421 - 427 |
Myco-protein from Fusarium venenatum: a well-established product for human consumption Wiebe MG |
428 - 434 |
An update on the use of unconventional substrates for biosurfactant production and their new applications Makkar RS, Cameotra SS |
435 - 438 |
Draw-fill batch culture mode for production of xylanases by Cellulomonas flavigena on sugar cane bagasse Vega-Estrada J, Flores-Cotera LB, Santiago A, Magana-Plaza I, Montes-Horcasitas C |
439 - 445 |
Purification and characterization of a recombinant beta-galactosidase with transgalactosylation activity from Bifidobacterium infantis HL96 Hung MN, Lee BH |
446 - 453 |
High production of heterologous proteins in Escherichia coli using the thermo-regulated T7 expression system Chao YP, Law WS, Chen PT, Hung WB |
454 - 460 |
Transformation of the Pseudonocardiaceae Amycolatopsis sp strain HR167 is highly dependent on the physiological state of the cells Priefert H, Achterholt S, Steinbuchel A |
461 - 468 |
Constitutive expression of the Trichoderma reesei beta-1,4-xylanase gene (xyn2) and the beta-1,4-endoglucanase gene (egl) in Aspergillus niger in molasses and defined glucose media Rose SH, van Zyl WH |
469 - 475 |
Identification and characterization of the AgmR regulator of Pseudomonas putida: role in alcohol utilization Vrionis HA, Daugulis AJ, Kropinski AM |
476 - 481 |
Electrically enhanced ethanol fermentation by Clostridium thermocellum and Saccharomyces cerevisiae Shin HS, Zeikus JG, Jain MK |
482 - 486 |
Growth of sulfate-reducing bacteria with solid-phase electron acceptors Karnachuk OV, Kurochkina SY, Tuovinen OH |
487 - 494 |
Overproduction of BiP negatively affects the secretion of Aspergillus niger glucose oxidase by the yeast Hansenula polymorpha van der Heide M, Hollenberg CP, van der Klei IJ, Veenhuis M |
495 - 502 |
Growth physiology and dimorphism of Mucor circinelloides (syn. racemosus) during submerged batch cultivation McIntyre M, Breum J, Arnau J, Nielsen J |
503 - 510 |
Production of volatile compounds by cheese-ripening yeasts: requirement for a methanethiol donor for S-methyl thioacetate synthesis by Kluyveromyces lactis Arfi K, Spinnler HE, Tache R, Bonnarme P |
511 - 516 |
Controlled transient changes reveal differences in metabolite production in two Candida yeasts Granstrom T, Leisola M |
517 - 526 |
Metabolic response against sulfur-containing heterocyclic compounds by the lignin-degrading basidiomycete Coriolus versicolor Ichinose H, Nakamizo M, Wariishi H, Tanaka H |
527 - 531 |
Influence of spawn rate and commercial delayed release nutrient levels on Pleurotus cornucopiae (oyster mushroom) yield, size, and time to production Royse DJ |
532 - 538 |
Interactions between photoautotrophic and heterotrophic metabolism in photoheterotrophic cultures of Euglena gracilis Ogbonna JC, Ichige E, Tanaka H |
539 - 542 |
A lipoxygenase inhibitor from Aspergillus niger Rao KCS, Divakar S, Rao AGA, Karanth NG, Sattur AP |
543 - 546 |
Isolation of an Acinetobacter sp ST-550 which produces a high level of indigo in a water-organic solvent two-phase system containing high levels of indole Doukyu N, Nakano T, Okuyama Y, Aono R |
547 - 553 |
Bacillus naphthovorans sp nov from oil-contaminated tropical marine sediments and its role in naphthalene biodegradation Zhuang WQ, Tay JH, Maszenan AM, Tay STL |