Immobilized inclusion bodies of recombinant cold-adaptive lipase from Antarctic Pseudomonas sp. as catalysts

IF 4.3 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Muhammad Nura Bello, Suriana Sabri, Normi Mohd Yahaya, Fairolniza Mohd Shariff, Mohd Shukuri Mohamad Ali
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Abstract

Immobilization of lipase has been receiving attention for a long time; this is because of the need for robust catalysts by industries. Numerous literature has reported improvements in the properties of immobilized lipase in terms of stability when exposed to extreme conditions of temperature, pH, and organic solvents commonly encountered in most industrial settings. However, some microbial lipases that have the potential to catalyze significant reactions do occur in the form of inclusion bodies when expressed in Escherichia coli. This research aimed to immobilize catalytically active inclusion bodies (CatIBs) of LipAMS8 lipase onto Seplite LX120 as the adsorption material. Scanning electron microscopy and Fourier infrared spectroscopy were used to ascertain the immobilization. Immobilized CatIBs have an optimum temperature of 20 °C and pH of 9.0. They exhibit high stability to broad temperatures, pH levels, and organic solvents, with excellent storage stability and reusability, retaining 50% of their residual activity after ten cycles. They demonstrated excellent activity in the transesterification of waste cooking oil with methanol, in which 2% of the immobilized CatIBs produced up to 98% biodiesel in a ratio of 1:9 at 25 °C for 7 h at 200 rpm. LipAMS8 CatIBs immobilization improved their stability and capability to produce biodiesel at lower temperatures.

Catalytically active inclusion bodies from recombinant AMS8 lipase occurring naturally were successfully immobilized onto seplite LX120. Morphological and structural analyses using SEM and FITR confirmed the immobilization.

Characterization revealed the immobilized LipAMS8 CatIBs to maintain the residual activity of up to 50% at a broad temperature (10–80 °C) and pH (4–12).

Interactions with metal ions and various organic solvents manifest their stability. Transesterification reaction with methanol using palm cooking oil to produce biodiesel at 25 °C which revealed their synthetic capacity.

固定化南极假单胞菌重组冷适应脂肪酶包涵体作为催化剂。
脂肪酶的固定化一直受到人们的关注。这是因为工业需要强大的催化剂。许多文献报道了固定化脂肪酶在暴露于温度、pH值和大多数工业环境中常见的有机溶剂的极端条件下的稳定性方面的改进。然而,一些具有催化重要反应潜力的微生物脂肪酶在大肠杆菌中表达时确实以包涵体的形式发生。本研究旨在将LipAMS8脂肪酶的催化活性包合体(CatIBs)固定在Seplite LX120上作为吸附材料。采用扫描电镜和傅里叶红外光谱对固定化进行了验证。固定化CatIBs的最佳温度为20℃,pH为9.0。它们在广泛的温度、pH值和有机溶剂中表现出很高的稳定性,具有优异的储存稳定性和可重复使用性,在10次循环后保留50%的剩余活性。它们在废食用油与甲醇的酯交换反应中表现出优异的活性,其中2%的固定化CatIBs在25°C、200 rpm、7 h下以1:9的比例生产高达98%的生物柴油。LipAMS8 CatIBs的固定化提高了其稳定性和低温生产生物柴油的能力。•天然存在的重组AMS8脂肪酶具有催化活性的包体体成功地固定在分离物LX120上。利用扫描电镜和红外光谱进行形态学和结构分析,证实了固定。•表征表明固定化的LipAMS8 CatIBs在宽温度(10-80℃)和pH(4-12)下保持高达50%的残留活性。•与金属离子和各种有机溶剂的相互作用表明其稳定性。用棕榈油与甲醇在25℃条件下进行酯交换反应制备生物柴油,揭示了其合成能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Applied Microbiology and Biotechnology
Applied Microbiology and Biotechnology 工程技术-生物工程与应用微生物
CiteScore
10.00
自引率
4.00%
发文量
535
审稿时长
2 months
期刊介绍: Applied Microbiology and Biotechnology focusses on prokaryotic or eukaryotic cells, relevant enzymes and proteins; applied genetics and molecular biotechnology; genomics and proteomics; applied microbial and cell physiology; environmental biotechnology; process and products and more. The journal welcomes full-length papers and mini-reviews of new and emerging products, processes and technologies.
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