Post harvest changes in the juice quality parameters in relation to storage time were investigated in three sugarcane genotypes varying in maturity behaviour viz.CoJ83

In the present study, in vitro selection technique using pathogen culture filtrate of Colletotrichum falcatum Went was employed with the aim to identify associations (if any), between selection at the cellular and plant level for red rot resistance in sugarcane (Saccharum sp.). Five to eight months old sugarcane calli of genotypes CoJ 88 and CoJ 64 were screened in vitro against pathogen culture filtrate for two selection cycles. Effect of pathogen culture filtrate on callus survival and/or proliferation was observed to be directly related to its concentration in the selection media. Calli survived and exhibited further proliferation at 5, 10 and 15% v/v pathogen culture filtrate concentrations whereas, at higher concentrations (20 and 25% v/v) proliferation was completely inhibited. Shoot regeneration percent was higher in calli selected on 5% pathogen culture filtrate concentration than those selected on 10 and 15% concentrations. In vivo screening of field transferred somaclones against two pathtypes (Cf 03 and Cf 08) showed considerable variation for red rot resistance. Somaclones regenerated from resistant and/or tolerant calli exhibited better resistance than the parental genotypes. The results indicated that in vitro selection for red rot resistance was effective and expressed when somaclones were screened in the field. This indicated a positive association between in vitro and in vivo methods of selection for disease resistance in sugarcane.

Two field experiments were conducted to ascertain the potential of micropropagation technique for faster production of seed cane by using tissue culture plants raised through apical meristem culture in first generation (TC 0) followed by clonal propagation through cane setts in next generation (TC1). About 18, 520 plants, produced from a single shoot through micropropagation, were required at row to row and plant to plant spacing of 90 and 60 cm, respectively as compared to 88 quintal of cane seed in conventional methods for planting in an area of one hectare. Multiplication ratio was 100-150 times using tissue culture plants as compared to 11-12 using conventional cane setts, leading to drastic reduction in seed cane requirement. The TC 1 exhibited superiority over vegetatively propagated conventional crop for millable canes and stalk yield by 17 and 10.4 per cent, respectively. Though the single cane weight and cane diameter (non-significantly) were slightly lesser in TC1 as compared to conventional crop, this did not distress its potential as seed crop. The incidence of Ratoon Stunting Disease (RSD) and Leaf Scald Disease (LSD) was very low in TC 1 crop as compared to conventional crop. The findings established the potential of tissue culture technique for the production of quality seed free of pests and pathogens in the existing varieties and rapid multiplication of newly released varieties for quick adoption by the growers.

Sugarcane (Saccharum spp.) is a commercially important crop, vulnerable to fungal disease red rot caused by Colletotrichum falcatum Went. The pathogen attacks sucrose accumulating parenchyma cells of cane stalk leading to severe losses in cane yield and sugar recovery. We report development of red rot resistant transgenic sugarcane through expression of β-1,3-glucanase gene from Trichoderma spp. The transgene integration and its expression were confirmed by quantitative reverse transcription-PCR in first clonal generation raised from T0 plants revealing up to 4.4-fold higher expression, in comparison to non-transgenic sugarcane. Bioassay of transgenic plants with two virulent C. falcatum pathotypes, Cf 08 and Cf 09 causing red rot disease demonstrated that some plants were resistant to Cf 08 and moderately resistant to Cf 09. The electron micrographs of sucrose storing stalk parenchyma cells from these plants displayed characteristic sucrose-filled cells inhibiting Cf 08 hyphae and lysis of Cf 09 hyphae; in contrast, the cells of susceptible plants were sucrose depleted and prone to both the pathotypes. The transgene expression was up-regulated (up to 2.0-fold in leaves and 5.0-fold in roots) after infection, as compared to before infection in resistant plants. The transgene was successfully transmitted to second clonal generation raised from resistant transgenic plants. β-1,3-glucanase protein structural model revealed that active sites Glutamate 628 and Aspartate 569 of the catalytic domain acted as proton donor and nucleophile having role in cleaving β-1,3-glycosidic bonds and pathogen hyphal lysis.

Genetic divergence among the twenty four sugarcane genotypes collected from various sugarcane research institutions of northern India were tested in a randomized complete block design with three replicates during the cropping seasons 2013 -14. The assessment of the genetic diversity was based on the eighteen cane yield and quality characters. The results of the study indicated that, the genotypes were grouped into five clusters based on the genetic distance using Mahalanobis's statistics. Higher inter-cluster distance was recorded between cluster II and V (89.668) indicating high genetic diversity among these two clusters. Thus, exploitation of genotypes within these two clusters as parents for crossing could produce good sugarcane segregants. The lowest intra cluster distance was reported in the cluster III (14.897) revealed that clones are identical and can not to be used as parents in crossing that results hybrid not desirable for the characters studied. A critical analysis of cluster means for different traits indicated that cluster I was desirable for cane yield, CCS (t/ha), single cane weight, stalk diameter, germination (%), cluster II was better for juice extraction percentage, cluster III for better juice purity percent, brix (%), sucrose (%) and CCS (%) for 12 months and cluster V was the best source for NMC (000/ha), stalk length with other good cane and sugar yield traits. The average D 2 values among clones ranged from 29.998 (CoH 08262) to 69.791 (CoPb 09214).