Bacillus caviae - PMC

Mohammad Amir, Naushin Bano, Abu Baker, Qamar Zia, Saeed Banawas, Mohd. Rehan Zaheer, Mohammad Shariq, Md Sarfaraz Nawaz, Mohd. Farhan Khan, Z. R. Azaz Ahmad Azad, Anamika Gupta, Danish Iqbal, Roohi

PLoS One. 2022; 17(4): e0264207. Published online 2022 Apr 14. doi: 10.1371/journal.pone.0264207

PMCID:: PMC9009665

Abstract Article PDF–1.9M

Select item 101363004.

Endochitinase and Chitobiosidase Production by Marine Aeromonas caviae CHZ306: Establishment of Nitrogen Supplementation

Flavio Cardozo, Valker Feitosa, Omar Pillaca-Pullo, Adalberto Pessoa

Bioengineering (Basel) 2023 Apr; 10(4): 431. Published online 2023 Mar 29. doi: 10.3390/bioengineering10040431

PMCID:: PMC10136300

Abstract Article PDF–1.6M

Select item 40296325.

Quorum Sensing Activity of Aeromonas Caviae Strain YL12, A Bacterium Isolated from Compost

Yan-Lue Lim, Robson Ee, Wai-Fong Yin, Kok-Gan Chan

Sensors (Basel) 2014 Apr; 14(4): 7026–7040. Published online 2014 Apr 22. doi: 10.3390/s140407026

PMCID:: PMC4029632

Abstract Article PDF–932K

Select item 99891986.

Exploring Class I polyhydroxyalkanoate synthases with broad substrate specificity for polymerization of structurally diverse monomer units

Ramamoorthi M Sivashankari, Maierwufu Mierzati, Yuki Miyahara, Shoji Mizuno, Christopher T. Nomura, Seiichi Taguchi, Hideki Abe, Takeharu Tsuge

Front Bioeng Biotechnol. 2023; 11: 1114946. Published online 2023 Feb 21. doi: 10.3389/fbioe.2023.1114946

PMCID:: PMC9989198

Abstract Article PDF–1.3M

Select item 76693557.

Identification and Characterization of a Newly Isolated Chitinase-Producing Strain Bacillus licheniformis SSCL-10 for Chitin Degradation

Abirami Sasi, Nagarajan Duraipandiyan, Kannan Marikani, Sugapriya Dhanasekaran, Noura Al-Dayan, Divya Venugopal

Archaea. 2020; 2020: 8844811. Published online 2020 Nov 9. doi: 10.1155/2020/8844811

PMCID:: PMC7669355

Abstract Article PDF–824K

Select item 106652918.

De novo assembly and comparative genome analysis for polyhydroxyalkanoates-producing Bacillus sp. BNPI-92 strain

Seid Mohammed Ebu, Lopamudra Ray, Ananta N. Panda, Sudhansu K. Gouda

J Genet Eng Biotechnol. 2023 Dec; 21: 132. Published online 2023 Nov 22. doi: 10.1186/s43141-023-00578-7

PMCID:: PMC10665291

Abstract Article PDF–3.6M

Select item 86103499.

Isolation and identification of high fluoride resistant bacteria from water samples of Dindigul district, Tamil Nadu, South India

Edward Raja Chellaiah, Pandeeswari Ravi, Ramesh Uthandakalaipandian

Curr Res Microb Sci. 2021 Dec; 2: 100038. Published online 2021 May 12. doi: 10.1016/j.crmicr.2021.100038

PMCID:: PMC8610349

Abstract Article PDF–1.6M

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MICROBIC VIRULENCE AND HOST SUSCEPTIBILITY IN PARATYPHOID-ENTERITIDIS INFECTION OF WHITE MICE : VII. SEASONAL VARIATION IN THE SUSCEPTIBILITY OF DIFFERENT STRAINS OF MICE TO PER Os INFECTION WITH THE TYPE II BACILLUS OF MOUSE TYPHOID (BACILLUS PESTIS CAVIÆ).

Ida W. Pritchett

J Exp Med. 1925 Jan 31; 41(2): 209–214. doi: 10.1084/jem.41.2.209

PMCID:: PMC2130938

Summary PDF–387K

Select item 213106811.

MICROBIC VIRULENCE AND HOST SUSCEPTIBILITY IN PARATYPHOID-ENTERITIDIS INFECTION OF WHITE MICE : XI. SEASONAL VARIATION IN THE SUSCEPTIBILITY OF DIFFERENT STRAINS OF MICE TO PER OS INFECTION WITH THE TYPE II BACILLUS OF MOUSE TYPHOID (BACILLUS PESTIS CAVIÆ). FURTHER STUDIES.

Ida W. Pritchett

J Exp Med. 1926 Jan 31; 43(2): 173–177. doi: 10.1084/jem.43.2.173

PMCID:: PMC2131068

Summary PDF–292K

Select item 213094212.

