Evidence map›Paper›PMID 28922869›Full record

ArticleGenome biology and evolution2017

Genome Organization of Sphingobium indicum B90A: An Archetypal Hexachlorocyclohexane (HCH) Degrading Genotype.

Helianthous Verma, Abhay Bajaj, Roshan Kumar, Jasvinder Kaur, Shailly Anand, Namita Nayyar, Akshita Puri, Yogendra Singh, Jitendra P Khurana, Rup Lal

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Article in Genome biology and evolution, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

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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

7 citing papers in PubMed, 18 citations in OpenAlex.

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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

10 authors at 1 institution in 1 country.

Helianthous VermaMolecular Biology Laboratory, Department of Zoology, University of Delhi, India.
Abhay BajajMolecular Biology Laboratory, Department of Zoology, University of Delhi, India.
Roshan KumarMolecular Biology Laboratory, Department of Zoology, University of Delhi, India.
Jasvinder KaurMolecular Biology Laboratory, Department of Zoology, University of Delhi, India.
Shailly AnandMolecular Biology Laboratory, Department of Zoology, University of Delhi, India.
Namita NayyarMolecular Biology Laboratory, Department of Zoology, University of Delhi, India.
Akshita PuriMolecular Biology Laboratory, Department of Zoology, University of Delhi, India.
Yogendra SinghBacterial Pathogenesis Laboratory, Department of Zoology, University of Delhi, India.
Jitendra P KhuranaDepartment of Plant Molecular Biology, Interdisciplinary Centre for Plant Genomics, University of Delhi South Campus, India.
Rup LalMolecular Biology Laboratory, Department of Zoology, University of Delhi, India.
University of Delhi · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Among sphingomonads, Sphingobium indicum B90A is widely investigated for its ability to degrade a manmade pesticide, γ-hexachlorocyclohexane (γ-HCH) and its isomers (α-, β-, δ-, and ε-HCH). In this study, complete genome of strain B90A was constructed using Single Molecule Real Time Sequencing (SMRT) and Illumina platform. The complete genome revealed that strain B90A harbors four replicons: one chromosome (3,654,322 bp) and three plasmids designated as pSRL1 (139,218 bp), pSRL2 (108,430 bp) and pSRL3 (43,761 bp). The study determined the precise location of lin genes (genes associated with the degradation of HCH isomers), for example, linA2, linB, linDER, linF, linGHIJ, and linKLMN on the chromosome; linA1, linC, and linF on pSRL1 and linDEbR on pSRL3. Strain B90A contained 26 copies of IS6100 element and most of them (15 copies) was found to be associated with lin genes. Duplication of several lin genes including linA, linDER, linGHIJ, and linF along with two variants of linE, that is, linEa (hydroquinone 1,2-dioxygenase) and linEb (chlorohydroquinone/hydroquinone 1,2-dioxygenase) were identified. This suggests that strain B90A not only possess efficient machinery for upper and lower HCH degradation pathways but it can also act on both hydroquinone and chlorohydroquinone metabolites produced during γ-HCH degradation. Synteny analysis revealed the duplication and transposition of linA gene (HCH dehydrochlorinase) between the chromosome and pSRL1, possibly through homologous recombination between adjacent IS6100 elements. Further, in silico analysis and laboratory experiments revealed that incomplete tyrosine metabolism was responsible for the production of extracellular brown pigment which distinguished strain B90A from other HCH degrading sphingomonads. The precise localization of lin genes, and transposable elements (IS6100) on different replicons now opens up several experimental avenues to elucidate the functions and regulatory mechanism of lin genes acquisition and transfer that were not completely known among the bacterial population inhabiting the HCH contaminated environment.

Indexed as

Genes, BacterialGenome, BacterialBiodegradation, EnvironmentalChromosome MappingChromosomes, BacterialGenotypeHexachlorocyclohexaneHomogentisate 1,2-DioxygenaseHomogentisic AcidPlasmidsSphingomonadaceaeHexachlorocyclohexaneHomogentisate 1,2-DioxygenaseHomogentisic AcidhexachlorocyclohexaneIS6100lin genesSingle Molecule Real Time SequencingSphingobium indicum B90A

Identifiers

PMID28922869
PMCPMC5737386
OpenAlexW2736986636

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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.