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开发内生青霉(Penicillium oxalicum)作为木质纤维素酶的来源,以增强生物炼制相关预处理水稻秸秆的水解。

Developing endophytic Penicillium oxalicum as a source of lignocellulolytic enzymes for enhanced hydrolysis of biorefinery relevant pretreated rice straw.

机构信息

Department of Microbiology, Guru Nanak Dev University, Amritsar, 143005, Punjab, India.

Center for Structural and Functional Genomics, Concordia University, 7141 Sherbrooke Street West, Montreal, QC, H4B 1R6, Canada.

出版信息

Bioprocess Biosyst Eng. 2024 Dec;47(12):2055-2073. doi: 10.1007/s00449-024-03085-2. Epub 2024 Sep 9.

Abstract

Endophytic fungi, as plant symbionts, produce an elaborate array of enzymes for efficient disintegration of lignocellulosic biomass into constituent monomeric sugars, making them novel source of lignocellulolytic CAZymes with immense potential in future biorefineries. The present study reports lignocellulolytic enzymes production potential of an endophytic halotolerant Penicillium oxalicum strain isolated from Citrus limon, under submerged and solid-state fermentation (SmF & SSF, respectively), in the presence and absence of salt (1 M NaCl). The comparative QTOF-LC/MS-based exoproteome analysis of the culture extracts unveiled differential expression of CAZymes, with the higher abundance of GH6 and GH7 family cellobiohydrolase in the presence of 1 M salt. The strain improvement program, employing cyclic mutagenesis and diploidization, was utilized to develop hyper-cellulase producing mutant strains of P. oxalicum. The enzyme production of the developed strain (POx-M35) was further enhanced through statistical optimization of the culture conditions utilizing glucose mix disaccharides (GMDs) as an inducer. This optimization process resulted in the lignocellulolytic cocktail that contained high titers (U/mL) of endoglucanase (EG) (146.16), cellobiohydrolase (CBHI) (6.99), β-glucosidase (β-G) (26.21), xylanase (336.05) and FPase (2.02 U/mL), which were 5.47-, 5.54-, 8.55-, 4.96-, and 4.39-fold higher when compared to the enzyme titers obtained in wild HP1, respectively. Furthermore, the lignocellulolytic cocktails designed by blending secretome produced by mutant POx-M35 with xylanases (GH10 and GH11) derived from Malbranchea cinnamomea resulted in efficient hydrolysis of unwashed acid pretreated (UWAP) rice straw slurry and mild alkali deacetylated (MAD) rice straw. This study underscores the potential of bioprospecting novel fungus and developing an improved strain for optimized production and constitution of lignocellulolytic cocktails that can be an important determinant in advancing biomass conversion technologies.

摘要

内生真菌作为植物共生体,产生了一系列复杂的酶,用于将木质纤维素生物质高效分解为组成单糖,使它们成为未来生物炼制厂中具有巨大潜力的新型木质纤维素 CAZymes 来源。本研究报告了从柠檬中分离出的耐盐内生青霉(Penicillium oxalicum)菌株在液体和固态发酵(分别为 SmF 和 SSF)条件下,在有盐(1 M NaCl)和无盐条件下,产木质纤维素酶的潜力。基于 QTOF-LC/MS 的外肽组分析揭示了 CAZymes 的差异表达,在有 1 M 盐的情况下,GH6 和 GH7 家族纤维二糖水解酶的丰度更高。采用循环诱变和二倍化的菌株改良方案,开发了产高纤维素酶的青霉突变株。通过利用葡萄糖混合二糖(GMDs)作为诱导剂,对开发菌株(POx-M35)的培养条件进行统计优化,进一步提高了酶的产量。该优化过程产生了含有高浓度(U/mL)内切葡聚糖酶(EG)(146.16)、纤维二糖水解酶(CBHI)(6.99)、β-葡萄糖苷酶(β-G)(26.21)、木聚糖酶(336.05)和纤维二糖酶(FPase)(2.02 U/mL)的木质纤维素酶制剂,与野生型 HP1 相比,分别提高了 5.47、5.54、8.55、4.96 和 4.39 倍。此外,通过将突变株 POx-M35 分泌的 secretome 与 Malbranchea cinnamomea 衍生的木聚糖酶(GH10 和 GH11)混合设计的木质纤维素酶制剂可有效水解未经洗涤的酸预处理(UWAP)水稻秸秆浆和温和碱脱乙酰(MAD)水稻秸秆。本研究强调了生物勘探新型真菌和开发改良菌株以优化木质纤维素酶制剂的生产和组成的潜力,这可能是推进生物质转化技术的重要决定因素。

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