Paper · 30530516

Exonuclease III (XthA) Enforces In Vivo DNA Cloning of Escherichia coli To Create Cohesive Ends.

Nozaki S and 1 other. J Bacteriol, 2019. Cited by 79 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Exonuclease III (XthA) Enforces In Vivo DNA Cloning of Escherichia coli To Create Cohesive Ends. Papers, record 30530516. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/30530516

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Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title: Exonuclease III (XthA) Enforces In Vivo DNA Cloning of Escherichia coli To Create Cohesive Ends.; PubMed
Journal: J Bacteriol; PubMed
Year: 2019; PubMed
Publication types: Journal Article, Research Support, Non-U.S. Gov't; PubMed
PubMed: https://pubmed.ncbi.nlm.nih.gov/30530516/; PubMed
DOI: https://doi.org/10.1128/jb.00660-18; PubMed
PMC: https://pmc.ncbi.nlm.nih.gov/articles/PMC6379578/; PubMed
The journal: https://conductscience.org/library/journal-index/2985120R; PubMed
Citations, by iCite: 79; iCite
Relative citation ratio, by iCite: 3.41; iCite
Revised in PubMed: 2020-12-09; PubMed

Authors2

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

Order	Author	Forename	Kind	ORCID iD
1	Nozaki S	Shingo
2	Niki H	Hironori		https://orcid.org/0000-0002-5391-6595

Source PubMed

Topics8

NLM's MeSH indexing of the paper, its major topics first.

MeSH term	Major
DNA, Bacterial	Major topic
Escherichia coli	Major topic
Exodeoxyribonucleases	Major topic
Recombination, Genetic	Major topic
Cloning, Molecular
DNA Polymerase I
Nucleic Acid Hybridization
Transformation, Genetic

Source PubMed

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Trials0

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Comments and corrections0

PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.

None in this release.

References31

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

Order	PMID	Title	Journal	Year	In Papers	Source
1	22,404,288	DNA replication fidelity in Escherichia coli: a multi-DNA polymerase affair.	FEMS Microbiol Rev	2012	https://conductscience.org/library/papers/22404288	PubMed
2	9,765,205	Negative control of replication initiation by a novel chromosomal locus exhibiting exceptional affinity for Escherichia coli DnaA protein.	Genes Dev	1998	https://conductscience.org/library/papers/9765205	PubMed
3	16,738,554	Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants: the Keio collection.	Mol Syst Biol	2006	https://conductscience.org/library/papers/16738554	PubMed
4	6,255,295	The hsd (host specificity) genes of E. coli K 12.	Mol Gen Genet	1980	https://conductscience.org/library/papers/6255295	PubMed
5	26,037,246	A simple and efficient seamless DNA cloning method using SLiCE from Escherichia coli laboratory strains and its application to SLiP site-directed mutagenesis.	BMC Biotechnol	2015	https://conductscience.org/library/papers/26037246	PubMed
6	10,197,989	The RecBC enzyme loads RecA protein onto ssDNA asymmetrically and independently of chi, resulting in constitutive recombination activation.	Genes Dev	1999	https://conductscience.org/library/papers/10197989	PubMed
7	10,829,079	One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products.	Proc Natl Acad Sci U S A	2000	https://conductscience.org/library/papers/10829079	PubMed
8	21,992,524	FastCloning: a highly simplified, purification-free, sequence- and ligation-independent PCR cloning method.	BMC Biotechnol	2011	https://conductscience.org/library/papers/21992524	PubMed
9	6,233,260	Method for determining whether a gene of Escherichia coli is essential: application to the polA gene.	J Bacteriol	1984	https://conductscience.org/library/papers/6233260	PubMed
10	26,360,249	AQUA Cloning: A Versatile and Simple Enzyme-Free Cloning Approach.	PLoS One	2015	https://conductscience.org/library/papers/26360249	PubMed

1 to 10 of 31

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Cited by55

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 79 citations.

PMID	Title	Journal	Year	In Papers	Source
42,436,197	Phage portal proteins counteract stringent-response-mediated restriction.	Nat Commun	2026	https://conductscience.org/library/papers/42436197	PubMed
42,406,626	A self-replicating artificial module-genome that generates bacterial chromosome replication system in vitro.	Nucleic Acids Res	2026	https://conductscience.org/library/papers/42406626	PubMed
42,185,385	Directed mutagenesis of large multi-subunit protein complexes by plasmid sub-fragmentation.	Sci Rep	2026	https://conductscience.org/library/papers/42185385	PubMed
42,094,760	Amorphous-to-rodlet structural transition governs the interfacial functions of Aspergillus oryzae hydrophobin RolA.	Front Microbiol	2026	https://conductscience.org/library/papers/42094760	PubMed
42,052,402	Cell-Size Confinement Drives Size-Dependent Scaling of Intracellular Reaction-Diffusion Waves for Robust Patterning.	Small Sci	2026	https://conductscience.org/library/papers/42052402	PubMed
41,983,697	FtsZ forms biomolecular condensates in a polar-growing Alphaproteobacterium.	mBio	2026	https://conductscience.org/library/papers/41983697	PubMed
41,931,560	Enhancement of RecET-mediated in vivo linear DNA assembly by a xonA mutation.	PLoS One	2026	https://conductscience.org/library/papers/41931560	PubMed
41,721,466	SanA Plays a Role in Peptidoglycan Integrity in Escherichia coli.	Mol Microbiol	2026	https://conductscience.org/library/papers/41721466	PubMed
41,402,526	Involvement of the inner surface residues of bacterial SMC protein MukB in the ssDNA binding in vitro.	Commun Biol	2025	https://conductscience.org/library/papers/41402526	PubMed
40,287,593	Emergence of transferable daptomycin resistance in Gram-positive bacteria.	NPJ Antimicrob Resist	2025	https://conductscience.org/library/papers/40287593	PubMed

1 to 10 of 55

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Data dates

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PubMed: 2026-11-06; PubMed
iCite: 2026-11-05; iCite
PMC's ID file: 2026-11-05; PMC's ID file
NIH RePORTER's grant and paper links: 2026-11-01; NIH RePORTER's grant and paper links
Trials: 2026-11-12
Gene search: 2026-11-11
Pipelines: 2026-09-18

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ClinicalTrials.govNo license stated
HGNCCC0
iCiteCC BY 4.0
NCBI GenePublic domain (US government)
NIH RePORTER's grant and paper linksPublic domain
Open TargetsCC0 1.0
PMC's ID filePublic domain (US government)
PubMedNLM's terms
PubTator 3Public domain
UniProtCC BY 4.0

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ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
ClinicalTrials.govnone stated
HGNCCC0: https://www.genenames.org/about/license/
iCiteCC BY 4.0
NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
PubMedNLM's terms
PubTator 3Public domain
UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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