LaoABCR, a Novel System for Oxidation of Long-Chain Alcohols Derived from SDS and Alkane Degradation in Pseudomonas aeruginosa

被引:20
作者
Panasia, Gianna [1 ]
Philipp, Bodo [1 ]
机构
[1] Westfalische Wilhelms Univ Munster, Inst Mol Mikrobiol & Biotechnol, Munster, Germany
关键词
Pseudomonas aeruginosa; SDS; alcohol dehydrogenase; alkanes; biodegradation; long-chain alcohol; SODIUM DODECYL-SULFATE; QUINOPROTEIN ETHANOL DEHYDROGENASE; CELL-AGGREGATION; EXPRESSION; STRAIN; GENES; PROTEINS; SURVIVAL; GROWTH; BIODEGRADATION;
D O I
10.1128/AEM.00626-18
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The opportunistic pathogen Pseudomonas aeruginosa strain PAO1 is able to use a variety of organic pollutants as growth substrates, including the anionic detergent sodium dodecyl sulfate (SDS) and long-chain alkanes. While the enzymes initiating SDS and alkane degradation are well known, the subsequent enzymatic steps for degradation of the derived primary long-chain alcohols have not yet been identified. By evaluating genes specifically induced during growth with SDS, a gene cluster encoding a putative alcohol dehydrogenase (PA0364/LaoA), a probable inner membrane protein (PA0365/ LaoB), and a presumable aldehyde dehydrogenase (PA0366/LaoC) was identified and designated the Lao (long-chain-alcohol/aldehyde-oxidation) system. Growth experiments with deletion mutants with SDS, 1-dodecanol, and alkanes revealed that LaoA and LaoB are involved in the degradation of primary long-chain alcohols. Moreover, detection of 1-dodecanol oxidation in cell extracts by activity staining revealed an interdependency of LaoA and LaoB for efficient 1-dodecanol oxidation. An in silico analysis yielded no well-characterized homologue proteins for LaoA and LaoB. Furthermore, a gene adjacent to the lao gene cluster encodes a putative transcriptional regulator (PA0367/LaoR). A laoR deletion mutant exhibited constitutive expression of LaoA and LaoB, indicating that LaoR is a repressor for the expression of laoABC. Taken together, these results showed that the proteins LaoA and LaoB constitute a novel oxidation system for long-chain alcohols derived from pollutants. IMPORTANCE The versatile and highly adaptive bacterium Pseudomonas aeruginosa is able to colonize a variety of habitats, including anthropogenic environments, where it is often challenged with toxic compounds. Its ability to degrade such compounds and to use them as growth substrates can significantly enhance spreading of this opportunistic pathogen in hygienic settings, such as clinics or water distribution systems. Thus, knowledge about the metabolism of P. aeruginosa can contribute to novel approaches for preventing its growth and reducing nosocomial infections. As the Lao system is important for the degradation of two different classes of pollutants, the identification of these novel enzymes can be a useful contribution for developing effective antibacterial strategies.
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页数:17
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共 67 条
  • [1] Gapped BLAST and PSI-BLAST: a new generation of protein database search programs
    Altschul, SF
    Madden, TL
    Schaffer, AA
    Zhang, JH
    Zhang, Z
    Miller, W
    Lipman, DJ
    [J]. NUCLEIC ACIDS RESEARCH, 1997, 25 (17) : 3389 - 3402
  • [2] AZOULAY E, 1963, BIOCHIM BIOPHYS ACTA, V73, P1
  • [3] The Biofilm-Specific Antibiotic Resistance Gene ndvB Is Important for Expression of Ethanol Oxidation Genes in Pseudomonas aeruginosa Biofilms
    Beaudoin, Trevor
    Zhang, Li
    Hinz, Aaron J.
    Parr, Christopher J.
    Thien-Fah Mah
    [J]. JOURNAL OF BACTERIOLOGY, 2012, 194 (12) : 3128 - 3136
  • [4] Pseudomonas aeruginosa in premise plumbing of large buildings
    Bedard, Emilie
    Prevost, Michele
    Deziel, Eric
    [J]. MICROBIOLOGYOPEN, 2016, 5 (06): : 937 - 956
  • [5] GMC OXIDOREDUCTASES - A NEWLY DEFINED FAMILY OF HOMOLOGOUS PROTEINS WITH DIVERSE CATALYTIC ACTIVITIES
    CAVENER, DR
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1992, 223 (03) : 811 - 814
  • [6] PQQ-Dependent Alcohol Dehydrogenase (QEDH) of Pseudomonas aeruginosa is involved in catabolism of acyclic terpenes
    Chattopadhyay, Ava
    Foerster-Fromme, Karin
    Jendrossek, Dieter
    [J]. JOURNAL OF BASIC MICROBIOLOGY, 2010, 50 (02) : 119 - 124
  • [7] THE METABOLIC VERSATILITY OF PSEUDOMONADS
    CLARKE, PH
    [J]. ANTONIE VAN LEEUWENHOEK JOURNAL OF MICROBIOLOGY, 1982, 48 (02): : 105 - 130
  • [8] SiaA/D Interconnects c-di-GMP and RsmA Signaling to Coordinate Cellular Aggregation of Pseudomonas aeruginosa in Response to Environmental Conditions
    Colley, Brendan
    Dederer, Verena
    Carnell, Michael
    Kjelleberg, Staffan
    Rice, Scott A.
    Klebensberger, Janosch
    [J]. FRONTIERS IN MICROBIOLOGY, 2016, 7
  • [9] CLONING AND SEQUENCING OF PSEUDOMONAS GENES DETERMINING SODIUM DODECYL-SULFATE BIODEGRADATION
    DAVISON, J
    BRUNEL, F
    PHANOPOULOS, A
    PROZZI, D
    TERPSTRA, P
    [J]. GENE, 1992, 114 (01) : 19 - 24
  • [10] SOLUBILIZATION AND GEL ELECTROPHORESIS OF MEMBRANE ENZYMES BY USE OF DETERGENTS
    DULANEY, JT
    TOUSTER, O
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1970, 196 (01) : 29 - &