Showing posts with label Growth. Show all posts
Showing posts with label Growth. Show all posts

Thursday, 29 September 2016

Applied Microbiology and Biotechnology, 2016, 100 (18), 7899–790
DOI: 10.1007/s00253-016-7558-9


Nisin production by Lactococcus lactis CECT 539 was followed in batch cultures in whey supplemented with different concentrations of glucose and in two realkalized fed-batch fermentations in unsupplemented whey, which were fed, respectively, with concentrated solutions of lactose and glucose. In the batch fermentations, supplementation of whey with glucose inhibited both the growth and bacteriocin production. However, fed-batch cultures were characterized with high productions of biomass (1.34 and 1.51 g l−1) and nisin (50.6 and 60.3 BU ml−1) in comparison to the batch fermentations in unsupplemented whey (0.48 g l−1 and 22.5 BU ml−1) and MRS broth (1.59 g l−1 and 50.0 BU ml−1). In the two realkalized fed-batch fermentations, the increase in bacteriocin production parallels both the biomass production and pH drop generated in each realkalization and feeding cycle, suggesting that nisin was synthesized as a pH-dependent primary metabolite. A shift from homolactic to heterolactic fermentation was observed at the 108 h of incubation, and other metabolites (acetic acid and butane-2,3-diol) in addition to lactic acid accumulated in the medium. On the other hand, the feeding with glucose improved the efficiencies in glucose, nitrogen, and phosphorus consumption as compared to the batch cultures. The realkalized fed-batch fermentations showed to be an effective strategy to enhance nisin production in whey by using an appropriate feeding strategy to avoid the substrate inhibition.

Thursday, 7 January 2016

Biochemical, physiological and isotopic responses to natural product p-hydroxybenzoic acid in Cocksfoot (Dactylis glomerata L.)

Plant Growth Regulation
DOI: 10.1007/s10725-014-9981-1


The present study was conducted to evaluate the role of natural compound p-hydroxybenzoic acid (pHBA) on physiological, biochemical and isotopic responses of Dactylis glomerata L. Application of pHBA in the range 0.5–1.5 mM reduced the leaf fresh/dry biomass, shoot/root length, relative water content and leaf osmotic potential of D. glomerata. pHBA decreased the photosynthetic efficiency and quantum yield of photosystem II photochemistry in D. glomerata seedlings following treatment at all concentrations. Photochemical and non-photochemical fluorescence quenching were reduced after treatment with 1.5 mM pHBA. Carbon isotope composition ratio in D. glomerata leaves was significantly less negative following treatment with pHBA than the control. Carbon isotope discrimination value was declined by pHBA. The leaf protein content was lower after treatment with 1.5 mM pHBA. Our results suggest that pHBA possesses allelopathic potential against D. glomerata and this study provide new insights into the physiological, biochemical and isotopic action mechanism of pHBA.