摘要:
The present invention relates to recombinant DNA which encodes the AsiSI restriction endonuclease as well as AsiSI methylase, expression of AsiSI restriction endonuclease and AsiSI methylase in E. coli cells containing the recombinant DNA.
摘要:
The present invention relates to recombinant DNA which encodes the BpmI restriction endonuclease as well as BpmI methyltransferase, expression of BpmI restriction endonuclease from E. coli cells containing the recombinant DNA. BpmI endonuclease is a fusion of two distinct elements with a possible structural domains of restriction-methylation-specificity (R-M-S). This domain organization is analogous to the type I restriction-modification system with three distinct subunits, restriction, methylation, and specificity (R, M, and S). Because BpmI is quite distinct to other type IIs restriction enzymes, it is proposed that BpmI belongs to a subgroup of type II restriction enzymes called type IIf (f stands for fusion of restriction-modification-specificity domains). The Type IIf group of restriction enzyme includes Eco57I, BpmI, GsuI, BseRI and some other restriction enzymes that cut downstream sequences at long distance, 10-20 bp downstream of recognition sequence, such as MmeI (N20/N18)).
摘要:
Described is an apparatus comprising a first interface, a second interface, a third interface, and an interconnection fabric. The first interface may transfer a first stream of data traffic. The second interface, which may be an enhanced Serial Peripheral Interface (eSPI) interface, may transfer a second stream of data traffic and a third stream of data traffic. The third interface may transfer a fourth stream of data traffic. The interconnection fabric may couple the first interface to the second interface and may couple the second interface to the third interface. The second interface may initiate a transfer of an outbound data stream from one of the second stream of data traffic or the third stream of data traffic based on an available-space credit indicator. The second interface may receive an inbound data stream based upon the outbound data stream.
摘要:
This is a process, with supporting apparatus, to facilitate modular software application and knowledgebase development and usage in a searchable, cumulative and automated manner.Developer and users deploy and access the application/knowledgebase with integrated process through the application call manager. A standardized data container is used to store various types of data in the entire process. Depends of user action, the process can automatically record or use parametric information of the target applications to manual or batch call applications or load knowledgebase of the applications.The standardized data container also serves a data and application call knowledgebase template and facilitates knowledge transfer between users and developers.
摘要:
Methods and compositions are provided for engineering mutant enzymes with reduced star activity where the mutant enzymes have a fidelity index (FI) in a specified buffer that is greater than the FI of the non-mutated enzyme in the same buffer.
摘要:
Described herein are embodiments of USB device control using endpoint type detection during enumeration. An apparatus configured for USB device control using endpoint type detection during enumeration may include a host controller configured to selectively disable enumeration of a USB device based at least in part on an endpoint type of the USB device. The apparatus may include a management engine configured to store in the host controller a USB lock policy defining endpoint types disallowed to be enumerated by the apparatus. Other embodiments may be described and/or claimed.
摘要:
The present invention relates to compositions including: (1) isolated DNA encoding the StuI restriction endonuclease and isolated DNA encoding cognate and non-cognate methylase; (2) vectors and cells containing the isolated DNA; and (3) methods for producing the StuI restriction endonuclease.
摘要:
Methods and compositions are provided for engineering mutant enzymes with reduced star activity where the mutant enzymes have a fidelity index (FI) in a specified buffer that is greater than the FI of the non-mutated enzyme in the same buffer.
摘要:
A nicking endonuclease is described which has an amino acid sequence with at least 70% identity to SEQ ID NO:6 and comprising a mutation at least one of an arginine or gutamic acid corresponding to position 507 and position 546 respectively in SEQ ID NO:6.
摘要翻译:描述了一种切口内切核酸酶,其具有与SEQ ID NO:6具有至少70%同一性的氨基酸序列,并且包含分别对应于SEQ ID NO:6中的位置507和位置546的精氨酸或谷氨酸中的至少一种的突变 。
摘要:
Compositions and methods are provided for enzymes with altered properties that involve a systematic approach to mutagenesis and a screening assay that permits selection of the desired proteins. Embodiments of the method are particularly suited for modifying specific properties of restriction endonucleases such as star activity. The compositions include restriction endonucleases with reduced star activity as defined by an overall fidelity index improvement factor.