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Cloning, Expression and Characterization of Histidine-Tagged Biotin Synthase of Mycobacterium Tuberculosis

Cloning, Expression and Characterization of Histidine-Tagged Biotin Synthase of Mycobacterium Tuberculosis

Clement Chedza Magwamba, Kamolchanok Rukseree, Prasit Palittapongarnpim

Tuberculosis (Edinb). 2016 May;98:42-9.

PMID: 27156617

Abstract:

The emergence of Mycobacterium tuberculosis strains that are resistant to the current anti-tuberculosis (TB) drugs necessitates a need to develop a new class of drugs whose targets are different from the current ones. M. tuberculosis biotin synthase (MtbBS) is one such target that is essential for the survival of the bacteria. In this study, MtbBS was cloned, overexpressed and purified to homogeneity for biochemical characterization. It is likely to be a dimer in its native form. Its pH and temperature optima are 8.0 and 37 °C, respectively. Km for DTB and SAM was 2.81 ± 0.35 and 9.95 ± 0.98 μM, respectively. The enzyme had a maximum velocity of 0.575 ± 0.015 μM min(-1), and a turn-over of 0.0935 min(-1). 5'-deoxyadenosine (dAH), S-(5'-Adenosyl)-l-cysteine (AdoCy) and S-(5'-Adenosyl)-l-homocysteine (AdoHcy) were competitive inhibitors of MtbBS with the following inactivation parameters: Ki = 24.2 μM, IC50 = 267.4 μM; Ki = 0.84 μM, IC50 = 9.28 μM; and Ki = 0.592 μM, IC50 = 6.54 μM for dAH, AdoCy and AdoHcy respectively. dAH could inhibit the growth of M. tuberculosis H37Ra with an MIC of 392.6 μg/ml. This information should be useful for the discovery of inhibitors of MtbBS.

Chemicals Related in the Paper:

Catalog Number	Product Name	Structure	CAS Number	Price
AP979920	S-(5′-Adenosyl)-L-homocysteine		979-92-0	Price

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