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Biotechnology and Bioengineering: Volume 114, Number 6, June 2017.

Biotechnology and bioengineering

[No authors listed]
PMID: 28425633
Biotechnol Bioeng. 2017 Jun;114(6):1123-1127. doi: 10.1002/bit.26136.

No abstract available.

Cite
Biotechnology and Bioengineering: Volume 114, Number 6, June 2017. Biotechnol Bioeng. 2017;114(6):1123-1127doi: 10.1002/bit.26136.
(2017). Biotechnology and Bioengineering: Volume 114, Number 6, June 2017. Biotechnology and bioengineering, 114(6), 1123-1127. https://doi.org/10.1002/bit.26136
"Biotechnology and Bioengineering: Volume 114, Number 6, June 2017." Biotechnology and bioengineering vol. 114,6 (2017): 1123-1127. doi: https://doi.org/10.1002/bit.26136
Biotechnology and Bioengineering: Volume 114, Number 6, June 2017. Biotechnol Bioeng. 2017 Jun;114(6):1123-1127. doi: 10.1002/bit.26136. PMID: 28425633.
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Adapting viral safety assurance strategies to continuous processing of biological products.

Biotechnology and bioengineering

Johnson SA, Brown MR, Lute SC, Brorson KA.
PMID: 28425635
Biotechnol Bioeng. 2017 Jun;114(6):1362. doi: 10.1002/bit.26245.

No abstract available.

Cite
Johnson SA, Brown MR, Lute SC, et al. Adapting viral safety assurance strategies to continuous processing of biological products. Biotechnol Bioeng. 2017;114(6):1362doi: 10.1002/bit.26245.
Johnson, S. A., Brown, M. R., Lute, S. C., & Brorson, K. A. (2017). Adapting viral safety assurance strategies to continuous processing of biological products. Biotechnology and bioengineering, 114(6), 1362. https://doi.org/10.1002/bit.26245
Johnson, Sarah A, et al. "Adapting viral safety assurance strategies to continuous processing of biological products." Biotechnology and bioengineering vol. 114,6 (2017): 1362. doi: https://doi.org/10.1002/bit.26245
Johnson SA, Brown MR, Lute SC, Brorson KA. Adapting viral safety assurance strategies to continuous processing of biological products. Biotechnol Bioeng. 2017 Jun;114(6):1362. doi: 10.1002/bit.26245. PMID: 28425635.
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Biotechnology and Bioengineering: Volume 113, Number 11, November 2016.

Biotechnology and bioengineering

[No authors listed]
PMID: 27668413
Biotechnol Bioeng. 2016 Nov;113(11):2307-11. doi: 10.1002/bit.25801.

No abstract available.

Cite
Biotechnology and Bioengineering: Volume 113, Number 11, November 2016. Biotechnol Bioeng. 2016;113(11):2307-11doi: 10.1002/bit.25801.
(2016). Biotechnology and Bioengineering: Volume 113, Number 11, November 2016. Biotechnology and bioengineering, 113(11), 2307-11. https://doi.org/10.1002/bit.25801
"Biotechnology and Bioengineering: Volume 113, Number 11, November 2016." Biotechnology and bioengineering vol. 113,11 (2016): 2307-11. doi: https://doi.org/10.1002/bit.25801
Biotechnology and Bioengineering: Volume 113, Number 11, November 2016. Biotechnol Bioeng. 2016 Nov;113(11):2307-11. doi: 10.1002/bit.25801. PMID: 27668413.
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Low pH bioproduction of succinic acid in yeast.

Biotechnology and bioengineering

[No authors listed]
PMID: 27668414
Biotechnol Bioeng. 2016 Nov;113(11):2312. doi: 10.1002/bit.25797.

No abstract available.

Cite
Low pH bioproduction of succinic acid in yeast. Biotechnol Bioeng. 2016;113(11):2312doi: 10.1002/bit.25797.
(2016). Low pH bioproduction of succinic acid in yeast. Biotechnology and bioengineering, 113(11), 2312. https://doi.org/10.1002/bit.25797
"Low pH bioproduction of succinic acid in yeast." Biotechnology and bioengineering vol. 113,11 (2016): 2312. doi: https://doi.org/10.1002/bit.25797
Low pH bioproduction of succinic acid in yeast. Biotechnol Bioeng. 2016 Nov;113(11):2312. doi: 10.1002/bit.25797. PMID: 27668414.
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Self-immobilizing enzymes for biosensing.

