Literature DB >> 27419196

Secretome data from Trichoderma reesei and Aspergillus niger cultivated in submerged and sequential fermentation methods.

Camila Florencio1, Fernanda M Cunha2, Alberto C Badino3, Cristiane S Farinas4, Eduardo Ximenes5, Michael R Ladisch5.   

Abstract

The cultivation procedure and the fungal strain applied for enzyme production may influence levels and profile of the proteins produced. The proteomic analysis data presented here provide critical information to compare proteins secreted by Trichoderma reesei and Aspergillus niger when cultivated through submerged and sequential fermentation processes, using steam-explosion sugarcane bagasse as inducer for enzyme production. The proteins were organized according to the families described in CAZy database as cellulases, hemicellulases, proteases/peptidases, cell-wall-protein, lipases, others (catalase, esterase, etc.), glycoside hydrolases families, predicted and hypothetical proteins. Further detailed analysis of this data is provided in "Secretome analysis of Trichoderma reesei and Aspergillus niger cultivated by submerged and sequential fermentation process: enzyme production for sugarcane bagasse hydrolysis" C. Florencio, F.M. Cunha, A.C Badino, C.S. Farinas, E. Ximenes, M.R. Ladisch (2016) [1].

Entities:  

Keywords:  Aspergillus Niger; Enzyme Production; Secretome; Tricoderma reesei

Year:  2016        PMID: 27419196      PMCID: PMC4936598          DOI: 10.1016/j.dib.2016.05.080

Source DB:  PubMed          Journal:  Data Brief        ISSN: 2352-3409


Specifications Table Value of the data This data set will be of value to the scientific community aiming to analyze the identified proteins secreted by T. reesei and A. niger under different cultivation methods. The data can be a useful tool to effectively select fungal strain and cultivation procedure for the production of proteins of interest. The data provided here identify key enzymes from T. reesei and A. niger for combined use to effectively degrade lignocellulose substrates, and therefore provide an opportunity to help researchers in the field to formulate enzyme cocktails in according to characteristics of lignocellulose biomass and enzyme activities found in the secretome.

Data

In Table 1, the proteins identified by proteomic analysis of enzymatic cocktails from Trichoderma reesei and Aspergillus niger, cultivated on pretreated sugarcane bagasse by either submerged or sequential fermentation processes, are presented according to the families classification from CAZy database.
Table 1

Major proteins identified in the secretome of Trichoderma reesei and Aspergillus niger cultivated under submerged (A) and sequential (B) fermentation methods.

Gene IDEnzymeFamilyT. reesei
A. niger
ABAB
21842121CellulasesEndoglucanaseGH12xx
3757552Endoglucanase AGH12xx
145235569Endo-beta-1,4-glucanase AGH12x
145228915Endo-beta-1,4-glucanase AGH12x
2833231Endoglucanase IGH7xx
121794Endoglucanase IIGH5x
201066457Endoglucanase IV (AA9)GH61xx
145235523Glucan endo-1,3-beta-glucosidase eglCxx
320592482Beta-glucanasex
403314396Endoglucanase VIGH61x
145229151Endo-1,3(4)-beta-glucanaseGH16xx
202072834Cellobiohydrolase IGH7xx
95115828Cellobiohydrolase IIGH6xx
746984991,4-beta-D-glucan cellobiohydrolaseGH7xx
201066459GlucosidaseGH3x
126046487β-glucosidaseGH3xx
145242946β-glucosidase M 4GH3x
145255120Glucan 1,3-beta-glucosidase AGH5xx
400602153Glucan 1,3-β-glucosidaseGH17x
257187Alpha-glucosidase P2 subunit 5GH31x



