Methenyl-Dephosphotetrahydromethanopterin Is a Regulatory Signal for Acclimation to Changes in Substrate Availability in Methylobacterium extorquens AM1

被引:6
|
作者
Martinez-Gomez, N. Cecilia [1 ]
Good, Nathan M. [2 ]
Lidstrom, Mary E. [1 ,2 ]
机构
[1] Univ Washington, Dept Chem Engn, Seattle, WA 98195 USA
[2] Univ Washington, Dept Microbiol, Seattle, WA 98195 USA
关键词
METHYLENE-TETRAHYDROMETHANOPTERIN DEHYDROGENASE; SERINE CYCLE GENES; METHYLOTROPHIC METABOLISM; C-4; METABOLISM; GROWTH; METHANOL; RECONSTRUCTION; BACTERIA; FORMATE; POINT;
D O I
10.1128/JB.02595-14
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
During an environmental perturbation, the survival of a cell and its response to the perturbation depend on both the robustness and functionality of the metabolic network. The regulatory mechanisms that allow the facultative methylotrophic bacterium Methylobacterium extorquens AM1 to effect the metabolic transition from succinate to methanol growth are not well understood. Methenyl-dephosphotetrahydromethanopterin (methenyl-dH(4)MPT), an early intermediate during methanol metabolism, transiently accumulated 7- to 11-fold after addition of methanol to a succinate-limited culture. This accumulation partially inhibited the activity of the methylene-H4MPT dehydrogenase, MtdA, restricting carbon flux to the assimilation cycles. A strain overexpressing the gene (mch) encoding the enzyme that consumes methenyl-dH(4)MPT did not accumulate methenyl-dH(4)MPT and had a growth rate that was 2.7-fold lower than that of the wild type. This growth defect demonstrates the physiological relevance of this enzymatic regulatory mechanism during the acclimation period. Changes in metabolites and enzymatic activities were analyzed in the strain overexpressing mch. Under these conditions, the activity of the enzyme coupling formaldehyde with dH(4)MPT (Fae) remained constant, with concomitant formaldehyde accumulation. Release of methenyl-dH(4)MPT regulation did not affect the induction of the serine cycle enzyme activities immediately after methanol addition, but after 1 h, the activity of these enzymes decreased, likely due to the toxicity of formaldehyde accumulation. Our results support the hypothesis that in a changing environment, the transient accumulation of methenyl-dH(4)MPT and inhibition of MtdA activity are strategies that permit flexibility and acclimation of the metabolic network while preventing the accumulation of the toxic compound formaldehyde. IMPORTANCE The identification and characterization of regulatory mechanisms for methylotrophy are in the early stages. We report a non-transcriptional regulatory mechanism that was found to operate as an immediate response for acclimation during changes in substrate availability. Methenyl-dH(4)MPT, an early intermediate during methanol oxidation, reversibly inhibits the methylene-H4MPT dehydrogenase, MtdA, when Methylobacterium extorquens is challenged to switch from succinate to methanol growth. Bypassing this regulatory mechanism causes formaldehyde to accumulate. Fae, the enzyme catalyzing the conversion of formaldehyde to methylene-dH(4)MPT, was also identified as another potential regulatory target using this strategy. The results herein further our understanding of the complex regulatory network in methylotrophy and will allow us to improve metabolic engineering strategies of methylotrophs for the production of value-added products.
引用
收藏
页码:2020 / 2026
页数:7
相关论文
共 50 条
  • [31] QscR regulates expression of the formate dehydrogenase genes in Methylobacterium extorquens AM1
    Valdez, Rachael
    Skovran, Elizabeth
    FASEB JOURNAL, 2014, 28 (01):
  • [32] Generation of formate by the formyltransferase/hydrolase complex (Fhc) from Methylobacterium extorquens AM1
    Pomper, BK
    Saurel, O
    Milon, A
    Vorholt, JA
    FEBS LETTERS, 2002, 523 (1-3) : 133 - 137
  • [33] Structural insight into a molecular mechanism of methenyltetrahydrofolate cyclohydrolase from Methylobacterium extorquens AM1
    Kim, Seongmin
    Lee, Seul Hoo
    Kim, Il-Kwon
    Seo, Hogyun
    Kim, Kyoung-Jin
    INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2022, 202 : 234 - 240
  • [34] GENETIC ORGANIZATION OF METHYLAMINE UTILIZATION GENES FROM METHYLOBACTERIUM-EXTORQUENS AM1
    CHISTOSERDOV, AY
    TSYGANKOV, YD
    LIDSTROM, ME
    JOURNAL OF BACTERIOLOGY, 1991, 173 (18) : 5901 - 5908
  • [35] Biochemical characterization of a dihydromethanopterin reductase involved in tetrahydromethanopterin biosynthesis in Methylobacterium extorquens AM1
    Caccamo, MA
    Malone, CS
    Rasche, ME
    JOURNAL OF BACTERIOLOGY, 2004, 186 (07) : 2068 - 2073
  • [36] Comprehensive molecular characterization of Methylobacterium extorquens AM1 adapted for 1-butanol tolerance
    Hu, Bo
    Yang, Yi-Ming
    Beck, David A. C.
    Wang, Qian-Wen
    Chen, Wen-Jing
    Yang, Jing
    Lidstrom, Mary E.
    Yang, Song
    BIOTECHNOLOGY FOR BIOFUELS, 2016, 9
  • [37] Comprehensive molecular characterization of Methylobacterium extorquens AM1 adapted for 1-butanol tolerance
    Bo Hu
    Yi-Ming Yang
    David A. C. Beck
    Qian-Wen Wang
    Wen-Jing Chen
    Jing Yang
    Mary E. Lidstrom
    Song Yang
    Biotechnology for Biofuels, 9
  • [38] Comparison of the proteome of Methylobacterium extorquens AM1 grown under methylotrophic and nonmethylotrophic conditions
    Laukel, M
    Rossignol, M
    Borderies, G
    Völker, U
    Vorholt, JA
    PROTEOMICS, 2004, 4 (05) : 1247 - 1264
  • [39] Ethylmalonyl Coenzyme A Mutase Operates as a Metabolic Control Point in Methylobacterium extorquens AM1
    Good, Nathan M.
    Martinez-Gomez, N. Cecilia
    Beck, David A. C.
    Lidstrom, Mary E.
    JOURNAL OF BACTERIOLOGY, 2015, 197 (04) : 727 - 735
  • [40] CHARACTERIZATION OF TRANSPOSON INSERTION MUTANTS OF METHYLOBACTERIUM-EXTORQUENS AM1 (METHYLOBACTERIUM STRAIN-AM1) WHICH ARE DEFECTIVE IN METHANOL OXIDATION
    LEE, KE
    STONE, S
    GOODWIN, PM
    HOLLOWAY, BW
    JOURNAL OF GENERAL MICROBIOLOGY, 1991, 137 : 895 - 904