Example of Journal of Bacteriology format
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Example of Journal of Bacteriology format Example of Journal of Bacteriology format Example of Journal of Bacteriology format Example of Journal of Bacteriology format Example of Journal of Bacteriology format Example of Journal of Bacteriology format Example of Journal of Bacteriology format Example of Journal of Bacteriology format
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Example of Journal of Bacteriology format Example of Journal of Bacteriology format Example of Journal of Bacteriology format Example of Journal of Bacteriology format Example of Journal of Bacteriology format Example of Journal of Bacteriology format Example of Journal of Bacteriology format Example of Journal of Bacteriology format
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open access Open Access

Journal of Bacteriology — Template for authors

Categories Rank Trend in last 3 yrs
Microbiology #57 of 150 down down by 26 ranks
Molecular Biology #173 of 382 down down by 56 ranks
journal-quality-icon Journal quality:
Good
calendar-icon Last 4 years overview: 1071 Published Papers | 5755 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 10/06/2020
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Journal Performance & Insights

Impact Factor

CiteRatio

Determines the importance of a journal by taking a measure of frequency with which the average article in a journal has been cited in a particular year.

A measure of average citations received per peer-reviewed paper published in the journal.

3.004

7% from 2018

Impact factor for Journal of Bacteriology from 2016 - 2019
Year Value
2019 3.004
2018 3.234
2017 3.219
2016 3.143
graph view Graph view
table view Table view

5.4

CiteRatio for Journal of Bacteriology from 2016 - 2020
Year Value
2020 5.4
2019 5.4
2018 5.8
2017 6.2
2016 6.8
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has decreased by 7% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

insights Insights

  • This journal’s CiteRatio is in the top 10 percentile category.

SCImago Journal Rank (SJR)

Source Normalized Impact per Paper (SNIP)

Measures weighted citations received by the journal. Citation weighting depends on the categories and prestige of the citing journal.

Measures actual citations received relative to citations expected for the journal's category.

1.652

10% from 2019

SJR for Journal of Bacteriology from 2016 - 2020
Year Value
2020 1.652
2019 1.843
2018 1.841
2017 1.885
2016 1.943
graph view Graph view
table view Table view

0.899

1% from 2019

SNIP for Journal of Bacteriology from 2016 - 2020
Year Value
2020 0.899
2019 0.904
2018 0.886
2017 0.911
2016 0.891
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has decreased by 10% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has decreased by 1% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

Journal of Bacteriology

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American Society for Microbiology

Journal of Bacteriology

The Journal of Bacteriology (JB) has been disseminating important results from basic research studies of bacteria and other microorganisms since 1916. Topics include structure and function, biochemistry, enzymology, metabolism and its regulation, molecular biology, genetics, p...... Read More

Microbiology

Molecular Biology

Immunology and Microbiology

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Last updated on
10 Jun 2020
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ISSN
0021-9193
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Impact Factor
High - 1.012
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Open Access
Yes
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Sherpa RoMEO Archiving Policy
Green faq
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Plagiarism Check
Available via Turnitin
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Endnote Style
Download Available
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Bibliography Name
unsrt asm custom citation
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Citation Type
Numbered
(25)
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Bibliography Example
Blonder, G. E., Tinkham, M., and Klapwijk, T. M. 1982. Transition from metallic to tunneling regimes in superconducting microconstrictions: Excess current, charge imbalance, and supercurrent conversion. Phys. Rev. B, 25(7):4515–4532.

