Evidence map›Paper›PMID 42845956›Full record

ReviewQuantitative biology (Beijing, China)2026

Advances in large DNA fragment assembly for microbial cell factory engineering.

Yu Zhang, Wenqian Liu, Dongyuan Cheng, Jiazhang Lian, Xian Fu, Yue Shen

Abstract readReview
In one paragraph

Review in Quantitative biology (Beijing, China), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Yu ZhangKey Laboratory of Biomass Chemical Engineering of Ministry of Education & State Key Laboratory of Biobased Transportation Fuel Technology College of Chemical and Biological Engineering Zhejiang University Hangzhou China.ORCID https://orcid.org/0009-0003-5453-5545
Wenqian LiuKey Laboratory of Biomass Chemical Engineering of Ministry of Education & State Key Laboratory of Biobased Transportation Fuel Technology College of Chemical and Biological Engineering Zhejiang University Hangzhou China.ORCID https://orcid.org/0000-0002-4930-8116
Dongyuan ChengState Key Laboratory of Genome and Multi-omics Technologies BGI Research Hangzhou China.ORCID https://orcid.org/0009-0002-0141-8540
Jiazhang LianKey Laboratory of Biomass Chemical Engineering of Ministry of Education & State Key Laboratory of Biobased Transportation Fuel Technology College of Chemical and Biological Engineering Zhejiang University Hangzhou China.ORCID https://orcid.org/0000-0001-9784-9876
Xian FuBGI Research Changzhou China.ORCID https://orcid.org/0000-0001-9044-8850
Yue ShenBGI Research Changzhou China.ORCID https://orcid.org/0000-0002-3276-7295

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The efficient, rapid, and reliable assembly of DNA fragments is essential for advancing metabolic engineering and synthetic biology. With the rapid advancement of DNA synthesis and assembly technologies, the scale of DNA assembly has expanded from single genes to metabolic pathways and even genomes. Large DNA fragment assembly, in particular, has developed into a pivotal tool for microbial cell factory engineering, significantly contributing to the understanding and construction of biological systems. This review summarizes recent advancements in large DNA fragment assembly methods, encompassing in vitro and in vitro methods for multiple-gene assemblies, as well as genome-scale technologies, including synthetic genome and neochromosome construction. We systematically compare their key features in terms of assembly principle, capacity, and efficiency. Especially, we highlight their applications in microbial cell factory engineering, including heterologous pathway construction, reprogramming host metabolism, and expanding complex biosynthetic networks. Finally, we discuss the challenges and prospects of applying large DNA fragment assembly to advance cell factories. In summary, this review provides a theoretical and technical framework for engineering high-performance microbial cell factories, contributing to the advancement of industrial biomanufacturing.

Indexed as

in vitro and in vitro assemblylarge DNA fragment assemblymicrobial cell factoriesneochromosomesynthetic genome

Identifiers

PMID42845956
PMCPMC13642171

What OpenQuestion holds

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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.