Biotechnology and bioengineering

[No authors listed]
PMID: 27902852
Biotechnol Bioeng. 2017 Jan;114(1):6. doi: 10.1002/bit.26095.

No abstract available.

Cite
Self-immobilizing enzymes for biosensing. Biotechnol Bioeng. 2017;114(1):6doi: 10.1002/bit.26095.
(2017). Self-immobilizing enzymes for biosensing. Biotechnology and bioengineering, 114(1), 6. https://doi.org/10.1002/bit.26095
"Self-immobilizing enzymes for biosensing." Biotechnology and bioengineering vol. 114,1 (2017): 6. doi: https://doi.org/10.1002/bit.26095
Self-immobilizing enzymes for biosensing. Biotechnol Bioeng. 2017 Jan;114(1):6. doi: 10.1002/bit.26095. PMID: 27902852.
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New bioprocess tool for phototrophic cultivation.

Biotechnology and bioengineering

[No authors listed]
PMID: 27902851
Biotechnol Bioeng. 2017 Jan;114(1):6. doi: 10.1002/bit.26096.

No abstract available.

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New bioprocess tool for phototrophic cultivation. Biotechnol Bioeng. 2017;114(1):6doi: 10.1002/bit.26096.
(2017). New bioprocess tool for phototrophic cultivation. Biotechnology and bioengineering, 114(1), 6. https://doi.org/10.1002/bit.26096
"New bioprocess tool for phototrophic cultivation." Biotechnology and bioengineering vol. 114,1 (2017): 6. doi: https://doi.org/10.1002/bit.26096
New bioprocess tool for phototrophic cultivation. Biotechnol Bioeng. 2017 Jan;114(1):6. doi: 10.1002/bit.26096. PMID: 27902851.
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Demonstration of efficient trichloroethylene biodegradation in a hollow-fiber membrane bioreactor .

Biotechnology and bioengineering

Pressman JG, Georgiou G, Speitel GE.
PMID: 10404245
Biotechnol Bioeng. 1999 Sep 05;64(5):630. doi: 10.1002/(sici)1097-0290(19990905)64:5<630::aid-bit15>3.0.co;2-n.

No abstract available.

Cite
Pressman JG, Georgiou G, Speitel GE. Demonstration of efficient trichloroethylene biodegradation in a hollow-fiber membrane bioreactor . Biotechnol Bioeng. 1999;64(5):630doi: 10.1002/(sici)1097-0290(19990905)64:5<630::aid-bit15>3.0.co;2-n.
Pressman, J. G., Georgiou, G., & Speitel, G. E. (1999). Demonstration of efficient trichloroethylene biodegradation in a hollow-fiber membrane bioreactor . Biotechnology and bioengineering, 64(5), 630. https://doi.org/10.1002/(sici)1097-0290(19990905)64:5<630::aid-bit15>3.0.co;2-n
Pressman, et al. "Demonstration of efficient trichloroethylene biodegradation in a hollow-fiber membrane bioreactor ." Biotechnology and bioengineering vol. 64,5 (1999): 630. doi: https://doi.org/10.1002/(sici)1097-0290(19990905)64:5<630::aid-bit15>3.0.co;2-n
Pressman JG, Georgiou G, Speitel GE. Demonstration of efficient trichloroethylene biodegradation in a hollow-fiber membrane bioreactor . Biotechnol Bioeng. 1999 Sep 05;64(5):630. doi: 10.1002/(sici)1097-0290(19990905)64:5<630::aid-bit15>3.0.co;2-n. PMID: 10404245.
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Looking good at forty.

Biotechnology and bioengineering

Clark DS.
PMID: 10699865
Biotechnol Bioeng. 2000 Mar;67(6):VII. doi: 10.1002/(sici)1097-0290(20000320)67:63.0.co;2-l.

No abstract available.

Cite
Clark DS. Looking good at forty. Biotechnol Bioeng. 2000;67(6):VIIdoi: 10.1002/(sici)1097-0290(20000320)67:63.0.co;2-l.
Clark, D. S. (2000). Looking good at forty. Biotechnology and bioengineering, 67(6), VII. https://doi.org/10.1002/(sici)1097-0290(20000320)67:63.0.co;2-l
Clark. "Looking good at forty." Biotechnology and bioengineering vol. 67,6 (2000): VII. doi: https://doi.org/10.1002/(sici)1097-0290(20000320)67:63.0.co;2-l
Clark DS. Looking good at forty. Biotechnol Bioeng. 2000 Mar;67(6):VII. doi: 10.1002/(sici)1097-0290(20000320)67:63.0.co;2-l. PMID: 10699865.
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Scale-up of citric acid fermentation by redox potential control .

