Evidence map›Paper›PMID 33276774›Full record

ArticleBMC biotechnology2020

An effective combination of codon optimization, gene dosage, and process optimization for high-level production of fibrinolytic enzyme in Komagataella phaffii (Pichia pastoris).

Zhiqun Che, Xiaoyan Cao, Guiguang Chen, Zhiqun Liang

Open access · goldAbstract read
In one paragraph

Article in BMC biotechnology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.6field-weighted citation impact, top 18% of its field
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

13 citing papers in PubMed, 25 citations in OpenAlex.

  1. Transcriptome study ofMicrobiology spectrum · 2026
    Article
  2. Article
  3. Global research trends and therapeutic potential of fibrinolytic enzymes.Journal, genetic engineering & biotechnology · 2025
    Review
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  13. Role of Fibrinolytic Enzymes in Anti-Thrombosis Therapy.Frontiers in molecular biosciences · 2021
    Review
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

4 authors at 3 institutions in 1 country.

Zhiqun CheState Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, Guangxi Microorganism and Enyme Research Center of Engineering Technology, College of Life Science and Technology, Guangxi University, Nanning, 530004, China.
Xiaoyan CaoCollege of Agriculture and Forestry Science, Linyi University, Linyi, 276000, China.
Guiguang ChenState Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, Guangxi Microorganism and Enyme Research Center of Engineering Technology, College of Life Science and Technology, Guangxi University, Nanning, 530004, China.
Zhiqun LiangState Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, Guangxi Microorganism and Enyme Research Center of Engineering Technology, College of Life Science and Technology, Guangxi University, Nanning, 530004, China. zqliang@gxu.edu.cn.
Guangxi University · CNLinyi University · CNState Key Laboratory For Conservation and Utilization of Subtropical Agro-Bioresources

Funding

the National Natural Science Foundation of China 31560448, 21062001the Natural Science Foundation of Guangxi 2016GXNSFAA380130
6 · The paper itself

Abstract

backgroundAs a main drug for diseased thrombus, some clinically used thrombolytic agents have various disadvantages, safer novel thrombolytic agents are of great demand. This study aimed to achieve high and efficient production of a fibrinolytic enzyme with superior enzymatic properties, by a combination strategy of codon optimization, gene dosage and process optimization in Komagataella phaffii (K. phaffii).

resultsAfter codon optimization, the fibase from a marine Bacillus subtilis was expressed and secreted in K. phaffii GS115. Recombinant strains harboring different copies of the fib gene (fib-nc) were successfully obtained via Geneticin (0.25-4 mg/ml) screening on minimal dextrose selection plates and assessment via real-time quantitative PCR. The respective levels of fibase produced by strains expressing fib-5.4c, fib-6c, fib-8c, fib-9c, and fib-12c were 4428, 5781, 7323, 7930, and 2472 U/ml. Levels increased as the copy number increased from 4 to 9, but decreased dramatically at copy number 12. After high cell density fermentation optimization, the highest fibase activity of the strain expressing fib-9c was 7930 U/ml in a shake flask and increased to 12,690 U/ml after 3 days of continuous culture in a 5-L fermenter, which is one of the highest levels of production reported. The recombinant fibase was maximally active at pH 9.0 and 45 °C, and was remarkably stable at pH levels ranging from 5 to 10 and temperatures up to 50 °C. As a metal-dependent serine protease, fibase did not cause hemolysis in vitro and preferentially degraded fibrin directly.

conclusionsThe combination of codon optimization, gene dosage, and process optimization described herein could be used for the expression of other therapeutic proteins difficult to express. The characteristics of the recombinant fibase suggest that it has potential applications for thrombosis prevention and therapy.

Indexed as

Gene DosageBacillus subtilisBioreactorsCodonFermentationFibrinolytic AgentsFungal ProteinsGene Expression Regulation, FungalHydrogen-Ion ConcentrationIndustrial MicrobiologyKineticsRecombinant ProteinsSaccharomycetalesTemperatureThrombosisCodonFibrinolytic AgentsFungal ProteinsRecombinant ProteinsCharacteristicsFermentation optimizationFibrinolytic enzymeReal-time quantification PCRRecombinant engineered strain

Identifiers

PMID33276774
PMCPMC7716587
OpenAlexW3107361181

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LicenceCC BY
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Registered trials

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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.