Top papers written in this journal

open accessOpen access Journal Article DOI: 10.1128/JB.173.2.697-703.1991
16S ribosomal DNA amplification for phylogenetic study.
01 Jan 1991 - Journal of Bacteriology

Abstract:

A set of oligonucleotide primers capable of initiating enzymatic amplification (polymerase chain reaction) on a phylogenetically and taxonomically wide range of bacteria is described along with methods for their use and examples. One pair of primers is capable of amplifying nearly full-length 16S ribosomal DNA (rDNA) from man... A set of oligonucleotide primers capable of initiating enzymatic amplification (polymerase chain reaction) on a phylogenetically and taxonomically wide range of bacteria is described along with methods for their use and examples. One pair of primers is capable of amplifying nearly full-length 16S ribosomal DNA (rDNA) from many bacterial genera; the additional primers are useful for various exceptional sequences. Methods for purification of amplified material, direct sequencing, cloning, sequencing, and transcription are outlined. An obligate intracellular parasite of bovine erythrocytes, Anaplasma marginale, is used as an example; its 16S rDNA was amplified, cloned, sequenced, and phylogenetically placed. Anaplasmas are related to the genera Rickettsia and Ehrlichia. In addition, 16S rDNAs from several species were readily amplified from material found in lyophilized ampoules from the American Type Culture Collection. By use of this method, the phylogenetic study of extremely fastidious or highly pathogenic bacterial species can be carried out without the need to culture them. In theory, any gene segment for which polymerase chain reaction primer design is possible can be derived from a readily obtainable lyophilized bacterial culture. read more read less

Topics:

Amplified Ribosomal DNA Restriction Analysis (59%)59% related to the paper, Ribosomal DNA (57%)57% related to the paper, Polymerase chain reaction (54%)54% related to the paper, Ribosomal RNA (53%)53% related to the paper, Primer (molecular biology) (51%)51% related to the paper
10,245 Citations
open accessOpen access Journal Article DOI: 10.1128/JB.153.1.163-168.1983
Transformation of intact yeast cells treated with alkali cations.
H Ito, Y Fukuda, Kousaku Murata, A Kimura
01 Jan 1983 - Journal of Bacteriology

Abstract:

Intact yeast cells treated with alkali cations took up plasmid DNA. Li+, Cs+, Rb+, K+, and Na+ were effective in inducing competence. Conditions for the transformation of Saccharomyces cerevisiae D13-1A with plasmid YRp7 were studied in detail with CsCl. The optimum incubation time was 1 h, and the optimum cell concentration ... Intact yeast cells treated with alkali cations took up plasmid DNA. Li+, Cs+, Rb+, K+, and Na+ were effective in inducing competence. Conditions for the transformation of Saccharomyces cerevisiae D13-1A with plasmid YRp7 were studied in detail with CsCl. The optimum incubation time was 1 h, and the optimum cell concentration was 5 x 10(7) cells per ml. The optimum concentration of Cs+ was 1.0 M. Transformation efficiency increased with increasing concentrations of plasmid DNA. Polyethylene glycol was absolutely required. Heat pulse and various polyamines or basic proteins stimulated the uptake of plasmid DNA. Besides circular DNA, linear plasmid DNA was also taken up by Cs+-treated yeast cells, although the uptake efficiency was considerably reduced. The transformation efficiency with Cs+ or Li+ was comparable with that of conventional protoplast methods for a plasmid containing ars1, although not for plasmids containing a 2 microns origin replication. Images read more read less

Topics:

Calcium chloride transformation (64%)64% related to the paper, Transformation efficiency (61%)61% related to the paper, Transformation (genetics) (55%)55% related to the paper, Plasmid (53%)53% related to the paper, Protoplast (50%)50% related to the paper
6,673 Citations
open accessOpen access Journal Article DOI: 10.1128/JB.177.14.4121-4130.1995
Tight regulation, modulation, and high-level expression by vectors containing the arabinose PBAD promoter.
Luz-Maria Guzman1, Dominique Belin1, M. J. Carson1, Jon Beckwith1
01 Jul 1995 - Journal of Bacteriology

Abstract:

