Evidence map›Paper›PMID 27034716›Full record

ArticleBiotechnology for biofuels2016

Production of a high-efficiency cellulase complex via β-glucosidase engineering in Penicillium oxalicum.

Guangshan Yao, Ruimei Wu, Qinbiao Kan, Liwei Gao, Meng Liu, Piao Yang, Jian Du, Zhonghai Li, Yinbo Qu

Abstract read
In one paragraph

Article in Biotechnology for biofuels, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed.

  1. Article
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  3. Profiling of the β-glucosidases identified in the genome ofApplied and environmental microbiology · 2023
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  4. Optimisation ofInternational journal of molecular sciences · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Guangshan Yao *State Key Laboratory of Microbial Technology, Shandong University, Jinan City, 250100 Shandong Province China.
Ruimei Wu *State Key Laboratory of Microbial Technology, Shandong University, Jinan City, 250100 Shandong Province China.
Qinbiao Kan *State Key Laboratory of Microbial Technology, Shandong University, Jinan City, 250100 Shandong Province China.
Liwei GaoState Key Laboratory of Microbial Technology, Shandong University, Jinan City, 250100 Shandong Province China.
Meng LiuState Key Laboratory of Microbial Technology, Shandong University, Jinan City, 250100 Shandong Province China.
Piao YangState Key Laboratory of Microbial Technology, Shandong University, Jinan City, 250100 Shandong Province China.
Jian DuState Key Laboratory of Microbial Technology, Shandong University, Jinan City, 250100 Shandong Province China.
Zhonghai LiDepartment of Bioengineering, Qilu University of Technology, Jinan City, 250353 Shandong Province China.
Yinbo QuState Key Laboratory of Microbial Technology, Shandong University, Jinan City, 250100 Shandong Province China.ORCID 0000-0003-3405-9396

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTrichoderma reesei is a widely used model cellulolytic fungus, supplying a highly effective cellulase production system. Recently, the biofuel industry discovered filamentous fungi from the Penicillium genus as a promising alternative to T. reesei.

resultsIn our study, we present a systematic over-expression analysis of nine β-glucosidase encoding genes in the wild-type strain 114-2 of Penicillium oxalicum. We found that the over-expression of BGL1, BGL4, or BGL5 significantly enhanced both β-glucosidase activity and hydrolysis efficiency of the enzyme system on filter paper. We utilised two strategies to over-express β-glucosidase in the strain RE-10 that-although over-producing cellulase, does so at the cost of the cellulase mixture deficiency. The constitutive promoter of gene pde_02864 encoding 40S ribosomal protein S8 was used to over-express three β-glucosidases: BGL1, BGL4, and BGL5. We found that all mutants show significantly enhanced levels of β-glucosidase at transcriptional, protein, and activity levels. Furthermore, the inducible promoter from bgl2 was used to conditionally over-express the β-glucosidases BGL1 and BGL4. Surprisingly, this induced expression strategy enables significantly improved expression efficiency. The BGL1 over-expressing mutant I1-13 particularly improved the β-glucosidase activity at a factor of 65-folds, resulting in levels of up to 150 U/ml. All our BGL over-expression mutants displayed significant enhancement of cellulolytic ability on both microcrystalline cellulose and filter paper. In addition, they substantially reduced the enzyme loads in the saccharification of a natural lignocellulose material delignified corncob residue (DCCR). The mutant I4-32 with over-expression of BGL4 achieved the highest glucose yield in the saccharification of DCCR at only 25 % enzyme load compared to the parental strain RE-10.

conclusionsIn summary, genetically engineering P. oxalicum to significantly improve β-glucosidase activity is a potent strategy to substantially boost the hydrolytic efficiency of the cellulase cocktail, which will ultimately lead to a considerable reduction of cost for biomass-based biofuel.

Indexed as

BiofuelGenetic engineeringPenicillium oxalicumβ-glucosidase

Identifiers

PMID27034716
PMCPMC4815182

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.