Evidence map›Paper›PMID 39061053›Full record

ArticleMicrobial cell factories2024

A convenient broad-host counterselectable system endowing rapid genetic manipulations of Kluyveromyces lactis and other yeast species.

Yanli Zheng, Yuhui Deng, Ping Hu, Shiqing Wang, Jiawen Wu, Siqi Luo, Lei Lei, Jiangke Yang, Wenfang Peng

Abstract read
In one paragraph

Article in Microbial cell factories, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Unlocking genome engineering inMicrobiology spectrum · 2026
    Article
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.

Yanli ZhengCollege of Life Science and Technology, Wuhan Polytechnic University, Wuhan, 430023, P. R. China.
Yuhui DengCollege of Life Science and Technology, Wuhan Polytechnic University, Wuhan, 430023, P. R. China.
Ping HuCollege of Life Science and Technology, Wuhan Polytechnic University, Wuhan, 430023, P. R. China.
Shiqing WangCollege of Life Science and Technology, Wuhan Polytechnic University, Wuhan, 430023, P. R. China.
Jiawen WuCollege of Life Science and Technology, Wuhan Polytechnic University, Wuhan, 430023, P. R. China.
Siqi LuoCollege of Life Science and Technology, Wuhan Polytechnic University, Wuhan, 430023, P. R. China.
Lei LeiCollege of Life Science and Technology, Wuhan Polytechnic University, Wuhan, 430023, P. R. China.
Jiangke YangCollege of Life Science and Technology, Wuhan Polytechnic University, Wuhan, 430023, P. R. China.
Wenfang PengState Key Laboratory of Biocatalysis and Enzyme Engineering, Hubei Engineering Research Center for Bio-enzyme Catalysis, Environmental Microbial Technology Center of Hubei Province, School of Life Sciences, Hubei University, Wuhan, 430062, P.R. China. wenfang@hubu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Being generally regarded as safe, Kluyveromyces lactis has been widely taken for food, feed, and pharmaceutical applications, owing to its ability to achieve high levels of protein secretion and hence being suitable for industrial production of heterologous proteins. Production platform strains can be created through genetic engineering; while prototrophic cells without chromosomally accumulated antibiotics resistance genes have been generally preferred, arising the need for dominant counterselection. We report here the establishment of a convenient counterselection system based on a Frs2 variant, Frs2v, which is a mutant of the alpha-subunit of phenylalanyl-tRNA synthase capable of preferentially incorporating a toxic analog of phenylalanine, r-chloro-phenylalanine (4-CP), into proteins to bring about cell growth inhibition. We demonstrated that expression of Frs2v from an episomal plasmid in K. lactis could make the host cells sensitive to 2 mM 4-CP, and a Frs2v-expressing plasmid could be efficiently removed from the cells immediately after a single round of cell culturing in a 4-CP-contianing YPD medium. This Frs2v-based counterselection helped us attain scarless gene replacement in K. lactis without any prior engineering of the host cells. More importantly, counterselection with this system was proven to be functionally efficient also in Saccharomyces cerevisiae and Komagataella phaffii, suggestive of a broader application scope of the system in various yeast hosts. Collectively, this work has developed a strategy to enable rapid, convenient, and high-efficiency construction of prototrophic strains of K. lactis and possibly many other yeast species, and provided an important reference for establishing similar methods in other industrially important eukaryotic microbes.

Indexed as

KluyveromycesPlasmidsGenetic EngineeringPhenylalaninePhenylalanine-tRNA LigaseSaccharomyces cerevisiaePhenylalaninePhenylalanine-tRNA Ligase

Identifiers

PMID39061053
PMCPMC11282862

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.