had no effect on feed efficiency. This difference in performance responses appeared to be 'rotein driven'as the combination increased (p<0.05) nitrogen retention in Experiment 2 but not in Experiment 3; whereas phytase plus xylanase significantly increased AME in both experiments. In Experiments 2 and 3 the combined inclusion levels of phytase and xylanase were lower that the individual additions, which demonstrates the benefits of simultaneously including phytase and xylanase in wheat-based poultry diets.

• 펄프종이기술
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• 제35권1호
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• pp.34-40
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• 2003

This study was carried out to select the useful bacteria which secret extracellula enzymes for enzymatic deinking agent of old newspaper. CMCase, FPase and xylanase activities of the bacteria liquid culture were measured at optimal growth conditions. Clear zone test was checked on the solid culture. The results of this study were as follow: Eight strains of 28 bacteria isolated from a paper mill soil ground were shown strong CMCase and xylanase activity with the clear zone test. The optimal pH and temperature for culture growth were 6~8 and 26~$34^{\circ}C$, respectively and optimal culture period were less than 60 hours. Based on CMCase, FPase and xylanase activity, strain No. 18, 21, 22 and 28 which were relatively higher than the other strains, were selected for further enzymatic deinking research.

• 한국인쇄학회지
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• 제26권1호
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• pp.113-124
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• 2008

Viscosity of cellulose pulp was greatly decreased with endo-xylanase treatment but tiny decreased with exo-xylanase treatment. Change of freeness was greatly influenced with exo-xylanase treatment. The first stage of refining(5,000 revolution), freeness was greatly decreased with exo-xylanase treatment. After middle stage of refining(10,000 revolution) change of freeness was similar to endo-xylanase treatment. WRV(water retention value) was more effective exo-xylanas than endo-xylanase treatment. Interfiber bonding of cellulose fiber was disintegrated with exo-xylanse treatment.

• Journal of Microbiology and Biotechnology
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• 제12권1호
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• pp.153-156
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• 2002

The characterization of a partially purified, cellulase-free, thermostable alkaline xylanase from thermoalkalophilic Bacillus sp. JB-99 was investigated. The xylanase production was the highest when birchwood xylan was added to a medium containing finely powdered rice bran, showing 4,826 IU$ml^-1$ of activity for 15 h of incubation. The partially purified xylanase exhibited an optimum temperature and pH at $70^C{\circ}$ and 10, respectively. The enzyme was stable at pH 5-11 at $50^C{\circ}$. The xylanase activity was strongly inhibited by $Hg^2+$, while dithiothreitol, cysteine, and ${\beta}$-mercaptoethanol enhanced the activity.

• 한국식품영양학회지
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• 제7권1호
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• pp.1-7
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• 1994

To investigate the characteristics of active sites of the D-xylanase and $\beta$-xylosidase purified from Penicillium verruculosum, effects of various chemicals on the enzyme activity were analyzed. The D-xylanase was activated by Cua), however it was inhibited by metal ions, Hg2+ and Mna+, by chemicals, N-bromosuccinimide, iodine, diethylpyrocarbonate, and 2,3-butanedione. These results suggested that the D-xylanase from Penicillium verruculosum contained tyrosine, histidine, arginine and tryptophan at the active center. The $\beta$-xylosidase was inhibited by Hg2+, N-bromosuccinimide and sodium dodecyl sulfate, however it was not effected by Mn2+ and Cu2). It was suggested that the enzyme contained tryptophan at the active center.

• Journal of Microbiology and Biotechnology
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• 제7권6호
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• pp.386-390
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• 1997

A xylanase from the Bacillus sp. strain DSNC 101, isolated from soil, was purified to homogeneity by anion-exchange and hydrophobic interaction chromatography followed by gel filtration chromatography. The enzyme cleaved xylan, but not carboxymethyl cellulose, Avicel, soluble starch, and pNPX. The main product of oat spelts xylan hydrolysates was xylobiose. The xylanase had a molecular weight of 25 kDa determined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. Optimum temperature and pH for the xylanase activity were $50^{\circ}C$ and 6.0, respectively. $K_{m}\;and\;V_{max}$ of the enzyme for oat spelts xylan were 12.5 mg of xylan/ml and 869.5 unit/mg of protein, respectively. Xylanase was completely inhibited by Hg, Cu, and N-bromosuccinimide, but was stimulated by Ca, Co, and Mg.

• 펄프종이기술
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• 제30권3호
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• pp.7-14
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• 1998

It is well known that the recycling of pulp generates a lot of fines, and cause the hornification of fiber. Both phenomena have been contributed to a limited use of recycled fiber. Among several means which can improve the properties of recycled fiber, enzymatic treatments are considered as an effective means. Thus the effects of xylanase on the properties of recycled pulp were investigated in this study Xylanase treatment showed some refining effect at a small dosage while the fines and fibrils were reduced at higher dosage as shown in the treatment with cellulase-hemicellulase. The interesting finding is that the WRV of recycled fiber treated with xylanase was higher than that treated with the mixture of cellulase and hemicellulase. Breaking length and tear index of recycled fiber treated with xylanase were also higher.

• 한국미생물·생명공학회지
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• 제31권4호
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• pp.383-388
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• 2003

가축 사료첨가용 효소생산을 목적으로 xylanase 및 CMCase를 동시에 분비하는 미생물을 분리한 후 가장 생산성이 높은 균주를 선발하였다. 선발된 미생물을 동정한 결과 Bacillus sp.에 속하는 균주로 Bacillus sp. A-7로 명명하였으며, B. licheniformis로 동정되었다. 효소생산을 위한 최적 액상배양조건은 탄소원으로 glucose 2.0%(w/v), 질소원으로 yeast extract 0.3%(w/v), 미네랄은 CaCl$_2$ 0.1% (w/v)인 것으로 나타났다. 저렴한 효소생산을 위한 배지조성을 얻기 위해 가축사료로 이용되는 저가의 원료사료를 이용하여 효소생산성을 파악한 결과 대두박 1.0%(w/v)와 당밀 0.5%(w/v)가 특히 xylanase 생산성이 높은 것으로 나타났다. 특히, 대두박 1.0%(w/v)를 기본배지로 하여 ammonium nitrate 0.3%(w/v) 및$ CaCl_2$ 0.1% 첨가가 적합한 배지조성으로 나타났다.

• Journal of Microbiology and Biotechnology
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• 제28권4호
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• pp.638-644
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• 2018

In this study, the immobilization of xylanase using a protein-inorganic hybrid nanoflower system was assessed to improve the enzyme properties. The synthesis of hybrid xylanase nanoflowers was very effective at $4^{\circ}C$ for 72 h, using 0.25 mg/ml protein, and efficient immobilization of xylanase was observed, with a maximum encapsulation yield and relative activity of 78.5% and 148%, respectively. Immobilized xylanase showed high residual activity at broad pH and temperature ranges. Using birchwood xylan as a substrate, the $V_{max}$ and $K_m$ values of xylanase nanoflowers were 1.60 mg/ml and $455{\mu}mol/min/mg$ protein, compared with 1.42 mg/ml and $300{\mu}mol/min/mg$ protein, respectively, for the free enzyme. After 5 and 10 cycles of reuse, the xylanase nanoflowers retained 87.5% and 75.8% residual activity, respectively. These results demonstrate that xylanase immobilization using a proteininorganic hybrid nanoflower system is an effective approach for its potential biotechnological applications.