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Table 1 Comparison of studies on [FeFe] hydrogenase genes expression in various conditions available in literature and the present study

From: Improving sustainable hydrogen production from green waste: [FeFe]-hydrogenases quantitative gene expression RT-qPCR analysis in presence of autochthonous consortia

Organism(s)

Methodological approach

Growth conditions

Focused metabolism studied

[FeFe] hydrogenase genes expression monitored

Refs.

C. beijerinckii SM10

Semi-quantitative

RT-PCR

Clostridial medium, pure culture

Hydrogen production

Cbei_1773

Cbei_0327

Cbei_1901

Cbei_4110

Cbei_3796

Cbei_4000

[35]

C. butyricum SM32

Semi-quantitative

RT-PCR

Clostridial medium, pure culture

Hydrogen production

CBY_3049

CBY_2300

CBY_2047

CBY_2676

[35]

C. perfringens SM09

Semi-quantitative

RT-PCR

Clostridial medium, pure cultures

Hydrogen production

CPF_2655

CPF_1076

CPF_0270

CPF_2900

[35]

C. tyrobutyricum KCTC 5387 (ATCC 25,755)

Shotgun proteomics

2xYTG medium

Pure culture

General metabolism

CTK_C05160

CTK_C26290

CTK_C29580

[43]

Proteobacteria,

Firmicutes,

Bacteroidetes, and Chloroflexi

DGGE analysis of hydA in time

Paddy Field Soil during rice straw decomposition with autochthonous microbiota

Hydrogen production

hydA sequences of uncultured strains deposited to the DDBJ database under accession numbers LC041370-LC041941

[45]

Clostridium beijerinckii NRRL B-598

RNA-Seq

Batch fermentation, pure culture in culture broths with a glucose concentration of 50 g/L at pH 6.3

Acidogenesis, solventogenesis, metabolic stress response and life cycle changes

X276_17350, X276_06930 X276_05300 (sharing high similarity with Cbei_1901, Cbei_3796 and Cbei_4110, respectively)

[46]

Clostridium butyricum CWBI 1009

Transcriptomic (RNA-seq and RT-qPCR) and proteomic analyses

Glucose fermentation, unregulated pH with Argon atmosphere

pure culture

Hydrogen production

hydA2,

hydA8

hydB2

hydB3

(changes only observed in Argon atmosphere, not in N2)

[49]

Clostridium sp. strain H2

RT-qPCR

Under fermentation conditions,

Widdel’s freshwater medium

pure cultures

Hydrogen production

H2hydA1

H2hydA2

H2hydA3

H2hydA4

H2hydA5 corresponding to hydA genes of C. bifermentans ATCC 638 (AVNC00000000) and ATCC 19,299 (AVNB00000000)

[50]

Desulfovibrio sp. strain A1 and AH1

RT-qPCR

Under sulphate-reducing conditions

modified Widdel’s freshwater medium

pure cultures

Hydrogen production

A1hydA1

A1hydA2 corresponding to hydA genes of D. vulgaris Hildenborough (AE017285)

[50]

Clostridium butyricum CGS5

RT-PCR and qPCR

PM medium

Pure culture

Hydrogen production

hydA

[51]

Thermotoga neapolitana and Caldicellulosiruptor saccharolyticus

Quantitative Real-time PCR

Synthetic co-culture

Hydrogen production

hydA

from Thermotoga neapolitana

[52]

Clostridium thermocellum ATCC 27,405

Real-time quantitative PCR

Continuous pure culture on Modified Dehority medium containing (per litre) 3.0 g of cellobiose or 2.7 to 3.1 g of Sigmacell 20 microcrystalline cellulose

Fermentation of Cellulose or Cellobiose

hydA

[53]

Clostridium beijerinckii AM2 and

Clostridium tyrobutyricum AM6

RT-qPCR

Green waste with autochthonous microbiota and co-addition of both strains

Hydrogen production on green waste

Cbei_1773

Cbei_0327

Cbei_1901

Cbei_4110

Cbei_3796

Cbei_4000

Ctyr_hydA (FJ226584)

This study

  1. The genes with changes in expression levels are highlighted in bold