Accelerated bioethanol fermentation by using a novel yeast immobilization technique: Microtube array membrane

•A novel cell immobilization technique for bioethanol production was introduced.•Microtube array membrane was stable in 15% ethanol during shaking cultivation.•MTAM-encapsulated yeasts showed better bioethanol productivity. Cell immobilization is a way to isolate or localize intact cells in a certai...

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Published inProcess biochemistry (1991) Vol. 50; no. 10; pp. 1509 - 1515
Main Authors Chen, Chien-Chung, Wu, Chien-Hui, Wu, Jhih-Jhong, Chiu, Chien-Chih, Wong, Chien-Hsuan, Tsai, Min-Lang, Lin, Hong-Ting Victor
Format Journal Article
LanguageEnglish
Published Elsevier Ltd 01.10.2015
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Abstract •A novel cell immobilization technique for bioethanol production was introduced.•Microtube array membrane was stable in 15% ethanol during shaking cultivation.•MTAM-encapsulated yeasts showed better bioethanol productivity. Cell immobilization is a way to isolate or localize intact cells in a certain space and maintain their catalytic activity. Immobilized cells can effectively reduce the negative effects of inhibitors and the processing cost of inoculum preparation for continuous or fed-batch fermentation of microorganisms. In this study, a novel yeast immobilization technique using renewable poly-l-lactic acid (PLLA) microtube array membrane (MTAM) was thoroughly evaluated for bioethanol fermentation. PLLA-MTAM was shown to be stable in 15% (v/v) ethanol solution during shaking cultivation. A yeast encapsulation efficiency of 67–70% was obtained, and the yeasts in MTAMs with greater porosity showed greater bioethanol productivity. The MTAM-immobilized Kluyveromyces marxianus, prepared using in situ and siphon methods, were evaluated using 5% (w/v) glucose fermentation. Improved glucose consumption and bioethanol production were observed in batch bioethanol fermentation. In 7 cycles during repeated-batch fermentation, the immobilized yeasts prepared using the in situ method showed a maximum CEtOH of 24.23g/L, maximum YP/S of 0.48g/g, and r PEtOH of 2.69g/L h. Our data indicated that the PLLA-MTAM immobilized yeasts significantly enhanced bioethanol productivity and was a novel, promising technology for bioethanol fermentation.
AbstractList Cell immobilization is a way to isolate or localize intact cells in a certain space and maintain their catalytic activity. Immobilized cells can effectively reduce the negative effects of inhibitors and the processing cost of inoculum preparation for continuous or fed-batch fermentation of microorganisms. In this study, a novel yeast immobilization technique using renewable poly-l-lactic acid (PLLA) microtube array membrane (MTAM) was thoroughly evaluated for bioethanol fermentation. PLLA-MTAM was shown to be stable in 15% (v/v) ethanol solution during shaking cultivation. A yeast encapsulation efficiency of 67–70% was obtained, and the yeasts in MTAMs with greater porosity showed greater bioethanol productivity. The MTAM-immobilized Kluyveromyces marxianus, prepared using in situ and siphon methods, were evaluated using 5% (w/v) glucose fermentation. Improved glucose consumption and bioethanol production were observed in batch bioethanol fermentation. In 7 cycles during repeated-batch fermentation, the immobilized yeasts prepared using the in situ method showed a maximum CEtOH of 24.23g/L, maximum YP/S of 0.48g/g, and r PEtOH of 2.69g/L h. Our data indicated that the PLLA-MTAM immobilized yeasts significantly enhanced bioethanol productivity and was a novel, promising technology for bioethanol fermentation.