We have constructed a series of plasmid vectors (pBAD vectors) containing the PBAD promoter of the araBAD (arabinose) operon and the gene encoding the positive and negative regulator of this promoter, araC. Using the phoA gene and phoA fusions to monitor expression in these vectors, we show that the ratio of induction/repress... We have constructed a series of plasmid vectors (pBAD vectors) containing the PBAD promoter of the araBAD (arabinose) operon and the gene encoding the positive and negative regulator of this promoter, araC. Using the phoA gene and phoA fusions to monitor expression in these vectors, we show that the ratio of induction/repression can be 1,200-fold, compared with 50-fold for PTAC-based vectors. phoA expression can be modulated over a wide range of inducer (arabinose) concentrations and reduced to extremely low levels by the presence of glucose, which represses expression. Also, the kinetics of induction and repression are very rapid and significantly affected by the ara allele in the host strain. Thus, the use of this system which can be efficiently and rapidly turned on and off allows the study of important aspects of bacterial physiology in a very simple manner and without changes of temperature. We have exploited the tight regulation of the PBAD promoter to study the phenotypes of null mutations of essential genes and explored the use of pBAD vectors as an expression system. read more read less

Topics:

PBAD promoter (76%)76% related to the paper, Arabinose (56%)56% related to the paper, Operon (52%)52% related to the paper, Phage shock (52%)52% related to the paper, Regulation of gene expression (51%)51% related to the paper
4,997 Citations
open accessOpen access Journal Article DOI: 10.1128/JB.134.3.1141-1156.1978
Construction and characterization of amplifiable multicopy DNA cloning vehicles derived from the P15A cryptic miniplasmid.
01 Jun 1978 - Journal of Bacteriology

Abstract:

Construction and characterization of a class of multicopy plasmid cloning vehicles containing the replication system of miniplasmid P15A are described. The constructed plasmids have cleavage sites within antibiotic resistance genes for a variety of commonly employed site-specific endonucleases, permitting convenient use of th... Construction and characterization of a class of multicopy plasmid cloning vehicles containing the replication system of miniplasmid P15A are described. The constructed plasmids have cleavage sites within antibiotic resistance genes for a variety of commonly employed site-specific endonucleases, permitting convenient use of the insertional inactivation procedure for the selection of clones that contain hybrid DNA molecules. Although the constructed plasmids showed DNA sequence homology with the ColE1 plasmid within the replication region, were amplifiable by chloramphenicol or spectinomycin, required DNA polymerase I for replication, and shared other replication properties with ColE1, they were nevertheless compatible with ColE1. P15A-derived plasmids were not self-transmissible and were mobilized poorly by Hfr strains; however, mobilization was complemented by the presence of a ColE1 plasmid within the same cell. read more read less

Topics:

Plasmid (62%)62% related to the paper, Plasmid preparation (61%)61% related to the paper, Molecular cloning (59%)59% related to the paper, In vitro recombination (57%)57% related to the paper, pSC101 (56%)56% related to the paper
4,372 Citations
open accessOpen access Journal Article DOI: 10.1128/JB.172.8.4238-4246.1990
Rapid genetic identification and mapping of enzymatically amplified ribosomal DNA from several Cryptococcus species.
Rytas Vilgalys1, M Hester1
01 Aug 1990 - Journal of Bacteriology

Abstract:

Detailed restriction analyses of many samples often require substantial amounts of time and effort for DNA extraction, restriction digests, Southern blotting, and hybridization. We describe a novel approach that uses the polymerase chain reaction (PCR) for rapid simplified restriction typing and mapping of DNA from many diffe... Detailed restriction analyses of many samples often require substantial amounts of time and effort for DNA extraction, restriction digests, Southern blotting, and hybridization. We describe a novel approach that uses the polymerase chain reaction (PCR) for rapid simplified restriction typing and mapping of DNA from many different isolates. DNA fragments up to 2 kilobase pairs in length were efficiently amplified from crude DNA samples of several pathogenic Cryptococcus species, including C. neoformans, C. albidus, C. laurentii, and C. uniguttulatus. Digestion and electrophoresis of the PCR products by using frequent-cutting restriction enzymes produced complex restriction phenotypes (fingerprints) that were often unique for each strain or species. We used the PCR to amplify and analyze restriction pattern variation within three major portions of the ribosomal DNA (rDNA) repeats from these fungi. Detailed mapping of many restriction sites within the rDNA locus was determined by fingerprint analysis of progressively larger PCR fragments sharing a common primer site at one end. As judged by PCR fingerprints, the rDNA of 19 C. neoformans isolates showed no variation for four restriction enzymes that we surveyed. Other Cryptococcus spp. showed varying levels of restriction pattern variation within their rDNAs and were shown to be genetically distinct from C. neoformans. The PCR primers used in this study have also been successfully applied for amplification of rDNAs from other pathogenic and nonpathogenic fungi, including Candida spp., and ought to have wide applicability for clinical detection and other studies. read more read less

