Combination of ARTP mutagenesis and color-mediated high-throughput screening to enhance 1-naphthol yield from microbial oxidation of naphthalene in aqueous system

Abstract Strain QCG of the aerobic bacteria Bacillus cereus is capable of producing 1-naphthol from naphthalene, this strain was first isolated and characterized in this study. Strain QCG was mutagenized to enhance 1-naphthol production, using atmospheric and room temperature plasma (ARTP) technolog...
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Autor*in:	Qiu, Chenggang [verfasserIn] Zhang, Alei [verfasserIn] Tao, Sha [verfasserIn] Li, Kang [verfasserIn] Chen, Kequan [verfasserIn] Ouyang, Pingkai [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2020

Schlagwörter:	QCG naphthalene 1-naphthol ARTP mutagenesis high-throughput screening 4-aminoantipyrine

Übergeordnetes Werk:	Enthalten in: Frontiers of chemical engineering in China - Beijing : Higher Education Press, 2007, 14(2020), 5 vom: 03. Jan., Seite 793-801
Übergeordnetes Werk:	volume:14 ; year:2020 ; number:5 ; day:03 ; month:01 ; pages:793-801

Links:	Volltext

DOI / URN:	10.1007/s11705-019-1876-2

Katalog-ID:	SPR039882136

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520			\|a Abstract Strain QCG of the aerobic bacteria Bacillus cereus is capable of producing 1-naphthol from naphthalene, this strain was first isolated and characterized in this study. Strain QCG was mutagenized to enhance 1-naphthol production, using atmospheric and room temperature plasma (ARTP) technology. Then, a microbial clone screening system was used to accelerate the operation. Meanwhile, a novel color-mediated high-throughput screening using 4-aminoantipyrine was performed to screen mutants. The optimal mutant strain QCG4 produced 19.58±0.34 mg∙$ L^{−1} $ 1-naphthol from naphthalene that was 47.32% higher than that of the original strain (13.29±0.28 mg∙$ L^{−1} $). In addition, the optimal conditions for 1-naphthol production via whole-cell catalysis of strain QCG4 were determined to be an $ OD_{600} $ of 40,150 mg∙$ L^{−1} $ naphthalene, and 7.5% dimethyl formamide as a co-solvent at pH 7.5 and 26°C for 3 h, resulting in 41.18±0.12 mg-$ L^{−1} $ 1-naphthol, i.e., the mutant strain produces a 2.1-fold higher yield compared to the original strain.
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allfields	10.1007/s11705-019-1876-2 doi (DE-627)SPR039882136 (SPR)s11705-019-1876-2-e DE-627 ger DE-627 rakwb eng 540 ASE Qiu, Chenggang verfasserin aut Combination of ARTP mutagenesis and color-mediated high-throughput screening to enhance 1-naphthol yield from microbial oxidation of naphthalene in aqueous system 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Strain QCG of the aerobic bacteria Bacillus cereus is capable of producing 1-naphthol from naphthalene, this strain was first isolated and characterized in this study. Strain QCG was mutagenized to enhance 1-naphthol production, using atmospheric and room temperature plasma (ARTP) technology. Then, a microbial clone screening system was used to accelerate the operation. Meanwhile, a novel color-mediated high-throughput screening using 4-aminoantipyrine was performed to screen mutants. The optimal mutant strain QCG4 produced 19.58±0.34 mg∙$ L^{−1} $ 1-naphthol from naphthalene that was 47.32% higher than that of the original strain (13.29±0.28 mg∙$ L^{−1} $). In addition, the optimal conditions for 1-naphthol production via whole-cell catalysis of strain QCG4 were determined to be an $ OD_{600} $ of 40,150 mg∙$ L^{−1} $ naphthalene, and 7.5% dimethyl formamide as a co-solvent at pH 7.5 and 26°C for 3 h, resulting in 41.18±0.12 mg-$ L^{−1} $ 1-naphthol, i.e., the mutant strain produces a 2.1-fold higher yield compared to the original strain. QCG (dpeaa)DE-He213 naphthalene (dpeaa)DE-He213 1-naphthol (dpeaa)DE-He213 ARTP mutagenesis (dpeaa)DE-He213 high-throughput screening (dpeaa)DE-He213 4-aminoantipyrine (dpeaa)DE-He213 Zhang, Alei verfasserin aut Tao, Sha verfasserin aut Li, Kang verfasserin aut Chen, Kequan verfasserin aut Ouyang, Pingkai verfasserin aut Enthalten in Frontiers of chemical engineering in China Beijing : Higher Education Press, 2007 14(2020), 5 vom: 03. Jan., Seite 793-801 (DE-627)545787602 (DE-600)2388862-3 1673-7474 nnns volume:14 year:2020 number:5 day:03 month:01 pages:793-801 https://dx.doi.org/10.1007/s11705-019-1876-2 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_152 GBV_ILN_161 GBV_ILN_171 GBV_ILN_187 GBV_ILN_224 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 AR 14 2020 5 03 01 793-801
spelling	10.1007/s11705-019-1876-2 doi (DE-627)SPR039882136 (SPR)s11705-019-1876-2-e DE-627 ger DE-627 rakwb eng 540 ASE Qiu, Chenggang verfasserin aut Combination of ARTP mutagenesis and color-mediated high-throughput screening to enhance 1-naphthol yield from microbial oxidation of naphthalene in aqueous system 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Strain QCG of the aerobic bacteria Bacillus cereus is capable of producing 1-naphthol from naphthalene, this strain was first isolated and characterized in this study. Strain QCG was mutagenized to enhance 1-naphthol production, using atmospheric and room temperature plasma (ARTP) technology. Then, a microbial clone screening system was used to accelerate the operation. Meanwhile, a novel color-mediated high-throughput screening using 4-aminoantipyrine was performed to screen mutants. The optimal mutant strain QCG4 produced 19.58±0.34 mg∙$ L^{−1} $ 1-naphthol from naphthalene that was 47.32% higher than that of the original strain (13.29±0.28 mg∙$ L^{−1} $). In addition, the optimal conditions for 1-naphthol production via whole-cell catalysis of strain QCG4 were determined to be an $ OD_{600} $ of 40,150 mg∙$ L^{−1} $ naphthalene, and 7.5% dimethyl formamide as a co-solvent at pH 7.5 and 26°C for 3 h, resulting in 41.18±0.12 mg-$ L^{−1} $ 1-naphthol, i.e., the mutant strain produces a 2.1-fold higher yield compared to the original strain. QCG (dpeaa)DE-He213 naphthalene (dpeaa)DE-He213 1-naphthol (dpeaa)DE-He213 ARTP mutagenesis (dpeaa)DE-He213 high-throughput screening (dpeaa)DE-He213 4-aminoantipyrine (dpeaa)DE-He213 Zhang, Alei verfasserin aut Tao, Sha verfasserin aut Li, Kang verfasserin aut Chen, Kequan verfasserin aut Ouyang, Pingkai verfasserin aut Enthalten in Frontiers of chemical engineering in China Beijing : Higher Education Press, 2007 14(2020), 5 vom: 03. Jan., Seite 793-801 (DE-627)545787602 (DE-600)2388862-3 1673-7474 nnns volume:14 year:2020 number:5 day:03 month:01 pages:793-801 https://dx.doi.org/10.1007/s11705-019-1876-2 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_152 GBV_ILN_161 GBV_ILN_171 GBV_ILN_187 GBV_ILN_224 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 AR 14 2020 5 03 01 793-801
allfields_unstemmed	10.1007/s11705-019-1876-2 doi (DE-627)SPR039882136 (SPR)s11705-019-1876-2-e DE-627 ger DE-627 rakwb eng 540 ASE Qiu, Chenggang verfasserin aut Combination of ARTP mutagenesis and color-mediated high-throughput screening to enhance 1-naphthol yield from microbial oxidation of naphthalene in aqueous system 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Strain QCG of the aerobic bacteria Bacillus cereus is capable of producing 1-naphthol from naphthalene, this strain was first isolated and characterized in this study. Strain QCG was mutagenized to enhance 1-naphthol production, using atmospheric and room temperature plasma (ARTP) technology. Then, a microbial clone screening system was used to accelerate the operation. Meanwhile, a novel color-mediated high-throughput screening using 4-aminoantipyrine was performed to screen