317035725HemicellulasesEndo-arabinaseGH43x
145234699Alpha-L-arabinofuranosidase axhAGH62xx
358375978Arabinoxylan arabinofuranohydrolaseGH62xx
145233623Endo-1,5-alpha-L-arabinosidase CGH43xx
145250511Alpha-N-arabinofuranosidase Bxx
78101601Anfaea-ferulic Acid Complexx
23821545Feruloyl esterase Bx
145246174Feruloyl esterase Cxx
48425840Ferulic acid esterasex
145247672Feruloyl esterase B-1x
145230716Beta-galactosidase EGH35xx
350630290Alpha-galactosidase extracellularx
74626383Alpha-galactosidase Bxx
317034650Alpha-galactosidase Dx
307776646Beta-mannanaseGH5xx
358367813Alpha-mannosidaseGH38x
145233855Alpha-mannosidaseGH38x
572273984Beta-mannosidase AGH2x
572273001Putative beta-mannosidase AGH2xx
317032967Beta-mannosidase AGH2xX
358369379Beta-mannosidase (MndA)GH2x
145230794Alpha-1,2-mannosidase 1BGH47xx
145256261Pectate lyase plyBx
572278177Pectin lyase-like proteinxx
165906534EndoxylanaseGH10xx
11513450Acetyl Xylan Esterasexx
292495278Endo-1,4-beta-xylanase CGH10xx



549461HemicellulasesEndo-1,4-beta-xylanase 2GH11xx
145250044Endo-1,4-beta-xylanase 5GH11xx
157488002SwolleninCBM1xx
9858848XylanaseGH11x
42716406XylanaseGH11xx
13242071XylanaseGH11x
26514830XylanaseGH11x
83638302XylanaseGH11x
380293098Xylanase IIGH11xx
145242002Alpha-xylosidaseGH31xx
145230215Exo-1,4-beta-xylosidase xlnDGH3xx
145243586Xylosidase/arabinosidasexx



145228611Proteases/ PeptidasesAorsinx
530795Pepsinogenxx
589101183Aminopeptidasex
145257498Aminopeptidase 2x
145242728Vaculolar aspartyl aminopeptidase Lap4xx
145583569Aspartic endopeptidasex
145254317Aspartic-type endopeptidase opsBx
145248205Aspartic-type endopeptidase opsBx
145256471Dipeptidyl peptidase IIIx
145249068Tripeptidyl-peptidase sed2x
629687989Tripeptidyl peptidase precursorx
145246822Extracellular serine carboxypeptidasex
1093596Ser carboxypeptidasex
145235505Serine carboxypeptidasexx
317026828Serine-type carboxypeptidasexx
134077081Endoprotease Endo-Pro-A. nigerxx
62002221Subtilase proteasex
115111226Subtilisin-like proteasexx
589111601Serine proteasex
29421423Extracellular serine proteasex
124295071SprT - serine proteasexx
464359Subtilisin-like serine protease pepCx
589099267Trypsin-like serine proteasexx
193735605Vacuolar protease Ax
387772861Aspartic proteinasexx



38256986Cell-wall proteinCell wall proteinx
47028077Cell-wall protein - CwpAx
145252266GPI anchored cell wall proteinGH64xx
589109601Ceramidase family proteinx
145255556Alkaline nonlysosomal ceramidasex
387772865Cerato-plataninxx
270160616ChitinaseGH18xx
145232927Endochitinase 1GH18xx
1839391ExochitinaseGH20x
145256696Protein ecm33xx



145241592LipasesLysophospholipase 1x
145234164Lysophospholipase 1x
145231236Phospholipase C PLC-Cx
109677003Triacylglycerol lipase precursorx
110431975Triacyglycerol lipase Bx



589114715OthersAmidasexx
145239143Aminotransferase, class Vx
145241960Alpha-amylasex
350631148Alpha-amylase ACBM20x
145243632Alpha-amylase a type-1/2xx
224027Glucoamylase G1GH15xx
145241784N-acetylglucosaminidaseGH20x
113206519Acetyl esterasex
589098125Carbohydrate esterasexx
358388255Carbohydrate esterase family 15 proteinCBM15xx
572279065Carboxylesterasex
145233451Cholinesterasexx
1705640Catalase Rx
589115621Catalase/peroxidasex
145228625Catalase Rx
119474019Mycelial catalase Cat1x
404312830Cellulose Induced Protein, CIP1xx
589107171Oxalate decarboxylasexx
380482942Oxalate decarboxylase family bicupinx
1169291Aldehyde dehydrogenasex
572279542Dihydrolipoyl dehydrogenasexx
350631179FAD/FMN-containing dehydrogenasex
589113573Malate dehydrogenasex
19702487Malate dehydrogenasex
145257405Short-chain dehydrogenasexx
145230419Glycosidase crf1x
1452561301,3-beta-glucanosyltransferase gel1GH72xx
1452404071,3-beta-glucanosyltransferase gel2GH72xx
1452414901,3-beta-glucanosyltransferase gel3GH72x
145234270Glutaminase GtaAxx
145247260InulinaseGH32xx
145242650Nucleoside diphosphate kinasex
589102565Acid phosphatase-like proteinxx
130734Phosphate-repressible acid phosphatasex
145232002Phosphatidylglycerolxx
145251519Phosphoglycerate mutase family proteinx