Biotechnology and bioengineering

Berovic M.
PMID: 10404235
Biotechnol Bioeng. 1999 Sep 05;64(5):552-7. doi: 10.1002/(sici)1097-0290(19990905)64:5<552::aid-bit5>3.0.co;2-2.

To obtain high citric acid productivity in Aspergillus niger fermentation on beet molasses substrate, a certain redox potential profile with two maxima (260 and 280 mV) and two minima (180 and 80 mV) must be maintained. The most effective...

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Berovic M. Scale-up of citric acid fermentation by redox potential control . Biotechnol Bioeng. 1999;64(5):552-7doi: 10.1002/(sici)1097-0290(19990905)64:5<552::aid-bit5>3.0.co;2-2.
Berovic, M. (1999). Scale-up of citric acid fermentation by redox potential control . Biotechnology and bioengineering, 64(5), 552-7. https://doi.org/10.1002/(sici)1097-0290(19990905)64:5<552::aid-bit5>3.0.co;2-2
Berovic. "Scale-up of citric acid fermentation by redox potential control ." Biotechnology and bioengineering vol. 64,5 (1999): 552-7. doi: https://doi.org/10.1002/(sici)1097-0290(19990905)64:5<552::aid-bit5>3.0.co;2-2
Berovic M. Scale-up of citric acid fermentation by redox potential control . Biotechnol Bioeng. 1999 Sep 05;64(5):552-7. doi: 10.1002/(sici)1097-0290(19990905)64:5<552::aid-bit5>3.0.co;2-2. PMID: 10404235.
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Spectroscopic investigation of lipase from pseudomonas cepacia solubilized in 1,4-dioxane by non-covalent complexation with methoxypoly(ethylene glycol) .

Biotechnology and bioengineering

Secundo F, Carrea G, Vecchio G, Zambianchi F.
PMID: 10404244
Biotechnol Bioeng. 1999 Sep 05;64(5):624-9. doi: 10.1002/(sici)1097-0290(19990905)64:5<624::aid-bit14>3.0.co;2-p.

Lipase from Pseudomonas cepacia was made soluble in 1,4-dioxane by lyophilization of the enzyme from aqueous solutions containing methoxypoly(ethylene glycol) (PEG). The solubility of the enzyme-PEG complex depended both on protein concentration and PEG protein ratio. Intrinsic protein fluorescence...

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Secundo F, Carrea G, Vecchio G, et al. Spectroscopic investigation of lipase from pseudomonas cepacia solubilized in 1,4-dioxane by non-covalent complexation with methoxypoly(ethylene glycol) . Biotechnol Bioeng. 1999;64(5):624-9doi: 10.1002/(sici)1097-0290(19990905)64:5<624::aid-bit14>3.0.co;2-p.
Secundo, F., Carrea, G., Vecchio, G., & Zambianchi, F. (1999). Spectroscopic investigation of lipase from pseudomonas cepacia solubilized in 1,4-dioxane by non-covalent complexation with methoxypoly(ethylene glycol) . Biotechnology and bioengineering, 64(5), 624-9. https://doi.org/10.1002/(sici)1097-0290(19990905)64:5<624::aid-bit14>3.0.co;2-p
Secundo, et al. "Spectroscopic investigation of lipase from pseudomonas cepacia solubilized in 1,4-dioxane by non-covalent complexation with methoxypoly(ethylene glycol) ." Biotechnology and bioengineering vol. 64,5 (1999): 624-9. doi: https://doi.org/10.1002/(sici)1097-0290(19990905)64:5<624::aid-bit14>3.0.co;2-p
Secundo F, Carrea G, Vecchio G, Zambianchi F. Spectroscopic investigation of lipase from pseudomonas cepacia solubilized in 1,4-dioxane by non-covalent complexation with methoxypoly(ethylene glycol) . Biotechnol Bioeng. 1999 Sep 05;64(5):624-9. doi: 10.1002/(sici)1097-0290(19990905)64:5<624::aid-bit14>3.0.co;2-p. PMID: 10404244.
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Fermentability of the hemicellulose-derived sugars from steam-exploded softwood (douglas fir) .