mutants. The optimal mutant strain QCG4 produced 19.58±0.34 mg∙$ L^{−1} $ 1-naphthol from naphthalene that was 47.32% higher than that of the original strain (13.29±0.28 mg∙$ L^{−1} $). In addition, the optimal conditions for 1-naphthol production via whole-cell catalysis of strain QCG4 were determined to be an $ OD_{600} $ of 40,150 mg∙$ L^{−1} $ naphthalene, and 7.5% dimethyl formamide as a co-solvent at pH 7.5 and 26°C for 3 h, resulting in 41.18±0.12 mg-$ L^{−1} $ 1-naphthol, i.e., the mutant strain produces a 2.1-fold higher yield compared to the original strain. QCG (dpeaa)DE-He213 naphthalene (dpeaa)DE-He213 1-naphthol (dpeaa)DE-He213 ARTP mutagenesis (dpeaa)DE-He213 high-throughput screening (dpeaa)DE-He213 4-aminoantipyrine (dpeaa)DE-He213 Zhang, Alei verfasserin aut Tao, Sha verfasserin aut Li, Kang verfasserin aut Chen, Kequan verfasserin aut Ouyang, Pingkai verfasserin aut Enthalten in Frontiers of chemical engineering in China Beijing : Higher Education Press, 2007 14(2020), 5 vom: 03. Jan., Seite 793-801 (DE-627)545787602 (DE-600)2388862-3 1673-7474 nnns volume:14 year:2020 number:5 day:03 month:01 pages:793-801 https://dx.doi.org/10.1007/s11705-019-1876-2 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_152 GBV_ILN_161 GBV_ILN_171 GBV_ILN_187 GBV_ILN_224 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 AR 14 2020 5 03 01 793-801
allfieldsGer	10.1007/s11705-019-1876-2 doi (DE-627)SPR039882136 (SPR)s11705-019-1876-2-e DE-627 ger DE-627 rakwb eng 540 ASE Qiu, Chenggang verfasserin aut Combination of ARTP mutagenesis and color-mediated high-throughput screening to enhance 1-naphthol yield from microbial oxidation of naphthalene in aqueous system 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Strain QCG of the aerobic bacteria Bacillus cereus is capable of producing 1-naphthol from naphthalene, this strain was first isolated and characterized in this study. Strain QCG was mutagenized to enhance 1-naphthol production, using atmospheric and room temperature plasma (ARTP) technology. Then, a microbial clone screening system was used to accelerate the operation. Meanwhile, a novel color-mediated high-throughput screening using 4-aminoantipyrine was performed to screen mutants. The optimal mutant strain QCG4 produced 19.58±0.34 mg∙$ L^{−1} $ 1-naphthol from naphthalene that was 47.32% higher than that of the original strain (13.29±0.28 mg∙$ L^{−1} $). In addition, the optimal conditions for 1-naphthol production via whole-cell catalysis of strain QCG4 were determined to be an $ OD_{600} $ of 40,150 mg∙$ L^{−1} $ naphthalene, and 7.5% dimethyl formamide as a co-solvent at pH 7.5 and 26°C for 3 h, resulting in 41.18±0.12 mg-$ L^{−1} $ 1-naphthol, i.e., the mutant strain produces a 2.1-fold higher yield compared to the original strain. QCG (dpeaa)DE-He213 naphthalene (dpeaa)DE-He213 1-naphthol (dpeaa)DE-He213 ARTP mutagenesis (dpeaa)DE-He213 high-throughput screening (dpeaa)DE-He213 4-aminoantipyrine (dpeaa)DE-He213 Zhang, Alei verfasserin aut Tao, Sha verfasserin aut Li, Kang verfasserin aut Chen, Kequan verfasserin aut Ouyang, Pingkai verfasserin aut Enthalten in Frontiers of chemical engineering in China Beijing : Higher Education Press, 2007 14(2020), 5 vom: 03. Jan., Seite 793-801 (DE-627)545787602 (DE-600)2388862-3 1673-7474 nnns volume:14 year:2020 number:5 day:03 month:01 pages:793-801 https://dx.doi.org/10.1007/s11705-019-1876-2 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_152 GBV_ILN_161 GBV_ILN_171 GBV_ILN_187 GBV_ILN_224 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 AR 14 2020 5 03 01 793-801