572278887Glycoside Hydrolases familiesGlycoside Hydrolase (GH)GHx
572275960GH, partialGHx
358381827GH family 2 proteinGH2x
589104105GH family 3GH3x
358388254GH family 5 proteinGH5x
589100793GH family 10GH10xx
261825113GH family 15 protein (glucoamylase)GH15xx
589113453GH family 16GH16x
358382969GH family 16 proteinGH17x
589111611GH family 17GH17x
589113629GH 18 protein (chitinase)GH18xx
317028062GH, family 18GH18x
589109851GH family 28GH28x
358380963GH family 28 proteinGH28x
572273805Family 31 GHGH31xx
589103027GH family 38 proteinGH38x
358387943GH family 43 proteinGH43x
589101105GH family 47GH47xx
631371154GH family 47 proteinGH47xx
589100379GH family 54 (lignin-degrading)GH57xx
589115645GH family 55GH55x
589114155GH familiy 67GH67x
358384989GH family 71 proteinGH71x
589103161GH family 71 proteinGH71x
589109155GH family 71 proteinGH71xx
589111135GH family 72 (lignin-degrading)GH72x
589108435GH 74GH74xx
358380926GH family 74 proteinGH74x
589098631GH 92GH92xx
589100807GH family 92GH92x



255722211Predicted proteinsPredicted proteinx
589105897Predicted proteinxx
589101909Predicted proteinxx
589110563Predicted proteinGH16xx
589113917Predicted proteinx
589109549Predicted proteinGH67xx
589108581Pr Predicted proteinGH16x
403411875Predicted proteinx
589105505Predicted proteinx
589107107Predicted proteinxx
589100041Predicted proteinxx
589115849Predicted proteinx
589099057Predicted proteinx
589112857Predicted proteinx
589116001Predicted proteinx
589113291Predicted proteinx
589115927Predicted proteinx
154322591Predicted proteinx



