André Soibelmann Glock Lorenzoni

André Soibelmann Glock Lorenzoni
  • MS
  • PhD Student at University of Groningen

About

13
Publications
49,634
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743
Citations
Introduction
André Soibelmann Glock Lorenzoni currently works at the Groningen Biomolecular Sciences and Biotechnology Institute (GBB), University of Groningen. André does research in cell biology and antimicrobial mode of action.
Current institution
University of Groningen
Current position
  • PhD Student
Additional affiliations
July 2014 - December 2018
University of Groningen
Position
  • PhD Student
March 2012 - April 2014
Federal University of Rio Grande do Sul
Position
  • Master of Science Student
Education
July 2014 - December 2018
University of Groningen
Field of study
  • Molecular microbiology

Publications

Publications (13)
Article
Full-text available
Xanthomonas citri subsp. citri (X. citri) is an important phytopathogen and causes Asiatic Citrus Canker (ACC). To control ACC, copper sprays are commonly used. As copper is an environmentally damaging heavy metal, new antimicrobials are needed to combat citrus canker. Here, we explored the antimicrobial activity of chalcones, specifically the meth...
Article
Full-text available
Xanthomonas citri subsp. citri (Xac) is the causative agent of citrus canker, a plant disease that significantly impacts citriculture. In earlier work, we showed that alkylated derivatives of gallic acid have antibacterial action against Xac and target both the cell division protein FtsZ and membrane integrity in Bacillus subtilis. Here, we have pu...
Article
Full-text available
Xanthomonas citri (Xac) is the causal agent of citrus canker, a disease that affects citrus crops and causes economic impact worldwide. To further characterize cell division in this plant pathogen, we investigated the role of the protein MinC in cell division, chromosome segregation, and peptidoglycan incorporation by deleting the gene minC using a...
Article
A new bioprocess for the synthesis of lactosucrose was studied using a covalently immobilized β-galactosidase on macrospheres of chitosan. The effects of temperature and pH on the production of lactosucrose and other oligosaccharides were evaluated. At 30 °C and pH 7.0, the maximum concentration of lactosucrose reached to 79 g L⁻¹. The change of th...
Article
Abstract In order to develop safer processes for the food industry, we prepared a chitosan support with the naturally occurring crosslinking reagent, genipin, for enzyme. As application model, it was tested the immobilization of β-D-galactosidase from Aspergillus oryzae. Chitosan particles were obtained by precipitation followed by adsorption of th...
Article
In this work, β-fructofuranosidase and β-fructosyltransferase were covalently immobilized on chitosan spheres, using glutaraldehyde as a coupling agent, in order to produce invert sugar and fructooligosaccharides (FOS). Maxinvert L was used to make β-fructofuranosidase biocatalyst yielding 7000 HU/g. A partial purified β-fructosyltransferase from V...
Article
The enzymatic synthesis of fructooligosaccharides (FOS) was carried out using a partially purified β-fructofuranosidase from the commercial enzyme preparation Viscozyme L. Partial purification of β-fructofuranosidase from Viscozyme L was done by batch adsorption using ion-exchange resin DEAE-Sepharose, showing a 6-fold increase in specific activity...
Article
Full-text available
Studies show children suffer fro m adverse effects to food additives, in both acute and chronic forms. Children are among the biggest consumers of processed products and have more susceptibility to these adverse effects. In Brazil, there are few data about the exposure to food additives. Therefore, the objective of this article is to elaborate a da...
Article
A new biocatalyst of lipase B from Candida antarctica (MCI-CALB) immobilized on styrene-divinylbenzene beads (MCI GEL CHP20P) was compared with the commercial Novozym 435 (immobilized lipase) in terms of their performances as biocatalysts for the esterification of acetic acid and n-butanol. The effects of experimental conditions on reaction rates d...
Article
The synthesis of pineapple flavour (butyl butyrate) catalysed by lipase from Rhizomucor miehei has been optimized using central composite design and response surface methodology. Initially, the best butyric acid concentration in the mixture was defined and found that 1 m butyric acid presented the highest initial reaction rate. The reaction paramet...
Article
In this paper is described the optimization of the esterification reaction of butyl acetate synthesis catalyzed by Candida antarctica lipase B (Novozym 435). The reaction parameters temperature, substrate molar ratio, enzyme content, and added water, and their responses measured as conversion yields, were evaluated using central composite design an...
Article
Full-text available
β-Galactosidase was immobilized in an ionic liquid-cellulose film that presents properties as increased flexibility and formability. A polyamine was added during the preparation of the film and their presence was detected by infrared analysis. Glutaraldehyde was used to activate the films in order to generate conditions for enzyme immobilization th...

Questions

Questions (5)
Question
I'm trying to grow Enterococcus faecium in 96-well plates in BHI using a plate incubator at 35 °C, 100 rpm.The cells grow normally in tubes with BHI at 35 °C, but when I dilute them to the micro plates they stop growing. I fill 200 µL in ~370 µL wells.
Is this because of oxygen diffusion limitations? Any other reason?
Question
In the bottle of a M17 medium they recommend to autoclave the medium without lactose, wait cool down to 50 °C and add (filter sterilized) lactose (or glucose).
The medium (37.25 g) is composed by:
Pancreatic Digest of Casein 5.0 g
Soy Peptone 5.0 g
Beef Extract 5.0 g
Yeast Extract 2.5 g
Ascorbic Acid 0.5 g
Magnesium Sulfate 0.25 g
Disodium-β-glycerophosphate 19.0 g
I thought it maybe because of Maillard reaction. However if this is the case waiting to cool down at 80 °C should be already fine.
Question
I'm going to start testing some compounds against the so called ESKAPE bugs, Enterococcus faecium, S. aureus, K. pneumoniae, A. baumannii, P. aeruginosa and Enterobacter species.
I know some of them grow in LB medium at 30 °C and 37 °C with regular shaking. But is that true for all of them?
Any specific remarks?
Question
Usually I wait the agar solution to cool down bellow 50 °C to add kanamycin and pour on the petri dishes. However, I wanted to know if this is really necessary, providing kanamycin is more stable than other antibiotics, such as ampicillin.
Question
Horses had been domesticated long ago, but this didn't happened with zebras, even though they are prettier.

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