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. 2018 Mar 13;9(2):e00188-18. doi: 10.1128/mBio.00188-18

Erratum for Mor et al., “Identification of a New Class of Antifungals Targeting the Synthesis of Fungal Sphingolipids”

Visesato Mor a, Antonella Rella a, Amir M Farnoud a, Ashutosh Singh a, Mansa Munshi a, Arielle Bryan a, Shamoon Naseem a, James B Konopka a, Iwao Ojima b, Erika Bullesbach c, Alan Ashbaugh d, Michael J Linke d,e, Melanie Cushion d,e, Margaret Collins e, Hari Krishna Ananthula f, Larry Sallans q, Pankaj B Desai f, Nathan P Wiederhold g, Annette W Fothergill g, William R Kirkpatrick h, Thomas Patterson h, Lai Hong Wong i, Sunita Sinha i, Guri Giaever i, Corey Nislow i, Patrick Flaherty j, Xuewen Pan k, Gabriele Vargas Cesar l, Patricia de Melo Tavares l, Susana Frases m, Kildare Miranda l,n, Marcio L Rodrigues l,o, Chiara Luberto p, Leonardo Nimrichter l, Maurizio Del Poeta a,
PMCID: PMC5850322  PMID: 29535196

ERRATUM

Volume 6, no. 3, e00647-15, 2015, https://doi.org/10.1128/mBio.00647-15. The compound that was used in our article was N′-(3-bromo-6-hydroxybenzylidene)-2-methylbenzohydrazide (BHBM) and not N′-(3-bromo-4-hydroxybenzylidene)-2-methylbenzohydrazide. All experiments described in the paper were done using BHBM [N′-(3-bromo-6-hydroxybenzylidene)-2-methylbenzohydrazide], and the structure noted in Fig. 1B of our original article should be as indicated in Fig. 1 here.

FIG 1 .

FIG 1 

Corrected structure of BHBM to replace the structure in Fig. 1B of our original article.

The structure of BHBM used in the mBio studies was confirmed by proton nuclear magnetic resonance (NMR), which indicated the following chemical shifts: 1H NMR (500 MHz, dimethyl sulfoxide-d6) δ 2.38 (s, 3H), 6.90 (d, 1H, J = 8.8 Hz), 7.28 to 7.32 (m, 3H), 7.37 to 7.43 (m, 2H), 7.47 (d, 1H, J = 7.5 Hz), 7.78 (s, 1H), 8.47 (s, 1H), 11.19 (s, 1H), 12.05 (s, 1H).

All findings illustrated in the paper are correct.


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