How Do You Spell ACYLCARNITINE TRANSLOCASE?

Pronunciation: [ɐkˈɪlkɑːnˌɪtiːn tɹanslˈɒke͡ɪs] (IPA)

Acylcarnitine translocase is a complex term that refers to a type of mitochondrial transport protein. The word is spelled using the International Phonetic Alphabet (IPA) to represent the exact sounds of the word. The IPA transcription of "Acylcarnitine Translocase" is /əˌsaɪlˈkɑrnɪtiːn ˈtrænzloʊkeɪs/. The first syllable "acyl" is pronounced "uh-sil" and the second syllable "carnitine" is pronounced "kahr-ni-teen." The final syllable "translocase" is pronounced "trans-loh-kayce." Overall, the word is quite complex and requires careful attention to its exact spelling and pronunciation.

ACYLCARNITINE TRANSLOCASE Meaning and Definition

  1. Acylcarnitine translocase is an enzyme that plays a crucial role in the transport of fatty acids across the inner mitochondrial membrane. It facilitates the exchange of acylcarnitines and free carnitine, enabling the transport of long-chain fatty acids into the mitochondria for β-oxidation, a key metabolic pathway involved in energy production.

    The enzyme is primarily located in the inner mitochondrial membrane of various tissues, including skeletal and cardiac muscles, liver, and kidneys. It is a member of the carnitine-acylcarnitine translocase protein family and consists of multiple subunits that work together to fulfill its function.

    The transport of acylcarnitines through the inner mitochondrial membrane is crucial for the maintenance of energy homeostasis. It allows long-chain fatty acids, derived from dietary sources or stored triglycerides, to enter the mitochondria where they can be broken down to produce ATP, the universal energy currency of cells.

    Defects or deficiencies in acylcarnitine translocase can lead to metabolic disorders such as carnitine palmitoyltransferase II deficiency, which impairs the transport of long-chain fatty acids into the mitochondria and results in the accumulation of harmful fatty acid byproducts. This can lead to symptoms such as muscle weakness, exercise intolerance, and low blood sugar levels.

    In summary, acylcarnitine translocase is a vital enzyme involved in the transport of fatty acids into the mitochondria for energy production through β-oxidation. Its dysregulation can result in metabolic disorders with a wide range of clinical manifestations.

Common Misspellings for ACYLCARNITINE TRANSLOCASE

  • zcylcarnitine translocase
  • scylcarnitine translocase
  • wcylcarnitine translocase
  • qcylcarnitine translocase
  • axylcarnitine translocase
  • avylcarnitine translocase
  • afylcarnitine translocase
  • adylcarnitine translocase
  • actlcarnitine translocase
  • acglcarnitine translocase
  • achlcarnitine translocase
  • aculcarnitine translocase
  • ac7lcarnitine translocase
  • ac6lcarnitine translocase
  • acykcarnitine translocase
  • acypcarnitine translocase
  • acyocarnitine translocase
  • acylxarnitine translocase
  • acylvarnitine translocase
  • acylfarnitine translocase

Etymology of ACYLCARNITINE TRANSLOCASE

The word "Acylcarnitine Translocase" has its etymology rooted in the scientific terminology and naming conventions. Here is a breakdown of its components:

1. Acyl: The term "acyl" refers to a chemical group derived from a carboxylic acid, characterized by having a carbon-oxygen double bond.

2. Carnitine: Carnitine is a compound that plays a vital role in transporting fatty acids into the mitochondria, the powerhouses of cells, for energy production.

3. Translocase: The suffix "-ase" is commonly used in biology to denote an enzyme or a protein involved in a specific biochemical reaction. "Translocase" indicates a protein that is responsible for the transport or movement of a molecule across cellular membranes.

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