JMB

Cited by CrossRef (20)

  1. Yanxia Yang, Yunjuan Yang, Qin Fan, Zunxi Huang, Junjun Li, Qian Wu, Xianghua Tang, Junmei Ding, Nanyu Han, Bo Xu. Molecular and Biochemical Characterization of Salt-Tolerant Trehalose-6-Phosphate Hydrolases Identified by Screening and Sequencing Salt-Tolerant Clones From the Metagenomic Library of the Gastrointestinal Tract. Front. Microbiol. 2020;11
    https://doi.org/10.3389/fmicb.2020.01466
  2. Jonathan B. Clayton, Andres Gomez, Katherine Amato, Dan Knights, Dominic A. Travis, Ran Blekhman, Rob Knight, Steven Leigh, Rebecca Stumpf, Tiffany Wolf, Kenneth E. Glander, Francis Cabana, Timothy J. Johnson. The gut microbiome of nonhuman primates: Lessons in ecology and evolution. American J Primatol 2018;80
    https://doi.org/10.1002/ajp.22867
  3. Tawseef Ahmad, Ram Sarup Singh, Gaganjot Gupta, Anshula Sharma, Baljinder Kaur. Advances in Enzyme Technology. 2018.
    https://doi.org/10.1016/B978-0-444-64114-4.00015-7
  4. Filipe Carvalho, Pedro Fernandes. Green Bio-processes. 2018.
    https://doi.org/10.1007/978-981-13-3263-0_9
  5. Arvind Bangaru, Kamasani Aarya Sree, Chandana Kruthiventi, Meenakshi Banala, Vadapalli Shreya, Y. Vineetha, A. Shalini, Bishwambhar Mishra, Rajasri Yadavalli, K. Chandrasekhar, C. Nagendranatha Reddy. Bio-Clean Energy Technologies: Volume 1. 2018.
    https://doi.org/10.1007/978-981-16-8090-8_4
  6. Hye-Yeon Jeon, Na-Ri Kim, Hye-Won Lee, Hye-Jeong Choi, Woo-Jae Choung, Ye-Seul Koo, Dam-Seul Ko, Jae-Hoon Shim. Characterization of a Novel Maltose-Forming α-Amylase from Lactobacillus plantarum subsp. plantarum ST-III. J. Agric. Food Chem. 2016;64:2307
    https://doi.org/10.1021/acs.jafc.5b05892
  7. F. Cabana, J. B. Clayton, K. A. I. Nekaris, W. Wirdateti, D. Knights, H. Seedorf. Nutrient-based diet modifications impact on the gut microbiome of the Javan slow loris (Nycticebus javanicus). Sci Rep 2019;9
    https://doi.org/10.1038/s41598-019-40911-0
  8. Raveendran Sindhu, Parameswaran Binod, Aravind Madhavan, Ummalyma Sabeela Beevi, Anil Kuruvilla Mathew, Amith Abraham, Ashok Pandey, Vinod Kumar. RETRACTED: Molecular improvements in microbial α-amylases for enhanced stability and catalytic efficiency. Bioresource Technology 2017;245:1740
    https://doi.org/10.1016/j.biortech.2017.04.098
  9. Deepika Mehta, Tulasi Satyanarayana. Bacterial and Archaeal α-Amylases: Diversity and Amelioration of the Desirable Characteristics for Industrial Applications. Front. Microbiol. 2016;7
    https://doi.org/10.3389/fmicb.2016.01129
  10. Pramod Kumar Sahu, Renu Singh, Manoj Shrivastava, Sibanada Darjee, Vellaichamy Mageshwaran, Laccy Phurailtpam, Bharti Rohatgi. Microbial production of α-amylase from agro-waste: An approach towards biorefinery and bio-economy. Energy Nexus 2024;14:100293
    https://doi.org/10.1016/j.nexus.2024.100293
  11. Krishna Bharwad, Satyamitra Shekh, Niraj Kumar Singh, Amrutlal Patel, Chaitanya Joshi. Heterologous expression and biochemical characterization of novel multifunctional thermostable α-amylase from hot-spring metagenome. International Journal of Biological Macromolecules 2023;242:124810
    https://doi.org/10.1016/j.ijbiomac.2023.124810
  12. Francesca Berini, Carmine Casciello, Giorgia Letizia Marcone, Flavia Marinelli. Metagenomics: novel enzymes from non-culturable microbes. 2017;364
    https://doi.org/10.1093/femsle/fnx211
  13. Dhanya Gangadharan, Anu Jose, K. Madhavan Nampoothiri. Recapitulation of stability diversity of microbial α-amylases. 2020;4:11
    https://doi.org/10.1515/amylase-2020-0002
  14. Débora Farage Knupp dos Santos, Paula Istvan, Betania Ferraz Quirino, Ricardo Henrique Kruger. Functional Metagenomics as a Tool for Identification of New Antibiotic Resistance Genes from Natural Environments. Microb Ecol 2017;73:479
    https://doi.org/10.1007/s00248-016-0866-x
  15. Roohi, Mohammed Kuddus. Strain improvement studies on Microbacterium foliorum GA2 for production of α-amylase in solid state fermentation: Biochemical characteristics and wash performance analysis at low temperatures. J. Gen. Appl. Microbiol. 2017;63:347
    https://doi.org/10.2323/jgam.2017.02.005
  16. Sharma Pooja, Muthuirulan Pushpanathan, Sathyanarayanan Jayashree, Paramasamy Gunasekaran, Jeyaprakash Rajendhran. Identification of Periplasmic α-Amlyase from Cow Dung Metagenome by Product Induced Gene Expression Profiling (Pigex). Indian J Microbiol 2015;55:57
    https://doi.org/10.1007/s12088-014-0487-3
  17. A K Wani, F Rahayu, F T Kadarwati, C Suhara, R Singh, D S Dhanjal, N Akhtar, T G Mir, C Chopra. Metagenomic screening strategies for bioprospecting enzymes from environmental samples. IOP Conf. Ser.: Earth Environ. Sci. 2022;974:012003
    https://doi.org/10.1088/1755-1315/974/1/012003
  18. Nobutada Kimura. Metagenomics. 2022.
    https://doi.org/10.1016/B978-0-08-102268-9.00014-8
  19. Harisree P. Nair, Sarita G. Bhat. Arabian Sea metagenome derived - α-amylase P109 and its potential applications. Ecological Genetics and Genomics 2020;16:100060
    https://doi.org/10.1016/j.egg.2020.100060
  20. Hongling Wang, Darren J. Hart, Yingfeng An. Functional Metagenomic Technologies for the Discovery of Novel Enzymes for Biomass Degradation and Biofuel Production. Bioenerg. Res. 2019;12:457
    https://doi.org/10.1007/s12155-019-10005-w