Wikipedia

Draft:The Branched Chain Amino Acid Exporter (LIV-E) Family

Branched Chain Amino Acid Exporters (LIV-E) are transmembrane protein complexes that mediate the export of branched chain amino acids — isoleucine, leucine, and valine — out of prokaryotic cells. LIV-E transporters are categorized as electrochemical potential-driven transporters, subcategory porters (2.A.78) in the Transporter Classification Database.[1] LIV-E transporters are antiporters that use the proton motive force, catalyzing the transport of two hydrogen ions inside the cell, to obtain the energy to export one amino acid out of the cell.[2]

All LIV-E complexes are formed from two separate transmembrane proteins.[3] Though no structure of a LIV-E transporter exists, both proteins are necessary for function and it is assumed they form a heterodimeric complex within the membrane [3].[4][5][6]

LIV-E Family Phylogeny edit

One study in the early 2000's investigated the phylogeny of the LIV-E family[3]. It found that LIV-E transporters are prevalent across many prokaryotic organisms, including archaea and both Gram-positive and Gram-negative bacteria. While many species only encode one LIV-E transporter, other species encode multiple paralogues. Notably, these paralogues are highly divergent, suggesting early gene duplication events and independent functions for each paralogue. By contrast, in some species like Methanococcus jannaschii and Neisseria meningitidis, only one of the two components of the transporter, and consistently only the larger component, are found. It is not known if these single genes encode a functional transporter.[3] Multiple instances of highly similar LIV-E transporters have been found in both closely related and distantly related species, suggesting inheritance of LIV-E transporters has occurred both from ancestral lineages and by horizontal gene transfer across divergent species.[3]

LIV-E Transporter Function edit

Characterized LIV-E transporters include BrnFE in Corynebacterium glutamicum.[3][5], AzlCD in Bacillus subtilis[4],[7] and YgaZH in Escherichia coli[6]. The most comprehensive functional characterizations have been performed for BrnFE. However, the earliest functional role of a LIV-E transporter was described for AzlCD. In Bacillus subtilis, overexpression of AzlCD causes resistance to 4-azaleucine, a toxic analogue of leucine[4]. Despite this function, AzlCD does not likely play a major role in branched-chain amino acid homeostasis in this species[7]

In Corynebacterium glutamicum, BrnFE exports branched chain amino acids isoleucine, leucine, and valine, as well as methionine and homoserine.[3][5].[8] The greatest induction of BrnFE expression occurs under high methionine concentrations, suggesting that methionine may actually be the native substrate rather than a branched-chain amino acid[5]

LIV-E Transporter Regulation edit

LIV-E transporters in Gram-negative bacteria have often been found to be regulated by, or even co-transcribed in one operon with, the important nutrient regulator Lrp (leucine responsive protein)[3][4][6]. The regulon for Lrp is not entirely conserved across species, but often regulates amino acid uptake and biosynthesis. Lrp activity is induced by interaction with leucine, such that in environments rich in leucine the cell does not expend energy acquiring or producing its own branched-chain amino acids.[9] Co-transcription of Lrp and a LIV-E amino acid exporter creates a negative regulatory feedback loop. Lrp is first expressed and activated under high nutrient conditions, then the LIV-E transporter exports nutrients to lower intracellular concentrations and reduce activation of Lrp, turning off the system.

Applications of LIV-E Transporter Regulation in Industrial Amino Acid Production edit

The regulatory relationship between Lrp and a LIV-E transporter has been used in both Corynebacterium glutamicum and Escherichia coli, where alterations to either or both Lrp and BrnFE or AzlCD, respectively, lead to an increase in amino acid biosynthesis[6][10][11].  As Corynebacterium glutamicum is commonly used in the industrial production of amino acids, these alterations have made important improvements in amino acid yields.

Studies into BrnFE have also been applied to create a biosensor of high nutrient concentration. As the promoter for BrnFE in Corynebacterium glutamicum is induced under high concentrations of methionine and branched-chain amino acids, and Lrp is induced under the same conditions, researchers have created a hybrid construct of Lrp driven by the promoter for BrnFE (Lrp-PbrnFE). Further engineering of a desired target genes with an Lrp-binding sequence allows for the specific activation of target gene expression under high concentrations of branched-chain amino acids. This system has been utilized to drive expression of YFP as a visual marker for cells with high intracellular methionine or branched-chain amino acid concentration, which is then used to screen for genetic mutants that produce higher concentrations of these amino acids for industrial production.[12]