Cell immobilization is a way to isolate or localize intact cells in a certain space and maintain their catalytic activity. Immobilized cells can effectively reduce the negative effects of inhibitors and the processing cost of inoculum preparation for continuous or fed-batch fermentation of microorganisms. In this study, a novel yeast immobilization technique using renewable poly-L-lactic acid (PLLA) microtube array membrane (MTAM) was thoroughly evaluated for bioethanol fermentation. PLLA-MTAM was shown to be stable in 15% (v/v) ethanol solution during shaking cultivation. A yeast encapsulation efficiency of 67-70% was obtained, and the yeasts in MTAMs with greater porosity showed greater bioethanol productivity. The MTAM-immobilized Kluyveromyces marxianus, prepared using in situ and siphon methods, were evaluated using 5% (w/v) glucose fermentation. Improved glucose consumption and bioethanol production were observed in batch bioethanol fermentation. In 7 cycles during repeated-batch fermentation, the immobilized yeasts prepared using the in situ method showed a maximum C sub(EtOH) of 24.23 g/L, maximum Y sub(P/S) of 0.48 g/g, and r P sub(EtOH) of 2.69 g/L h. Our data indicated that the PLLA-MTAM immobilized yeasts significantly enhanced bioethanol productivity and was a novel, promising technology for bioethanol fermentation.
•A novel cell immobilization technique for bioethanol production was introduced.•Microtube array membrane was stable in 15% ethanol during shaking cultivation.•MTAM-encapsulated yeasts showed better bioethanol productivity. Cell immobilization is a way to isolate or localize intact cells in a certain space and maintain their catalytic activity. Immobilized cells can effectively reduce the negative effects of inhibitors and the processing cost of inoculum preparation for continuous or fed-batch fermentation of microorganisms. In this study, a novel yeast immobilization technique using renewable poly-l-lactic acid (PLLA) microtube array membrane (MTAM) was thoroughly evaluated for bioethanol fermentation. PLLA-MTAM was shown to be stable in 15% (v/v) ethanol solution during shaking cultivation. A yeast encapsulation efficiency of 67–70% was obtained, and the yeasts in MTAMs with greater porosity showed greater bioethanol productivity. The MTAM-immobilized Kluyveromyces marxianus, prepared using in situ and siphon methods, were evaluated using 5% (w/v) glucose fermentation. Improved glucose consumption and bioethanol production were observed in batch bioethanol fermentation. In 7 cycles during repeated-batch fermentation, the immobilized yeasts prepared using the in situ method showed a maximum CEtOH of 24.23g/L, maximum YP/S of 0.48g/g, and r PEtOH of 2.69g/L h. Our data indicated that the PLLA-MTAM immobilized yeasts significantly enhanced bioethanol productivity and was a novel, promising technology for bioethanol fermentation.
Author Wu, Jhih-Jhong
Wong, Chien-Hsuan
Chen, Chien-Chung
Chiu, Chien-Chih
Wu, Chien-Hui
Tsai, Min-Lang
Lin, Hong-Ting Victor
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  surname: Chen
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  organization: Department of Seafood Science, National Kaohsiung Marine University, No. 142 Hai-Chuan Road, Nan-Tzu, Kaohsiung 81143, Taiwan, ROC
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  givenname: Min-Lang
  surname: Tsai
  fullname: Tsai, Min-Lang
  organization: Department of Food Science, National Taiwan Ocean University, No. 2, Pei-Ning Road, Keelung 202, Taiwan, ROC
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  givenname: Hong-Ting Victor
  surname: Lin
  fullname: Lin, Hong-Ting Victor
  email: hl358@ntou.edu.tw
  organization: Department of Food Science, National Taiwan Ocean University, No. 2, Pei-Ning Road, Keelung 202, Taiwan, ROC
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Keywords Repeated-batch
Kluyveromyces marxianus
Bioethanol
Microtube array membrane (MTAM)
Fermentation
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Snippet •A novel cell immobilization technique for bioethanol production was introduced.•Microtube array membrane was stable in 15% ethanol during shaking...
Cell immobilization is a way to isolate or localize intact cells in a certain space and maintain their catalytic activity. Immobilized cells can effectively...
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SubjectTerms adverse effects
Arrays
batch fermentation
Bioethanol
catalytic activity
encapsulation
ethanol fermentation
ethanol production
Fermentation
Glucose
Immobilization
immobilized cells
inoculum
Kluyveromyces marxianus
Membranes
Microtube array membrane (MTAM)
Polylactic acid
porosity
Productivity
Repeated-batch
Yeast
yeasts
Title Accelerated bioethanol fermentation by using a novel yeast immobilization technique: Microtube array membrane
URI https://dx.doi.org/10.1016/j.procbio.2015.06.006
https://www.proquest.com/docview/1762356690
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Volume 50
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