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Table 1 Characterization of precursors tested using the agar-plate screening test

From: Whole-cell fungal transformation of precursors into dyes

Name of precursor

Acronym

Substituents

Eo(mV)

Er(mV)

benzene derivatives

    

1,2-dihydroxybenzene

Cat

1-OH, 2-OH

548

285

aniline-2-sulfonic acid

A2SA

1-SO3H, 2-NH2

1013

-0.5

3-aminobenzenesulfonic acid

3ABS

1-SO3H, 3-NH2

968

5.4a

3-amino-4-hydroxybenzenesulfonic acid

AHBS

1-SO3H, 3-NH2, 4-OH

518

-103

2,4-diaminobenzenesulfonic acid

2,4DABS

1-SO3H, 2-NH2, 4-NH2

818

 

2,5-diaminobenzenesulfonic acid

2,5DABS

1-SO3H, 2-NH2, 5-NH2

433

-356a

3-amino-4-hydroxy-5-nitrobenzenesulfonic acid

AHNBS

1-SO3H, 3-NH2, 4-OH, 5-NO2

339a, 579

-92

5-sulfosalicylic acid hydrate

5SSA

1-COOH, 2-OH, 5-SO3H

-

-

2-formylbenzenesulfonic acid sodium salt

2FBSA

1-SO3Na, 2-CHO

-

-

4,5-dihydroxy-1,3-benzene-disulfonic acid

dHBdSA

1-SO3Na, 3-SO3Na, 4-OH, 5-OH

914b

 

2-amino-3-hydroxypyridine

2A3HP

2-NH2, 3-OH

647

144, 6.8

2-phenylphenol sodium salt tetrahydrate

2PP

2-ONa

790

 

naphtalene derivatives

    

2,7-dihydroxynaphtalene

DHN

2-OH, 7-OH

672

 

6-hydroxy-2-naphthalenesulfonic acid sodium salt

HNSA

2-SO3Na, 6-OH

893

-144

4-amino-3-hydroxy-1-naphthalenesulfonic acid

4AHNS

1-SO3Na, 3-OH, 4-NH2

251

194,-1.4

6-amino-4-hydroxy-2-naphthalenesulfonic acid

6AHNS

2-SO3Na, 4-OH, 6-NH2

499

 

5-amino-1-naphthalenesulfonic acid

ANS

1-SO3Na, 5-NH2

680

 
  1. Table summarizes the chemical structure of precursors in comparison with their oxidation (Eo) and reduction (Er) potentials. The potentials of the precursors were obtained at the scan rate 50 mV/s with the exception of dHBdSA, which was tested at the scan rate 25 mV/s. a very small peak, b scan rate - 25 mV/s.