References edit

  1. ^ "TCDB » HOME". www.tcdb.org. Retrieved 2024-04-10.
  2. ^ Hermann, T; Kramer, R (September 1996). "Mechanism and Regulation of Isoleucine Excretion in Corynebacterium glutamicum". Applied and Environmental Microbiology. 62 (9): 3238–3244. Bibcode:1996ApEnM..62.3238H. doi:10.1128/aem.62.9.3238-3244.1996. ISSN 0099-2240. PMC 1388935. PMID 16535397.
  3. ^ a b c d e f g h Kennerknecht, Nicole; Sahm, Hermann; Yen, Ming-Ren; Pátek, Miroslav; Saier, Milton H.; Eggeling, Lothar (2002-07-15). "Export of l -Isoleucine from Corynebacterium glutamicum : a Two-Gene-Encoded Member of a New Translocator Family". Journal of Bacteriology. 184 (14): 3947–3956. doi:10.1128/JB.184.14.3947-3956.2002. ISSN 0021-9193. PMC 135157. PMID 12081967.
  4. ^ a b c d Belitsky, B R; Gustafsson, M C; Sonenshein, A L; Von Wachenfeldt, C (September 1997). "An lrp-like gene of Bacillus subtilis involved in branched-chain amino acid transport". Journal of Bacteriology. 179 (17): 5448–5457. doi:10.1128/jb.179.17.5448-5457.1997. ISSN 0021-9193. PMC 179416. PMID 9287000.
  5. ^ a b c d Trötschel, Christian; Deutenberg, Dietrich; Bathe, Brigitte; Burkovski, Andreas; Krämer, Reinhard (June 2005). "Characterization of Methionine Export in Corynebacterium glutamicum". Journal of Bacteriology. 187 (11): 3786–3794. doi:10.1128/JB.187.11.3786-3794.2005. ISSN 0021-9193. PMC 1112045. PMID 15901702.
  6. ^ a b c d Park, Jin Hwan; Lee, Kwang Ho; Kim, Tae Yong; Lee, Sang Yup (2007-05-08). "Metabolic engineering of Escherichia coli for the production of l -valine based on transcriptome analysis and in silico gene knockout simulation". Proceedings of the National Academy of Sciences. 104 (19): 7797–7802. Bibcode:2007PNAS..104.7797P. doi:10.1073/pnas.0702609104. ISSN 0027-8424. PMC 1857225. PMID 17463081.
  7. ^ a b Belitsky, Boris R. (2015-04-15). Gourse, R. L. (ed.). "Role of Branched-Chain Amino Acid Transport in Bacillus subtilis CodY Activity". Journal of Bacteriology. 197 (8): 1330–1338. doi:10.1128/JB.02563-14. ISSN 0021-9193. PMC 4372739. PMID 25645558.
  8. ^ Li, Ning; Xu, Sha; Du, Guocheng; Chen, Jian; Zhou, Jingwen (September 2020). "Efficient production of L-homoserine in Corynebacterium glutamicum ATCC 13032 by redistribution of metabolic flux". Biochemical Engineering Journal. 161: 107665. Bibcode:2020BioEJ.16107665L. doi:10.1016/j.bej.2020.107665. ISSN 1369-703X.
  9. ^ Ziegler, Christine A.; Freddolino, Peter L. (2021-07-04). "The leucine-responsive regulatory proteins/feast-famine regulatory proteins: an ancient and complex class of transcriptional regulators in bacteria and archaea". Critical Reviews in Biochemistry and Molecular Biology. 56 (4): 373–400. doi:10.1080/10409238.2021.1925215. ISSN 1040-9238. PMC 9239533. PMID 34151666.
  10. ^ Yin, L.; Shi, F.; Hu, X.; Chen, C.; Wang, X. (May 2013). "Increasing l -isoleucine production in Corynebacterium glutamicum by overexpressing global regulator Lrp and two-component export system BrnFE". Journal of Applied Microbiology. 114 (5): 1369–1377. doi:10.1111/jam.12141. PMID 23331988.
  11. ^ Yu, Shengzhu; Zheng, Bo; Chen, Zhenya; Huo, Yi-Xin (December 2021). "Metabolic engineering of Corynebacterium glutamicum for producing branched chain amino acids". Microbial Cell Factories. 20 (1): 230. doi:10.1186/s12934-021-01721-0. ISSN 1475-2859. PMC 8709942. PMID 34952576.
  12. ^ Mustafi, Nurije; Grünberger, Alexander; Kohlheyer, Dietrich; Bott, Michael; Frunzke, Julia (July 2012). "The development and application of a single-cell biosensor for the detection of l-methionine and branched-chain amino acids". Metabolic Engineering. 14 (4): 449–457. doi:10.1016/j.ymben.2012.02.002. PMID 22583745.
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