木腐真菌KLUM2在Kirk培养基碱木质素Kayu Jati(MK-ALKJ)中产漆酶的酶谱分析及优化

S. Mutmainah, E. Susanti
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引用次数: 0

摘要

木腐菌产生木质素酶受碳源和生长条件的影响。本研究的目的是确定以栎木碱性木质素为碳源的WRF KLUM2在Kirk培养基中产生的木质素酶谱,即Kirk Medium- alkali lignin Kayu Jati (MK-ALKJ),与在Kirk培养基中以葡萄糖为碳源(MK-Glucose)产生的木质素酶相比,MK-ALKJ中木质素酶产量的优势优化。本研究在实验室内进行,包括:(1)孢子悬浮液的制备,(2)不同生长时期的木质素酶谱分析,(3)不同温度变化下的木质素酶谱分析,(4)优化漆酶的产量,包括pH和氮源的量。根据木质素过氧化物酶(LiP)、锰过氧化物酶(MnP)和漆酶的比活性鉴定其生长情况。结果表明,木腐菌KLUM2在MK-ALJK中产生的LiP、MnP和漆酶3种木质素酶含量相对相同。3个品种产量最高,分别为55.65;52.48;57.64 U /毫克。在37℃、pH = 3.5、氮源为20mM (NH4)2SO4的MK-ALKJ培养基中接种2.107个孢子细胞,培养6 d后,漆酶作为优势木质素酶可达到83.52 U/mg。由此可见,本地WRF KLUM2在MK-ALJK培养基中的木质素酶活性高于MK-Glucose培养基。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ligninase Profiling and Optimization of Laccase Production from Indigenous Wood Rot Fungus (WRF) KLUM2 in Kirk Medium-Alkali Lignin Kayu Jati (MK-ALKJ)
The production of ligninase by wood rot fungus (WRF) is determined by carbon source and growth condition. The goal of this study is to determine the ligninase profile produced by WRF KLUM2 in Kirk Medium using teak wood alkaline lignin as a carbon source known as Kirk Medium-Alkali lignin Kayu Jati (MK-ALKJ), optimization of dominant ligninase production in the MK-ALKJ compared to the one that is produced in the Kirk’s medium with glucose as a carbon source (MK-Glucose). This research was conducted in an experimental laboratory consisting of: (1) spore suspension preparation, (2) ligninase profiling at various growth times, (3) ligninase profiling at various temperature variations, (4) optimization of laccase production including pH and the amount of nitrogen source. Growth was identified based on the specific activity of lignin peroxidase (LiP), manganese peroxidase (MnP), and laccase. The results showed that relatively the three types of ligninase, namely LiP, MnP, and laccase, were produced in the same amount by the wood rotting fungus isolates KLUM2 in MK-ALJK. All three were produced with the highest yield of respectively 55.65; 52.48; 57.64 U/mg. Laccase as the dominant ligninase can be optimized to reach 83.52 U/mg by inoculating 2.107 spore cells in MK-ALKJ in 37 °C, pH = 3.5, and a nitrogen source of 20mM (NH4)2SO4 for 6 days. Therefore, it can be concluded that the ligninase activity of indigenous WRF KLUM2 in MK-ALJK medium is higher than in the MK-Glucose.
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CiteScore
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