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Maize protein quality is deficit in essential amino acids, lysine and tryptophan. These constraints of o2 (opaque2) are corrected in genetically improved, hard endosperm QPM (Quality Protein Maize). An integrated strategy of phenotypic selection for endosperm modifiers and molecular marker-assisted foreground and background selection has been used in present study. The QPM donors were, CML 161, DMRQPM 58, CML 176 and CML 141 whereas, normal maize inbreds were CM 212, V338, V361, V336, V341, V351, CM 141 and V335. The inbreds were subjected to parental polymorphism survey between non-QPM and QPM using CIMMYT based three SSR markers, viz. phi057, umc1066 and phi112. Two markers, viz. phi057 and umc1066 exhibited co-dominant reactions, while phi112 was dominant in nature. Finally, two combinations V335 × CML 141 and V351 × CML 141 were considered for conversion program. Foreground selection was exercised using o2 specific marker umc1066 in BC1 and BC2 generations, while background as well as foreground selection was exercised in BC2F3 generation to recover the genome of recurrent parent up to extent of 80 to 100% with the help of SSR markers distributed across the whole maize genome. The tryptophan concentration in endosperm protein was significantly enhanced and the converted maize lines had almost twice the amount of lysine and tryptophan than normal maize inbreds

SSR marker aided introgression for opaque2 allele for development of quality protein maize inbreds