358390109Hypothetical proteinsHypothetical protein TRIATDRAFT_129231x
358386311Hypothetical protein TRIVIDRAFT_45439x
358390537Hypothetical protein TRIATDRAFT_302472xx
572280833Hypothetical protein M419DRAFT_97005x
116199677Conserved hypothetical proteinx
589112113Hypothetical protein TRIREDRAFT_66935xx
358386247Hypothetical protein TRIVIDRAFT_179276x
572280092Hypothetical protein M419DRAFT_62371x
572273052Hypothetical protein M419DRAFT_125562x
358380920Hypothetical protein TRIVIDRAFT_118319x
572284103Hypothetical protein M419DRAFT_94877GH71xx
589108875Hypothetical protein TRIREDRAFT_122487x
380490319Hypothetical protein CH063_07742x
358394718Hypothetical protein TRIATDRAFT_300431x
345562011Hypothetical protein AOL_s00173g184CBM1x
440640361Hypothetical protein GMDG_04666x
358381566Hypothetical protein TRIVIDRAFT_49497x
358385331Hypothetical protein TRIVIDRAFT_60255x
358388440Hypothetical protein TRIVIDRAFT_141673x
358381654Hypothetical protein TRIVIDRAFT_4609x
46127631Hypothetical protein FG08193.1x
310800235Hypothetical protein GLRG_10272x
598027367Hypothetical protein AURDEDRAFT_162084x
646290693Hypothetical protein BOTBODRAFT_162340x
598062595Hypothetical protein SPAPADRAFT_57777x
350636308Hypothetical protein ASPNIDRAFT_182100GH43x
350629486Hypothetical protein ASPNIDRAFT_47677GH43x
350632025Hypothetical protein ASPNIDRAFT_128537xx
145246196Hypothetical protein ANI_1_1560104x
350635020Hypothetical protein ASPNIDRAFT_197780x
568447829Hypothetical protein AGABI2DRAFT_199975GH3x
350631594Hypothetical protein ASPNIDRAFT_53033GH72xx
46122475Hypothetical protein FG05615.1x
134082115Hypothetical protein An15g00620x
350637823Hypothetical protein ASPNIDRAFT_52061GH75xx
145258972Hypothetical protein ANI_1_2174184xx
145254751Hypothetical protein ANI_1_1218164xx
145233749Hypothetical protein ANI_1_1558024xx
350633910Hypothetical protein ASPNIDRAFT_54865xx
350639816Hypothetical protein ASPNIDRAFT_124700x
350638529Hypothetical protein ASPNIDRAFT_119858GH31x
350638823Hypothetical protein ASPNIDRAFT_205361x
350636991Hypothetical protein ASPNIDRAFT_56689x
350633205Hypothetical protein ASPNIDRAFT_55058x
350629696Hypothetical protein ASPNIDRAFT_126535x
145243362Hypothetical protein ANI_1_1704094GH1x
563290941Hypothetical protein SBOR_8115x
398407925Hypothetical protein MYCGRDRAFT_30155x
350636557Hypothetical protein ASPNIDRAFT_53540x
The enzymatic hydrolysis of pretreated sugarcane bagasse was performed with combined extracts from T. reesei Rut C30 and A. niger A12, and the data of proteomic analysis of this combination of identified proteins is shown in Table 2. The indicated enzyme loadings were applied for steam-explosion sugarcane bagasse saccharification as described by Florencio et al. [1].
Table 2

Major proteins identified in the submerged (A) and sequential (B) fermentation enzymatic extracts from Trichoderma reesei + Aspergillus niger, which were used in the hydrolysis process of the pretreated sugarcane bagasse at a 1:5 ratio, respectively.

Gene IDEnzymeFamilyT. reesei+A. niger(1:5)
AB
21842121CellulasesEndoglucanaseGH12xx
3757552Endoglucanase AGH12xx
145235569Endo-beta-1,4-glucanase AGH12x
145228915Endo-beta-1,4-glucanase AGH12x
2833231Endoglucanase IGH7xx
121794Endoglucanase IIGH5x
201066457Endoglucanase IV (AA9)GH61xx
145235523Glucan endo-1,3-beta-glucosidase eglCxx
320592482Beta-glucanasex
403314396Endoglucanase VI (AA9)GH61x
145229151Endo-1,3(4)-beta-glucanaseGH16xx
202072834Cellobiohydrolase IGH7xx
95115828Cellobiohydrolase IIGH6xx
746984991,4-beta-D-glucan cellobiohydrolaseGH7xx
201066459GlucosidaseGH3x
126046487β-glucosidaseGH3xx
145242946β-glucosidase M 4GH3x
145255120Glucan 1,3-beta-glucosidase AGH5xx
400602153Glucan 1,3-β-glucosidaseGH17x
257187Alpha-glucosidase P2 subunit 5GH31x



317035725HemicellulasesEndo-arabinaseGH43x
145234699Alpha-L-arabinofuranosidase axhAGH62xx
358375978Arabinoxylan arabinofuranohydrolaseGH62xx
145233623Endo-1,5-alpha-L-arabinosidase CGH43xx
145250511Alpha-N-arabinofuranosidase Bxx
78101601Anfaea-ferulic Acid Complexx
23821545Feruloyl esterase Bx
145246174Feruloyl esterase Cxx
48425840Ferulic acid esterasex
145247672Feruloyl esterase B-1x
145230716Beta-galactosidase EGH35xx
350630290Alpha-galactosidase extracellularx
74626383Alpha-galactosidase Bxx
317034650Alpha-galactosidase Dx
307776646Beta-mannanaseGH5xx
358367813Alpha-mannosidaseGH38x
145233855Alpha-mannosidaseGH38x
572273984Beta-mannosidase AGH2x
572273001Putative beta-mannosidase AGH2xx
317032967Beta-mannosidase AGH2xx
358369379Beta-mannosidase (MndA)GH2x
145230794Alpha-1,2-mannosidase 1BGH47xx
145256261Pectate lyase plyBx
572278177Pectin lyase-like proteinxx
165906534EndoxylanaseGH10xx
11513450Acetyl Xylan Esterasexx
292495278Endo-1,4-beta-xylanase CGH10xx
549461Endo-1,4-beta-xylanase 2GH11xx
145250044Endo-1,4-beta-xylanase 5GH11xx



