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    <subfield code="a">Optimization of xylonic acid production using recombinant e. coli bl21 (de3) with inserted gene from ralstonia pickettii /</subfield>
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    <subfield code="a">&#x1D05;-Xylonic acid  (XA)  is a five-carbon  sugar acid  compound that has  made the list of top  30  value-added  chemicals  from  biomass  with  promising  potentials.  XA  have  similar  properties as gluconic acid (GA) which is used in many different fields such as food, construction and textile industries. Production of GA however uses glucose as substrate  therefore  making  its  production  competes  with  food  production.  With  the  increasing  glucose price in the market, XA that is produced from non-food carbohydrate  would be a  valuable  and  cheaper  substitute  to  GA.  In  recent  years,  XA  is  produced  through  microbial  conversion  of  genetically  engineered  microorganism  rather  than  extracting  naturally oxidized XA from xylose. However, production of XA is yet to be produced at  an industrial scale as the bio-based industry is still facing certain limitations such as low  XA yield, slow production rate and certain bacterial species that produce XA  requires  complex  growth  medium.  In  this  study,  one-factor-at-a-time  (OFAT)  and  central  composite design (CCD)  using Design Expert Software  were employed to screen and  optimize  the  effect  of  temperature,  initial  pH  of  medium  and  agitation  rate  on  XA  production from recombinant E. coli BL21 (DE3)  fermentation in shake flask, followed  by  kinetic  study  using  Leudeking-Piret  equation  to  compare  and  evaluate  XA  production in shake flask and 2 L bioreactor  fermentation.  In screening, temperature,  initial pH  of medium  and agitation rate were  varied from 25&#xB0;C to 40&#xB0;C, pH 5.5 to pH  8.5 and 50 rpm to 250 rpm respectively. Meanwhile in optimization, process parameters  were set at 35&#xB0;C to 39&#xB0;C, pH 6.5 to pH 7.5 and 150 rpm to 250 rpm  which generated a  total  of  17  experiments  with  three  centre  points.  Fermentation  samples  were  analyse  using  Hydroxamate  method  and  DNS  method  to  determine  XA  and  xylose  concentration  respectively.  OFAT  results  show  that  the  highest  concentration  of  XA  (9.82  &#xB1;  0.22 g/L) was obtained at 37&#xB0;C, pH 7 and 200 rpm. Optimization results show  that  the developed  quadratic  model is fitted with the experimental data with R and R2 value  of  0.9661  and  0.9333  respectively.  The  optimize  condition  for  XA  production were 36.8&#xB0;C, initial pH of 6.8 and the agitation rate of 208 rpm. Concentration of XA as  high  as  11.15  &#xB1;  0.80  g/L  was  obtained  when  fermentation  was  governed  under  the  optimize  culture  conditions.  During  fermentation  in  bioreactor  using  optimized  parameters, XA production reduces to 6.89 g/L XA  from 10 g/L xylose. This shows  a  24%  reduction  of  XA  produced  from  fermentation  in  bioreactor  compared  to  shake  flask.  Higher  specific  growth  rate  of  recombinant  E.  coli  BL21  (DE3)  and  higher  concentration of XA was obtained by fermentation in shake flask which is 0.273 h-1and 9.06 g L-1  XA  respectively.  The kinetic  study using Leudeking-Piret equation  illustrates  that  XA  is  growth-associated  product.  Hence,  to  increase  concentration  of  XA  in  bioreactor  fermentation,  recombinant  E.  coli  BL21  (DE3)&#x2019;s  growth  rate  must  also  be  increase.  Overall,  optimization  process  for  temperature,  pH  and  agitation  rate  had  further increased XA from recombinant E. coli BL21 (DE3) by 13.5% higher compared  to OFAT process.  These results suggest a promising industrial-scale production of XA  from recombinant E. coli BL21 (DE3) with inserted gene from Ralstonia pickettii.</subfield>
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