Novozymes A/s

Telefonaktiebolaget Lm Ericsson (publ)

Vivek Srivastava

Sohel Dalal

Padmavathi Balumuri

Carsten Schau Andersen

Vinayak Joshi

Rakhi Saikia

Vasudeva Prahlada Rao

Partha Pratim Chakrabarti

Allan Svendsen

Thomas Agersten Poulsen

Jens Erik Nielsen

Marco Malten

Preethi Ramaiya

Shikha Gupta

Markus Klinger

Ashvin Lakshmikantha

Vijaya Shankar Nataraj

Beth Nelson

Prashant Anand

Rajendra Kulothungan Sainathan

Kendra Stallings

The present invention relates to alpha-amylase variants. The present invention also relates to polynucleotides encoding the variants; nucleic acid constructs, vectors, and host cells comprising the polynucleotides; and methods of using the variants.

Alpha-amylase variants and polynucleotides encoding same

The present invention relates to mannanase variants. The present invention also relates to polynucleotides encoding the variants; nucleic acid constructs, vectors, and host cells comprising the polynucleotides; and methods of using the variants.

Mannanase variants and polynucleotides encoding same

The present invention relates to alpha-amylase variants comprising a substitution at a position corresponding to position 188 and at least one further substitution at a position corresponding to position 242 or 279 or 275 of SEQ ID NO: 1, in particular one or more combinations of substitutions selected from the group consisting of E188P+S242Y, E188P+S242F, E188P+S242H, E188P+S242W, E188P+S242P, E188P+S242I, E188P+S242T, E188P+S242L, E188P+K279W, E188P+K279Y, E188P+K279F, E188P+K279H, E188P+K279I, E188P+K279L, E188P+K279D, E188P+K279M, E188P+K279S, E188P+K279T E188P+K279N, E188P+K279Q, E188P+K279V, E188P+K279A, E188P+N275F, E188P+N275Y, E188P+N275W, and E188P+N275H, wherein the variant has at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99%, but less than 100% sequence identity to a parent alpha amylase selected from the group consisting of: SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, SEQ ID NO: 13, SEQ ID NO: 14, SEQ ID NO: 15, SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, and SEQ ID NO: 27. The present invention also relates to polynucleotides encoding the variants; nucleic acid constructs, vectors, and host cells comprising the polynucleotides; and methods of using the variants.

A data center failure management system and method in a Software Defined Networking (SDN) deployment. In one embodiment, an SDN controller associated with the data center is configured to learn new flows entering the data center and determine which flows require flow stickiness. Responsive to the determination, the SDN controller generates commands to one or more switching nodes and/or one or more border gateway nodes to redirect the sticky flows arriving at the switching nodes via ECMP routes from the gateway nodes or avoid the ECMP routes by the gateway nodes in order to overcome certain failure conditions encountered in the data center, an external network, or both.

Data center failure management in an SDN deployment using border gateway node control

The present invention relates to glucoamylase variants, polynucleotides encoding the variants, methods of producing the variants, and methods of using the variants. Also described are the use of glucoamylases of the invention for starch conversion to produce fermentation products, such as ethanol, and syrups, such as glucose. The invention also relates to a composition comprising a glucoamylase variant of the invention.

Glucoamylase variants and polynucleotides encoding same

Data center failure management in an SDN deployment using switching node control

The present invention relates to glucoamylase variants having an increase in specific activity and/or an increase in melting temperature measured by TSA of at least 0.5 degrees Celsius, and further wherein the variants have at least at least 85%, at least 90%, at least 95% identity, at least 96%, at least 97%, at least 98%, or at least 99%, but less than 100%, sequence identity to the amino acid sequence of SEQ ID NO: 3. The present invention also relates to polynucleotides encoding the variants; nucleic acid constructs, vectors, and host cells comprising the polynucleotides; and methods of using the variants.

A method for generating a high-precision packet train includes configuring an initial packet generation flow of duration T in a network node and sending a packet to a loopback port to initiate the initial packet generation flow in the network node, where the loopback port loops packets back to the network node or recirculates packets within the network node, and where the loopback port is configured for traffic shaping that establishes a pre-determined inter-packet gap for packets output by the loopback port. The method further includes configuring a main packet generation flow having a duration tthat commences on expiration of the duration T. Looped back packets in the network node are sent to the loopback port for the entirety of durations T and t, while one copy of each looped back packet in the network node is sent to a network port during the duration t

High-precision packet train generation

Growing community of inventors

Bengaluru, India

Vivek Srivastava