MICROBIC VIRULENCE AND HOST SUSCEPTIBILITY IN PARATYPHOID-ENTERITIDIS INFECTION OF WHITE MICE : VI. THE RELATIVE SUSCEPTIBILITY OF DIFFERENT STRAINS OF MICE TO PER Os INFECTION WITH THE TYPE II BACILLUS OF MOUSE TYPHOID (BACILLUS PESTIS CAVIÆ).

Ida W. Pritchett

J Exp Med. 1925 Jan 31; 41(2): 195–208. doi: 10.1084/jem.41.2.195

PMCID:: PMC2130942

Summary PDF–487K

Select item 687414513.

Effect of Bacillus velezensis on Aeromonas veronii-Induced Intestinal Mucosal Barrier Function Damage and Inflammation in Crucian Carp (Carassius auratus)

Dong-Xing Zhang, Yuan-Huan Kang, Sheng Zhan, Ze-Lin Zhao, Sheng-Nan Jin, Chong Chen, Lei Zhang, Jin-Yu Shen, Chun-Feng Wang, Gui-Qin Wang, Xiao-Feng Shan, Ai-Dong Qian

Front Microbiol. 2019; 10: 2663. Published online 2019 Nov 15. doi: 10.3389/fmicb.2019.02663

PMCID:: PMC6874145

Abstract Article PDF–11M

Select item 212840814.

THE VIRULENCE OF AN EPIDEMIC STRAIN OF BACILLUS PESTIS CAVIÆ

Leslie T. Webster

J Exp Med. 1923 May 31; 37(6): 781–787. doi: 10.1084/jem.37.6.781

PMCID:: PMC2128408

Summary PDF–297K

Select item 281113115.

Comprehensive in silico prediction and analysis of chlamydial outer membrane proteins reflects evolution and life style of the Chlamydiae

Eva Heinz, Patrick Tischler, Thomas Rattei, Garry Myers, Michael Wagner, Matthias Horn

BMC Genomics. 2009; 10: 634. Published online 2009 Dec 29. doi: 10.1186/1471-2164-10-634

PMCID:: PMC2811131

Abstract Article PDF–486K

Select item 9785616.

Role of flm Locus in Mesophilic Aeromonas Species Adherence

Ioannis Gryllos, Jonathan G. Shaw, Rosalina Gavín, Susana Merino, Juan M. Tomás

Infect Immun. 2001 Jan; 69(1): 65–74. doi: 10.1128/IAI.69.1.65-74.2001

PMCID:: PMC97856

Abstract Article PDF–4.0M

Select item 12702417.

Type II Topoisomerase Quinolone Resistance-Determining Regions of Aeromonas caviae, A. hydrophila, and A. sobria Complexes and Mutations Associated with Quinolone Resistance

Marisol Goñi-Urriza, Corinne Arpin, Michèle Capdepuy, Véronique Dubois, Pierre Caumette, Claudine Quentin

Antimicrob Agents Chemother. 2002 Feb; 46(2): 350–359. doi: 10.1128/AAC.46.2.350-359.2002

PMCID:: PMC127024

Abstract Article PDF–304K

Select item 1070775718.

Plant-Associated Bacillus thuringiensis and Bacillus cereus: Inside Agents for Biocontrol and Genetic Recombination in Phytomicrobiome

Antonina Sorokan, Venera Gabdrakhmanova, Zilya Kuramshina, Ramil Khairullin, Igor Maksimov

Plants (Basel) 2023 Dec; 12(23): 4037. Published online 2023 Nov 30. doi: 10.3390/plants12234037

PMCID:: PMC10707757

Abstract Article PDF–489K

Select item 9448819.

Expression and Characterization of the Chitin-Binding Domain of Chitinase A1 from Bacillus circulans WL-12

Masayuki Hashimoto, Takahisa Ikegami, Shizuka Seino, Nobuhumi Ohuchi, Harumi Fukada, Junji Sugiyama, Masahiro Shirakawa, Takeshi Watanabe

J Bacteriol. 2000 Jun; 182(11): 3045–3054. doi: 10.1128/jb.182.11.3045-3054.2000

PMCID:: PMC94488

Abstract Article PDF–786K

Select item 1010081920.

