PREVIOUS MAJOR RESEARCH EXPERIENCE

In vitro interaction between whey protein, lactoferrin and bifidobacteria

In vitro interaction of lactoferrin and bifidobacteria  was studied and the possible mechanism was investigated.

Results   showed   that  lactoferrin   had   the  ability   to promote the growth of bifidobacteria and played role in autoaggregation  and  surface  hydrophobicity  process. Under microscope, lactoferrin binding was appeared at one pole of bacterial  cell instead  of entire surface. 50-kDa  lactoferrin-binding   protein  was  detected  and was purified from the extracted surface proteins of bifidobacteria.  The  binding  region  of  lactoferrin molecule was appeared to be N-lobe. The binding was suggested to be specific for lactoferrin.

Structure-function  and mechanism  of action  of a potent  antibacterial  peptide  derived  from

Haemaphysalis longicornis

This study was carried out to investigate the structural characterization, cytolytic activity and mechanisms of action of a potent antibacterial peptide. The potent peptide was identified as a conserved antimicrobial domain having anti-parallel beta sheet but adopt alpha helix in a membrane mimicking condition. The antimicrobial mechanism of the peptide followed defensin-like  chronological  events  such  as binding  to lipopolysaccharides,  outer membrane permeabilization and cytoplasmic membrane permeabilization.  The peptide can also bind with bacterial intracellular components such as DNA.

Potential of ovomucin enzymatic hydrolysates as multifunctional bioactive agents

Ovomucin is a highly glycosylated glycoprotein contributing  2.0  to  4.0  %  of  the  total  egg  albumin protein. Ovomucin consists of a carbohydrate-poor subunit  (α-ovomucin)  that has ~11-15%  carbohydrate and a carbohydrate-rich  subunit (β-ovomucin) that has

~50-57%  carbohydrate.  In  this  research,  high  purity (more  than  93%)  ovomucin  was  isolated  and hydrolyzed   by   various   food   grade   enzymes.   The resulting   soluble   hydrolysates   were  tested  for  bio- activity such as antioxidative, antihypertensive and adhesion  ability  to pathogenic  bacteria.  Some  of the hydrolysates showed significant bio-activity.

Attempt to regulate biological activity of the cells in hair follicle using microbial metabolites

In this study, Generally Recognized As Safe (GRAAS) microbes were grown on agricultural by-products using solid-state-fermentation techniques. The resulting metabolites  were extracted  and tested for their ability to induce or retard anagen progression and to elongate the   anagen   phase   of   hair   cycle.   Some   of   the metabolites were found to retard the anagen phase progression   of   hair   cycle.   In   addition,   couple   of microbial  metabolites  identified  as  potent  agents  for the elongation of the anagen phase of hair cycle.

RESEARCH EXPERTISE

  • I am experienced in working with diversified  protein (milk proteins, insect proteins, egg proteins, marine  transferrin  family  proteins,  bacterial  proteins).  I carried  out experiments  for isolating  the target proteins,  for enzymatic  digestion of them and also for estimating  their bioactivity  such as growth  stimulating   factor  for  probiotics  including   mechanism,   antimicrobial   activity  including structure-function relationship, antihypertensive activity, antioxidant activity.
  • I have hands  on  experience  in  different  proteomic  tools  such  as  chromatographic  separation, MALDI-TOF Mass spectrometry, Bioinformatics, Western and far-western blotting, Protein labeling, Elisa etc. I am also experienced with basic molecular biology work.
  • I am also experienced in conducting various biochemical assays using fluorescence spectrometer, luminometer, in performing  cytolytic  assay,  in carrying  out microscopic  analysis  using  confocal laser scanning microscope and transmission electron microscope.
  • I have  expertise   on  handling   various   pathogenic   and  fastidious   microorganisms,   parasites (Babesia) and fungi (especially those are generally recognized as safe).
  • I am experienced in working  with mouse model and also in carrying  out histomorphometry  and immunohistochemistry  of mouse dorsal skin.