allfieldsSound	10.1007/s11705-019-1876-2 doi (DE-627)SPR039882136 (SPR)s11705-019-1876-2-e DE-627 ger DE-627 rakwb eng 540 ASE Qiu, Chenggang verfasserin aut Combination of ARTP mutagenesis and color-mediated high-throughput screening to enhance 1-naphthol yield from microbial oxidation of naphthalene in aqueous system 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Strain QCG of the aerobic bacteria Bacillus cereus is capable of producing 1-naphthol from naphthalene, this strain was first isolated and characterized in this study. Strain QCG was mutagenized to enhance 1-naphthol production, using atmospheric and room temperature plasma (ARTP) technology. Then, a microbial clone screening system was used to accelerate the operation. Meanwhile, a novel color-mediated high-throughput screening using 4-aminoantipyrine was performed to screen mutants. The optimal mutant strain QCG4 produced 19.58±0.34 mg∙$ L^{−1} $ 1-naphthol from naphthalene that was 47.32% higher than that of the original strain (13.29±0.28 mg∙$ L^{−1} $). In addition, the optimal conditions for 1-naphthol production via whole-cell catalysis of strain QCG4 were determined to be an $ OD_{600} $ of 40,150 mg∙$ L^{−1} $ naphthalene, and 7.5% dimethyl formamide as a co-solvent at pH 7.5 and 26°C for 3 h, resulting in 41.18±0.12 mg-$ L^{−1} $ 1-naphthol, i.e., the mutant strain produces a 2.1-fold higher yield compared to the original strain. QCG (dpeaa)DE-He213 naphthalene (dpeaa)DE-He213 1-naphthol (dpeaa)DE-He213 ARTP mutagenesis (dpeaa)DE-He213 high-throughput screening (dpeaa)DE-He213 4-aminoantipyrine (dpeaa)DE-He213 Zhang, Alei verfasserin aut Tao, Sha verfasserin aut Li, Kang verfasserin aut Chen, Kequan verfasserin aut Ouyang, Pingkai verfasserin aut Enthalten in Frontiers of chemical engineering in China Beijing : Higher Education Press, 2007 14(2020), 5 vom: 03. Jan., Seite 793-801 (DE-627)545787602 (DE-600)2388862-3 1673-7474 nnns volume:14 year:2020 number:5 day:03 month:01 pages:793-801 https://dx.doi.org/10.1007/s11705-019-1876-2 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_152 GBV_ILN_161 GBV_ILN_171 GBV_ILN_187 GBV_ILN_224 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 AR 14 2020 5 03 01 793-801
language	English
source	Enthalten in Frontiers of chemical engineering in China 14(2020), 5 vom: 03. Jan., Seite 793-801 volume:14 year:2020 number:5 day:03 month:01 pages:793-801
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topic_facet	QCG naphthalene 1-naphthol ARTP mutagenesis high-throughput screening 4-aminoantipyrine
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container_title	Frontiers of chemical engineering in China
authorswithroles_txt_mv	Qiu, Chenggang @@aut@@ Zhang, Alei @@aut@@ Tao, Sha @@aut@@ Li, Kang @@aut@@ Chen, Kequan @@aut@@ Ouyang, Pingkai @@aut@@
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Strain QCG was mutagenized to enhance 1-naphthol production, using atmospheric and room temperature plasma (ARTP) technology. Then, a microbial clone screening system was used to accelerate the operation. Meanwhile, a novel color-mediated high-throughput screening using 4-aminoantipyrine was performed to screen mutants. The optimal mutant strain QCG4 produced 19.58±0.34 mg∙$ L^{−1} $ 1-naphthol from naphthalene that was 47.32% higher than that of the original strain (13.29±0.28 mg∙$ L^{−1} $). 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author	Qiu, Chenggang
spellingShingle	Qiu, Chenggang ddc 540 misc QCG misc naphthalene misc 1-naphthol misc ARTP mutagenesis misc high-throughput screening misc 4-aminoantipyrine Combination of ARTP mutagenesis and color-mediated high-throughput screening to enhance 1-naphthol yield from microbial oxidation of naphthalene in aqueous system
authorStr	Qiu, Chenggang
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topic_title	540 ASE Combination of ARTP mutagenesis and color-mediated high-throughput screening to enhance 1-naphthol yield from microbial oxidation of naphthalene in aqueous system QCG (dpeaa)DE-He213 naphthalene (dpeaa)DE-He213 1-naphthol (dpeaa)DE-He213 ARTP mutagenesis (dpeaa)DE-He213 high-throughput screening (dpeaa)DE-He213 4-aminoantipyrine (dpeaa)DE-He213
