Cloning, Expression and Characterization of NAD Kinase from Staphylococcus aureus Involved in the Formation of NADP (H): A Key Molecule in the Maintaining of Redox Status and Biofilm Formation

Background:Staphylococcus aureus has the ability to form biofilms on any niches, a key pathogenic factor of this organism and this phenomenon is directly related to the concentration of NADPH. The formation of NADP is catalyzed by NAD kinase (NADK) and this gene of S. aureus ATCC 12600 was cloned, s...

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Main Authors: U Venkateswara Prasad, D Vasu, R Rishi Gowtham, Krishna Pradeep, V Swarupa, S Yeswanth, Abhijit Choudhary, P. V. G. K. Sarma
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2017-01-01
Series:Advanced Biomedical Research
Subjects:
Online Access:http://www.advbiores.net/article.asp?issn=2277-9175;year=2017;volume=6;issue=1;spage=97;epage=97;aulast=Prasad
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spelling doaj-820ae46656f945d5a8a37f560f5f8a372020-11-24T21:15:15ZengWolters Kluwer Medknow PublicationsAdvanced Biomedical Research2277-91752017-01-0161979710.4103/2277-9175.211833Cloning, Expression and Characterization of NAD Kinase from Staphylococcus aureus Involved in the Formation of NADP (H): A Key Molecule in the Maintaining of Redox Status and Biofilm FormationU Venkateswara PrasadD VasuR Rishi GowthamKrishna PradeepV SwarupaS YeswanthAbhijit ChoudharyP. V. G. K. SarmaBackground:Staphylococcus aureus has the ability to form biofilms on any niches, a key pathogenic factor of this organism and this phenomenon is directly related to the concentration of NADPH. The formation of NADP is catalyzed by NAD kinase (NADK) and this gene of S. aureus ATCC 12600 was cloned, sequenced, expressed and characterized. Materials and Methods: The NADK gene was polymerase chain reaction amplified from the chromosomal DNA of S. aureus ATCC 12600 and cloned in pQE 30 vector, sequenced and expressed in Escherichia coli DH5α. The pure protein was obtained by passing through nickel metal chelate agarose column. The enzyme kinetics of the enzyme and biofilm assay of the S. aureus was carried out in both aerobic and anaerobic conditions. The kinetics was further confirmed by the ability of the substrates to dock to the NADK structure. Results: The recombinant NADK exhibited single band with a molecular weight of 31kDa in sodium dodecyl sulfate-polyacrylamide gel electrophoresis and the gene sequence (GenBank: JN645814) revealed presence of only one kind of NADK in all S. aureus strains. The enzyme exhibited very high affinity for NAD compared to adenosine triphosphate concurring with the docking results. A root-mean-square deviation value 14.039Š observed when NADK structure was superimposed with its human counterpart suggesting very low homology. In anaerobic conditions, higher biofilm units were found with decreased NADK activity. Conclusion: The results of this study suggest increased NADPH concentration in S. aureus plays a vital role in the biofilm formation and survival of this pathogen in any environmental conditions.http://www.advbiores.net/article.asp?issn=2277-9175;year=2017;volume=6;issue=1;spage=97;epage=97;aulast=PrasadAdenosine triphosphatebiofilmsNAD kinaseNADPHroot-mean-square deviation
collection DOAJ
language English
format Article
sources DOAJ
author U Venkateswara Prasad
D Vasu
R Rishi Gowtham
Krishna Pradeep
V Swarupa
S Yeswanth
Abhijit Choudhary
P. V. G. K. Sarma
spellingShingle U Venkateswara Prasad
D Vasu
R Rishi Gowtham
Krishna Pradeep
V Swarupa
S Yeswanth
Abhijit Choudhary
P. V. G. K. Sarma
Cloning, Expression and Characterization of NAD Kinase from Staphylococcus aureus Involved in the Formation of NADP (H): A Key Molecule in the Maintaining of Redox Status and Biofilm Formation
Advanced Biomedical Research
Adenosine triphosphate
biofilms
NAD kinase
NADPH
root-mean-square deviation
author_facet U Venkateswara Prasad
D Vasu
R Rishi Gowtham
Krishna Pradeep
V Swarupa
S Yeswanth
Abhijit Choudhary
P. V. G. K. Sarma
author_sort U Venkateswara Prasad
title Cloning, Expression and Characterization of NAD Kinase from Staphylococcus aureus Involved in the Formation of NADP (H): A Key Molecule in the Maintaining of Redox Status and Biofilm Formation
title_short Cloning, Expression and Characterization of NAD Kinase from Staphylococcus aureus Involved in the Formation of NADP (H): A Key Molecule in the Maintaining of Redox Status and Biofilm Formation
title_full Cloning, Expression and Characterization of NAD Kinase from Staphylococcus aureus Involved in the Formation of NADP (H): A Key Molecule in the Maintaining of Redox Status and Biofilm Formation
title_fullStr Cloning, Expression and Characterization of NAD Kinase from Staphylococcus aureus Involved in the Formation of NADP (H): A Key Molecule in the Maintaining of Redox Status and Biofilm Formation
title_full_unstemmed Cloning, Expression and Characterization of NAD Kinase from Staphylococcus aureus Involved in the Formation of NADP (H): A Key Molecule in the Maintaining of Redox Status and Biofilm Formation
title_sort cloning, expression and characterization of nad kinase from staphylococcus aureus involved in the formation of nadp (h): a key molecule in the maintaining of redox status and biofilm formation
publisher Wolters Kluwer Medknow Publications
series Advanced Biomedical Research
issn 2277-9175
publishDate 2017-01-01
description Background:Staphylococcus aureus has the ability to form biofilms on any niches, a key pathogenic factor of this organism and this phenomenon is directly related to the concentration of NADPH. The formation of NADP is catalyzed by NAD kinase (NADK) and this gene of S. aureus ATCC 12600 was cloned, sequenced, expressed and characterized. Materials and Methods: The NADK gene was polymerase chain reaction amplified from the chromosomal DNA of S. aureus ATCC 12600 and cloned in pQE 30 vector, sequenced and expressed in Escherichia coli DH5α. The pure protein was obtained by passing through nickel metal chelate agarose column. The enzyme kinetics of the enzyme and biofilm assay of the S. aureus was carried out in both aerobic and anaerobic conditions. The kinetics was further confirmed by the ability of the substrates to dock to the NADK structure. Results: The recombinant NADK exhibited single band with a molecular weight of 31kDa in sodium dodecyl sulfate-polyacrylamide gel electrophoresis and the gene sequence (GenBank: JN645814) revealed presence of only one kind of NADK in all S. aureus strains. The enzyme exhibited very high affinity for NAD compared to adenosine triphosphate concurring with the docking results. A root-mean-square deviation value 14.039Š observed when NADK structure was superimposed with its human counterpart suggesting very low homology. In anaerobic conditions, higher biofilm units were found with decreased NADK activity. Conclusion: The results of this study suggest increased NADPH concentration in S. aureus plays a vital role in the biofilm formation and survival of this pathogen in any environmental conditions.
topic Adenosine triphosphate
biofilms
NAD kinase
NADPH
root-mean-square deviation
url http://www.advbiores.net/article.asp?issn=2277-9175;year=2017;volume=6;issue=1;spage=97;epage=97;aulast=Prasad
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