Literature DB >> 7322186

Respiration of Leishmania mexicana amastigotes and promastigotes.

D T Hart, K Vickerman, G H Coombs.   

Abstract

Promastigotes of Leishmania mexicana mexicana recently derived from amastigotes by transformation in vitro respired at a rate (17 nmol O2/min per 10(8) parasites) 4-5 times higher than that of amastigotes, but when the difference in cell protein content between the two preparations was taken into account the rates were not significantly different (32 nmol O2/min per mg protein). The respiration of both amastigotes and promastigotes was sensitive to cyanide, azide, antimycin A, 2-n-heptyl-4-hydroxyquinoline-N-oxide and high concentrations of amytal, but insensitive to rotenone and salicyl-hydroxamic acid, indicating that the two developmental forms possess a similar cytochrome-containing respiratory chain. D-Glucose and non-esterified fatty acids stimulated promastigote respiration and amastigote transformation to promastigotes in vitro; possibly these substances are important exogenous energy substrates for both forms of the parasites. Amino acids (incuding L-proline) and proteins did not appear to be used as energy substrates. The respiration rate of promastigotes was found to rise significantly upon continued sub-culture in vitro; at the same time cell size and protein content increased.

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Year:  1981        PMID: 7322186     DOI: 10.1016/0166-6851(81)90027-x

Source DB:  PubMed          Journal:  Mol Biochem Parasitol        ISSN: 0166-6851            Impact factor:   1.759


  11 in total

1.  Leishmania mexicana amazonensis: plasma membrane adenine nucleotide translocator and chemotaxis.

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Journal:  Mol Microbiol       Date:  2010-05-24       Impact factor: 3.501

4.  A glucose transporter can mediate ribose uptake: definition of residues that confer substrate specificity in a sugar transporter.

Authors:  Christina M Naula; Flora J Logan; Flora M Logan; Pui Ee Wong; Michael P Barrett; Richard J Burchmore
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5.  RNA editing and mitochondrial activity in promastigotes and amastigotes of Leishmania donovani.

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6.  Experimental visceral leishmaniasis: role of trans-aconitic acid in combined chemotherapy.

Authors:  S Kar; K Kar; P K Bhattacharya; D K Ghosh
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7.  An essential type I nitroreductase from Leishmania major can be used to activate leishmanicidal prodrugs.

Authors:  Andrew A Voak; Vithurshaa Gobalakrishnapillai; Karin Seifert; Edina Balczo; Longqin Hu; Belinda S Hall; Shane R Wilkinson
Journal:  J Biol Chem       Date:  2013-08-14       Impact factor: 5.157

8.  Identification and characterization of genes involved in leishmania pathogenesis: the potential for drug target selection.

Authors:  Robert Duncan; Sreenivas Gannavaram; Ranadhir Dey; Alain Debrabant; Ines Lakhal-Naouar; Hira L Nakhasi
Journal:  Mol Biol Int       Date:  2011-06-26

9.  The mitochondrial SIR2 related protein 2 (SIR2RP2) impacts Leishmania donovani growth and infectivity.

Authors:  Nimisha Mittal; Rohini Muthuswami; Rentala Madhubala
Journal:  PLoS Negl Trop Dis       Date:  2017-05-11

10.  Universal minicircle sequence binding protein of Leishmania donovani regulates pathogenicity by controlling expression of cytochrome-b.

Authors:  Ruby Singh; Bidyut Purkait; Kumar Abhishek; Savita Saini; Sushmita Das; Sudha Verma; Abhishek Mandal; Ayan Kr Ghosh; Yousuf Ansari; Ashish Kumar; Abul H Sardar; Ajay Kumar; Pradeep Parrack; Pradeep Das
Journal:  Cell Biosci       Date:  2016-02-17       Impact factor: 9.584

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