157488002HemicellulasesSwolleninCBM1xx
9858848XylanaseGH11x
42716406XylanaseGH11xx
13242071XylanaseGH11x
26514830XylanaseGH11x
83638302XylanaseGH11x
380293098Xylanase IIGH11xx
145242002Alpha-xylosidaseGH31xx
145230215Exo-1,4-beta-xylosidase xlnDGH3xx
145243586Xylosidase/arabinosidasexx



572278887Glycoside Hydrolases familiesGlycoside Hydrolase (GH)GHx
572275960GH, partialGHx
358381827GH family 2 proteinGH2x
589104105GH family 3GH3x
358388254GH family 5 proteinGH5x
589100793GH family 10GH10xx
261825113GH family 15 protein (glucoamylase)GH15xx
589113453GH family 16GH16x
358382969GH family 16 proteinGH17x
589111611GH family 17GH17x
589113629GH 18 protein (chitinase)GH18xx
317028062GH, family 18GH18x
589109851GH family 28GH28x
358380963GH family 28 proteinGH28x
572273805Family 31 GHGH31xx
589103027GH family 38 proteinGH38x
358387943GH family 43 proteinGH43x
589101105GH family 47GH47xx
631371154GH family 47 proteinGH47xx
589100379GH family 54 (lignin-degrading)GH57xx
589115645GH family 55GH55x
589114155GH familiy 67GH67x
358384989GH family 71 proteinGH71x
589103161GH family 71 proteinGH71x



589109155GH familiesGH family 71 proteinGH71xx
589111135GH family 72 (lignin-degrading)GH72x
589108435GH 74GH74xx
358380926GH family 74 proteinGH74x
589098631GH 92GH92xx
589100807GH family 92GH92x



255722211Predicted proteinsPredicted proteinx
589105897Predicted proteinxx
589101909Predicted proteinxx
589110563Predicted proteinGH16xx
589113917Predicted proteinx
589109549Predicted proteinGH67xx
589108581Predicted proteinGH16x
403411875Predicted proteinx
589105505Predicted proteinx
589107107Predicted proteinxx
589100041Predicted proteinxx
589115849Predicted proteinx
589099057Predicted proteinx
589112857Predicted proteinx
589116001Predicted proteinx
589113291Predicted proteinx
589115927Predicted proteinx
154322591Predicted proteinx



358390109Hypothetical proteinsHypothetical protein TRIATDRAFT_129231x
358386311Hypothetical protein TRIVIDRAFT_45439x
358390537Hypothetical protein TRIATDRAFT_302472xx
572280833Hypothetical protein M419DRAFT_97005x
116199677Conserved hypothetical proteinx
589112113Hypothetical protein TRIREDRAFT_66935xx
358386247Hypothetical protein TRIVIDRAFT_179276x
572280092Hypothetical protein M419DRAFT_62371x
572273052Hypothetical protein M419DRAFT_125562x
358380920Hypothetical protein TRIVIDRAFT_118319x
572284103Hypothetical protein M419DRAFT_94877GH71xx
589108875Hypothetical protein TRIREDRAFT_122487x
380490319Hypothetical protein CH063_07742x
358394718Hypothetical protein TRIATDRAFT_300431x
345562011Hypothetical protein AOL_s00173g184CBM1x
440640361Hypothetical protein GMDG_04666x
358381566Hypothetical protein TRIVIDRAFT_49497x
358385331Hypothetical protein TRIVIDRAFT_60255x
358388440Hypothetical protein TRIVIDRAFT_141673x
358381654Hypothetical protein TRIVIDRAFT_4609x
46127631Hypothetical protein FG08193.1x
310800235Hypothetical protein GLRG_10272x
598027367Hypothetical protein AURDEDRAFT_162084x
646290693Hypothetical protein BOTBODRAFT_162340x
598062595Hypothetical protein SPAPADRAFT_57777x
350636308Hypothetical protein ASPNIDRAFT_182100GH43x
350629486Hypothetical protein ASPNIDRAFT_47677GH43x
350632025Hypothetical protein ASPNIDRAFT_128537xx
145246196Hypothetical protein ANI_1_1560104x
350635020Hypothetical protein ASPNIDRAFT_197780x



