新发现的聚酯聚氨酯降解甲基细菌aquaticum菌株A1的表征。

IF 3.5 4区 生物学 Q2 MICROBIOLOGY
Seong Hyeon Lee, Haemin Jeong, Injun Jung, Myounghyun Choi, Ah-Ram Kim
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引用次数: 0

摘要

在这项研究中,我们提出了一种能够降解聚酯聚氨酯(PE-PUR)的新型菌株——水甲基细菌A1。利用扫描电镜(SEM)和傅里叶变换红外光谱(FT-IR)验证了M. aquaticum A1在PE-PUR上的附着及其降解能力。通过对水草参比基因组的分析,揭示了具有PE-PUR降解活性的酶编码基因,包括酯酶、脂肪酶、蛋白酶和酰胺酶,如tesA、pgpB、aes、aprE、lon、degQ和gatA。采用对硝基苯乙酸酯(p-NPA)进行的酯酶活性测定显示,当M. aquaticum A1暴露于聚氨酯二醇(PU-diol)时,酯键裂解活性增加,表明酶活性参与了PE-PUR的降解。这些发现突出了M. aquaticum A1作为PE-PUR降解生物催化剂的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characterization of Newly Discovered Polyester Polyurethane-Degrading Methylobacterium aquaticum Strain A1.

In this study, we present Methylobacterium aquaticum A1, a novel strain capable of degrading polyester polyurethane (PE-PUR). The attachment of M. aquaticum A1 to PE-PUR and its degradation capabilities were verified using Scanning Electron Microscopy (SEM) and Fourier-Transform Infrared Spectroscopy (FT-IR). Analysis of the reference genome of M. aquaticum revealed genes encoding enzymes with potential PE-PUR degrading activity, including esterases, lipase, proteases and amidase such as tesA, pgpB, aes, aprE, lon, degQ, and gatA. An esterase activity assay using p-nitrophenyl acetate (p-NPA) showed increased ester bond-cleaving activity when M. aquaticum A1 was exposed to polyurethane diol (PU-diol), suggesting inducible enzymatic activity involved in PE-PUR degradation. These findings highlight the potential of M. aquaticum A1 as a promising biocatalyst for PE-PUR degradation.

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来源期刊
Journal of Basic Microbiology
Journal of Basic Microbiology 生物-微生物学
CiteScore
6.10
自引率
0.00%
发文量
134
审稿时长
1.8 months
期刊介绍: The Journal of Basic Microbiology (JBM) publishes primary research papers on both procaryotic and eucaryotic microorganisms, including bacteria, archaea, fungi, algae, protozoans, phages, viruses, viroids and prions. Papers published deal with: microbial interactions (pathogenic, mutualistic, environmental), ecology, physiology, genetics and cell biology/development, new methodologies, i.e., new imaging technologies (e.g. video-fluorescence microscopy, modern TEM applications) novel molecular biology methods (e.g. PCR-based gene targeting or cassettes for cloning of GFP constructs).
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