Enterobacter asburiae E7, a Novel Potential Probiotic, Enhances Resistance to Aeromonas veronii Infection via Stimulating the Immune Response in Common Carp (Cyprinus carpio)

Jing Li, Zhao Zhang, Zhi-Bin Wu, Shen-Ye Qu, Gao-Xue Wang, Dong-Dong Wei, Peng-Fei Li, Fei Ling

Microbiol Spectr. 2023 Mar-Apr; 11(2): e04273-22. Published online 2023 Mar 28. doi: 10.1128/spectrum.04273-22

PMCID:: PMC10100819

Abstract Article PDF–4.5M

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Figure 2

Alignment of Aeromonas caviae Sch3 AHA0618 (AcAHA0618) and Helicobacter pylori 26695 HP0518 (HpHP0518) with other members of the YkuD superfamily: Bacillus subtilis (Bs) (accession NP_389287), Aeromonas hydrophila (Ah) (accession AHE48181), Aeromonas salmonicida (As) (accession WP_021138855), Shewanella oneidensis (So) (accession NP_717783), Plesiomonas shigelloides (Ps) (accession WP_010864114), and Vibrio cholera (Vc) (accession NP_232564). The conserved histidine and cysteine residues from the his/cys motif in the predicted YkuD catalytic domain is highlighted.

The Aeromonas caviae AHA0618 gene modulates cell length and influences swimming and swarming motility

Microbiologyopen. 2015 Apr;4(2):220-234.
FIG. 3.

Comparison of P. furiosus ChiA_BD with other chitin- and cellulose-binding domains in CBM family 5. Absolute conserved aromatic residues responsible for the interaction of binding domain and sugar molecules are indicated by the “@” symbol. Pfu ChiA_BD, Pyrococcus furiosus chitinase A, chitin-binding domain; Tko ChiA_BD1, Thermococcus kodakaraensis chitinase A, binding domain 1; CparChiB, Clostridium paraputrificum chitinase B (AB001874); AcaChiA, Aeromonas caviae chitinase A (U09139); BlicChit, Bacillus lichenformis chitinase A (U71214); Vfu ChiD, Vibrio furnissii periplasmic chitodextrinase (U41418); BsubChi, Bacillus subtilus chitinase (AF069131); VharChiA, Vibrio harveyi chitinase A (U81496); BagCel5A, Bacillus agaradhaerens alkaline cellulase Cel5A (AF067428); BcN4endoA and -endoB, Bacillus sp. strain N-4 endoglucanase A and endoglucanase B (M14729); ArChiA_BD1 and ArChiA_BD2, Arthrobacter chitinase A binding domains 1 and 2 (AJ250585); ArChiB_BD, Arthrobacter chitinase B chitin-binding domain (AJ250586).

Growth of Hyperthermophilic Archaeon Pyrococcus furiosus on Chitin Involves Two Family 18 Chitinases

Appl Environ Microbiol. 2003 Jun;69(6):3119-3128.
Fig. 7

Sequence alignment of TtXyn30A and other GH30 xylanases, either of bacterial or fungal origin. The R46 residue (as in Xyn30B) is indicated by a blue arrow. Red arrows indicate the strictly conserved catalytic glutamate residues. The residue R293 of E. chrysanthemi XynA is indicated by a green arrow. The identical residues are shown in white on a red background, while similar residues are shown in red on a white background. Talaromyces cellulolyticus Xyn30B (GAM36763), Aeromonas caviae XynD (AAB63573.1), Bacillus sp. BP7 Xyn5B (ADM15019.1), Bacillus subtilis BsXynC (CAA97612.1), Clostridium thermocellum CtXyn30A (ABN54208.1), Clostridium papyrosolvens CpXyn30A (EGD48159.1), Erwinia chrysanthemi XynA (AAB53151.1), Paenibacillus barcinonensis Xyn30D (AEY82463.1), Bispora sp. MEY-1 XylD (ADG62369.1), Penicillium purpurogenum XynC (AKH40280), Trichoderma reesei XYN IV (AAP64786.1), Trichoderma reesei XYN VI (G0RV92)

A novel fungal GH30 xylanase with xylobiohydrolase auxiliary activity

Biotechnol Biofuels. 2019;12:120.
Fig 5Specificity of the K. pneumoniae-MCDA-LFB assay.

Biosensor 1, K. pneumoniae (ATCC2146). Biosensors 2–6, different K. pneumoniae strains from sputum. Biosensors 7–8, different K. pneumoniae strains from urine. Biosensors 9–12, K. pneumoniae strains from blood, pharyngeal swabs, puncture fluid, and wounds, respectively. Biosensors 13–24, Aeromonas caviae, Bacillus cereus, Citrobacter braakii, Corynebacterium stationis, Enterobacter sakazakii, Enterotoxigenic Escherichia coli, Listeria monocytogenes, Salmonella enterica, Shigella flexneri, Staphylococcus aureus, Streptococcus pneumoniae, and Streptococcus suis. MCDA, multiple cross displacement amplification; LFB, gold nanoparticle lateral flow biosensor.

Isothermal amplification and rapid detection of Klebsiella pneumoniae based on the multiple cross displacement amplification (MCDA) and gold nanoparticle lateral flow biosensor (LFB)

PLoS One. 2018;13(10):e0204332.