568447829Hypothetical proteinsHypothetical protein AGABI2DRAFT_199975GH3x
350631594Hypothetical protein ASPNIDRAFT_53033GH72xx
46122475Hypothetical protein FG05615.1x
134082115Hypothetical protein An15g00620x
350637823Hypothetical protein ASPNIDRAFT_52061GH75xx
145258972Hypothetical protein ANI_1_2174184xx
145254751Hypothetical protein ANI_1_1218164xx
145233749Hypothetical protein ANI_1_1558024xx
350633910Hypothetical protein ASPNIDRAFT_54865xx
350639816Hypothetical protein ASPNIDRAFT_124700x
350638529Hypothetical protein ASPNIDRAFT_119858GH31x
350638823Hypothetical protein ASPNIDRAFT_205361x
350636991Hypothetical protein ASPNIDRAFT_56689x
350633205Hypothetical protein ASPNIDRAFT_55058x
350629696Hypothetical protein ASPNIDRAFT_126535x
145243362Hypothetical protein ANI_1_1704094GH1x
563290941Hypothetical protein SBOR_8115x
398407925Hypothetical protein MYCGRDRAFT_30155x
350636557Hypothetical protein ASPNIDRAFT_53540x

Experimental design, materials and methods

Fungal strains

The strains used for enzyme production were T. reesei Rut-C30 and A. niger wild type A12 obtained from Centre for Agricultural Bioscience International (CABI) culture collection (United Kingdom) and Embrapa Food Technology collection (Rio de Janeiro, Brazil), respectively. The conditions in which strains were maintained are described in Florencio et al. [1].

Cultivation conditions

Submerged and sequential fermentations carried out to obtain the enzymatic cocktails from T. reesei and A. niger are described in detail in Florencio et al. [1]. Briefly, the submerged fermentation was initiated with a 48 h pre-culture that contained a final conidia concentration of 107 spores/mL in 100 mL of nutrient medium with 30 g/L of glucose, as described initially from Mandels and Stenberg [2] and adapted by Cunha et al. [3]. In the sequential fermentation, solid state fermentation was initiated using 5 g of dry sugarcane bagasse as solid substrate, and substrate moisture was adjusted through the addition of 12 mL of nutrient medium. The inoculum was added for a final concentration of 107 spores/g of dry bagasse in the pre-culture, which was maintained under static conditions for 24 h. Then, the pre-culture step was continued as a submerged fermentation after the addition of 100 mL of nutrient medium enriched with 30 g/L of glucose per 5 g of dry bagasse. After 48 h for both submerged and sequential fermentation, a volume of pre-culture suspension corresponding to 10% (v/v) was transferred to 100 mL of culture medium for enzyme production, which was supplemented with 10 g/L of glucose and 1% (w/v) of steam-exploded non-washed sugarcane bagasse. All cultivation experiments were carried out in triplicate, and the averaged data presented with standard deviations.