topic	ddc 540 misc QCG misc naphthalene misc 1-naphthol misc ARTP mutagenesis misc high-throughput screening misc 4-aminoantipyrine
topic_unstemmed	ddc 540 misc QCG misc naphthalene misc 1-naphthol misc ARTP mutagenesis misc high-throughput screening misc 4-aminoantipyrine
topic_browse	ddc 540 misc QCG misc naphthalene misc 1-naphthol misc ARTP mutagenesis misc high-throughput screening misc 4-aminoantipyrine
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title	Combination of ARTP mutagenesis and color-mediated high-throughput screening to enhance 1-naphthol yield from microbial oxidation of naphthalene in aqueous system
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title_full	Combination of ARTP mutagenesis and color-mediated high-throughput screening to enhance 1-naphthol yield from microbial oxidation of naphthalene in aqueous system
author_sort	Qiu, Chenggang
journal	Frontiers of chemical engineering in China
journalStr	Frontiers of chemical engineering in China
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author_browse	Qiu, Chenggang Zhang, Alei Tao, Sha Li, Kang Chen, Kequan Ouyang, Pingkai
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title_sort	combination of artp mutagenesis and color-mediated high-throughput screening to enhance 1-naphthol yield from microbial oxidation of naphthalene in aqueous system
title_auth	Combination of ARTP mutagenesis and color-mediated high-throughput screening to enhance 1-naphthol yield from microbial oxidation of naphthalene in aqueous system
abstract	Abstract Strain QCG of the aerobic bacteria Bacillus cereus is capable of producing 1-naphthol from naphthalene, this strain was first isolated and characterized in this study. Strain QCG was mutagenized to enhance 1-naphthol production, using atmospheric and room temperature plasma (ARTP) technology. Then, a microbial clone screening system was used to accelerate the operation. Meanwhile, a novel color-mediated high-throughput screening using 4-aminoantipyrine was performed to screen mutants. The optimal mutant strain QCG4 produced 19.58±0.34 mg∙$ L^{−1} $ 1-naphthol from naphthalene that was 47.32% higher than that of the original strain (13.29±0.28 mg∙$ L^{−1} $). In addition, the optimal conditions for 1-naphthol production via whole-cell catalysis of strain QCG4 were determined to be an $ OD_{600} $ of 40,150 mg∙$ L^{−1} $ naphthalene, and 7.5% dimethyl formamide as a co-solvent at pH 7.5 and 26°C for 3 h, resulting in 41.18±0.12 mg-$ L^{−1} $ 1-naphthol, i.e., the mutant strain produces a 2.1-fold higher yield compared to the original strain.
abstractGer	Abstract Strain QCG of the aerobic bacteria Bacillus cereus is capable of producing 1-naphthol from naphthalene, this strain was first isolated and characterized in this study. Strain QCG was mutagenized to enhance 1-naphthol production, using atmospheric and room temperature plasma (ARTP) technology. Then, a microbial clone screening system was used to accelerate the operation. Meanwhile, a novel color-mediated high-throughput screening using 4-aminoantipyrine was performed to screen mutants. The optimal mutant strain QCG4 produced 19.58±0.34 mg∙$ L^{−1} $ 1-naphthol from naphthalene that was 47.32% higher than that of the original strain (13.29±0.28 mg∙$ L^{−1} $). In addition, the optimal conditions for 1-naphthol production via whole-cell catalysis of strain QCG4 were determined to be an $ OD_{600} $ of 40,150 mg∙$ L^{−1} $ naphthalene, and 7.5% dimethyl formamide as a co-solvent at pH 7.5 and 26°C for 3 h, resulting in 41.18±0.12 mg-$ L^{−1} $ 1-naphthol, i.e., the mutant strain produces a 2.1-fold higher yield compared to the original strain.
