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    <subfield code="a">Ficus carica  (F. carica) or fig tree from mulberry family (Moraceae) known as &#x201E;buah  tin&#x201F;  among  Malaysians  highly  demand  from  pharmaceutical  area  for  its  nutritional  value. The objective of this research is to determine the optimize sterilization technique  and concentrations of plant growth regulator and SMC use.  In vitro  culture of fig plant  under  controlled  environment  was  introduced  in  fulfilling  the  demand  for  mass  propagation of high quality planting material  and  Pleurotus ostreatus  spent mushroom  compost (SMC) which is a waste substrate was used as an alternative nutrient supplier.  Upon  in  vitro  culture  of  fig  plant,  phytochemical  test  and  Fourier  transform  infrared  spectrophotometer  (FTIR)  analysis  were  also  conducted  to  highlight  the  important  functional groups of secondary metabolites related to this plant that can give benefits to  medicinal  area.  The  first  part  is  production  of  aseptic  plantlets  through  sterilization  process for  in vitro  fig&#x201F;s culture. The  best sterilization technique was treatment 3 (T3)  of 70% ethanol for 10 minutes, 30% clorox added with two drops of Tween 20 for 10  minutes and 0.01% silver acetate for 5 minutes. The second part is the shoots and root  inductions conducted in different types of media that supplemented with plant growth  regulator, SMC and combination of PGR and SMC. The highest shoot proliferations in  presence of plant hormone were achieved at 15 &#xB5;M Kinetin. For roots proliferation, the  highest  number  of  root  was  found  in  30  &#xB5;M  IAA  cultures.  For  media  supplemented  with SMC, the highest number of shoots was obtained in 10% SMC media. However,  new roots were failed to grow in media supplemented with SMC only. PGR (15 &#xB5;M  Kinetin and 30 &#xB5;M IAA) and SMC (10%) were combine with highest proliferations of  shoots  in  combination  media  were  15  &#xB5;M  Kinetin  with  10%  SMC  media  with  maximum  number  of  shoot  proliferation  achieved  (3.00  &#xB1;  1.27)  and  length  of  shoots  (0.23 cm &#xB1; 0.08). The maximum number of root (0.50 &#xB1; 0.84) and length of root  (0.10  &#xB1;  0.16)  was  achieved  in  30  &#xB5;M  IAA  +  10%  SMC  culture.  The  phytochemical  test  conducted for extracts of  F.carica  leaves indicates the presence of functional group of  secondary metabolites such as amine, aromatic, nitrile, carbonyl, alkene, nitro and alkyl  halide  which  is  align  with  FTIR  result.  In  conclusion,  optimal  use  of  plant  growth  regulator and SMC enables the promoting of new shoots and roots for fig nodal culture.  SMC  can  be  innovate  from  waste  material  to  provide  carbon  and  nutrient  and  minimizes the usage of plant hormone in micropropagation of fig plant.</subfield>
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