Topics:

Restriction map (68%)68% related to the paper, Amplified fragment length polymorphism (66%)66% related to the paper, Restriction fragment length polymorphism (65%)65% related to the paper, Restriction site (64%)64% related to the paper, Restriction digest (64%)64% related to the paper
4,187 Citations
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Journal of Bacteriology format uses unsrt asm custom citation citation style.

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Frequently asked questions

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Absolutely not! Our tool has been designed to help you focus on writing. You can write your entire paper as per the Journal of Bacteriology guidelines and auto format it.

2. Do you follow the Journal of Bacteriology guidelines?

Yes, the template is compliant with the Journal of Bacteriology guidelines. Our experts at SciSpace ensure that. If there are any changes to the journal's guidelines, we'll change our algorithm accordingly.

3. Can I cite my article in multiple styles in Journal of Bacteriology?

Of course! We support all the top citation styles, such as APA style, MLA style, Vancouver style, Harvard style, and Chicago style. For example, when you write your paper and hit autoformat, our system will automatically update your article as per the Journal of Bacteriology citation style.

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Sign up for our free trial, and you'll be able to use all our features for seven days. You'll see how helpful they are and how inexpensive they are compared to other options, Especially for Journal of Bacteriology.

5. Can I use a manuscript in Journal of Bacteriology that I have written in MS Word?

Yes. You can choose the right template, copy-paste the contents from the word document, and click on auto-format. Once you're done, you'll have a publish-ready paper Journal of Bacteriology that you can download at the end.

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After writing your paper autoformatting in Journal of Bacteriology, you can download it in multiple formats, viz., PDF, Docx, and LaTeX.

12. Is Journal of Bacteriology's impact factor high enough that I should try publishing my article there?

To be honest, the answer is no. The impact factor is one of the many elements that determine the quality of a journal. Few of these factors include review board, rejection rates, frequency of inclusion in indexes, and Eigenfactor. You need to assess all these factors before you make your final call.

13. What is Sherpa RoMEO Archiving Policy for Journal of Bacteriology?

SHERPA/RoMEO Database

We extracted this data from Sherpa Romeo to help researchers understand the access level of this journal in accordance with the Sherpa Romeo Archiving Policy for Journal of Bacteriology. The table below indicates the level of access a journal has as per Sherpa Romeo's archiving policy.

RoMEO Colour Archiving policy
Green Can archive pre-print and post-print or publisher's version/PDF
Blue Can archive post-print (ie final draft post-refereeing) or publisher's version/PDF
Yellow Can archive pre-print (ie pre-refereeing)
White Archiving not formally supported
FYI:
  1. Pre-prints as being the version of the paper before peer review and
  2. Post-prints as being the version of the paper after peer-review, with revisions having been made.

14. What are the most common citation types In Journal of Bacteriology?

The 5 most common citation types in order of usage for Journal of Bacteriology are:.

S. No. Citation Style Type
1. Author Year
2. Numbered
3. Numbered (Superscripted)
4. Author Year (Cited Pages)
5. Footnote

15. How do I submit my article to the Journal of Bacteriology?

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16. Can I download Journal of Bacteriology in Endnote format?

Yes, SciSpace provides this functionality. After signing up, you would need to import your existing references from Word or Bib file to SciSpace. Then SciSpace would allow you to download your references in Journal of Bacteriology Endnote style according to Elsevier guidelines.

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