abstract_unstemmed	Abstract Strain QCG of the aerobic bacteria Bacillus cereus is capable of producing 1-naphthol from naphthalene, this strain was first isolated and characterized in this study. Strain QCG was mutagenized to enhance 1-naphthol production, using atmospheric and room temperature plasma (ARTP) technology. Then, a microbial clone screening system was used to accelerate the operation. Meanwhile, a novel color-mediated high-throughput screening using 4-aminoantipyrine was performed to screen mutants. The optimal mutant strain QCG4 produced 19.58±0.34 mg∙$ L^{−1} $ 1-naphthol from naphthalene that was 47.32% higher than that of the original strain (13.29±0.28 mg∙$ L^{−1} $). In addition, the optimal conditions for 1-naphthol production via whole-cell catalysis of strain QCG4 were determined to be an $ OD_{600} $ of 40,150 mg∙$ L^{−1} $ naphthalene, and 7.5% dimethyl formamide as a co-solvent at pH 7.5 and 26°C for 3 h, resulting in 41.18±0.12 mg-$ L^{−1} $ 1-naphthol, i.e., the mutant strain produces a 2.1-fold higher yield compared to the original strain.
collection_details	GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_152 GBV_ILN_161 GBV_ILN_171 GBV_ILN_187 GBV_ILN_224 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702
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title_short	Combination of ARTP mutagenesis and color-mediated high-throughput screening to enhance 1-naphthol yield from microbial oxidation of naphthalene in aqueous system
url	https://dx.doi.org/10.1007/s11705-019-1876-2
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author2	Zhang, Alei Tao, Sha Li, Kang Chen, Kequan Ouyang, Pingkai
author2Str	Zhang, Alei Tao, Sha Li, Kang Chen, Kequan Ouyang, Pingkai
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doi_str	10.1007/s11705-019-1876-2
up_date	2024-07-04T01:59:11.066Z
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Strain QCG was mutagenized to enhance 1-naphthol production, using atmospheric and room temperature plasma (ARTP) technology. Then, a microbial clone screening system was used to accelerate the operation. Meanwhile, a novel color-mediated high-throughput screening using 4-aminoantipyrine was performed to screen mutants. The optimal mutant strain QCG4 produced 19.58±0.34 mg∙$ L^{−1} $ 1-naphthol from naphthalene that was 47.32% higher than that of the original strain (13.29±0.28 mg∙$ L^{−1} $). In addition, the optimal conditions for 1-naphthol production via whole-cell catalysis of strain QCG4 were determined to be an $ OD_{600} $ of 40,150 mg∙$ L^{−1} $ naphthalene, and 7.5% dimethyl formamide as a co-solvent at pH 7.5 and 26°C for 3 h, resulting in 41.18±0.12 mg-$ L^{−1} $ 1-naphthol, i.e., the mutant strain produces a 2.1-fold higher yield compared to the original strain.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">QCG</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">naphthalene</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">1-naphthol</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">ARTP mutagenesis</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">high-throughput screening</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">4-aminoantipyrine</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Zhang, Alei</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Tao, Sha</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Li, Kang</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Chen, Kequan</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Ouyang, Pingkai</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">Frontiers of chemical engineering in China</subfield><subfield code="d">Beijing : Higher Education Press, 2007</subfield><subfield code="g">14(2020), 5 vom: 03. Jan., Seite 793-801</subfield><subfield code="w">(DE-627)545787602</subfield><subfield code="w">(DE-600)2388862-3</subfield><subfield code="x">1673-7474</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:14</subfield><subfield code="g">year:2020</subfield><subfield code="g">number:5</subfield><subfield code="g">day:03</subfield><subfield code="g">month:01</subfield><subfield code="g">pages:793-801</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://dx.doi.org/10.1007/s11705-019-1876-2</subfield><subfield code="z">lizenzpflichtig</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_SPRINGER</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-PHA</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_20</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_22</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_23</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_24</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_31</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_32</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_39</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_40</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_60</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_62</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_65</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_69</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_70</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_73</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_74</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_90</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_95</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_100</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_101</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_105</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_110</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_120</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_138</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_152</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_161</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_171</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_187</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_224</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_250</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_281</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_285</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_293</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_370</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_602</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_702</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">14</subfield><subfield code="j">2020</subfield><subfield code="e">5</subfield><subfield code="b">03</subfield><subfield code="c">01</subfield><subfield code="h">793-801</subfield></datafield></record></collection>
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Combination of ARTP mutagenesis and color-mediated high-throughput screening to enhance 1-naphthol yield from microbial oxidation of naphthalene in aqueous system

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