Biotechnology and bioengineering

Boussaid A, Robinson J, Cai Yj, Gregg DJ, Saddler JN.
PMID: 10397865
Biotechnol Bioeng. 1999 Aug 05;64(3):284-9. doi: 10.1002/(sici)1097-0290(19990805)64:3<284::aid-bit4>3.0.co;2-c.

Steam explosion ofDouglas fir wood chips under low-severity conditions (log Ro = 3.08 corresponding to 175 degrees C, 7.5 min, and 4.5% SO2) resulted in the recovery of around 87% of the original hemicellulose component in the water-soluble stream....

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Boussaid A, Robinson J, Cai Yj, et al. Fermentability of the hemicellulose-derived sugars from steam-exploded softwood (douglas fir) . Biotechnol Bioeng. 1999;64(3):284-9doi: 10.1002/(sici)1097-0290(19990805)64:3<284::aid-bit4>3.0.co;2-c.
Boussaid, A., Robinson, J., Cai, Y. j., Gregg, D. J., & Saddler, J. N. (1999). Fermentability of the hemicellulose-derived sugars from steam-exploded softwood (douglas fir) . Biotechnology and bioengineering, 64(3), 284-9. https://doi.org/10.1002/(sici)1097-0290(19990805)64:3<284::aid-bit4>3.0.co;2-c
Boussaid, et al. "Fermentability of the hemicellulose-derived sugars from steam-exploded softwood (douglas fir) ." Biotechnology and bioengineering vol. 64,3 (1999): 284-9. doi: https://doi.org/10.1002/(sici)1097-0290(19990805)64:3<284::aid-bit4>3.0.co;2-c
Boussaid A, Robinson J, Cai Yj, Gregg DJ, Saddler JN. Fermentability of the hemicellulose-derived sugars from steam-exploded softwood (douglas fir) . Biotechnol Bioeng. 1999 Aug 05;64(3):284-9. doi: 10.1002/(sici)1097-0290(19990805)64:3<284::aid-bit4>3.0.co;2-c. PMID: 10397865.
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Process intensification by direct product sequestration from batch fermentations: application of a fluidised bed, multi-bed external loop contactor .

Biotechnology and bioengineering

Hamilton GE, Morton PH, Young TW, Lyddiatt A.
PMID: 10397868
Biotechnol Bioeng. 1999 Aug 05;64(3):310-21. doi: 10.1002/(sici)1097-0290(19990805)64:3<310::aid-bit7>3.0.co;2-j.

A critical comparison has been made of the relative efficacy of the primary purification of an extracellular acid protease produced by the yeast Yarrowia lipolytica. The performance of conventional, discrete sequences of fermentation, broth clarification and fixed bed, anion...

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Hamilton GE, Morton PH, Young TW, et al. Process intensification by direct product sequestration from batch fermentations: application of a fluidised bed, multi-bed external loop contactor . Biotechnol Bioeng. 1999;64(3):310-21doi: 10.1002/(sici)1097-0290(19990805)64:3<310::aid-bit7>3.0.co;2-j.
Hamilton, G. E., Morton, P. H., Young, T. W., & Lyddiatt, A. (1999). Process intensification by direct product sequestration from batch fermentations: application of a fluidised bed, multi-bed external loop contactor . Biotechnology and bioengineering, 64(3), 310-21. https://doi.org/10.1002/(sici)1097-0290(19990805)64:3<310::aid-bit7>3.0.co;2-j
Hamilton, et al. "Process intensification by direct product sequestration from batch fermentations: application of a fluidised bed, multi-bed external loop contactor ." Biotechnology and bioengineering vol. 64,3 (1999): 310-21. doi: https://doi.org/10.1002/(sici)1097-0290(19990805)64:3<310::aid-bit7>3.0.co;2-j
Hamilton GE, Morton PH, Young TW, Lyddiatt A. Process intensification by direct product sequestration from batch fermentations: application of a fluidised bed, multi-bed external loop contactor . Biotechnol Bioeng. 1999 Aug 05;64(3):310-21. doi: 10.1002/(sici)1097-0290(19990805)64:3<310::aid-bit7>3.0.co;2-j. PMID: 10397868.
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Showing 1 to 12 of 5445 entries