| 193 - 201 |
Biogas from microalgae: an overview emphasizing pretreatment methods and their energy return on investment (EROI)
Marques AD, Araujo ODF, Cammarota MC |
| 203 - 220 |
Solvent stable microbial lipases: current understanding and biotechnological applications
Priyanka P, Tan YQ, Kinsella GK, Henehan GT, Ryan BJ |
| 221 - 230 |
Progress in antibiotic susceptibility tests: a comparative review with special emphasis on microfluidic methods
Khan ZA, Siddiqui MF, Park S |
| 231 - 239 |
Improved yield of rhEPO in CHO cells with synthetic 5 UTR
Costello A, Lao NT, Barron N, Clynes M |
| 241 - 252 |
Comparative features between recombinant lipases CALA-like from U-maydis and CALA from C-antarctica in thermal stability and selectivity
Robles-Machuca M, del Campo MM, Camacho-Ruiz MA, Ordaz E, Zamora-Gonzalez EO, Muller-Santos M, Rodriguez JA |
| 253 - 262 |
Green asymmetric reduction of acetophenone derivatives: Saccharomyces cerevisiae and aqueous natural deep eutectic solvent
Panic M, Delac D, Roje M, Redovnikovic IR, Bubalo MC |
| 263 - 272 |
Oligosaccharides as co-encapsulating agents: effect on oral Lactobacillus fermentum survival in a simulated gastrointestinal tract
Liao N, Luo BL, Gao J, Li XJ, Zhao ZX, Zhang Y, Ni YQ, Tian FW |
| 273 - 281 |
The marine Gram-negative bacterium Novosphingobium sp. PP1Y as a potential source of novel metabolites with antioxidant activity
Petruk G, Roxo M, De Lise F, Mensitieri F, Notomista E, Wink M, Izzo V, Monti DM |
| 283 - 292 |
Thermophilin 109 is a naturally produced broad spectrum bacteriocin encoded within the blp gene cluster of Streptococcus thermophilus
Renye JA, Somkuti GA, Steinberg DH |
| 293 - 303 |
Chemical transformation mediated CRISPR/Cas9 genome editing in Escherichia coli
Sun DC, Wang L, Mao XD, Fei MY, Chen YY, Shen MJ, Qiu JP |