Secretome analysis

Sample preparation

Sequence grade Lys–C/Trypsin (Promega) was used to enzymatically digest the samples. Acetone precipitation was performed prior to sample digestion. The protein samples were reduced with a 10 mM dithiothreitol (DTT)/25 mM ammonium bicarbonate solution at 37 °C for 1 h and alkylated at 37 °C also for 1 h using a solution of 97% acetonitrile (ACN), 2% iodoethanol, and 0.5% triethylphosphine (v/v). Samples were dried before adding Lys–C/trypsin to them in a 25:1 ratio of protease to protein. Digestions were carried out in a barocycler NEP2320 (PBI) at 50 °C and 20 kpsi for 2 h. The samples were cleaned over C18 columns (MicroSpin, Nest Group), dried and resuspended in 97% purified water/3% ACN/0.1% formic acid (FA). A volume of 1 µL was used for LC-MS/MS analysis.

LC-MS/MS analysis

A nanoLC system (1100 Series LC, Agilent Technologies, Santa Clara, CA) was used to separate the peptides for downstream MS analysis using a C18 reversed phase ZORBAX 300SB-C18 analytical column (0.75 μm×150 mm, 3.5 um) from Agilent. The column was directly connected to New Objective׳s emission tip coupled to the nano-electrospray ionization (ESI) source of the high resolution hybrid ion trap mass spectrometer LTQ-Orbitrap XL (Thermo Scientific). Elution was conducted using an ACN/0.1% FA (mobile phase B) linear gradient. The column was equilibrated initially for 5 min with 95% H2O /0.1% FA (mobile phase A) followed by the linear gradient of 5–40% B for 85 min at 0.3uL/min, then from 40–95% B for 12 min. Blank injections were performed in between experimental runs. The resulting eluents were analyzed by a data-dependent positive acquisition mode at full MS scan (30,000 resolution) where the eight most abundant molecular ions were selected and fragmented by collision induced dissociation (CID) using a normalized collision energy of 35% to acquire the data for the LTQ-Orbitrap XL.

Data analysis

Database search analyses were done using Mascot Daemon version 2.4.0 (Matrix Science) against an all fungal protein database from the NCBI database. Peptide and spectral count data were performed on the searches. For protein identification, at least two peptides detected were considered, and the false discovery rate (FDR) was set to 1%.
Subject areaBiochemistry
More specific subject areaProteomic
Type of dataTable
How data was acquiredLC MS/MS analysis using Mascot Daemon version 2.4.0 (Matrix Science)
Data formatAnalyzed
Experimental factorsConcentrated enzymatic cocktail from A. niger A12 and T. reesei Rut C30 produced by submerged fermentation and sequential fermentation
Experimental featuresPeptides from enzyme cocktail of A. niger A12 and T. reesei Rut C30 were analyzed by LC-MS/MS
Data source locationPurdue University, West Lafayette, USA.
Data accessibilityData is with this article
  1 in total

1.  Secretome analysis of Trichoderma reesei and Aspergillus niger cultivated by submerged and sequential fermentation processes: Enzyme production for sugarcane bagasse hydrolysis.

Authors:  Camila Florencio; Fernanda M Cunha; Alberto C Badino; Cristiane S Farinas; Eduardo Ximenes; Michael R Ladisch
Journal:  Enzyme Microb Technol       Date:  2016-04-28       Impact factor: 3.493

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Journal:  Mycopathologia       Date:  2017-05-08       Impact factor: 2.574

2.  Comparative systems analysis of the secretome of the opportunistic pathogen Aspergillus fumigatus and other Aspergillus species.

Authors:  R P Vivek-Ananth; Karthikeyan Mohanraj; Muralidharan Vandanashree; Anupam Jhingran; James P Craig; Areejit Samal
Journal:  Sci Rep       Date:  2018-04-26       Impact factor: 4.379

3.  Data on microbial and physicochemical assessment of mixed fruit wine produced from physically damaged fruits.

Authors:  Deborah O Oba; Oluwaseun J Okunola; Solomon U Oranusi; Hilary I Okagbue
Journal:  Data Brief       Date:  2018-05-23

Review 4.  Harnessing microbial wealth for lignocellulose biomass valorization through secretomics: a review.

Authors:  Sivasamy Sethupathy; Gabriel Murillo Morales; Yixuan Li; Yongli Wang; Jianxiong Jiang; Jianzhong Sun; Daochen Zhu
Journal:  Biotechnol Biofuels       Date:  2021-07-05       Impact factor: 6.040

  4 in total

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